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前列腺素D2在大鼠结肠中的抗分泌作用特性

Characterization of the antisecretory action of prostaglandin D2 in the rat colon.

作者信息

Diener M, Nobles M, Schmitt C, Rummel W

机构信息

Institute for Pharmacology and Toxicology, University of Saarland, Homburg, Saar, Germany.

出版信息

Acta Physiol Scand. 1992 May;145(1):19-24. doi: 10.1111/j.1748-1716.1992.tb09331.x.

Abstract

Previous studies have shown that prostaglandin D2 (PGD2) inhibits neuronally mediated secretion in the rat colon. This antisecretory action of PGD2 was further characterized by the use of a prostaglandin D receptor blocker. Prostaglandin D2 inhibited the neuronally mediated short-circuit current evoked by prostaglandin I2, which represents Cl- secretion. The concentration-response curve for the inhibition by PGD2 was shifted to the right in the presence of the prostaglandin D receptor blocker, AH 6809. AH 6809 had no effect on the short-circuit current response induced by prostaglandin E2 or iloprost, a stable prostaglandin I2 analogue, suggesting an interaction of the blocker with receptors specific for PGD2. A direct interaction of PGD2 with enteric neurones was studied by determining its effect on acetylcholine release from enteric neurones preloaded with [3H]choline. Prostaglandin D2 suppressed 3H release induced by electric field stimulation. It had, however, no effect on the release induced by depolarization with potassium. The results suggest that the inhibitory action of PGD2 on enteric cholinergic neurones is mediated by prostaglandin D receptors.

摘要

先前的研究表明,前列腺素D2(PGD2)可抑制大鼠结肠中神经介导的分泌。通过使用前列腺素D受体阻滞剂进一步表征了PGD2的这种抗分泌作用。前列腺素D2抑制了前列腺素I2诱发的神经介导的短路电流,该电流代表氯离子分泌。在存在前列腺素D受体阻滞剂AH 6809的情况下,PGD2抑制作用的浓度-反应曲线向右移动。AH 6809对前列腺素E2或伊洛前列素(一种稳定的前列腺素I2类似物)诱导的短路电流反应没有影响,这表明该阻滞剂与PGD2特异性受体存在相互作用。通过测定PGD2对预加载[3H]胆碱的肠神经元乙酰胆碱释放的影响,研究了PGD2与肠神经元的直接相互作用。前列腺素D2抑制电场刺激诱导的3H释放。然而,它对钾去极化诱导的释放没有影响。结果表明,PGD2对肠胆碱能神经元的抑制作用是由前列腺素D受体介导的。

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