[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""].[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""].[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]La respuesta inflamatoria al daño muscular puede comprometer la fuerza/masa al inducir la formación de tejido adiposo intermuscular (IMAT). IMAT se origina de la diferenciación adipogénica de células mesenquimales progenitoras fibro-adipogénicas (FAPs). Este proceso podría revertirse modulando la respuesta inflamatoria aguda. Sin embargo, el uso de antiinflamatorios inhibe la síntesis proteica y reduce la capacidad regenerativa muscular. Alternativamente, medidas físicas como el reposo funcional o la reincorporación temprana a la actividad han reportado efectos contradictorios sobre el proceso inflamatorio, lo que dificulta establecer indicaciones en el manejo de la lesión muscular. Por otro lado, se ha descrito un potente papel antinflamatorio local o sistémico del cuerpo cetónico β-hydroxybutirato (βHB); efecto mediado por la inhibición del inflamasoma NLRP3 y la secreción de citoquinas proinflamatorias. Importantemente, la activación del inflamasoma NLRP3 favorecería la adipogénesis de células mesenquimales, lo que sugiere un rol en la formación de IMAT. Se hipotetiza que la suplementación con βHB durante la recuperación de una lesión muscular aguda inhibe la diferenciación adipogénica de FAPs reduciendo la formación de IMAT lo que acelera la reparación y recuperación funcional del tejido muscular. Este efecto estaría mediado por la inhibición del inflamasoma NLRP3. Se inyectará una solución hiperosmótica al 25% de glicerol o salino en el músculo tibial anterior en ratones con o sin suplementación de 3 mg/g βHB durante 2 semanas post injuria. Se recolectará tejido muscular al 14dpi para análisis histológico de IMAT. Paralelamente, se aislarán FAPs del estroma vascular muscular al 3dpi. En FAPs aisladas se evaluarán proteínas de la vía NLPR3 inflamasoma y su capacidad adipogénica en respuesta al tratamiento in-vitro con 3mM βHB. Los resultados de esta propuesta nos permitirán mostrar los efectos terapéuticos de la suplementación dietaría con cuerpos cetónicos en la función y recuperación muscular post daño.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]La respuesta inflamatoria al daño muscular puede comprometer la fuerza/masa al inducir la formación de tejido adiposo intermuscular (IMAT). IMAT se origina de la diferenciación adipogénica de células mesenquimales progenitoras fibro-adipogénicas (FAPs). Este proceso podría revertirse modulando la respuesta inflamatoria aguda. Sin embargo, el uso de antiinflamatorios inhibe la síntesis proteica y reduce la capacidad regenerativa muscular. Alternativamente, medidas físicas como el reposo funcional o la reincorporación temprana a la actividad han reportado efectos contradictorios sobre el proceso inflamatorio, lo que dificulta establecer indicaciones en el manejo de la lesión muscular. Por otro lado, se ha descrito un potente papel antinflamatorio local o sistémico del cuerpo cetónico β-hydroxybutirato (βHB); efecto mediado por la inhibición del inflamasoma NLRP3 y la secreción de citoquinas proinflamatorias. Importantemente, la activación del inflamasoma NLRP3 favorecería la adipogénesis de células mesenquimales, lo que sugiere un rol en la formación de IMAT. Se hipotetiza que la suplementación con βHB durante la recuperación de una lesión muscular aguda inhibe la diferenciación adipogénica de FAPs reduciendo la formación de IMAT lo que acelera la reparación y recuperación funcional del tejido muscular. Este efecto estaría mediado por la inhibición del inflamasoma NLRP3. Se inyectará una solución hiperosmótica al 25% de glicerol o salino en el músculo tibial anterior en ratones con o sin suplementación de 3 mg/g βHB durante 2 semanas post injuria. Se recolectará tejido muscular al 14dpi para análisis histológico de IMAT. Paralelamente, se aislarán FAPs del estroma vascular muscular al 3dpi. En FAPs aisladas se evaluarán proteínas de la vía NLPR3 inflamasoma y su capacidad adipogénica en respuesta al tratamiento in-vitro con 3mM βHB. Los resultados de esta propuesta nos permitirán mostrar los efectos terapéuticos de la suplementación dietaría con cuerpos cetónicos en la función y recuperación muscular post daño.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""].[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""].[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Fondecyt de Postdoctorado 2025 Proyecto Nº 3250704, Universidad de Chile y Universidad de O'Higgins - Implementación de la investigación 'Exploración de las bases neuroanatómicas de la alteración del insight en la enfermedad de Alzheimer' como Investigador Postdoctoral[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Fondecyt de Postdoctorado 2025 Proyecto Nº 3250704, Universidad de Chile y Universidad de O'Higgins - Implementación de la investigación 'Exploración de las bases neuroanatómicas de la alteración del insight en la enfermedad de Alzheimer' como Investigador Postdoctoral[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Implementación de la investigación 'Uso de inteligencia artificial para la exploración de las bases neuroanatómicas del deterioro del insight en la enfermedad de Alzheimer' desde el cargo de Investigador Postdoctoral del Instituto de Ciencias de la Ingeniería de la Universidad de O’Higgins.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Implementación de la investigación 'Uso de inteligencia artificial para la exploración de las bases neuroanatómicas del deterioro del insight en la enfermedad de Alzheimer' desde el cargo de Investigador Postdoctoral del Instituto de Ciencias de la Ingeniería de la Universidad de O’Higgins.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Research project aimed at identifying neuropsychological and biological markers for the early detection of Alzheimer's disease.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Research project aimed at identifying neuropsychological and biological markers for the early detection of Alzheimer's disease.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]DISCA (Discapacidad y Ciudadanía) es un núcleo que desde 2022 está dedicado al estudio inter y transdisciplinario de los procesos y mecanismos a través de los cuales las personas con discapacidad (PcD) se transforman en ciudadanas. Su objetivo general es examinar críticamente cómo las PcD construyen y negocian su ciudadanía en los ámbitos de: L1. la participación política, L2. el acceso a la justicia y L3. el acceso a la salud mental. Cada uno de estos ámbitos será una línea de trabajo de DISCA en los tres años del proyecto. Una cuarta línea se centrará en el uso de metodologías inclusivas y participativas en investigación en discapacidad. Nuestro enfoque se basa en dos pilares. Primero, la ciudadanía como forma de integración social mediante la igual consideración de todos. Consideramos aspectos institucionales (derechos civiles, políticos y sociales) y relacionales (demandas de reconocimiento). Segundo, el modelo social de la discapacidad, que busca superar el enfoque biomédico y entiende la discapacidad como resultado de la interacción entre condiciones de salud o déficits individuales y barreras sociales que impiden la plena participación de las PcD. El modelo social no es la mirada predominante. Siguen vigentes visiones asistencialistas que restringen la inclusión y el ejercicio de la ciudadanía de las PcD. Es urgente que la academia cree sinergias, tanto con organizaciones de PcD como con las instituciones del Estado, para examinar las barreras que afectan a las PcD y las vías para su superación. La escasez de investigación en discapacidad en Chile, y la necesidad de incorporar a PcD en la generación de conocimiento, hace nuestro proyecto muy relevante. La incorporación de PcD en el mundo académico a través de DISCA es una valiosa oportunidad para realizar cambios que preparen el camino para una mayor participación de otras PcD. Esperamos que sus resultados generen políticas inclusivas y participativas en discapacidad. DISCA está dirigido por una PcD, cuenta con un consejo de Expertos por Experiencia (con 7 PcD) y observa los principios de la investigación inclusiva y participativa. Sus investigadores principales, pioneros en la investigación en discapacidad en Chile, utilizan metodologías mixtas, cuantitativas y cualitativas, integrando conocimientos de sociología, derecho, salud, economía, sociología y psicología en conjunto con el campo transdisciplinario de los estudios de la discapacidad. Los logros a corto plazo se dirigen a: i) producir investigación inter y transdisciplinaria en discapacidad, ii) consolidar redes de colaboración con otros centros de investigación en el mundo, iii) formar capital humano en varios niveles, incluyendo PcD en todo el quehacer de DISCA y iv) informar la política pública. La meta a mediano plazo es consolidar a DISCA como el primer centro de excelencia en investigación en discapacidad de Latinoamérica, contribuyendo al fortalecimiento de los estudios de la discapacidad en el mundo.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Es un centro de excelencia en salud mental[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]DISCA (Discapacidad y Ciudadanía) es un núcleo que desde 2022 está dedicado al estudio inter y transdisciplinario de los procesos y mecanismos a través de los cuales las personas con discapacidad (PcD) se transforman en ciudadanas. Su objetivo general es examinar críticamente cómo las PcD construyen y negocian su ciudadanía en los ámbitos de: L1. la participación política, L2. el acceso a la justicia y L3. el acceso a la salud mental. Cada uno de estos ámbitos será una línea de trabajo de DISCA en los tres años del proyecto. Una cuarta línea se centrará en el uso de metodologías inclusivas y participativas en investigación en discapacidad. Nuestro enfoque se basa en dos pilares. Primero, la ciudadanía como forma de integración social mediante la igual consideración de todos. Consideramos aspectos institucionales (derechos civiles, políticos y sociales) y relacionales (demandas de reconocimiento). Segundo, el modelo social de la discapacidad, que busca superar el enfoque biomédico y entiende la discapacidad como resultado de la interacción entre condiciones de salud o déficits individuales y barreras sociales que impiden la plena participación de las PcD. El modelo social no es la mirada predominante. Siguen vigentes visiones asistencialistas que restringen la inclusión y el ejercicio de la ciudadanía de las PcD. Es urgente que la academia cree sinergias, tanto con organizaciones de PcD como con las instituciones del Estado, para examinar las barreras que afectan a las PcD y las vías para su superación. La escasez de investigación en discapacidad en Chile, y la necesidad de incorporar a PcD en la generación de conocimiento, hace nuestro proyecto muy relevante. La incorporación de PcD en el mundo académico a través de DISCA es una valiosa oportunidad para realizar cambios que preparen el camino para una mayor participación de otras PcD. Esperamos que sus resultados generen políticas inclusivas y participativas en discapacidad. DISCA está dirigido por una PcD, cuenta con un consejo de Expertos por Experiencia (con 7 PcD) y observa los principios de la investigación inclusiva y participativa. Sus investigadores principales, pioneros en la investigación en discapacidad en Chile, utilizan metodologías mixtas, cuantitativas y cualitativas, integrando conocimientos de sociología, derecho, salud, economía, sociología y psicología en conjunto con el campo transdisciplinario de los estudios de la discapacidad. Los logros a corto plazo se dirigen a: i) producir investigación inter y transdisciplinaria en discapacidad, ii) consolidar redes de colaboración con otros centros de investigación en el mundo, iii) formar capital humano en varios niveles, incluyendo PcD en todo el quehacer de DISCA y iv) informar la política pública. La meta a mediano plazo es consolidar a DISCA como el primer centro de excelencia en investigación en discapacidad de Latinoamérica, contribuyendo al fortalecimiento de los estudios de la discapacidad en el mundo.