Hasebe K, Horie S, Komasaka M, Yano S, Watanabe K
Laboratory of Chemical Pharmacology, Department of Drug Evaluation and Toxicological Sciences, Faculty of Pharmaceutical Sciences, Chiba University, 263-8522, Chiba, Japan.
Eur J Pharmacol. 2001 May 25;420(2-3):159-64. doi: 10.1016/s0014-2999(01)00995-5.
We previously reported on the stimulatory role of endogenous nitric oxide (NO) in gastric acid secretion. In the present study, we investigated the effects of NO donors on acid secretion in isolated mouse stomach. Nitroprusside (100 microM(-1) x mM) inhibited the gastric acid secretion induced by histamine (500 microM) in a concentration-dependent manner. In addition, nitroprusside abolished the acid secretion induced by bethanechol (100 microM) and by electrical stimulation (10 Hz) of the vagus nerve. On the other hand, nitroprusside, 75 microM, which did not affect the acid secretion induced by histamine, itself elicited an increase in acid secretion. The acid secretion induced by 75 microM nitroprusside was inhibited by 10 microM famotidine, a histamine H2 receptor antagonist. These results suggest that NO donors at high doses act on gastric parietal cells, resulting in inhibition of the stimulated acid secretion, and, at lower doses, facilitate histamine release from histamine-containing cells, leading to the increased acid secretion.
我们之前报道了内源性一氧化氮(NO)在胃酸分泌中的刺激作用。在本研究中,我们研究了NO供体对离体小鼠胃中酸分泌的影响。硝普钠(100微摩尔/升×毫摩尔)以浓度依赖的方式抑制组胺(500微摩尔)诱导的胃酸分泌。此外,硝普钠消除了氨甲酰甲胆碱(100微摩尔)和迷走神经电刺激(10赫兹)诱导的酸分泌。另一方面,75微摩尔的硝普钠本身引起酸分泌增加,而该浓度的硝普钠不影响组胺诱导的酸分泌。75微摩尔硝普钠诱导的酸分泌被10微摩尔法莫替丁(一种组胺H2受体拮抗剂)抑制。这些结果表明,高剂量的NO供体作用于胃壁细胞,导致刺激的酸分泌受到抑制,而低剂量时则促进含组胺细胞释放组胺,从而导致酸分泌增加。