Yanagisawa K, Yang H, Walsh J H, Taché Y
Center for Ulcer Research and Education, Veterans' Administration Medical Center, Los Angeles, CA 90073.
Regul Pept. 1990 Feb 4;27(2):161-70. doi: 10.1016/0167-0115(90)90036-v.
The role of gastrin, acetylcholine and histamine in the acid response to central vagal activation induced by intracisternal injection of the stable analog, RX 77368, was further investigated in urethane-anesthetized rats with gastric fistula. The gastrin monoclonal antibody 28-2 injected intravenously, at a dose previously shown to prevent gastrin-induced stimulation of acid secretion, did not alter the peak acid response to intracisternal injection of RX 77368 (15 ng). The TRH analog (30 ng) injected into the cisterna magna increased levels of histamine measured in the hepatic portal blood. Cimetidine administered at a dose which completely blocked the stimulation of gastric acid secretion produced by intravenous infusion of histamine, inhibited by 62% the stimulatory effect of intracisternal RX 77368 (30 ng). The M1 muscarinic antagonist, pirenzepine, completely prevented the acid secretion induced by intracisternal RX 77368 (30 ng). These results indicate that the acid response to central vagal activation by the TRH analog in rats involved M1 muscarinic receptors along with histamine release acting on H2 histaminergic receptors whereas gastrin does not appear to play an important role.
在有胃瘘的氨基甲酸乙酯麻醉大鼠中,进一步研究了胃泌素、乙酰胆碱和组胺在对脑池内注射稳定类似物RX 77368诱导的中枢迷走神经激活的酸反应中的作用。静脉注射胃泌素单克隆抗体28-2,其剂量先前已证明可预防胃泌素诱导的胃酸分泌刺激,但并未改变对脑池内注射RX 77368(15纳克)的酸反应峰值。向脑池内注射促甲状腺激素释放激素类似物(30纳克)可提高肝门静脉血中组胺的水平。以完全阻断静脉输注组胺产生的胃酸分泌刺激的剂量给予西咪替丁,可抑制脑池内RX 77368(30纳克)的刺激作用62%。M1毒蕈碱拮抗剂哌仑西平完全阻止了脑池内RX 77368(30纳克)诱导的胃酸分泌。这些结果表明,大鼠中促甲状腺激素释放激素类似物对中枢迷走神经激活的酸反应涉及M1毒蕈碱受体以及作用于H2组胺能受体的组胺释放,而胃泌素似乎并未发挥重要作用。