Stein J, Zeuzem S, Uphoff K, Laube H
Department of Internal Medicine, Johann-Wolfgang-Goethe-University, Frankfurt 70, Germany.
Prostaglandins. 1994 Jan;47(1):31-40. doi: 10.1016/0090-6980(94)90072-8.
Prostaglandins have been shown to stimulate contraction of gastrointestinal smooth muscle in vitro, and their synthesis has been reported in different gastrointestinal diseases. The aim of this study was to determine the different effects of PGs and indomethacin on gastric emptying in the rat in vivo, and to investigate their possible role as modulators of osmolarity induced changes in gastric emptying. Rats were fed via gastric tube with suspensions of various osmolarity containing different prostaglandins or indomethacin. Gastric emptying, measured by the quantity of food remaining in the stomach, was studied by a noninvasive technique using orally administered nonabsorbable marker 141Cerium. PGE2 given orally and its synthetic analogue 16-16-dimethyl PGE2 given subcutaneously caused significant delay of gastric emptying, while PGF2 alpha increased gastric emptying regardless of the administration route. Tube-feeding with high osmolarity suspension significantly reduced emptying rate of 141Cerium compared to feeding with low osmolarity suspension. Gastric emptying rate of the tracer was significantly higher in rats fed with low osmolarity test meal, in comparison to those fed with high osmolarity test meal. This effect was completely antagonized by indomethacin. Due to the known inhibitory effect of indomethacin on cyclooxygenase, the effects observed in the present study are also presumably mediated by the action of prostaglandins.
前列腺素已被证明在体外能刺激胃肠道平滑肌收缩,且在不同的胃肠道疾病中也有其合成的报道。本研究的目的是确定前列腺素(PGs)和吲哚美辛对大鼠体内胃排空的不同影响,并研究它们作为渗透压诱导胃排空变化调节剂的可能作用。通过胃管给大鼠喂食含有不同前列腺素或吲哚美辛的各种渗透压的混悬液。采用口服不可吸收标记物141铈的非侵入性技术,通过测量胃内剩余食物量来研究胃排空情况。口服PGE2及其皮下注射合成类似物16,16-二甲基PGE2均导致胃排空显著延迟,而无论给药途径如何,PGF2α均增加胃排空。与喂食低渗混悬液相比,喂食高渗混悬液显著降低了141铈的排空率。与喂食高渗试验餐的大鼠相比,喂食低渗试验餐的大鼠示踪剂的胃排空率显著更高。吲哚美辛完全拮抗了这种作用。由于已知吲哚美辛对环氧化酶有抑制作用,本研究中观察到的效应也可能是由前列腺素的作用介导的。