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5-脂氧合酶产物参与调控培养的星形胶质细胞中脑啡肽原基因表达的证据。

Evidence for the involvement of 5-lipoxygenase products in the regulation of the expression of the proenkephalin gene in cultured astroglial cells.

作者信息

Mamot C, Hildebrand B, Olenik C, Simmet T, Meyer D K

机构信息

Department of Pharmacology, University of Freiburg, Germany.

出版信息

Brain Res Mol Brain Res. 1995 Oct;33(1):79-86. doi: 10.1016/0169-328x(95)00108-5.

DOI:10.1016/0169-328x(95)00108-5
PMID:8774948
Abstract

Cultured astroglial cells secrete eicosanoids which are produced by the cyclooxygenase and lipoxygenases. These cells also transcribe the proenkephalin gene. In the present study, it was investigated whether agents which inhibit the metabolism of arachidonic acid affect the basal and stimulated expression of the gene. Tetradecanoyl phorbol acetate (TPA; 1-1000 nmol/l) increases the concentration of proenkephalin mRNA in these cells by activating protein kinase C. The enhancement in proenkephalin mRNA caused by TPA (10 nmol/l) was not affected by the cyclooxygenase inhibitor indomethacin (5 mumol/l). However, nordihydroguaiaretic acid, which blocks cyclooxygenase and lipoxygenases, potentiated the effect of TPA on proenkephalin mRNA, when used at concentrations of 0.5-50 mumol/l. Two selective inhibitors of 5-lipoxygenase, i.e. MK886 (5 mumol/l) and BAY X1005 (1 mumol/l), also enhanced the effect of TPA (10 nmol/l) without affecting the basal expression of the gene. When added to the incubation medium, leukotriene E4 (10-1000 nmol/l) diminished in a dose-dependent manner the basal and TPA-induced expression of the proenkephalin gene. It is concluded that in astroglial cells derived from cortex of new-born rats products of 5-lipoxygenase can diminish the action of protein kinase C on the proenkephalin gene.

摘要

培养的星形胶质细胞分泌由环氧化酶和脂氧化酶产生的类二十烷酸。这些细胞还转录脑啡肽原基因。在本研究中,研究了抑制花生四烯酸代谢的试剂是否影响该基因的基础表达和刺激表达。十四酰佛波醇乙酸酯(TPA;1-1000 nmol/L)通过激活蛋白激酶C增加这些细胞中脑啡肽原mRNA的浓度。TPA(10 nmol/L)引起的脑啡肽原mRNA增强不受环氧化酶抑制剂吲哚美辛(5 μmol/L)的影响。然而,阻断环氧化酶和脂氧化酶的去甲二氢愈创木酸在0.5-50 μmol/L浓度下使用时,增强了TPA对脑啡肽原mRNA的作用。两种5-脂氧化酶的选择性抑制剂,即MK886(5 μmol/L)和BAY X1005(1 μmol/L),也增强了TPA(10 nmol/L)的作用,而不影响该基因的基础表达。当添加到孵育培养基中时,白三烯E4(10-1000 nmol/L)以剂量依赖性方式降低脑啡肽原基因的基础表达和TPA诱导的表达。得出的结论是,在新生大鼠皮质来源的星形胶质细胞中,5-脂氧化酶的产物可以减弱蛋白激酶C对脑啡肽原基因的作用。

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