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Acoustically targeted chemogenetics for the non-invasive control of neural circuits.
Szablowski, Jerzy O; Lee-Gosselin, Audrey; Lue, Brian; Malounda, Dina; Shapiro, Mikhail G.
Afiliación
  • Szablowski JO; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Lee-Gosselin A; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Lue B; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Malounda D; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Shapiro MG; Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA. mikhail@caltech.edu.
Nat Biomed Eng ; 2(7): 475-484, 2018 07.
Article en En | MEDLINE | ID: mdl-30948828
Neurological and psychiatric disorders are often characterized by dysfunctional neural circuits in specific regions of the brain. Existing treatment strategies, including the use of drugs and implantable brain stimulators, aim to modulate the activity of these circuits. However, they are not cell-type-specific, lack spatial targeting or require invasive procedures. Here, we report a cell-type-specific and non-invasive approach based on acoustically targeted chemogenetics that enables the modulation of neural circuits with spatiotemporal specificity. The approach uses ultrasound waves to transiently open the blood-brain barrier and transduce neurons at specific locations in the brain with virally encoded engineered G-protein-coupled receptors. The engineered neurons subsequently respond to systemically administered designer compounds to activate or inhibit their activity. In a mouse model of memory formation, the approach can modify and subsequently activate or inhibit excitatory neurons within the hippocampus, with selective control over individual brain regions. This technology overcomes some of the key limitations associated with conventional brain therapies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Drogas de Diseño / Receptores Acoplados a Proteínas G / Hipocampo / Neuronas Límite: Animals Idioma: En Revista: Nat Biomed Eng Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Drogas de Diseño / Receptores Acoplados a Proteínas G / Hipocampo / Neuronas Límite: Animals Idioma: En Revista: Nat Biomed Eng Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido