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儿茶素和茶黄素介导的心脏保护作用的特征。

Characteristics of catechin- and theaflavin-mediated cardioprotection.

作者信息

Dreger Henryk, Lorenz Mario, Kehrer Alexandra, Baumann Gert, Stangl Karl, Stangl Verena

机构信息

Medizinische Klinik m. S. Kardiologie und Angiologie (CCM), Charité - Universitätsmedizin Berlin, Charitéplatz 1, D - 10117 Berlin, Germany.

出版信息

Exp Biol Med (Maywood). 2008 Apr;233(4):427-33. doi: 10.3181/0710-RM-292.

Abstract

Catechins and theaflavins-the main polyphenolic substances of green and black tea, respectively-exert a plethora of beneficial effects on the cardiovascular system. In a model of H(2)O(2)-mediated oxidative stress, we investigated the effects of epigallocatechin-3-gallate (EGCG) and theaflavin-3,3'-digallate (TF3) on neonatal rat cardiomyocytes. Pretreatment with EGCG or TF3 1 hr prior to induction of oxidative stress by H(2)O(2) effectively protected cardiac myocytes as determined by measuring release of lactate dehydrogenase after 24 hrs. Longer pre-incubation times resulted in significant loss of protection. To enable further mechanistic insight, we investigated expression of antioxidative enzymes and activation of prosurvival signaling cascades. Whereas mRNA levels of glutathione peroxidase 3, superoxide dismutase 1, and catalase were not influenced by both polyphenols, heme oxygenase (HO-1) was selectively upregulated by EGCG-but not by TF3. However, inhibition of HO-1 did not diminish polyphenol-mediated cardioprotection. While EGCG and TF3 activated Akt, extracellular signal-regulated kinase 1/2, and p38 mitogen-activated protein kinase, inhibition of these kinases did not attenuate polyphenol-mediated protection. Loading of cardiomyocytes with dichlorofluorescein revealed that intracellular levels of reactive oxygen species were significantly reduced after treatment with EGCG or TF3 as early as 30 mins after induction of oxidative stress. In conclusion, activation of prosurvival signaling kinases and upregulation of antioxidative enzymes do not play a major role in tea polyphenol-mediated cardioprotection.

摘要

儿茶素和茶黄素分别是绿茶和红茶中的主要多酚类物质,它们对心血管系统具有众多有益作用。在过氧化氢介导的氧化应激模型中,我们研究了表没食子儿茶素-3-没食子酸酯(EGCG)和茶黄素-3,3'-双没食子酸酯(TF3)对新生大鼠心肌细胞的影响。在用过氧化氢诱导氧化应激前1小时用EGCG或TF3预处理,通过在24小时后测量乳酸脱氢酶的释放来确定,可有效保护心肌细胞。预孵育时间延长会导致保护作用显著丧失。为了深入了解其机制,我们研究了抗氧化酶的表达和促生存信号级联的激活。虽然谷胱甘肽过氧化物酶3、超氧化物歧化酶1和过氧化氢酶的mRNA水平不受这两种多酚的影响,但血红素加氧酶(HO-1)被EGCG选择性上调,而不被TF3上调。然而,抑制HO-1并没有减弱多酚介导的心脏保护作用。虽然EGCG和TF3激活了Akt、细胞外信号调节激酶1/2和p38丝裂原活化蛋白激酶,但抑制这些激酶并没有减弱多酚介导的保护作用。用二氯荧光素加载心肌细胞显示,在用EGCG或TF3处理后,早在氧化应激诱导后30分钟,细胞内活性氧水平就显著降低。总之,促生存信号激酶的激活和抗氧化酶的上调在茶多酚介导的心脏保护中并不起主要作用。

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