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亚油酸及其代谢产物氢过氧化十八碳二烯酸可刺激大鼠主动脉平滑肌细胞中c-Fos、c-Jun和c-Myc信使核糖核酸的表达、丝裂原活化蛋白激酶的激活以及细胞生长。

Linoleic acid and its metabolites, hydroperoxyoctadecadienoic acids, stimulate c-Fos, c-Jun, and c-Myc mRNA expression, mitogen-activated protein kinase activation, and growth in rat aortic smooth muscle cells.

作者信息

Rao G N, Alexander R W, Runge M S

机构信息

Division of Cardiology, University of Texas Medical Branch, Galveston 77555, USA.

出版信息

J Clin Invest. 1995 Aug;96(2):842-7. doi: 10.1172/JCI118130.

Abstract

Previous studies from other laboratories suggest that linoleic acid and its metabolites, hydroperoxyoctadecadienoic acids, play an important role in modulating the growth of some cells. A correlation has been demonstrated between hydroperoxyoctadecadienoic acids and conditions characterized by abnormal cell growth such as atherosclerosis and psoriasis. To determine if linoleic acid and its metabolites modulate cell growth in atherosclerosis, we measured DNA synthesis, protooncogene mRNA expression, and mitogen-activated protein kinase (MAPK) activation in vascular smooth muscle cells (VSMC). Linoleic acid induces DNA synthesis, c-fos, c-jun, and c-myc mRNA expression and MAPK activation in VSMC. Furthermore, nordihydroguaiaretic acid, a potent inhibitor of the lipoxygenase system, significantly reduced the growth-response effects of linoleic acid in VSMC, suggesting that conversion of linoleic acid to hydroperoxyoctadecadienoic acids (HPODEs) is required for these effects. HPODEs also caused significant induction of DNA synthesis, protooncogene mRNA expression, and MAPK activation in growth-arrested VSMC, suggesting that linoleic acid and its metabolic products, HPODEs, are potential mitogens in VSMC, and that conditions such as oxidative stress and lipid peroxidation which provoke the production of these substances may alter VSMC growth.

摘要

其他实验室先前的研究表明,亚油酸及其代谢产物氢过氧化十八碳二烯酸在调节某些细胞的生长中起重要作用。已证实氢过氧化十八碳二烯酸与以细胞生长异常为特征的病症(如动脉粥样硬化和牛皮癣)之间存在关联。为了确定亚油酸及其代谢产物是否调节动脉粥样硬化中的细胞生长,我们测量了血管平滑肌细胞(VSMC)中的DNA合成、原癌基因mRNA表达和丝裂原活化蛋白激酶(MAPK)激活。亚油酸可诱导VSMC中的DNA合成、c-fos、c-jun和c-myc mRNA表达以及MAPK激活。此外,去甲二氢愈创木酸是脂氧合酶系统的有效抑制剂,可显著降低亚油酸对VSMC的生长反应效应,这表明亚油酸转化为氢过氧化十八碳二烯酸(HPODEs)是产生这些效应所必需的。HPODEs还可显著诱导生长停滞的VSMC中的DNA合成、原癌基因mRNA表达和MAPK激活,这表明亚油酸及其代谢产物HPODEs是VSMC中的潜在促分裂原,并且诸如氧化应激和脂质过氧化等引发这些物质产生的状况可能会改变VSMC的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a4/185270/46b40c97357c/jcinvest00014-0198-a.jpg

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