Long-range inhibitory neurons mediate cortical neurovascular coupling

Cell Rep. 2024 Apr 23;43(4):113970. doi: 10.1016/j.celrep.2024.113970. Epub 2024 Mar 19.

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.

Keywords: CP: Cell biology; CP: Neuroscience; cerebral blood flow; hemodynamics; pericytes; somatostatin; tachykinin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cerebral Cortex / blood supply
  • Cerebral Cortex / physiology
  • Cerebrovascular Circulation / physiology
  • GABAergic Neurons / metabolism
  • GABAergic Neurons / physiology
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / metabolism
  • Neurons / physiology
  • Neurovascular Coupling* / physiology
  • Nitric Oxide Synthase Type I / metabolism
  • Vibrissae / physiology

Substances

  • Nitric Oxide Synthase Type I