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Nat Commun ; 8: 15557, 2017 05 23.
Article in English | MEDLINE | ID: mdl-28534495

ABSTRACT

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.


Subject(s)
Brain/blood supply , Neovascularization, Physiologic/physiology , Physical Conditioning, Animal/physiology , Receptors, G-Protein-Coupled/metabolism , Vascular Endothelial Growth Factor A/metabolism , Animals , Capillaries/cytology , Capillaries/drug effects , Capillaries/metabolism , Injections, Subcutaneous , Lactic Acid/administration & dosage , Lactic Acid/blood , Lactic Acid/metabolism , Male , Mice , Mice, Knockout , Models, Animal , Muscle, Skeletal/blood supply , Muscle, Skeletal/drug effects , Muscle, Skeletal/metabolism , Pericytes/metabolism , Receptors, G-Protein-Coupled/genetics
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