SKL of Marine Food Processing & Safety Control, National Engineering Research Center of Seafood, School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, China.
West China School of Pharmacy, Sichuan University, Chengdu 610207, China.
Int J Biol Macromol. 2024 Mar;261(Pt 2):129908. doi: 10.1016/j.ijbiomac.2024.129908. Epub 2024 Feb 4.
An alcohol-induced liver injury model was induced in C57BL/6 mice to assess the protective efficacy of Enteromorpha prolifera polysaccharides (EP) against liver damage. Histological alterations in the liver were examined following hematoxylin-eosin (H&E) staining. Biochemical assay kits and ELISA kits were employed to analyze serum and liver biochemical parameters, as well as the activity of antioxidant enzymes and alcohol metabolism-related enzymes. The presence of oxidative stress-related proteins in the liver was detected using western blotting. Liquid chromatography and mass spectrometry were used to profile serum metabolites in mice. The findings demonstrated that EP-H (100 mg/Kg) reduced serum ALT and AST activity by 2.31-fold and 2.32-fold, respectively, when compared to the alcohol-induced liver injury group. H&E staining revealed a significant attenuation of microvesicular steatosis and ballooning pathology in the EP-H group compared to the model group. EP administration was found to enhance alcohol metabolism by regulating metabolite-related enzymes (ADH and ALDH) and decreasing CYP2E1 expression. EP also modulated the Nrf2/HO-1 signaling pathway to bolster hepatic antioxidant capacity. Furthermore, EP restored the levels of lipid metabolites (Glycine, Butanoyl-CoA, and Acetyl-CoA) to normalcy. In summary, EP confers protection to the liver through the regulation of antioxidant activity and lipid metabolites in the murine liver.
采用 C57BL/6 小鼠建立酒精性肝损伤模型,评估浒苔多糖(EP)对肝损伤的保护作用。通过苏木精-伊红(H&E)染色观察肝组织学改变。采用生化试剂盒和 ELISA 试剂盒分析血清和肝生化参数以及抗氧化酶和酒精代谢相关酶的活性。采用 Western blot 检测肝组织中氧化应激相关蛋白的表达。采用液相色谱-质谱联用技术分析小鼠血清代谢物谱。结果表明,与酒精性肝损伤组相比,EP-H(100mg/kg)可使血清 ALT 和 AST 活性分别降低 2.31 倍和 2.32 倍。与模型组相比,EP-H 组的微泡性脂肪变性和气球样变病理明显减轻。EP 可通过调节代谢物相关酶(ADH 和 ALDH)和降低 CYP2E1 表达来促进酒精代谢。EP 还通过调节 Nrf2/HO-1 信号通路来增强肝抗氧化能力。此外,EP 还可使脂质代谢物(甘氨酸、丁酰辅酶 A 和乙酰辅酶 A)的水平恢复正常。综上所述,EP 通过调节抗氧化活性和肝内脂质代谢物对小鼠肝脏发挥保护作用。