Your browser doesn't support javascript.
loading
Long-range inhibitory neurons mediate cortical neurovascular coupling.
Ruff, Catherine F; Juarez Anaya, Fernanda; Dienel, Samuel J; Rakymzhan, Adiya; Altamirano-Espinoza, Alain; Couey, Jonathan J; Fukuda, Mitsuhiro; Watson, Alan M; Su, Aihua; Fish, Kenneth N; Rubio, Maria E; Hooks, Bryan M; Ross, Sarah E; Vazquez, Alberto L.
Afiliación
  • Ruff CF; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Juarez Anaya F; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Dienel SJ; Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
  • Rakymzhan A; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
  • Altamirano-Espinoza A; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
  • Couey JJ; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Fukuda M; Department of Radiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Watson AM; Center for Biologic Imaging, University of Pittsburgh, Pittsburgh, PA, USA.
  • Su A; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Fish KN; Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
  • Rubio ME; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Hooks BM; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Ross SE; Department of Neurobiology, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: saross@pitt.edu.
  • Vazquez AL; Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA; Department of Radiology, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: alv15@pitt.edu.
Cell Rep ; 43(4): 113970, 2024 Apr 23.
Article en En | MEDLINE | ID: mdl-38512868
ABSTRACT
To meet the high energy demands of brain function, cerebral blood flow (CBF) parallels changes in neuronal activity by a mechanism known as neurovascular coupling (NVC). However, which neurons play a role in mediating NVC is not well understood. Here, we identify in mice and humans a specific population of cortical GABAergic neurons that co-express neuronal nitric oxide synthase and tachykinin receptor 1 (Tacr1). Through whole-tissue clearing, we demonstrate that Tacr1 neurons extend local and long-range projections across functionally connected cortical areas. We show that whisker stimulation elicited Tacr1 neuron activity in the barrel cortex through feedforward excitatory pathways. Additionally, through optogenetic experiments, we demonstrate that Tacr1 neurons are instrumental in mediating CBF through the relaxation of mural cells in a similar fashion to whisker stimulation. Finally, by electron microscopy, we observe that Tacr1 processes contact astrocytic endfeet. These findings suggest that Tacr1 neurons integrate cortical activity to mediate NVC.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Acoplamiento Neurovascular Límite: Animals / Humans / Male Idioma: En Revista: Cell Rep Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Acoplamiento Neurovascular Límite: Animals / Humans / Male Idioma: En Revista: Cell Rep Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos