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综述:脂氧合酶抑制剂与肠道

Review: lipoxygenase inhibitors and the gut.

作者信息

Kennedy N P, Keeling P W

机构信息

Department of Clinical Medicine, Trinity College Dublin, Ireland.

出版信息

Aliment Pharmacol Ther. 1987 Aug;1(4):263-72. doi: 10.1111/j.1365-2036.1987.tb00626.x.

Abstract

Leukotriene synthesis is influenced by several drugs currently in use for the treatment of alimentary disease, including the corticosteroids, sulphasalazine and mesalazine. However, the use of selective lipoxygenase inhibitors in human gastrointestinal disease has not been investigated. The complexity of eicosanoid metabolism, and the incomplete knowledge of roles played by each metabolite in each tissue and disease condition, make rational pharmacological manipulation of arachidonate metabolism difficult. However, lipoxygenase inhibitors show promise in animal models of inflammation, including hepatitis, and studies in vitro suggest that therapeutic benefits may be achieved using inhibitors of leukotriene synthesis in other inflammatory disorders.

摘要

白三烯的合成受到目前用于治疗消化系统疾病的几种药物的影响,包括皮质类固醇、柳氮磺胺吡啶和美沙拉嗪。然而,选择性脂氧合酶抑制剂在人类胃肠道疾病中的应用尚未得到研究。类花生酸代谢的复杂性,以及对每种代谢产物在每种组织和疾病状态中所起作用的不完全了解,使得对花生四烯酸代谢进行合理的药理学调控变得困难。然而,脂氧合酶抑制剂在包括肝炎在内的炎症动物模型中显示出前景,并且体外研究表明,在其他炎症性疾病中使用白三烯合成抑制剂可能会获得治疗益处。

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