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水杨酰胺的肠道吸收及阿托品对其的影响。

Intestinal absorption of salicylamide and effect of atropine on it.

作者信息

Shibasaki S, Yokoyama M, Bando A, Nishigaki R, Umemura K

出版信息

J Pharmacobiodyn. 1985 Apr;8(4):296-304. doi: 10.1248/bpb1978.8.296.

Abstract

The effect of atropine (ATR), a parasynpatholytic agent, on the intestinal absorption of salicylamide (SAM) was studied using the absorption kinetic model proposed by Winne et al. The disappearance of SAM from perfusate and the appearance in intestinal blood were determined using perfused intestinal loop of the rat in vivo. The results showed that the absorption of SAM was simulated by the four compartment model consisting of luminal, interstitial, blood and serosal compartments. The model was assumed to have three rate determining factors, namely mucosal membrane permeability, clearance by blood flow and serosal membrane permeability. ATR decreased the absorption of SAM by decreasing the clearance factor relating to intestinal blood flow and increased the fraction of the transported amount of SAM from interstitial space to serosal compartment.

摘要

使用温内等人提出的吸收动力学模型,研究了抗胆碱药阿托品(ATR)对水杨酰胺(SAM)肠道吸收的影响。通过在体大鼠肠袢灌注法,测定了灌注液中SAM的消失情况以及肠血中SAM的出现情况。结果表明,SAM的吸收可用由管腔、间质、血液和浆膜腔室组成的四室模型来模拟。该模型假定有三个速率决定因素,即粘膜膜通透性、血流清除率和浆膜膜通透性。ATR通过降低与肠血流量相关的清除率来减少SAM的吸收,并增加了SAM从间质空间转运至浆膜腔室的转运量比例。

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