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无核黑果葡萄中的白藜芦醇多酚通过靶向坏死性凋亡和促纤维化介质协同作用抑制肝毒性。

Vitis vinifera polyphenols from seedless black fruit act synergistically to suppress hepatotoxicity by targeting necroptosis and pro-fibrotic mediators.

机构信息

Department of Medical Biotechnology, Genetic Engineering, and Biotechnology Research Institute, City of Scientific Research and Technological Applications (SRTA-City), New Borg EL-Arab, 21934, Alexandria, Egypt.

Biochemistry Department, Faculty of Science, Alexandria University, Alexandria, 21511, Egypt.

出版信息

Sci Rep. 2020 Feb 12;10(1):2452. doi: 10.1038/s41598-020-59489-z.

Abstract

Human is subjected from his surrounding to various hepatotoxins, which aggravates his liver. Nowadays, natural polyphenols have attracted great interest in health improvement, especially liver health. The present research, therefore, assessed the hepatotherapeutic potency of the isolated polyphenols (VVF1) from seedless (pulp and skin) black Vitis vinifera (VV) against CCl-induced hepatotoxicity in vitro and in vivo. Further, VVF1 was fractionated into resveratrol-enriched (VVF2) and phenolics-enriched (VVF3) fractions to study (in vitro) the possible synergism of their coexistence. The highest content of phenolics in VVF1 displayed in vitro synergistic antioxidant and anti-hepatotoxic activities comparing to VVF2, VVF3, and silymarin (SM, reference drug). More importantly, it exhibited multiple in vivo regulatory functions via diminishing oxidative stress and inflammation, which in turn decreased necroptosis and pro-fibrotic mediators (mixed lineage kinase domain-like protein (MLKL), collagen type I alpha 1 chain (COL1A1), and transforming growth factor (TGF)-β1). In addition to these novel findings, VVF1 had higher anti-hepatotoxic potency than that of SM in most of the studied parameters. The histopathological analysis confirmed the improving role of VVF1 in the serious hepatic damage induced by CCl. Thus, the synergistic functions of VVF1 polyphenols could be a promising new anti-hepatotoxic agent for targeting both necroptotic and profibrotic mediators.

摘要

人会受到周围环境中各种肝毒素的影响,从而加重肝脏负担。如今,天然多酚因其对改善健康状况的作用,尤其是对肝脏健康的作用,而受到了广泛关注。因此,本研究评估了从无籽(果肉和果皮)黑葡萄(VV)中分离得到的多酚(VVF1)对 CCl 诱导的体外和体内肝毒性的治疗潜力。此外,将 VVF1 进一步分离为富含白藜芦醇的(VVF2)和富含酚类的(VVF3)部分,以研究它们共存的可能协同作用。VVF1 中酚类物质含量最高,其体外抗氧化和抗肝毒性活性优于 VVF2、VVF3 和水飞蓟素(SM,参比药物)。更重要的是,它通过减少氧化应激和炎症表现出多种体内调节功能,从而减少坏死性凋亡和促纤维化介质(混合谱系激酶结构域样蛋白(MLKL)、I 型胶原α 1 链(COL1A1)和转化生长因子(TGF)-β1)。除了这些新发现之外,VVF1 在大多数研究参数中都表现出比 SM 更高的抗肝毒性效力。组织病理学分析证实了 VVF1 在 CCl 引起的严重肝损伤中的改善作用。因此,VVF1 多酚的协同作用可能是一种有前途的新型抗肝毒性药物,可靶向坏死性凋亡和促纤维化介质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5c9/7016101/afed76611c3b/41598_2020_59489_Fig1_HTML.jpg

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