Suppr超能文献

白皮杉醇通过新型蛋白激酶C和酪氨酸激酶途径上调内皮细胞血红素加氧酶-1的表达。

Piceatannol upregulates endothelial heme oxygenase-1 expression via novel protein kinase C and tyrosine kinase pathways.

作者信息

Wung Being-Sun, Hsu Ming-Chun, Wu Chun-Ching, Hsieh Chia-Wen

机构信息

Department of Applied Microbiology, National Chiayi University, No. 300, Shiuefu Road, Chiayi, Taiwan.

出版信息

Pharmacol Res. 2006 Feb;53(2):113-22. doi: 10.1016/j.phrs.2005.09.006. Epub 2005 Oct 21.

Abstract

Piceatannol is an anti-inflammatory and anti-proliferative plant-derived stilbene. Heme oxygenase-1 (HO-1) is a cytoprotective enzyme to activate by various phytochemicals. In this study, we examined the ability of piceatannol to upregulate HO-1 expression in endothelial cells. We found piceatannol at micromolar (10-50 microM) concentrations dramatically increased HO-1 protein levels in a time-dependent manner. Piceatannol was similarly potent in the induction of HO-1 as hemin, arsenate, and 15d-PGJ2, and was more potent than some other phytochemicals including curcumin, EGCG, baicalein, and quercetin. In contrast, the similar chemical structure compounds, trans-stilbene, stilbene oxide, and resveratrol had no HO-1-inducing effects, suggesting a critical role for the hydroxyl groups in HO-1 induction. No cytotoxicity and superoxide production was observed after 10-50 microM piceatannol treatments. Piceatannol-mediated HO-1 induction was abrogated in the presence of N-acetylcysteine and glutathione, but not by other antioxidants. Induction of HO-1 by piceatannol was further enhanced by using buthionine sulfoximine. In addition, we determined that tyrosine kinase was involved in the induction of HO-1 by using tyrosine kinase inhibitors, herbimycin A, erbstatin, and genistein; in contrast, no significant changes in the pretreatment of PI3 kinase or MAP kinase inhibitors was determined. HO-1 induction was blocked by the protein kinase C inhibitors calphostin C, rottlerin, and long PMA pretreatment, whereas conventional PKC inhibitors, Go6976, and Ca2+ chelator BAPTA/AM, had no effect. Elevated HO-1 protein levels were associated with the inhibition of tumor necrosis factor-alpha (TNFalpha)-induced intercellular adhesion molecule-1 (ICAM-1) expression. Treating ECs with zinc protoporphyrin, an HO-1 inhibito blocked the anti-inflammatory effect of piceatannol. In summary, this study identified piceatannol as a novel phytochemical inducer of HO-1 expression and identified the mechanisms involved in this process.

摘要

白皮杉醇是一种具有抗炎和抗增殖作用的植物源芪类化合物。血红素加氧酶-1(HO-1)是一种可被多种植物化学物质激活的细胞保护酶。在本研究中,我们检测了白皮杉醇上调内皮细胞中HO-1表达的能力。我们发现,微摩尔浓度(10 - 50微摩尔)的白皮杉醇能以时间依赖性方式显著增加HO-1蛋白水平。白皮杉醇诱导HO-1的效力与血红素、砷酸盐和15d - PGJ2相似,且比姜黄素、表没食子儿茶素没食子酸酯、黄芩素和槲皮素等其他一些植物化学物质更强。相比之下,化学结构相似的反式芪、氧化芪和白藜芦醇没有诱导HO-1的作用,这表明羟基在HO-1诱导过程中起关键作用。在10 - 50微摩尔白皮杉醇处理后未观察到细胞毒性和超氧阴离子生成。在存在N-乙酰半胱氨酸和谷胱甘肽的情况下,白皮杉醇介导的HO-1诱导作用被消除,但其他抗氧化剂则无此作用。使用丁硫氨酸亚砜胺可进一步增强白皮杉醇对HO-1的诱导作用。此外,我们通过使用酪氨酸激酶抑制剂、除莠霉素A、抑癌蛋白和染料木黄酮确定酪氨酸激酶参与了HO-1的诱导;相比之下,PI3激酶或MAP激酶抑制剂预处理后未观察到显著变化。HO-1的诱导被蛋白激酶C抑制剂钙泊三醇、rottlerin和长期PMA预处理所阻断,而传统的蛋白激酶C抑制剂Go6976和Ca2 +螯合剂BAPTA/AM则没有作用。HO-1蛋白水平升高与肿瘤坏死因子-α(TNFα)诱导的细胞间黏附分子-1(ICAM-1)表达的抑制有关。用HO-1抑制剂锌原卟啉处理内皮细胞可阻断白皮杉醇的抗炎作用。总之,本研究确定白皮杉醇是一种新型的HO-1表达植物化学诱导剂,并确定了该过程涉及的机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验