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乙醇刺激大鼠胃黏膜中白三烯C4的形成。

Ethanol stimulates formation of leukotriene C4 in rat gastric mucosa.

作者信息

Peskar B M, Lange K, Hoppe U, Peskar B A

出版信息

Prostaglandins. 1986 Feb;31(2):283-93. doi: 10.1016/0090-6980(86)90054-7.

Abstract

Ethanol-induced gastric mucosal damage is characterized by microcirculatory changes such as stasis and plasma leakage. Sluggish blood flow and stasis have also been observed after administration of exogenous leukotriene (LT) C4. The effect of ethanol on the release of LTC4 from rat gastric mucosa was therefore investigated. It was found that intragastric instillation of ethanol increases gastric mucosal release of LTC4 in a dose- and time-dependent manner parallel to the production of gastric lesions. The lipoxygenase inhibitor nordihydroguaiaretic acid (NDGA) and the anti-ulcer drug carbenoxolone (CX) inhibited mucosal release of LTC4 and simultaneously protected against gastric damage caused by ethanol. It is concluded that increased formation of LTC4 and/or other 5-lipoxygenase-derived products of arachidonate metabolism may be involved in ethanol-induced gastric damage. Furthermore, inhibition of the 5-lipoxygenase pathway may be an important mechanism of action of gastric protective drugs.

摘要

乙醇诱导的胃黏膜损伤的特征是微循环变化,如血流淤滞和血浆渗漏。在外源性白三烯(LT)C4给药后,也观察到血流缓慢和淤滞。因此,研究了乙醇对大鼠胃黏膜LTC4释放的影响。发现胃内滴注乙醇会以剂量和时间依赖性方式增加胃黏膜LTC4的释放,这与胃损伤的产生平行。脂氧合酶抑制剂去甲二氢愈创木酸(NDGA)和抗溃疡药物甘珀酸(CX)抑制LTC4的黏膜释放,同时预防乙醇引起的胃损伤。结论是,LTC4和/或花生四烯酸代谢的其他5-脂氧合酶衍生产物的生成增加可能参与乙醇诱导的胃损伤。此外,抑制5-脂氧合酶途径可能是胃保护药物的重要作用机制。

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