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Es un centro de excelencia en salud mental[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Mental health conditions and inequities in Chile have risen significantly over recent decades, fueled by factors such as social exclusion, precarious employment, and environmental challenges. In line with recent national legislation and policy reforms, including the recently proposed Mental Health Law (2024,) there is growing recognition that these issues require not only expanded clinical services but also a deeper focus on the socio-structural determinants of mental health (Breilh, 2023; Lund et al., 2018). The Centro de Investigación y Acción en Determinación Social y Salud Mental (Center for Research and Action in Social Determination and Mental Health) or CIADES responds to this urgency by adopting a Latin American–rooted Social Determination of Health (SDnH) framework, thereby situating mental health vulnerabilities and risks within broader historical, economic, and political contexts. CIADES will work in close collaboration with the Ministry of Social Development and Family (MIDESO) and the Ministry of Health (MINSAL), to generate robust evidence and policy guidance to address the social factors that affect and produce mental health problems beyond the individual. This collaboration ensures that the Center’s research advances academic knowledge and informs public-sector strategies and interventions. In doing so, CIADES seeks to address crucial social factors, including growing economic inequalities, stigma, and social disintegration, which have direct implications for mental well-being across the lifespan. Methodologically, CIADES employs a three-by-three matrix that interlinks three social determinants— Social Exclusion and Discrimination, Environmental Factors, and Employment—with three priority populations: migrants, older adults, and people with SMI (SMI). This matrix underpins interdisciplinary research lines, integrating quantitative (e.g., epidemiological surveys, geospatial risk mapping), qualitative (e.g., multimodal and sensory ethnography, focus groups), and participatory methods. AI-driven analyses, such as natural language processing for tracking stigma on social media, and economic evaluations that assess intervention feasibility also feature prominently within the Center’s approach. The significance of this research lies in its focus on macro-structural drivers—housing insecurity, workplace discrimination, socio-environmental conflicts—and how they contribute to mental health inequities. By examining these intersecting challenges, CIADES will move beyond an exclusively clinical perspective to propose and evaluate, in close collaboration with MIDESO and MINSAL, evidence-based strategies that can be implemented at multiple levels: local (community-based initiatives), regional (intersectoral policies), and national (legislative reforms). This holistic orientation positions CIADES as a transformative force in Chile’s public policy on mental health. Once established, the Center expects to identify and integrate other social determinants and priority groups. The Center’s work will be guided by four Specific Objectives. First, Generate Evidence for Strategic Interventions and Policy Reforms involves collaborating with MIDESO and MINSAL to systematically examine socio-structural determinants—such as discrimination, environmental stressors, and employment vulnerabilities—and generate robust evidence to inform and guide future interventions and policy actions. Second, Methodological Development uses participatory and mixed-methods approaches, emphasizing community involvement and local knowledge. Third, Capacity Building trains emerging researchers, policymakers, and practitioners to apply the SDnH framework. Finally, Knowledge Dissemination and Policy Advocacy entails translating findings into policy briefs, stakeholder workshops, and legislative recommendations that foreground structural change and equitable access to the exercise of rights, and to policies, programs and services. CIADES benefits from a multidisciplinary team involving principal and associate investigators with extensive track records in mental health, social sciences, environmental studies, and policy work. Their collective experience includes leading large-scale epidemiological surveys, designing culturally relevant interventions, and influencing legislative reforms. This breadth enables the Center to integrate cutting-edge methods—such as AI-driven stigma detection and geospatial modeling—within a robust theoretical framework. By drawing on a wide range of expertise, CIADES is uniquely positioned to undertake a comprehensive agenda that links empirical research to transformative actions in policy and practice. CIADES anticipates having a significant impact at the national level by influencing discussions on the design, implementation, and evaluation of policies related to labor laws, anti-discrimination statutes, community-oriented service models, environmental regulations, urban transformations, and other public policies with an impact on mental health. In the short term, the center aims to increase recognition of the structural factors that affect the mental health of different populations, factors that are often overlooked or ignored due to the current emphasis on individual-focused approaches. Collaborating with communities, CIADES will co-design initiatives and pilot projects that serve as scalable case studies. These efforts will lead to the production of policy briefs and guidelines, offering new frameworks to understand mental health challenges and proposing context-sensitive interventions. Over the