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磷脂酶A2与大鼠结肠黏膜短路电流激活的介导作用

Phospholipase A2 and mediation of the activation of short-circuit current in the rat colonic mucosa.

作者信息

Diener M, Rummel W

机构信息

Institut für Pharmakologie und Toxikologie, Universität des Saarlandes, Homburg/Saar, Federal Republic of Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1991 Jun;343(6):652-8. doi: 10.1007/BF00184298.

DOI:10.1007/BF00184298
PMID:1944607
Abstract

Melittin (0.5-2 micrograms ml-1) increased the short-circuit current (ISC) in mucosa-submucosa and mucosa preparations of the rat colon descendens in a dose-dependent manner. In the preparation with the submucosal plexus, quinacrine and indomethacin completely blocked the effect of melittin, indicating activation of phospholipase A2 and production of prostaglandins induced by the drug. The melittin response was also partially sensitive to the lipoxygenase inhibitor, nordihydroguaiaretic acid. Complete inhibition by tetrodotoxin and atropine gives evidence for the involvement of cholinergic neurons in the mediation of the response induced by melittin. In contrast, in the preparation without the submucosal plexus the effect of melittin was only partially inhibited by quinacrine, indomethacin, or by neuronal blockers, suggesting direct interactions of melittin with the epithelium in addition. The effect of melittin resembles to the action of bradykinin, which is neuronally mediated and quinacrine-sensitive in the mucosa-submucosa preparation, and quinacrine-resistant and not neuronally mediated in the mucosa preparation. In the mucosa-submucosa preparation, the melittin response is even partially sensitive to the bradykinin receptor antagonist [D-Phe7]-bradykinin. The results provide evidence for the presence of a quinacrine-sensitive phospholipase A2 in the preparation with and that without the submucosa.

摘要

蜂毒肽(0.5 - 2微克/毫升)以剂量依赖方式增加大鼠降结肠黏膜 - 黏膜下层和黏膜制剂中的短路电流(ISC)。在含有黏膜下神经丛的制剂中,奎纳克林和吲哚美辛完全阻断了蜂毒肽的作用,表明该药物诱导了磷脂酶A2的激活和前列腺素的产生。蜂毒肽反应对脂氧合酶抑制剂去甲二氢愈创木酸也部分敏感。河豚毒素和阿托品的完全抑制证明胆碱能神经元参与了蜂毒肽诱导反应的介导。相反,在没有黏膜下神经丛的制剂中,蜂毒肽的作用仅被奎纳克林、吲哚美辛或神经元阻滞剂部分抑制,这表明蜂毒肽还与上皮细胞有直接相互作用。蜂毒肽的作用类似于缓激肽的作用,缓激肽在黏膜 - 黏膜下层制剂中是由神经元介导且对奎纳克林敏感的,而在黏膜制剂中对奎纳克林耐药且不是由神经元介导的。在黏膜 - 黏膜下层制剂中,蜂毒肽反应甚至对缓激肽受体拮抗剂[D - Phe7] - 缓激肽部分敏感。这些结果为在有和没有黏膜下层的制剂中存在对奎纳克林敏感的磷脂酶A2提供了证据。

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Melittin as an epithelial permeability enhancer I: investigation of its mechanism of action in Caco-2 monolayers.蜂毒肽作为一种上皮通透性增强剂I:其在Caco-2单层细胞中作用机制的研究
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Modulation by fish oil diet of eicosanoid-induced anion secretion in the rat distal colon.

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