Endogenous muscarinic acetylcholine receptor signaling blunts α(1)-adrenergic vasoconstriction during higher-intensity handgrip exercise in humans

内源性毒蕈碱乙酰胆碱受体信号传导可减弱人体高强度握力运动期间的α(1)-肾上腺素能血管收缩。

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Abstract

Muscarinic acetylcholine receptors (mAChRs) are expressed ubiquitously in the human skeletal muscle vasculature. Prior studies have been unable to identify a contribution of mAChR signaling to exercise-mediated vasodilation; however, no studies have determined whether endogenous mAChR signaling regulates the ability of contracting skeletal muscle to attenuate sympathetic vasoconstriction, a phenomenon called "functional sympatholysis." We tested the hypothesis that endogenous mAChR signaling contributes to functional sympatholysis in humans. In healthy volunteers (8 F, 8 M; 26 ± 5 yr), changes in forearm vascular conductance (ΔFVC) were calculated in response to intra-arterial infusions of phenylephrine (PE; α(1)-agonist) during 1) infusion of a "nonmetabolic" vasodilator at rest (rest; adenosine or sodium nitroprusside), 2) dynamic handgrip exercise at 15% maximal voluntary contraction (MVC), and 3) higher-intensity exercise (25% MVC). Conditions were completed before and after intra-arterial infusion of atropine (mAChR antagonist). Under control conditions, vasoconstriction to PE was limited in parallel with exercise intensity (PE-induced %ΔFVC, rest: -40 ± 13%, 15% MVC: -20 ± 7%, 25% MVC: -12 ± 8%; P < 0.0001). There was no effect of atropine on PE vasoconstriction during rest (-38 ± 12%; P = 0.60 vs. control) or 15% MVC exercise (-23 ± 7%, P = 0.34 vs. control). However, PE-mediated vasoconstriction was approximately twofold greater during 25% MVC exercise after blockade of mAChRs (-22 ± 9%, P < 0.001 vs. control). These results provide evidence of a novel physiological role of endogenous mAChR signaling as a modulator of α(1)-adrenergic vasoconstriction during higher-intensity handgrip exercise in humans.NEW & NOTEWORTHY The present study demonstrates that muscarinic acetylcholine receptor (mAChR) signaling attenuates postjunctional α(1)-adrenergic signaling during higher-intensity exercise specifically within contracting skeletal muscle, thereby revealing endogenous mAChR signaling as a potential mechanism of functional sympatholysis. This is the first study to identify an endogenous signaling pathway that selectively modulates α(1)-adrenergic vasoconstriction specifically in contracting muscle in humans. These findings establish a novel physiological role for endogenous mAChR signaling in the regulation of muscle blood flow during exercise.

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