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水提物通过改善脂质积累和氧化应激诱导的细胞毒性发挥其肝保护作用。

Water Extract of L. Exhibits Hepatoprotective Effects Through Improvement of Lipid Accumulation and Oxidative Stress-Induced Cytotoxicity.

机构信息

Sungkyun Biotech Co., Ltd., Suwon, Korea.

Department of Biomedical Sciences and Seoul National University College of Medicine, Seoul, Korea.

出版信息

J Med Food. 2020 Dec;23(12):1312-1322. doi: 10.1089/jmf.2020.4696. Epub 2020 Nov 17.

Abstract

Nonalcoholic fatty liver disease (NAFLD) is a metabolic liver disease with a complex underlying mechanism that has not been completely understood. Thus, effective and safe drugs for this disease are not yet available. L. is a medicinal plant with potent antimicrobial and antioxidant activities. In this study, we prepared a water extract of (WEAA) and examined its potential for NAFLD treatment. First, we pretreated HepG2 cells (human hepatocarcinoma cell line) with WEAA and then treated the cells with oleic acid or -butylhydroperoxide to examine the effect of WEAA on the lipid accumulation and the cytotoxicity, respectively. WEAA not only inhibited lipid accumulation within HepG2 cells but also protected cells from oxidative stress-mediated damage through the activation of antioxidant enzymes (such as activation of superoxide dismutase and production of glutathione) and its own scavenging activity. Next, to confirm protective effect of the WEAA in , mice were intragastrically administered with WEAA, extract of or water once a day, and simultaneously provided with high-fat diet to induce fatty liver and hepatic steatosis. Oral administration of WEAA ameliorated weight gain and hepatic lipid accumulation in high-fat diet-fed mice. Moreover, the plasma levels of triglyceride, aspartate aminotransferase, and alanine aminotransferase were reduced in the WEAA-treated group. Our findings indicated that WEAA may be a potential intervention for preventing or treating hepatic lipid accumulation and liver damage.

摘要

非酒精性脂肪性肝病(NAFLD)是一种代谢性肝病,其潜在机制复杂,尚未完全阐明。因此,目前尚无针对这种疾病的有效和安全药物。L. 是一种具有强大抗菌和抗氧化活性的药用植物。在本研究中,我们制备了 L. 的水提取物(WEAA),并研究了其治疗非酒精性脂肪性肝病的潜力。首先,我们用 WEAA 预处理 HepG2 细胞(人肝癌细胞系),然后用油酸或 -丁基过氧化物处理细胞,分别研究 WEAA 对脂质积累和细胞毒性的影响。WEAA 不仅抑制 HepG2 细胞内的脂质积累,还通过激活抗氧化酶(如超氧化物歧化酶的激活和谷胱甘肽的产生)及其自身的清除活性来保护细胞免受氧化应激介导的损伤。接下来,为了确认 WEAA 在体内的保护作用,我们将 WEAA、L. 提取物或水每天一次灌胃给药,同时给予高脂肪饮食以诱导脂肪肝和肝脂肪变性。WEAA 口服给药可改善高脂肪饮食喂养小鼠的体重增加和肝脂质积累。此外,WEAA 治疗组的血浆甘油三酯、天冬氨酸转氨酶和丙氨酸转氨酶水平降低。我们的研究结果表明,WEAA 可能是预防或治疗肝内脂质积累和肝损伤的潜在干预措施。

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