medium to long term, CIADES aims to enhance intersectoral collaboration to drive structural-level interventions able to reduce mental health disparities— positioning Chile as a regional leader in addressing mental health through a justice-based perspective. The Center places a strong emphasis on capacity building and human capital formation as integral components of its mission. Students from undergraduate to postgraduate levels will benefit from interdisciplinary training in mental health, social epidemiology, qualitative methods, participatory methods and inclusive research, and implementation and dissemination science. This approach aims to nurture a new generation of scholars, practitioners, and other stakeholders equipped with the skills and knowledge necessary to advance the SDnH perspective. Furthermore, partnerships with leading international institutions, such as King’s College London and Columbia University, will facilitate knowledge exchange, foster global networks, and enhance CIADES’ reach and credibility on an international scale. Through proactive dissemination, outreach, and knowledge transfer, CIADES will engage with both public and private sectors to drive actionable change. Dissemination channels include academic publications, open-access materials, community forums, policy dialogues, and strategic communication through social media to ensure broader public penetration of the center's work. Regarding academic publications, CIADES is committed to publishing in high-impact international journals while also recognizing the strategic importance of positioning itself within Latin American and national contexts by contributing to academic journals in Spanish. Open-access materials will include the development of conceptual, methodological, and practical tools and guides, which will be freely available for public use. Community forums will serve both to share research findings and to identify emerging issues among the general population, while policy dialogues will aim to directly support and influence decision-making processes at the policy level based on the center’s research findings and experiences.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Mental health conditions and inequities in Chile have risen significantly over recent decades, fueled by factors such as social exclusion, precarious employment, and environmental challenges. In line with recent national legislation and policy reforms, including the recently proposed Mental Health Law (2024,) there is growing recognition that these issues require not only expanded clinical services but also a deeper focus on the socio-structural determinants of mental health (Breilh, 2023; Lund et al., 2018). The Centro de Investigación y Acción en Determinación Social y Salud Mental (Center for Research and Action in Social Determination and Mental Health) or CIADES responds to this urgency by adopting a Latin American–rooted Social Determination of Health (SDnH) framework, thereby situating mental health vulnerabilities and risks within broader historical, economic, and political contexts. CIADES will work in close collaboration with the Ministry of Social Development and Family (MIDESO) and the Ministry of Health (MINSAL), to generate robust evidence and policy guidance to address the social factors that affect and produce mental health problems beyond the individual. This collaboration ensures that the Center’s research advances academic knowledge and informs public-sector strategies and interventions. In doing so, CIADES seeks to address crucial social factors, including growing economic inequalities, stigma, and social disintegration, which have direct implications for mental well-being across the lifespan. Methodologically, CIADES employs a three-by-three matrix that interlinks three social determinants— Social Exclusion and Discrimination, Environmental Factors, and Employment—with three priority populations: migrants, older adults, and people with SMI (SMI). This matrix underpins interdisciplinary research lines, integrating quantitative (e.g., epidemiological surveys, geospatial risk mapping), qualitative (e.g., multimodal and sensory ethnography, focus groups), and participatory methods. AI-driven analyses, such as natural language processing for tracking stigma on social media, and economic evaluations that assess intervention feasibility also feature prominently within the Center’s approach. The significance of this research lies in its focus on macro-structural drivers—housing insecurity, workplace discrimination, socio-environmental conflicts—and how they contribute to mental health inequities. By examining these intersecting challenges, CIADES will move beyond an exclusively clinical perspective to propose and evaluate, in close collaboration with MIDESO and MINSAL, evidence-based strategies that can be implemented at multiple levels: local (community-based initiatives), regional (intersectoral policies), and national (legislative reforms). This holistic orientation positions CIADES as a transformative force in Chile’s public policy on mental health. Once established, the Center expects to identify and integrate other social determinants and priority groups. The Center’s work will be guided by four Specific Objectives. First, Generate Evidence for Strategic Interventions and Policy Reforms involves collaborating with MIDESO and MINSAL to systematically examine socio-structural determinants—such as discrimination, environmental stressors, and employment vulnerabilities—and generate robust evidence to inform and guide future interventions and policy actions. Second, Methodological Development uses participatory and mixed-methods approaches, emphasizing community involvement and local knowledge. Third, Capacity Building trains emerging researchers, policymakers, and practitioners to apply the SDnH framework. Finally, Knowledge Dissemination and Policy Advocacy entails translating findings into policy briefs, stakeholder