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      Acute exercise enhances receptor-mediated endothelium-dependent vasodilation by receptor upregulation.

      Journal of Biomedical Science
      Acetylcholine, pharmacology, Adrenergic alpha-Agonists, analysis, metabolism, Animals, Clonidine, Endothelium, Vascular, drug effects, physiology, In Vitro Techniques, Male, Muscarinic Antagonists, Physical Conditioning, Animal, Piperidines, Rats, Rats, Wistar, Receptor, Muscarinic M3, Receptors, Adrenergic, alpha-2, Receptors, Muscarinic, Thoracic Arteries, Tritium, Up-Regulation, Vasodilation

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          Abstract

          The effects of acute exercise on receptor-mediated endothelium-dependent vasodilation and its possible mechanisms were investigated in the presence of indomethacin. Male Wistar rats (16-20 weeks old) were divided into control and exercise groups. The exercise group ran on a drum exerciser until exhaustion, followed by immediate decapitation. Acetylcholine (ACh)- or clonidine (CLO)-induced vasodilating responses in thoracic aortae of the control and exercise groups were compared. Receptor-binding assays were performed to determine whether there were any upregulations of endothelial receptors after acute exercise. Our results indicated that acute exercise induced the following effects: (1) the dose-response curves of ACh and CLO shifted to the left; (2) the high-affinity M3 binding sites increased in number but not in affinity; (3) the alpha2 binding sites decreased in number but increased in affinity. We conclude that acute exercise enhances receptor-mediated vasodilation responses, at least in part, by regulating either endothelial receptor number or receptor affinity.

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