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脑池内促甲状腺激素释放激素类似物RX 77368刺激大鼠胃组胺释放。

Intracisternal TRH analogue RX 77368 stimulates gastric histamine release in rats.

作者信息

Yanagisawa K, Taché Y

机构信息

Center for Ulcer Research and Education, Veterans Administration Medical Center, Los Angeles, California.

出版信息

Am J Physiol. 1990 Oct;259(4 Pt 1):G599-604. doi: 10.1152/ajpgi.1990.259.4.G599.

Abstract

The influence of intracisternal injection of the stable thyrotropin-releasing hormone (TRH) analogue RX 77368 on histamine levels in gastric secretion, interstitial fluid of the fundic submucosa, and portal hepatic circulation was investigated in rats. Intracisternal injection of RX 77368 (10-300 ng) induced a dose-related increase in histamine and acid output measured in the gastric secretion of pylorus-ligated, conscious rats. Intracisternal RX 77368 (300 ng) induced within 20 min a significant twofold histamine increase in interstitial fluid sampled from dialysis fibers implanted into the fundic submucosa. Histamine levels in the hepatic portal circulation were also dose dependently increased by RX 77368 injected intracisternally (30-100 ng), whereas intravenous infusion of RX 77368 (300 ng/30 min) did not significantly modify portal histamine levels. Bilateral cervical vagotomy or atropine pretreatment prevented intracisternal RX 77368-induced rise in hepatic portal levels of histamine, whereas purified gastrin monoclonal antibody 9303, injected at a dose blocking gastrin-stimulated acid secretion, had no effect. These results indicate that RX 77368 acts in the brain to increase gastric histamine secretion through vagal-dependent, muscarinic, nongastrin-mediated mechanisms and suggest a possible role of medullary TRH in the vagal regulation of gastric histamine secretion.

摘要

在大鼠中研究了脑池内注射稳定的促甲状腺激素释放激素(TRH)类似物RX 77368对胃分泌、胃底黏膜下层组织液和肝门静脉循环中组胺水平的影响。脑池内注射RX 77368(10 - 300 ng)可使幽门结扎的清醒大鼠胃分泌中测得的组胺和酸分泌量呈剂量依赖性增加。脑池内注射RX 77368(300 ng)在20分钟内可使从植入胃底黏膜下层的透析纤维采集的组织液中的组胺显著增加两倍。脑池内注射RX 77368(30 - 100 ng)也可使肝门静脉循环中的组胺水平呈剂量依赖性增加,而静脉输注RX 77368(300 ng/30分钟)对门静脉组胺水平无显著影响。双侧颈迷走神经切断术或阿托品预处理可阻止脑池内注射RX 77368引起肝门静脉组胺水平升高,而以阻断胃泌素刺激的酸分泌剂量注射的纯化胃泌素单克隆抗体9303则无作用。这些结果表明,RX 77368在脑中通过迷走神经依赖性、毒蕈碱能、非胃泌素介导的机制增加胃组胺分泌,并提示延髓TRH在迷走神经对胃组胺分泌的调节中可能起作用。

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