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中国精品科技期刊2020
郝世奇,李雅菲,吴晓云,等. 骆驼乳对非酒精性脂肪肝小鼠糖脂代谢的影响[J]. 华体会体育,2023,44(6):376−383. doi: 10.13386/j.issn1002-0306.2022060164.
引用本文: 郝世奇,李雅菲,吴晓云,等. 骆驼乳对非酒精性脂肪肝小鼠糖脂代谢的影响[J]. 华体会体育,2023,44(6):376−383. doi: 10.13386/j.issn1002-0306.2022060164.
HAO Shiqi, LI Yafei, WU Xiaoyun, et al. Effects of Camel Milk on Glucolipid Metabolism in Mice with Nonalcoholic Fatty Liver Disease[J]. Science and Technology of Food Industry, 2023, 44(6): 376−383. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022060164.
Citation: HAO Shiqi, LI Yafei, WU Xiaoyun, et al. Effects of Camel Milk on Glucolipid Metabolism in Mice with Nonalcoholic Fatty Liver Disease[J]. Science and Technology of Food Industry, 2023, 44(6): 376−383. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022060164.

骆驼乳对非酒精性脂肪肝小鼠糖脂代谢的影响

Effects of Camel Milk on Glucolipid Metabolism in Mice with Nonalcoholic Fatty Liver Disease

  • 摘要: 目的:探究骆驼乳对高脂高糖高胆固醇饮食诱导的非酒精性脂肪性肝病(Non-alcoholic Fatty Liver Disease,NAFLD)小鼠糖脂代谢的影响。方法:将50只C57BL6/J雄性小鼠随机分为对照组(NC)、模型组(Mod)、对照骆驼乳组(NCM,3 g·kg−1 bw)、骆驼乳组(CaM,3 g·kg−1 bw)和水飞蓟素组(PC,200 mg·kg−1 bw)。试验12周,建立NAFLD模型,骆驼乳组和水飞蓟素组小鼠在每日固定时间分别灌胃相应剂量的骆驼乳和水飞蓟素。通过测定小鼠体重、空腹血糖、血清生化指标、胰岛素抵抗指数、胰岛素敏感指数、经口葡萄糖耐量及胰岛素耐量,探讨骆驼乳对高脂高糖高胆固醇饮食诱导的NAFLD小鼠糖脂代谢的影响。结果:骆驼乳能显著抑制NAFLD小鼠体重和血糖的升高,并且可以显著降低小鼠血清中总甘油三酯(total triglycerides,TG)、总胆固醇(total cholesterol,TC)、低密度脂蛋白胆固醇(low density lipoprotein cholesterin,LDL-c)、肿瘤坏死因子(tumor necrosis factor,TNF-α)、瘦素(leptin,LEP)和胰岛素(insulin,INS)水平(P<0.05),显著提高小鼠血清中脂联素(adiponectin,ADPN)水平(P<0.05)。骆驼乳组小鼠糖耐量显著升高,胰岛素抵抗减轻,胰岛素敏感度增加(P<0.05),糖脂代谢能力增强。结论:骆驼乳对高脂高糖高胆固醇饮食诱导的NAFLD小鼠糖脂代谢具有调节作用。骆驼乳可能通过减轻小鼠胰岛素抵抗,促进血清脂质转运,增强NAFLD小鼠糖脂代谢能力。

     

    Abstract: Objective: This study was designed to explore the effect of camel milk on glucose and lipid metabolism metabolism in mice with nonalcoholic fatty liver disease induced by high fat, high sugar and high cholesterol diet. Methods: 50 C57BL6/J male mice were randomly divided into control group (NC), model group (Mod), control camel milk group (NCM, 3g·kg−1 bw), camel milk group (CaM, 3 g·kg−1 bw) and silymarin group (PC, 200 mg·kg−1 bw). The model of nonalcoholic fatty liver was established for 12 weeks. The mice in the camel milk group and the silymarin group were gavaged with the corresponding doses of camel milk and silymarin at a fixed time every day, respectively. Body weight, fasting blood glucose, serum biochemical, insulin resistance and insulin sensitivity, oral glucose tolerance and insulin tolerance were measured to investigate the effect of camel milk on glucolipid metabolism in mice with non-alcoholic fatty liver disease induced by high fat, high sugar, and high cholesterol diet. Results: Camel milk significantly inhibited the increase of body weight and blood sugar of NAFLD mice and notably reduced the levels of total triglyceride (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-c), tumor necrosis factor (TNF-α), leptin (LEP) and insulin (INS) (P<0.05). While the adiponectin (ADPN) levels in mice serum was increased (P<0.05). In the camel milk group, the glucose tolerance were significantly increased, insulin resistance was reduced, and insulin sensitivity was significantly improved (P<0.05), indicating glucose and lipid metabolism was enhanced. Conclusion: Camel milk had a modulatory role in glucose and lipid metabolism in NAFLD mice induced by high-fat, high-sugar and high-cholesterol diet, which would increase the glucose and lipid metabolism by alleviating insulin resistance and promoting serum lipid transport.

     

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