workshops, and legislative recommendations that foreground structural change and equitable access to the exercise of rights, and to policies, programs and services. CIADES benefits from a multidisciplinary team involving principal and associate investigators with extensive track records in mental health, social sciences, environmental studies, and policy work. Their collective experience includes leading large-scale epidemiological surveys, designing culturally relevant interventions, and influencing legislative reforms. This breadth enables the Center to integrate cutting-edge methods—such as AI-driven stigma detection and geospatial modeling—within a robust theoretical framework. By drawing on a wide range of expertise, CIADES is uniquely positioned to undertake a comprehensive agenda that links empirical research to transformative actions in policy and practice. CIADES anticipates having a significant impact at the national level by influencing discussions on the design, implementation, and evaluation of policies related to labor laws, anti-discrimination statutes, community-oriented service models, environmental regulations, urban transformations, and other public policies with an impact on mental health. In the short term, the center aims to increase recognition of the structural factors that affect the mental health of different populations, factors that are often overlooked or ignored due to the current emphasis on individual-focused approaches. Collaborating with communities, CIADES will co-design initiatives and pilot projects that serve as scalable case studies. These efforts will lead to the production of policy briefs and guidelines, offering new frameworks to understand mental health challenges and proposing context-sensitive interventions. Over the medium to long term, CIADES aims to enhance intersectoral collaboration to drive structural-level interventions able to reduce mental health disparities— positioning Chile as a regional leader in addressing mental health through a justice-based perspective. The Center places a strong emphasis on capacity building and human capital formation as integral components of its mission. Students from undergraduate to postgraduate levels will benefit from interdisciplinary training in mental health, social epidemiology, qualitative methods, participatory methods and inclusive research, and implementation and dissemination science. This approach aims to nurture a new generation of scholars, practitioners, and other stakeholders equipped with the skills and knowledge necessary to advance the SDnH perspective. Furthermore, partnerships with leading international institutions, such as King’s College London and Columbia University, will facilitate knowledge exchange, foster global networks, and enhance CIADES’ reach and credibility on an international scale. Through proactive dissemination, outreach, and knowledge transfer, CIADES will engage with both public and private sectors to drive actionable change. Dissemination channels include academic publications, open-access materials, community forums, policy dialogues, and strategic communication through social media to ensure broader public penetration of the center's work. Regarding academic publications, CIADES is committed to publishing in high-impact international journals while also recognizing the strategic importance of positioning itself within Latin American and national contexts by contributing to academic journals in Spanish. Open-access materials will include the development of conceptual, methodological, and practical tools and guides, which will be freely available for public use. Community forums will serve both to share research findings and to identify emerging issues among the general population, while policy dialogues will aim to directly support and influence decision-making processes at the policy level based on the center’s research findings and experiences.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Experiencias del Movimiento Social de la Discapacidad en América Latina: Itinerarios de lucha por los derechos del Colectivo Nacional por la Discapacidad de Chile y la Asociación de Discapacidad del Guayas de Ecuador.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Experiencias del Movimiento Social de la Discapacidad en América Latina: Itinerarios de lucha por los derechos del Colectivo Nacional por la Discapacidad de Chile y la Asociación de Discapacidad del Guayas de Ecuador.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Consolidar y fortalecer una nueva red de nodos de innovación social que promueva la inclusión socio laboral en personas con alguna discapacidad, personas mayores, mujeres y personas en situación de vulnerabilidad enfocada en los sectores económicos priorizados en la Estrategia de Desarrollo Regional 2011-2020 (EDRE) y de innovación, priorizando el sector turístico, y agroalimentario y la puesta en valor de la identidad cultural.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Consolidar y fortalecer una nueva red de nodos de innovación social que promueva la inclusión socio laboral en personas con alguna discapacidad, personas mayores, mujeres y personas en situación de vulnerabilidad enfocada en los sectores económicos priorizados en la Estrategia de Desarrollo Regional 2011-2020 (EDRE) y de innovación, priorizando el sector turístico, y agroalimentario y la puesta en valor de la identidad cultural.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]l Núcleo Milenio Discapacidad y Ciudadanía (DISCA) es un centro de investigación interdisciplinario financiado por la Agencia Nacional de Investigación y Desarrollo (2023 a 2025). Con un abordaje multi y transdisciplinario, la agenda de DISCA se centra en el estudio de los procesos y mecanismos a través de los cuales las personas con discapacidad se transforman en ciudadanas. DISCA está dirigido por una persona con discapacidad, cuenta con un consejo de expertas y expertos por experiencia y esta alineado con los principios de la investigación inclusiva y participativa. Sus investigadores, pioneros en la investigación en discapacidad en el país, utilizan metodologías mixtas, cuantitativas y cualitativas, integrando conocimientos de la antropología social, el derecho, la salud, la economía, la sociología y la psicología, en conjunto con el campo transdisciplinario de los estudios de la discapacidad.