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缓激肽和趋化肽fMLP刺激大鼠肺组织中白三烯的生物合成及其受血管活性肠肽的抑制作用

Bradykinin- and chemotactic peptide fMLP-stimulated leukotriene biosynthesis in rat lungs and its inhibition by vasoactive intestinal peptide.

作者信息

Di Marzo V, Tippins J R, Morris H R

机构信息

Department of Biochemistry, Imperial College of Science & Technology, London.

出版信息

Biochem Int. 1988 Aug;17(2):235-42.

PMID:2847737
Abstract

The release/biosynthesis of peptidoleukotrienes (pLT) from rat lung tissue was stimulated with either bradykinin (Bk) or the chemotactic peptide formyl-methionyl-leucinyl-phenylalanine (fMLP). Bk- and fMLP-induced stimulation of pLT levels was dose-related for leukotriene D4 (LTD4), E4 (LTE4) and total pLTs and was maximal when a 10 microM concentration of either peptide was used. This stimulation was partially counteracted by vasoactive intestinal peptide (VIP), in agreement with the previously reported VIP inhibition of platelet activating factor- and IgG-stimulated pLT biosynthesis.

摘要

用缓激肽(Bk)或趋化肽甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)刺激大鼠肺组织中肽白三烯(pLT)的释放/生物合成。Bk和fMLP诱导的pLT水平刺激与白三烯D4(LTD4)、E4(LTE4)和总pLTs呈剂量相关,当使用10微摩尔浓度的任何一种肽时刺激最大。这种刺激被血管活性肠肽(VIP)部分抵消,这与先前报道的VIP抑制血小板活化因子和IgG刺激的pLT生物合成一致。

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