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β-肾上腺素能机制与幽门结扎大鼠溃疡形成

Beta-adrenergic mechanisms and ulcer formation in pylorus-ligated rats.

作者信息

Christensen K C, Stadil F, Hermansen K

出版信息

Scand J Gastroenterol. 1975;10(7):715-20.

PMID:1188304
Abstract

The importance of beta-adrenergic receptor activity for ulcer formation was studied. In rats fasted for 48 hours, ulcers in the rumen were produced constantly after 17 hours of pyloric ligation. d,1,Propranolol in doses of 1 to 30 mg/kg given 4 times during 12 hours caused a dose-dependent inhibition of ulcer formation. The ulcero-protective potency of d,1,propranolol was about 20 times that of d,propranolol. No explanation of the ulcero-protective effect was observed when the gastric acid secretion was studied after 17 hours. Serum gastrin concentration after 17 hours of ligation was in all animals less than 5 pmol per liter, i.e. below one-third of the normal fasting value. For all pharmacological effects apart from beta-adrenergic blockage, d,1, and d,propranolol do not differ, while the results presented here suggest that intact beta-adrenergic receptor activity is important for the development of gastric ulcers in the pylorus-ligated rat. The mechanism behind the ulcero-protective effect of beta-adrenergic blockage remains to be solved.

摘要

研究了β-肾上腺素能受体活性对溃疡形成的重要性。在禁食48小时的大鼠中,幽门结扎17小时后瘤胃中持续产生溃疡。在12小时内分4次给予剂量为1至30mg/kg的消旋普萘洛尔,可引起剂量依赖性的溃疡形成抑制。消旋普萘洛尔的溃疡保护效力约为右旋普萘洛尔的20倍。在17小时后研究胃酸分泌时,未观察到溃疡保护作用的解释。结扎17小时后所有动物的血清胃泌素浓度均低于每升5pmol,即低于正常空腹值的三分之一。除β-肾上腺素能阻断外,消旋普萘洛尔和右旋普萘洛尔的所有药理作用均无差异,而此处呈现的结果表明完整的β-肾上腺素能受体活性对幽门结扎大鼠胃溃疡的发展很重要。β-肾上腺素能阻断的溃疡保护作用背后的机制仍有待解决。

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