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齐留通可抑制白三烯通路的激活并减少皮脂生成。

Zileuton prevents the activation of the leukotriene pathway and reduces sebaceous lipogenesis.

出版信息

Exp Dermatol. 2010 Feb;19(2):148-50. doi: 10.1111/j.1600-0625.2009.00929.x. Epub 2009 Jul 23.

Abstract

Arachidonic acid (AA) activates the 5-lipoxygenase, induces leukotriene-B(4) (LTB(4)) synthesis, enhances interleukin-6 (IL-6) release and increases intracellular neutral lipids in human sebocytes. Moreover, the enzymes of LTB(4) biosynthesis are activated in acne-involved sebaceous glands. Zileuton a 5-lipoxygenase inhibitor, reduces the number of inflammatory acne lesions and lipogenesis in patients with acne. In this study, we investigated the activity of zileuton on LTB(4) generation, lipid content and IL-6 and -8 release from human SZ95 sebocytes in vitro. Pretreatment with zileuton partially prevented the AA-induced LTB(4) and IL-6 release and increased neutral lipid content. IL-6 release and neutral lipid content were also reduced under long-term zileuton treatment. In conclusion, zileuton prevents the activation of the leukotriene pathway and enhancement of lipogenesis by AA in human sebocytes in vitro.

摘要

花生四烯酸 (AA) 可激活 5-脂氧合酶,诱导白三烯-B4 (LTB4) 的合成,增强白细胞介素-6 (IL-6) 的释放,并增加人皮脂腺细胞内的中性脂质。此外,LTB4 生物合成的酶在痤疮相关的皮脂腺中被激活。齐留通是一种 5-脂氧合酶抑制剂,可减少痤疮患者的炎症性痤疮损伤和脂肪生成。在这项研究中,我们研究了齐留通对体外人 SZ95 皮脂腺细胞中 LTB4 生成、脂质含量以及 IL-6 和 -8 释放的活性。齐留通预处理部分阻止了 AA 诱导的 LTB4 和 IL-6 的释放,并增加了中性脂质含量。长期齐留通治疗也降低了 IL-6 释放和中性脂质含量。总之,齐留通可防止 AA 在体外激活人皮脂腺细胞中的白三烯途径并增强脂肪生成。

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