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巴氯芬在大鼠胃中与体温相关的作用。与胃酸分泌及致溃疡作用的关系。

Body temperature-dependent action of baclofen in rat stomach. Relation to acid secretion and ulcerogenicity.

作者信息

Takeuchi K, Nishiwaki H, Niida H, Okabe S

机构信息

Department of Applied Pharmacology, Kyoto Pharmaceutical University, Japan.

出版信息

Dig Dis Sci. 1990 Apr;35(4):458-66. doi: 10.1007/BF01536920.

Abstract

The effect of baclofen (PCPGABA) on acid secretion, motility, and mucosa was investigated in the anesthetized rat stomach under various body temperatures (BT: 28-38 degrees C), and they were compared with those of 2-deoxy-D-glucose (2DG), an acid stimulant through cytoglycopenia. Under these conditions PCPGABA induces lesions dose-dependently (greater than 1 mg/kg, subcutaneously) in both the stomach and duodenum, and this action was dependent on BT; lowering of BT enhanced the ulcerogenicity. PCPGABA (3 mg/kg) had no effect on acid secretion at higher BT (36-38 degrees C) but produced a marked increase of acid output at lower BT (30-32 degrees C). 2DG caused a stimulation of acid output and gastric lesions without BT dependency, but the duodenal ulcerogenicity enhanced at lower BT. Gastric motility was enhanced significantly by these two agents to similar degrees, at either high or low BT. Neither PCPGABA nor 2DG affected alkaline secretion in the duodenum, while lowering of BT by itself reduced alkaline secretory responses. The above changes caused by PCPGABA and 2DG were blocked by both atropine and vagotomy. These results suggest that (1) acid stimulatory and ulcerogenic action of PCPGABA may involve a temperature-dependent process but does not relate to a cytoglycopenia, and (2) the vagus nerve mediating acid secretion and motility may be different in the temperature dependency.

摘要

在不同体温(BT:28 - 38摄氏度)下,研究了巴氯芬(PCPGABA)对麻醉大鼠胃内酸分泌、运动及黏膜的影响,并与通过细胞糖原减少起作用的酸刺激剂2 - 脱氧 - D - 葡萄糖(2DG)的作用进行了比较。在这些条件下,PCPGABA在胃和十二指肠中均剂量依赖性地诱导损伤(大于1mg/kg,皮下注射),且该作用依赖于体温;体温降低会增强致溃疡作用。PCPGABA(3mg/kg)在较高体温(36 - 38摄氏度)时对酸分泌无影响,但在较低体温(30 - 32摄氏度)时会使酸分泌显著增加。2DG可刺激酸分泌并导致胃损伤,且不依赖于体温,但在较低体温时十二指肠致溃疡作用增强。这两种药物在高体温或低体温时均能显著增强胃运动,程度相似。PCPGABA和2DG均不影响十二指肠的碱性分泌,而体温降低本身会减少碱性分泌反应。PCPGABA和2DG引起的上述变化均可被阿托品和迷走神经切断术阻断。这些结果表明:(1)PCPGABA的酸刺激和致溃疡作用可能涉及温度依赖性过程,但与细胞糖原减少无关;(2)介导酸分泌和运动的迷走神经在温度依赖性方面可能有所不同。

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