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. 1994 Jul;112(3):831–836. doi: 10.1111/j.1476-5381.1994.tb13154.x

Contribution of both nitric oxide and a change in membrane potential to acetylcholine-induced relaxation in the rat small mesenteric artery.

G J Waldron 1, C J Garland 1
PMCID: PMC1910178  PMID: 7921609

Abstract

1. Acetylcholine stimulated repolarization and relaxation in isolated segments of rat small mesenteric artery (D100 = 325 +/- 9 microns) in which the smooth muscle cells were depolarized and contracted by submaximal concentrations of noradrenaline (0.75-2.5 microM). There was no significant difference either in the time taken to initiate relaxation or hyperpolarization, or for these parameters to reach maximum in response to acetylcholine. 2. The nitric oxide synthase inhibitor, NG-nitro L-arginine methyl ester (L-NAME, 100 microM) reduced the pD2 for acetylcholine-induced relaxation from 7.5 to 7 and depressed the maximum relaxation from 89% to 68% in tissues stimulated with noradrenaline. The pD2 for smooth muscle repolarization in these experiments was also reduced (7.4 to 6.6) but the maximum change in membrane potential in response to acetylcholine was unaltered. The increase in potential now clearly preceded relaxation by 3.7 s (to initiation) and 4.7 s (to maximum). 3. In the presence of noradrenaline and a raised potassium concentration (25 mM), the repolarization to acetylcholine was markedly attenuated. Simultaneous tension measurements also revealed a marked reduction in the maximal relaxation to acetylcholine, but the pD2 was unchanged at 7.4. 4. The residual relaxation recorded in the absence of marked repolarization (in the presence of noradrenaline and 25 mM potassium) was abolished by the addition of 100 microM L-NAME. 5. Nitric oxide gas in solution (0.2-2.2 microM; NOg) relaxed artery segments precontracted with noradrenaline. The magnitude of relaxation to NOg was not altered in the presence of noradrenaline and 25 mM potassium.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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