Yan Yamei, Wu Wanqiang, Lu Lu, Ren Jie, Mi Jia, Liu Xuebo, Cao Youlong
National Wolfberry Engineering Research Center Yinchuan China.
College of Food Science and Engineering Northwest A&F University Yangling China.
Food Sci Nutr. 2019 Sep 12;7(11):3435-3442. doi: 10.1002/fsn3.1182. eCollection 2019 Nov.
Both L. polysaccharides (LBP) and zinc have protective effects on liver injuries. In this paper, LBP and ZnSO were combined to study the effects on the prevention of alcoholic liver injury. The rats were divided into six groups, the normal group, alcohol group, zinc sulfate group, LBP group, low-dose group of ZnSO, and high-dose group of ZnSO and LBP, used to explore the impact of LBP and ZnSO complex on liver lipid metabolism of alcohol, alcohol-metabolizing enzymes, oxidative damage, and inflammation of the liver. The experimental model was established by gavage treatment, observation, and determination of indexes of rats. The results showed that the combination of LBP and ZnSO could significantly decrease the levels of triglyceride (TG), total cholesterol (TC), tumor necrosis factor-α(TNF-ɑ), malondialdehyde (MDA), alanine aminotransferase (ALT), aspartate aminotransferase (AST), and the activity of enzyme subtype 2E1 (CYP2E1). It also significantly increased the activities of total superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), glutathione peptide (GSH), and alcohol dehydrogenase, effectively improved the liver tissue lesion. What is more, the combination of LBP and ZnSO had a synergistic effect on the remission of alcoholic fatty liver, and alleviated chronic alcoholic liver injury by promoting lipid metabolism, inhibiting oxidative stress, controlling inflammatory responses, and regulating the expression and activity of alcohol-metabolizing enzymes in rats.
枸杞多糖(LBP)和锌对肝损伤均具有保护作用。本文将LBP与硫酸锌(ZnSO)联用,研究其对酒精性肝损伤的预防作用。将大鼠分为六组,即正常组、酒精组、硫酸锌组、LBP组、低剂量硫酸锌组以及高剂量硫酸锌与LBP组,用以探究LBP与ZnSO复合物对酒精性肝损伤大鼠肝脏脂质代谢、酒精代谢酶、氧化损伤及肝脏炎症的影响。通过灌胃处理、观察及测定大鼠各项指标建立实验模型。结果显示,LBP与ZnSO联用可显著降低甘油三酯(TG)、总胆固醇(TC)、肿瘤坏死因子-α(TNF-α)、丙二醛(MDA)、谷丙转氨酶(ALT)、谷草转氨酶(AST)的水平以及酶亚型2E1(CYP2E1)的活性。同时还显著提高了总超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)、谷胱甘肽(GSH)以及乙醇脱氢酶的活性,有效改善了肝组织损伤。此外,LBP与ZnSO联用对酒精性脂肪肝的缓解具有协同作用,并通过促进脂质代谢、抑制氧化应激、控制炎症反应以及调节大鼠酒精代谢酶的表达与活性,减轻慢性酒精性肝损伤。