Lee Beobyi, Lee Eo-Jin, Kim Dong-Il, Park Sung-Kyu, Kim Wun-Jae, Moon Sung-Kwon
Department of Anatomy, College of Medicine, Konkuk University, Chungju City, Chungbuk 380-701, South Korea.
Toxicol In Vitro. 2009 Oct;23(7):1284-91. doi: 10.1016/j.tiv.2009.07.023. Epub 2009 Jul 22.
Piceatannol (3,5,3',4'-tetrahydroxy- trans-stilbene), a resveratrol analogue, is a polyphenol present in the skins of grapes and in wine and other foods. The present study aimed to investigate for the first time the cardioprotective effects of piceatannol on vascular smooth muscle cells (VSMC). The treatment of cells with piceatannol inhibited cell proliferation by reducing extracellular signal-regulated kinase (ERK) 1/2 and JNK activity in cultured VSMC in the presence of tumor necrosis factor-alpha (TNF-alpha). These inhibitory effects were also associated with G1 cell cycle arrest, and resulted in a decrease in cyclin-dependent kinases (CDKs) and cyclins. Piceatannol treatment strongly induced the expression of p21WAF1 via independence of p27KIP and p53 expression. The effect of piceatannol was not restricted to cell proliferation, as TNF-alpha-induced invasion and migration was also suppressed in VSMC. Moreover, piceatannol treatment strongly decreased matrix metalloproteinase-9 (MMP-9) expression and promoter activity in a dose-dependent manner in response to TNF-alpha. It was further demonstrated that piceatannol abrogated the transcriptional activity of nuclear factor kappa B (NF-kappaB), an important nuclear transcription factor involved in MMP-9 expression. Overall, these results demonstrate that piceatannol inhibits proliferation and migration of VSMC treated with TNF-alpha. Therefore, piceatannol may be an effective therapeutic approach to treat atherosclerosis.
白皮杉醇(3,5,3',4'-四羟基-反式芪)是白藜芦醇的类似物,是一种存在于葡萄皮、葡萄酒及其他食物中的多酚。本研究旨在首次探究白皮杉醇对血管平滑肌细胞(VSMC)的心脏保护作用。在肿瘤坏死因子-α(TNF-α)存在的情况下,用白皮杉醇处理细胞可通过降低细胞外信号调节激酶(ERK)1/2和JNK活性来抑制培养的VSMC细胞增殖。这些抑制作用还与G1期细胞周期停滞有关,并导致细胞周期蛋白依赖性激酶(CDK)和细胞周期蛋白减少。白皮杉醇处理通过不依赖p27KIP和p53表达而强烈诱导p21WAF1的表达。白皮杉醇的作用不仅限于细胞增殖,因为TNF-α诱导的VSMC侵袭和迁移也受到抑制。此外,白皮杉醇处理以剂量依赖的方式强烈降低了TNF-α刺激下基质金属蛋白酶-9(MMP-9)的表达和启动子活性。进一步证明,白皮杉醇消除了参与MMP-9表达的重要核转录因子核因子κB(NF-κB)的转录活性。总体而言,这些结果表明白皮杉醇抑制TNF-α处理的VSMC的增殖和迁移。因此,白皮杉醇可能是治疗动脉粥样硬化的一种有效治疗方法。