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向大鼠迷走神经背侧复合体微量注射蛙皮素可抑制迷走神经刺激引起的胃酸分泌。

Bombesin microinjected into the dorsal vagal complex inhibits vagally stimulated gastric acid secretion in the rat.

作者信息

Ishikawa T, Taché Y

机构信息

Center for Ulcer Research and Education, Veterans' Administration Medical Center, Los Angeles, CA 90073.

出版信息

Regul Pept. 1989 Feb;24(2):187-94. doi: 10.1016/0167-0115(89)90237-1.

Abstract

Medullary sites of action for bombesin-induced inhibition of gastric acid secretion were investigated in urethane-anesthetized rats with gastric fistula. Unilateral microinjection of bombesin or vehicle into the dorsal vagal complex was performed using a glass micropipet and pressure ejection of 100 nl volume; gastric acid output was measured every 10 min by flushing the stomach. Microinjection of vehicle into the dorsal vagal complex did not alter gastric acid secretion (1.9 +/- mumol/10) from preinjection levels (2.9 +/- 0.8 mumol/10 min). Microinjection of the stable thyrotropin-releasing hormone (TRH) analog, RX 77368, at a 77 pmol dose into the dorsal vagal complex stimulated gastric acid secretion for 100 min with a peak response at 40 min (24.1 +/- 3.2 mumol/10 min). Concomitant microinjection of RX 77368 (77 pmol) with bombesin (0.6-6.2 pmol) into the dorsal vagal complex dose dependently inhibited by 35-86% the gastric acid response to the TRH analog. Bombesin (6.2 pmol) microinjected into the dorsal vagal complex inhibited by 17% pentagastrin infusion-induced stimulation of gastric acid secretion (13.2 +/- 0.8 mumol/10 min) whereas intracisternal injection induced a 69% inhibition of the pentagastrin response. These results demonstrate that the dorsal motor complex is a sensitive site of action for bombesin-induced inhibition of vagally stimulated gastric secretion. However, other medullary sites must be involved in mediating the inhibitory effect of intracisternal bombesin on pentagastrin-stimulated gastric acid secretion.

摘要

在具有胃瘘的氨基甲酸乙酯麻醉大鼠中,研究了蛙皮素诱导胃酸分泌抑制作用的延髓作用部位。使用玻璃微量移液器并以100 nl的体积压力喷射,将蛙皮素或赋形剂单侧微量注射到迷走神经背核复合体中;每10分钟通过冲洗胃来测量胃酸分泌量。向迷走神经背核复合体中微量注射赋形剂不会改变胃酸分泌(1.9±μmol/10),与注射前水平(2.9±0.8 μmol/10分钟)相比无变化。以77 pmol的剂量向迷走神经背核复合体中微量注射稳定的促甲状腺激素释放激素(TRH)类似物RX 77368,可刺激胃酸分泌100分钟,在40分钟时达到峰值反应(24.1±3.2 μmol/10分钟)。将RX 77368(77 pmol)与蛙皮素(0.6 - 6.2 pmol)同时向迷走神经背核复合体中微量注射,可使对TRH类似物的胃酸反应剂量依赖性地抑制35 - 86%。向迷走神经背核复合体中微量注射蛙皮素(6.2 pmol)可使五肽胃泌素输注诱导的胃酸分泌刺激作用抑制17%(13.2±0.8 μmol/10分钟),而脑池内注射则可使五肽胃泌素反应抑制69%。这些结果表明,迷走神经背核复合体是蛙皮素诱导的迷走神经刺激胃酸分泌抑制作用的敏感作用部位。然而,其他延髓部位必定参与介导脑池内蛙皮素对五肽胃泌素刺激胃酸分泌的抑制作用。

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