Affiliation:
1. University Laboratory of Physiology, Parks Road, Oxford OX1 3PT, United Kingdom
Abstract
The role of nitric oxide (NO) in the cholinergic regulation of heart rate (HR) recovery from an aspect of simulated exercise was investigated in atria isolated from guinea pig to test the hypothesis that NO may be involved in the cholinergic antagonism of the positive chronotropic response to adrenergic stimulation. Inhibition of NO synthesis with N G-monomethyl-l-arginine (l-NMMA, 100 μM) significantly slowed the time course of the reduction in HR without affecting the magnitude of the response elicited by bath-applied ACh (100 nM) or vagal nerve stimulation (2 Hz). The half-times ( t 1/2) of responses were 3.99 ± 0.41 s in control vs. 7.49 ± 0.68 s inl-NMMA ( P < 0.05). This was dependent on prior adrenergic stimulation (norepinephrine, 1 μM). The effect ofl-NMMA was reversed byl-arginine (1 mM; t 1/2 4.62 ± 0.39 s). The calcium-channel antagonist nifedipine (0.2 μM) also slowed the kinetics of the reduction in HR caused by vagal nerve stimulation. However, the t 1/2 for the reduction in HR with antagonists (2 mM Cs+ and 1 μM ZD-7288) of the hyperpolarization-activated current were significantly faster compared with control. There was no additional effect ofl-NMMA orl-NMMA+l-arginine on vagal stimulation in groups treated with nifedipine, Cs+, or ZD-7288. We conclude that NO contributes to the cholinergic antagonism of the positive cardiac chronotropic effects of adrenergic stimulation by accelerating the HR response to vagal stimulation. This may involve an interplay between two pacemaking currents (L-type calcium channel current and hyperpolarization-activated current). Whether NO modulates the vagal control of HR recovery from actual exercise remains to be determined.
Publisher
American Physiological Society
Subject
Physiology (medical),Physiology
Cited by
44 articles.
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