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]l Núcleo Milenio Discapacidad y Ciudadanía (DISCA) es un centro de investigación interdisciplinario financiado por la Agencia Nacional de Investigación y Desarrollo (2023 a 2025). Con un abordaje multi y transdisciplinario, la agenda de DISCA se centra en el estudio de los procesos y mecanismos a través de los cuales las personas con discapacidad se transforman en ciudadanas. DISCA está dirigido por una persona con discapacidad, cuenta con un consejo de expertas y expertos por experiencia y esta alineado con los principios de la investigación inclusiva y participativa. Sus investigadores, pioneros en la investigación en discapacidad en el país, utilizan metodologías mixtas, cuantitativas y cualitativas, integrando conocimientos de la antropología social, el derecho, la salud, la economía, la sociología y la psicología, en conjunto con el campo transdisciplinario de los estudios de la discapacidad.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Número de proyecto: 3220665[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Número de proyecto: 3220665[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]El present projecte pretén descriure la visió que els futurs professionals de la salut tenen del cos i els usos que li donen per tal d’afavorir la reflexió sobre el seu impacte en atenció a l’usuari (l’aproximació al cos de l’altre). Conèixer els discursos i les pràctiques realitzades amb el cos dels estudiants de primer curs de ciències de la salut (teràpia ocupacional i infermeria) que expliquem la seva relació amb el “cos”.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]El present projecte pretén descriure la visió que els futurs professionals de la salut tenen del cos i els usos que li donen per tal d’afavorir la reflexió sobre el seu impacte en atenció a l’usuari (l’aproximació al cos de l’altre). Conèixer els discursos i les pràctiques realitzades amb el cos dels estudiants de primer curs de ciències de la salut (teràpia ocupacional i infermeria) que expliquem la seva relació amb el “cos”.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]The proposal focuses on understanding the neuro-vascular aging mechanisms associated with alterations in fetal growth by intrauterine hypoxia using molecular biology and physiology as an area. The aim of the study is to demonstrate that impaired fetal growth conditions are associated with epigenetic programming of aging-related DNA methylation, chromatin remodeling, and miRNA-omic profile of junctional complex genes in the neuroendothelium, which can alter BBB integrity and permeability, increasing cerebral damage which impacts the juvenile and adulthood neurocognitive function.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]The proposal focuses on understanding the neuro-vascular aging mechanisms associated with alterations in fetal growth by intrauterine hypoxia using molecular biology and physiology as an area. The aim of the study is to demonstrate that impaired fetal growth conditions are associated with epigenetic programming of aging-related DNA methylation, chromatin remodeling, and miRNA-omic profile of junctional complex genes in the neuroendothelium, which can alter BBB integrity and permeability, increasing cerebral damage which impacts the juvenile and adulthood neurocognitive function.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]The brain is an energy intensive organ that requires a robust supply of nutrients and oxygen. The vasculature irrigating the brain is a huge and complex network of blood vessels fulfilling this requirement, while also protecting the neural tissue from blood-borne toxic substances. This regulated nutrient supply is accomplished by the formation of a highly selective molecular barrier, termed the blood-brain barrier (BBB). Dysfunction of the BBB or malformations of the vascular network are associated with pathological conditions that impair brain function, and can lead to death. Thus, appropriate morphogenesis and establishment of the brain vasculature is necessary for a healthy life. The brain vasculature forms during intrauterine development, matching brain growth in this same period. Anatomically, blood vessels grow first surrounding the brain primordium and then penetrate the parenchyma until they vascularize the periventricular zone. The molecular regulation of this patterned growth is not completely understood. Several signaling pathways are known to be involved in brain angiogenesis, including WNT, TGF-β, Hh, and NOTCH, which differentially regulate vascular growth. Recently, cholesterol has been shown to modulate angiogenic growth in other vascular beds by regulating the activity of the NOTCH pathway, suggesting that cholesterol levels could influence developmental angiogenesis in the brain. Interestingly, cholesterol is also required for signal transduction of the Hh pathway. In preliminary in vitro experiments, we have observed that brain endothelial cells activate an angiogenic program after cholesterol depletion. Here, we will extend those studies to in vivo models to determine the role of cholesterol in developmental brain angiogenesis. We propose that an increase in vascular cell cholesterol activates NOTCH and attenuates Hh signaling pathways, restricting sprouting angiogenesis and blood-brain barrier formation in mouse embryo brain vasculature. To test this hypothesis, we will study mouse embryos with altered cholesterol levels by dietary, pharmacological, and genetic manipulations. We expect these manipulations to induce a