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The secretory actions of histamine in rat small intestine.

机译:组胺在大鼠小肠中的分泌作用。

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摘要

1. Histamine caused a dose-dependent rise in the transintestinal potential difference in vivo that was competitively blocked by H1, but not by H2 antagonists. This effect of histamine was also reduced by the cyclo-oxygenase inhibitor indomethacin. 2. Histamine induced a net secretion of fluid by the small intestine and this effect was reduced by indomethacin. 3. In intestinal sheets histamine increased the potential difference, short-circuit current and tissue resistance. This response was decreased in the absence of Cl- and in the presence of furosemide, suggesting that Cl- secretion was responsible for the observed electrical changes. This was confirmed by direct measurement of ion fluxes which showed an increase in net Cl- secretion together with an inhibition of net Na+ absorption. 4. The response to histamine was Ca2+-dependent since it was inhibited by removal of serosal Ca2+ and by verapamil. 5. Indomethacin caused a dose-dependent reduction in the response of intestinal sheets to histamine, without affecting the rise in short-circuit current induced by mucosal glucose or serosal prostaglandin E2. Mepacrine also inhibited the response to histamine, but not that to prostaglandin E2. 6. It is concluded that histamine induces intestinal secretion by stimulating the production of prostaglandins which then activate the secretory process.
机译:1.组胺引起体内跨肠电位差异的剂量依赖性上升,该差异被H1竞争性阻断,但未被H2拮抗剂竞争性阻断。组胺的这种作用也被环加氧酶抑制剂吲哚美辛降低。 2.组胺引起小肠的液体净分泌,消炎痛使这种作用减弱。 3.在肠片中,组胺会增加电位差,短路电流和组织电阻。在不存在Cl-和存在速尿的情况下,该反应降低,表明Cl分泌是所观察到的电变化的原因。通过直接测量离子通量可以证实这一点,该离子通量显示出净Cl-分泌的增加以及净Na +吸收的抑制。 4.对组胺的反应是Ca2 +依赖性的,因为它被浆膜中Ca2 +的清除和维拉帕米抑制。 5.吲哚美辛引起肠片对组胺反应的剂量依赖性降低,而不影响粘膜葡萄糖或浆膜前列腺素E2引起的短路电流升高。美帕克林还抑制对组胺的反应,但不抑制对前列腺素E2的反应。 6.结论是,组胺通过刺激前列腺素的产生诱导肠道分泌,然后激活分泌过程。

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