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Vasculo-Neuronal Coupling: Retrograde Vascular Communication to Brain Neurons.
- Source :
-
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2016 Dec 14; Vol. 36 (50), pp. 12624-12639. Date of Electronic Publication: 2016 Nov 07. - Publication Year :
- 2016
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Abstract
- Continuous cerebral blood flow is essential for neuronal survival, but whether vascular tone influences resting neuronal function is not known. Using a multidisciplinary approach in both rat and mice brain slices, we determined whether flow/pressure-evoked increases or decreases in parenchymal arteriole vascular tone, which result in arteriole constriction and dilation, respectively, altered resting cortical pyramidal neuron activity. We present evidence for intercellular communication in the brain involving a flow of information from vessel to astrocyte to neuron, a direction opposite to that of classic neurovascular coupling and referred to here as vasculo-neuronal coupling (VNC). Flow/pressure increases within parenchymal arterioles increased vascular tone and simultaneously decreased resting pyramidal neuron firing activity. On the other hand, flow/pressure decreases evoke parenchymal arteriole dilation and increased resting pyramidal neuron firing activity. In GLAST-CreERT2; R26-lsl-GCaMP3 mice, we demonstrate that increased parenchymal arteriole tone significantly increased intracellular calcium in perivascular astrocyte processes, the onset of astrocyte calcium changes preceded the inhibition of cortical pyramidal neuronal firing activity. During increases in parenchymal arteriole tone, the pyramidal neuron response was unaffected by blockers of nitric oxide, GABA <subscript>A</subscript> , glutamate, or ecto-ATPase. However, VNC was abrogated by TRPV4 channel, GABA <subscript>B</subscript> , as well as an adenosine A <subscript>1</subscript> receptor blocker. Differently to pyramidal neuron responses, increases in flow/pressure within parenchymal arterioles increased the firing activity of a subtype of interneuron. Together, these data suggest that VNC is a complex constitutive active process that enables neurons to efficiently adjust their resting activity according to brain perfusion levels, thus safeguarding cellular homeostasis by preventing mismatches between energy supply and demand.<br />Significance Statement: We present evidence for vessel-to-neuron communication in the brain slice defined here as vasculo-neuronal coupling. We showed that, in response to increases in parenchymal arteriole tone, astrocyte intracellular Ca <superscript>2+</superscript> increased and cortical neuronal activity decreased. On the other hand, decreasing parenchymal arteriole tone increased resting cortical pyramidal neuron activity. Vasculo-neuronal coupling was partly mediated by TRPV4 channels as genetic ablation, or pharmacological blockade impaired increased flow/pressure-evoked neuronal inhibition. Increased flow/pressure-evoked neuronal inhibition was blocked in the presence of adenosine A1 receptor and GABA <subscript>B</subscript> receptor blockade. Results provide evidence for the concept of vasculo-neuronal coupling and highlight the importance of understanding the interplay between basal CBF and resting neuronal activity.<br /> (Copyright © 2016 the authors 0270-6474/16/3612624-16$15.00/0.)
- Subjects :
- Animals
Arterioles innervation
Arterioles physiology
Astrocytes physiology
Blood Vessels drug effects
Brain cytology
Calcium metabolism
Cell Communication drug effects
Cerebrovascular Circulation drug effects
Cerebrovascular Circulation physiology
Excitatory Amino Acid Transporter 1 genetics
Excitatory Amino Acid Transporter 1 physiology
In Vitro Techniques
Mice
Mice, Inbred C57BL
Muscle, Smooth, Vascular physiology
Neurons drug effects
Pyramidal Cells physiology
TRPV Cation Channels genetics
TRPV Cation Channels physiology
Blood Vessels innervation
Brain physiology
Cell Communication physiology
Neurons physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2401
- Volume :
- 36
- Issue :
- 50
- Database :
- MEDLINE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 27821575
- Full Text :
- https://doi.org/10.1523/JNEUROSCI.1300-16.2016