reduction or an increase in cholesterol levels in the brain vasculature during embryonic development, which we will evaluate by measuring cholesterol content in isolated vascular fragments. In all these models, we will (Specific aim 1) study vascularization in the brain during intrauterine development using immunofluorescence with specific antibodies against endothelium proteins. In addition, we will measure the levels of transcript and proteins of general key regulators of angiogenesis in isolated vascular fragments, using qPCR and Western blot. We will (Specific aim 2) also evaluate the state of the BBB in the brain vasculature of these models at a fetal stage when the barrier is already formed and functional. For this, we will use immunofluorescence to detect the presence of marker proteins of the BBB in vascular fragments, and we will measure their levels by Western blot. Further, we will test the functionality of the barrier by injecting a fluorescent tracer and evaluating its extravasation in the brain. Finally, we will (Specific aim 3) determine the activation of the NOTCH and Hh pathways in the brain vasculature of the models at the stage of maximal angiogenesis. We will use qPCR and Western blot to measure the levels of marker genes and proteins for these two pathways in vascular fragments, and Proximity Ligation In Situ Hybridization in tissue sections to evaluate the transcript levels of those markers in situ. We expect that the different models of dietary, pharmacological, and genetic interventions will increase or reduce cholesterol levels in the brain vasculature. These changes are expected to correlate with opposing effects on angiogenesis in the brain during development (i.e. low cholesterol will increase angiogenesis, while high cholesterol will inhibit it). In the same way, we expect that distinct cholesterol levels will have opposing effects on the integrity of the BBB. These changes in angiogenesis and BBB function are expected to be associated with concomitant disruption of the NOTCH and Hh pathways. In summary, in this proposal we aim to cover a knowledge gap regarding the role of cholesterol in the regulation of developmental angiogenesis in the brain. These experiments may uncover new mechanisms driving vascular growth and barrier establishment in the brain, which could lead to new strategies for the prevention and treatment of pathologies involving the brain vasculature.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]The brain is an energy intensive organ that requires a robust supply of nutrients and oxygen. The vasculature irrigating the brain is a huge and complex network of blood vessels fulfilling this requirement, while also protecting the neural tissue from blood-borne toxic substances. This regulated nutrient supply is accomplished by the formation of a highly selective molecular barrier, termed the blood-brain barrier (BBB). Dysfunction of the BBB or malformations of the vascular network are associated with pathological conditions that impair brain function, and can lead to death. Thus, appropriate morphogenesis and establishment of the brain vasculature is necessary for a healthy life. The brain vasculature forms during intrauterine development, matching brain growth in this same period. Anatomically, blood vessels grow first surrounding the brain primordium and then penetrate the parenchyma until they vascularize the periventricular zone. The molecular regulation of this patterned growth is not completely understood. Several signaling pathways are known to be involved in brain angiogenesis, including WNT, TGF-β, Hh, and NOTCH, which differentially regulate vascular growth. Recently, cholesterol has been shown to modulate angiogenic growth in other vascular beds by regulating the activity of the NOTCH pathway, suggesting that cholesterol levels could influence developmental angiogenesis in the brain. Interestingly, cholesterol is also required for signal transduction of the Hh pathway. In preliminary in vitro experiments, we have observed that brain endothelial cells activate an angiogenic program after cholesterol depletion. Here, we will extend those studies to in vivo models to determine the role of cholesterol in developmental brain angiogenesis. We propose that an increase in vascular cell cholesterol activates NOTCH and attenuates Hh signaling pathways, restricting sprouting angiogenesis and blood-brain barrier formation in mouse embryo brain vasculature. To test this hypothesis, we will study mouse embryos with altered cholesterol levels by dietary, pharmacological, and genetic manipulations. We expect these manipulations to induce a reduction or an increase in cholesterol levels in the brain vasculature during embryonic development, which we will evaluate by measuring cholesterol content in isolated vascular fragments. In all these models, we will (Specific aim 1) study vascularization in the brain during intrauterine development using immunofluorescence with specific antibodies against endothelium proteins. In addition, we will measure the levels of transcript and proteins of general key regulators of angiogenesis in isolated vascular fragments, using qPCR and Western blot. We will (Specific aim 2) also evaluate the state of the BBB in the brain vasculature of these models at a fetal stage when the barrier is already formed and functional. For this, we will use immunofluorescence to detect the presence of marker proteins of the BBB in vascular fragments, and we will measure their levels by Western blot. Further, we will test the functionality of the barrier by injecting a fluorescent tracer and evaluating its extravasation in the brain. Finally, we will (Specific aim 3) determine the activation of the NOTCH and Hh pathways in the brain vasculature of the models at the stage of maximal angiogenesis. We will use qPCR and Western blot to measure the levels of marker genes and proteins for these two pathways in vascular fragments, and Proximity Ligation In Situ Hybridization in tissue sections to evaluate the transcript levels of those markers in situ. We expect that the different models of dietary, pharmacological, and genetic interventions will increase or reduce cholesterol levels in the brain vasculature. These changes are expected to correlate with opposing effects on angiogenesis in the brain during development (i.e. low cholesterol will increase angiogenesis, while high cholesterol will inhibit it). In the same way, we expect that distinct cholesterol levels will have opposing effects on the integrity of the BBB. These changes in angiogenesis and BBB function are expected to be associated with concomitant disruption of the NOTCH and Hh pathways. In summary, in this proposal we aim to cover a knowledge gap regarding the role of cholesterol in the regulation of developmental angiogenesis in the brain. These experiments may uncover new mechanisms driving vascular growth and barrier establishment in the brain, which could lead to new strategies for the prevention and treatment of pathologies involving the brain vasculature.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Retinal vascular diseases are major causes of vision loss in the United States and around the world. To better treat these disorders, we need to understand the signaling pathways that control the growth and integrity of retinal blood vessels. Our recent publications and preliminary data detail a novel angiogenic signaling system centered around heme, a co-factor critical for oxygen transport, metabolism, and gene transcription. We found that heme promotes angiogenic growth in the retina by regulating tip/stalk selection, and that reduced heme production or import leads to reduced retinal vascularization and tissue hypoxia, similar to other retinal vasculopathies including retinopathy of prematurity, choroidal neovascularization, and the rare but important exudative vitreoretinopathies. Furthermore, we found that VEGF suppresses, while Norrin-bCatenin promotes, the expression of the obligate endothelial heme importer, Flvcr2. Based on these data, we hypothesize that heme, is involved in retinal angiogenesis and retinal vasculopathies. The Specific Aims of this proposal are to (1) determine how heme intersects with Notch signaling to control angiogenic tip/stalk selection, (2) characterize the role for Flvcr2/heme in VEGF-induced angiogenic proliferation and neo-vascularization, and (3) determine whether induction of Flvcr2/heme signaling is sufficient and necessary to reverse the vascular defects and downstream vision changes observed in mouse models of exudative vitreoretinopathy. To accomplish these aims, we developed new tools to directly manipulate heme in cultured retinal endothelial cells and assess heme transport and intracellular trafficking in vitro. We also generated new conditional knock-in and knock-out alleles to manipulate endothelial heme transport in vivo. Our studies will fundamentally impact our understanding of how endothelial heme levels are controlled, and the role of heme in retinal angiogenesis and vascular disease.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]

[vc_section el_class="container mx-auto align-items-center circle--pattern" css=".vc_custom_1648956589196{padding-top: 3rem !important;}"][vc_row el_class="pb-5"][vc_column][vc_wp_custommenu nav_menu="6"][uoh_breadcrumb_component automatic_breadcrumb="true"][uoh_title_component title_dropdown="big" title_decorator="true"]{{title}}[/uoh_title_component][vc_column_text css=""]Retinal vascular diseases are major causes of vision loss in the United States and around the world. To better treat these disorders, we need to understand the signaling pathways that control the growth and integrity of retinal blood vessels. Our recent publications and preliminary data detail a novel angiogenic signaling system centered around heme, a co-factor critical for oxygen transport, metabolism, and gene transcription. We found that heme promotes angiogenic growth in the retina by regulating tip/stalk selection, and that reduced heme production or import leads to reduced retinal vascularization and tissue hypoxia, similar to other retinal vasculopathies including retinopathy of prematurity, choroidal neovascularization, and the rare but important exudative vitreoretinopathies. Furthermore, we found that VEGF suppresses, while Norrin-bCatenin promotes, the expression of the obligate endothelial heme importer, Flvcr2. Based on these data, we hypothesize that heme, is involved in retinal angiogenesis and retinal vasculopathies. The Specific Aims of this proposal are to (1) determine how heme intersects with Notch signaling to control angiogenic tip/stalk selection, (2) characterize the role for Flvcr2/heme in VEGF-induced angiogenic proliferation and neo-vascularization, and (3) determine whether induction of Flvcr2/heme signaling is sufficient and necessary to reverse the vascular defects and downstream vision changes observed in mouse models of exudative vitreoretinopathy. To accomplish these aims, we developed new tools to directly manipulate heme in cultured retinal endothelial cells and assess heme transport and intracellular trafficking in vitro. We also generated new conditional knock-in and knock-out alleles to manipulate endothelial heme transport in vivo. Our studies will fundamentally impact our understanding of how endothelial heme levels are controlled, and the role of heme in retinal angiogenesis and vascular disease.[/vc_column_text][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649209804184{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5"][vc_row el_class="container mx-auto align-items-center p-md-0 pt-5"][vc_column el_class="p-0"][/vc_column][/vc_row][/vc_section][vc_section css=".vc_custom_1649210787516{background-color: #f6faff !important;}" el_class="p-md-0 pt-md-5 pb-md-5"][vc_row el_class="container mx-auto align-items-center"][vc_column][/vc_column][/vc_row][/vc_section]