表没食子儿茶素没食子酸酯 (EGCG) 在抗击和治疗性传播病毒感染中的作用。

Ozge Yilmaz, Alev Onder
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引用次数: 0

摘要

茶叶取自多年生常绿植物山茶(Camellia sinensis (L.) Kuntze)的嫩叶和嫩枝,是世界上最受欢迎和最常饮用的天然饮料产品。包括绿茶、红茶和乌龙茶在内的一些种类的茶叶因制造工艺不同而具有各种风味。多年来,人们一直在研究绿茶的重要功效,如抗癌、抗肥胖、抗糖尿病、抗炎、保护神经和心血管。这些作用主要与茶多酚有关,据报道,经常饮用绿茶可以降低一些慢性疾病的发病率。目前的研究支持绿茶儿茶素在治疗和改善许多疾病的病理方面发挥重要作用。表没食子儿茶素-3-棓酸盐(EGCG)是茶叶中含量最高的多酚类物质,因其在预防疾病方面的保护作用而备受关注。因此,本综述介绍了表儿茶素-3-没食子酸酯对性传播病毒的功效和可能的作用机制。此外,EGCG 及其衍生物被认为是安全、具有生物活性的植物化学物质,可用于外用和内服,预防和治疗病毒性性传播疾病和其他并发感染。要利用 EGCG 及其衍生物发现更便宜、更安全、更有效的治疗方法,改善病毒性 STI 药物的毒性和配方,就必须开展多学科研究。
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The Role of Epigallocatechin Gallate (EGCG) in Treatment and Management of Sexually Transmitted Viral Infections

Tea is obtained from the young leaves and shoots of the evergreen perennial plant Camellia sinensis (L.) Kuntze, the most popular and frequently consumed product using a natural beverage worldwide. Some kinds of tea products, such as green tea, black tea, and oolong tea, have assorted flavors depending on the manufacturing techniques. Green tea has been studied for many years for its important beneficial effects, including anticancer, anti-obesity, anti-diabetes, anti-inflammatory, neuroprotective, and cardiovascular effects. These effects are primarily associated with tea polyphenols, and regular consumption has been re-ported to decrease the incidence of some chronic diseases. Current studies support that green tea catechins play an important role in healing and improving the pathology of many diseases. Epigallocatechin-3-gallate (EGCG) is the most a highly found polyphenol in the leaves and is of great interest for its protective role in the prevention of diseases. Therefore, this review presents the efficacy and possible mechanisms of EGCG against sexually transmitted viruses. Moreover, EGCG and its derivatives are recognized as safe bioactive phytochemicals for external and internal use in preventing and treating viral STIs and other concurrent infections. Multidisciplinary studies are essential to discover cheaper, safer, and more effective treat-ments using EGCG and its derivatives to improve the toxicity and formulations of viral STI medications.

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