Taub M, Bonorris G, Chung A, Coyne M J, Schoenfield L J
Gastroenterology. 1977 Jan;72(1):101-5.
Stimulation of net secretion by deoxycholic acid (DCA) in the colon and by cholera enterotoxin (CE) in the jejunum is mediated by cAMP. Propranolol (Pr) inhibits adenylate cyclase (AC) activity and net secretion induced by bile acid in the colon. The aim of this study was to assess the organ specificity of DCA and CE as well as the selectivity of Pr inhibition. Three colonic and three jejunal loops were prepared in each of 8 rabbits treated intravenously with Pr, 4 mg per kg, 1/2 hr before loop construction and in each of 10 untreated control rabbits. One milliliter of DCA, 6 mM, CE, 10 mug per ml, or heat-inactivated CE or 0.9% NaCl, as basal controls were injected in random order into each of the loops. The volume of luminal fluid and mucosal AC were measured in each intestinal loop 5 hr later. DCA in the colon stimulated AC 2-fold (P less than 0.01) and luminal fluid 15-fold (P less than 0.01). CE in the jejunum stimulated AC 2.3-fold (P less than 0.01) and luminal fluid 9-fold (P less that 0.01). No significant effects on volume or AC occurred in response to CE in the colon or to DCA in the jejunum. Pr pretreatment completely prevented the stimulation of AC and luminal fluid by DCA in the colon but did not affect the action of CE in the jejunum of the same animals. Thus, DCA and CE are organ-specific stimulants of cAMP systems, and Pr is a selective inhibitor of certain inducers of cAMP and net secretion.
脱氧胆酸(DCA)在结肠中以及霍乱肠毒素(CE)在空肠中对净分泌的刺激是由环磷酸腺苷(cAMP)介导的。普萘洛尔(Pr)抑制腺苷酸环化酶(AC)活性以及胆汁酸在结肠中诱导的净分泌。本研究的目的是评估DCA和CE的器官特异性以及Pr抑制的选择性。在8只静脉注射Pr(每千克4毫克,在构建肠袢前半小时注射)的兔子和10只未处理的对照兔子中,每只兔子均制备3个结肠肠袢和3个空肠肠袢。将1毫升6毫摩尔的DCA、每毫升10微克的CE、热灭活的CE或作为基础对照的0.9%氯化钠随机注射到每个肠袢中。5小时后测量每个肠袢中的肠腔液体积和黏膜AC。结肠中的DCA使AC增加2倍(P<0.01),使肠腔液增加15倍(P<0.01)。空肠中的CE使AC增加2.3倍(P<0.01),使肠腔液增加9倍(P<0.01)。结肠中对CE或空肠中对DCA的反应对体积或AC无显著影响。Pr预处理完全阻止了结肠中DCA对AC和肠腔液的刺激,但不影响同一动物空肠中CE的作用。因此,DCA和CE是cAMP系统的器官特异性刺激物,而Pr是cAMP和净分泌某些诱导剂的选择性抑制剂。