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乙醇提取物对体内肝损伤的保肝活性。

The hepatoprotective activities of ethanol extract against liver injury in vivo.

作者信息

Wang Guo-Kai, Zhang Nan, Wang Yi, Liu Jin-Song, Wang Gang, Zhou Zhong-Yu, Lu Chi-Cheng, Yang Jai-Sing

机构信息

School of Pharmacy Anhui Key Laboratory of Modern Chinese Materia Medica Anhui University of Chinese Medicine Hefei China.

Bristol-Myers Squibb Lawrence NJ USA.

出版信息

Food Sci Nutr. 2019 Oct 18;7(11):3797-3807. doi: 10.1002/fsn3.1241. eCollection 2019 Nov.

Abstract

(L.) Sch. Bip. is a traditional Chinese medicine (TCM) and a portion of food used for cooking in China. It has been demonstrated that an ethanol extract of has an anti-inflammatory effect by inhibition of nitric oxide (NO) production on murine macrophage RAW264.7 cells after lipopolysaccharide (LPS) induction. In this study, the hepatoprotective effects of the total phenolics of (TPK), the total triterpenes of (TTK), and the total flavones of (TFK) from ethanol extracts of were evaluated in Bacille Calmette-Guerin (BCG)/LPS-induced liver injury in vivo. The treatments of TPK, TTK, and TFK improved liver injury in mice. Additionally, all treatments significantly not only reduced the hepatic malondialdehyde (MDA) content and hepatic total nitric oxide synthase (tNOS) but also induced the hepatic superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activity. The treatments of TPK and TTK significantly reduced the hepatic inducible nitric oxide synthase (iNOS). The treatments of TPK, TTK, and TFK reduced the serum total bilirubin (T-Bil), and only TFK treatment reduced the serum alanine aminotransferase (ALT). Our results suggest that TPK, TTK, and TFK from ethanol extracts of might play an essential protective role against BCG/LPS-induced liver injury in vivo.

摘要

(L.)Sch. Bip.是一种中药,在中国也是用于烹饪的一部分食材。已经证明,(L.)Sch. Bip.的乙醇提取物通过抑制脂多糖(LPS)诱导后小鼠巨噬细胞RAW264.7细胞中一氧化氮(NO)的产生而具有抗炎作用。在本研究中,在体内卡介苗(BCG)/LPS诱导的肝损伤模型中评估了(L.)Sch. Bip.乙醇提取物中的总酚(TPK)、总三萜(TTK)和总黄酮(TFK)的肝保护作用。TPK、TTK和TFK处理改善了小鼠的肝损伤。此外,所有处理不仅显著降低了肝脏丙二醛(MDA)含量和肝脏总一氧化氮合酶(tNOS),还诱导了肝脏超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)活性。TPK和TTK处理显著降低了肝脏诱导型一氧化氮合酶(iNOS)。TPK、TTK和TFK处理降低了血清总胆红素(T-Bil),只有TFK处理降低了血清丙氨酸氨基转移酶(ALT)。我们的结果表明,(L.)Sch. Bip.乙醇提取物中的TPK、TTK和TFK可能在体内对BCG/LPS诱导的肝损伤发挥重要的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d88/6848823/9d72c894f7c3/FSN3-7-3797-g001.jpg

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