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生长抑素类似物SMS 201-995刺激大鼠胃酸分泌的中枢作用。

Central action of somatostatin analog, SMS 201-995, to stimulate gastric acid secretion in rats.

作者信息

Yoneda M, Raybould H, Taché Y

机构信息

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

出版信息

Peptides. 1991 May-Jun;12(3):401-6. doi: 10.1016/0196-9781(91)90076-2.

Abstract

The effects of intracisternal and intravenous injections of the somatostatin analog, SMS 201-995, on gastric acid secretion were investigated in rats with pylorus ligation or gastric cannula. Intracisternal injection of SMS 201-995 induced a dose-related (0.1-0.3 microgram) and long-lasting stimulation of gastric acid output with a peak response at 3 h postinjection in conscious, pylorus-ligated rats. Intracisternal SMS 201-995 increased histamine levels in the portal blood, whereas plasma gastrin levels were not modified. Atropine, cimetidine and adrenalectomy abolished the stimulatory effect of intracisternal SMS 201-995 (0.3 microgram). SMS 201-995 (0.03 microgram), microinjected unilaterally into the dorsal vagal complex, increased gastric acid output in urethane anesthetized rats. SMS 201-995, injected intravenously at 0.5 microgram, did not alter gastric secretion, whereas higher doses (5-20 micrograms) resulted in a dose-related inhibition of gastric acid secretion in conscious pylorus-ligated rats. These data indicate that SMS 201-995, a selective ligand for somatostatin-1 receptor subtype, induces a centrally mediated stimulatory effect on gastric acid secretion in rats. The central action involves the parasympathetic system, muscarinic and H2 receptors as well as adrenal-dependent pathways.

摘要

在幽门结扎或胃插管的大鼠中,研究了脑池内和静脉注射生长抑素类似物SMS 201-995对胃酸分泌的影响。在清醒的幽门结扎大鼠中,脑池内注射SMS 201-995可诱导剂量相关(0.1-0.3微克)且持久的胃酸分泌刺激,注射后3小时出现峰值反应。脑池内注射SMS 201-995可使门静脉血中组胺水平升高,而血浆胃泌素水平未改变。阿托品、西咪替丁和肾上腺切除术可消除脑池内注射SMS 201-995(0.3微克)的刺激作用。在乌拉坦麻醉的大鼠中,单侧微量注射到背侧迷走神经复合体中的SMS 201-995(0.03微克)可增加胃酸分泌。静脉注射0.5微克的SMS 201-995不会改变胃液分泌,而更高剂量(5-20微克)会导致清醒的幽门结扎大鼠胃酸分泌出现剂量相关的抑制。这些数据表明,SMS 201-995是生长抑素-1受体亚型的选择性配体,可诱导对大鼠胃酸分泌的中枢介导的刺激作用。中枢作用涉及副交感神经系统、毒蕈碱和H2受体以及肾上腺依赖途径。

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