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Exercise induces cerebral VEGF and angiogenesis via the lactate receptor HCAR1

Physical exercise can improve brain function and delay neurodegeneration; however, the initial signal from muscle to brain is unknown. Here we show that the lactate receptor (HCAR1) is highly enriched in pial fibroblast-like cells that line the vessels supplying blood to the brain, and in pericyte-l...

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Detalles Bibliográficos
Autores principales: Morland, Cecilie, Andersson, Krister A., Haugen, Øyvind P., Hadzic, Alena, Kleppa, Liv, Gille, Andreas, Rinholm, Johanne E., Palibrk, Vuk, Diget, Elisabeth H., Kennedy, Lauritz H., Stølen, Tomas, Hennestad, Eivind, Moldestad, Olve, Cai, Yiqing, Puchades, Maja, Offermanns, Stefan, Vervaeke, Koen, Bjørås, Magnar, Wisløff, Ulrik, Storm-Mathisen, Jon, Bergersen, Linda H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457513/
https://www.ncbi.nlm.nih.gov/pubmed/28534495
http://dx.doi.org/10.1038/ncomms15557
Descripción
Sumario:Physical exercise can improve brain function and delay neurodegeneration; however, the initial signal from muscle to brain is unknown. Here we show that the lactate receptor (HCAR1) is highly enriched in pial fibroblast-like cells that line the vessels supplying blood to the brain, and in pericyte-like cells along intracerebral microvessels. Activation of HCAR1 enhances cerebral vascular endothelial growth factor A (VEGFA) and cerebral angiogenesis. High-intensity interval exercise (5 days weekly for 7 weeks), as well as L-lactate subcutaneous injection that leads to an increase in blood lactate levels similar to exercise, increases brain VEGFA protein and capillary density in wild-type mice, but not in knockout mice lacking HCAR1. In contrast, skeletal muscle shows no vascular HCAR1 expression and no HCAR1-dependent change in vascularization induced by exercise or lactate. Thus, we demonstrate that a substance released by exercising skeletal muscle induces supportive effects in brain through an identified receptor.