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阿托品对人体促胰液素作用及释放的影响。

Effects of atropine on the action and release of secretin in humans.

作者信息

You C H, Rominger J M, Chey W Y

出版信息

Am J Physiol. 1982 Jun;242(6):G608-11. doi: 10.1152/ajpgi.1982.242.6.G608.

Abstract

Using two groups of volunteers, we investigated the effects of atropine on pancreatic secretion of bicarbonate, protein, and trypsin stimulated by secretin. Secretin given intravenously in graded doses of 0.03, 0.06, and 0.125 clinical units.kg-1.h-1 produced significant increases in pancreatic secretion of bicarbonate in a dose-related manner. Pancreatic secretion of bicarbonate and protein was significantly suppressed by intravenous atropine, despite the dose of secretin infused. Intrajejunal perfusion of HCl at a rate of 3.3 mM/h, producing plasma secretin concentration comparable with that of the postprandial state, resulted in significant increases in the pancreatic secretion of bicarbonate. The increase in the pancreatic secretion of bicarbonate and trypsin was significantly suppressed by atropine. However, atropine did not affect the increase in the plasma secretin concentration produced by jejunal acidification or intravenous secretin. These studies indicate that atropine inhibits the pancreatic effect but not the intestinal release of secretin.

摘要

我们使用两组志愿者,研究了阿托品对促胰液素刺激的胰腺碳酸氢盐、蛋白质和胰蛋白酶分泌的影响。以0.03、0.06和0.125临床单位·千克⁻¹·小时⁻¹的分级剂量静脉注射促胰液素,可使胰腺碳酸氢盐分泌呈剂量依赖性显著增加。尽管输注了促胰液素,但静脉注射阿托品可显著抑制胰腺碳酸氢盐和蛋白质的分泌。以3.3 mM/h的速率空肠内灌注盐酸,使血浆促胰液素浓度达到与餐后状态相当的水平,可导致胰腺碳酸氢盐分泌显著增加。阿托品可显著抑制胰腺碳酸氢盐和胰蛋白酶分泌的增加。然而,阿托品并不影响空肠酸化或静脉注射促胰液素所引起的血浆促胰液素浓度升高。这些研究表明,阿托品抑制胰腺效应,但不影响促胰液素的肠道释放。

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