枸杞多糖联合有氧运动对非酒精性脂肪肝大鼠的保护作用

被引:5
作者
马佳敏
刘双
张梦伟
高璐璐
高清菡
陶秀娟
范彦娜
杨建军
机构
[1] 宁夏医科大学公共卫生与管理学院
关键词
非酒精性脂肪肝; 枸杞多糖; 有氧运动; 氧化应激; 大鼠;
D O I
10.16050/j.cnki.issn1674-6309.2021.05.002
中图分类号
R285.5 [中药实验药理];
学科分类号
1008 ;
摘要
目的探讨枸杞多糖(lycium barbarum polysaccharide,LBP)联合有氧运动(aerobic exercise,AE)对糖脂代谢异常的非酒精性脂肪肝(non-alcoholic fatty liver disease,NAFLD)大鼠的保护作用及其相关机制。方法 8周龄SD大鼠适应性喂养一周后,随机取9只为对照组,食用普通饲料,剩余大鼠为高脂组,食用高脂饲料。28周末进行葡萄糖耐量试验(oral glucose tolerance test,OGTT)后,将高脂组再随机分为4组(每组8只),分别为模型组、枸杞多糖组、有氧运动组、枸杞多糖联合有氧运动组;对照组食用普通饲料,其余各组继续食用高脂饲料,干预10周后重复OGTT试验。实验结束进行10%水合氯醛麻醉处死,取血液以及组织样本保留备用。肝组织冷冻固定切片,厚10μm,并用油红O染色以检测脂质沉积;血清甘油三酯(triacylglycerol,TG)、总胆固醇(total cholesterol,TC)、高密度脂蛋白(high density lipoprotein,HDL)、低密度脂蛋白(low density lipoprotein,LDL)、谷丙转氨酶(alanine aminotransferase,ALT)、谷草转氨酶(aspartate aminotransferase,AST)、血清空腹胰岛素(fasting insulin,FINS)、丙二醛(malondialdehyde,MDA)、超氧化物歧化酶(superoxide dismutase,SOD)采用相应试剂盒检测,Western blot检测大鼠肝脏组织中解偶联蛋白2(UCP2)、沉默信息调节因子-3(SIRT3)、锰超氧化物歧化酶(MnSOD)蛋白水平。结果与对照组相比,模型组肝细胞质中可见大小不等、不同数量的脂滴;与模型组相比,各干预组肝细胞脂质蓄积均有不同程度的减少。与对照组相比,模型组大鼠TG、TC、LDL、LDL/HDL、AST、ALT、MDA、FINS和胰岛素抵抗指数(HOMA-IR)均升高(P均<0.05),HDL和SOD均降低(P均<0.05)。与对照组大鼠相比,模型组大鼠肝脏组织UCP2、SIRT3和MnSOD蛋白表达降低(P均<0.05)。与模型组比较,各干预组大鼠TG、TC、LDL、LDL/HDL、AST、ALT、MDA、FINS和HOMA-IR水平均降低(P均<0.05),SOD水平增高(P均<0.05)。与模型组相比,各干预组大鼠肝脏组织UCP2、SIRT3和MnSOD蛋白表达均升高(P均<0.05)。与单独干预组相比,联合组大鼠FINS和HOMA-IR水平均降低,肝脏组织UCP2和MnSOD蛋白水平升高(P均<0.05)。结论与单独干预相比,LBP联合AE在改善NAFLD大鼠糖脂代谢、氧化应激和肝脏损伤方面效果更显著,其机制可能与UCP2-SIRT3通路的激活有关。
引用
收藏
页码:439 / 446
页数:8
相关论文
共 24 条
[11]   Berberine attenuates hepatic oxidative stress in rats with non-alcoholic fatty liver disease via the Nrf2/ARE signalling pathway [J].
Deng, Yuanjun ;
Tang, Kairui ;
Chen, Runsen ;
Nie, Huan ;
Liang, Shu ;
Zhang, Jinwen ;
Zhang, Yupei ;
Yang, Qinhe .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2019, 17 (03) :2091-2098
[12]  
A Systematic Review of Potential Therapeutic Use of Lycium Barbarum Polysaccharides in Disease.[J].Sum Sum Kwok;Yashan Bu;Amy Cheuk Yin Lo;Tommy Chung Yan Chan;Kwok Fai So;Jimmy Shiu Ming Lai;Kendrick Co Shih.BioMed Research International.2019,
[13]  
Genipin protects against cerebral ischemia-reperfusion injury by regulating the UCP2-SIRT3 signaling pathway.[J].Busi Zhao;Sun Lian-kun;Xianrui Jiang;Yong Zhang;Jinsong Kang;Hao Meng;Hongyan Li;Su Jing.European Journal of Pharmacology.2018,
[14]   Lycium barbarum polysaccharides protect rat liver from non-alcoholic steatohepatitis-induced injury [J].
Xiao, J. ;
Liong, E. C. ;
Ching, Y. P. ;
Chang, R. C. C. ;
Fung, M. L. ;
Xu, A. M. ;
So, K. F. ;
Tipoe, G. L. .
NUTRITION & DIABETES, 2013, 3 :e81-e81
[15]   Mechanisms of NAFLD development and therapeutic strategies [J].
Friedman, Scott L. ;
Neuschwander-Tetri, Brent A. ;
Rinella, Mary ;
Sanyal, Arun J. .
NATURE MEDICINE, 2018, 24 (07) :908-922
[16]   Current and future pharmacological therapies for NAFLD/NASH [J].
Sumida, Yoshio ;
Yoneda, Masashi .
JOURNAL OF GASTROENTEROLOGY, 2018, 53 (03) :362-376
[17]   Nonalcoholic Fatty Liver Disease and Risk of Incident Type 2 Diabetes: A Meta-analysis [J].
Mantovani, Alessandro ;
Byrne, Christopher D. ;
Bonora, Enzo ;
Targher, Giovanni .
DIABETES CARE, 2018, 41 (02) :372-382
[18]  
Cytoprotective Effect of the UCP2-SIRT3 Signaling Pathway by Decreasing Mitochondrial Oxidative Stress on Cerebral Ischemia–Reperfusion Injury.[J].Jing Su;Jie Liu;Xiao-Yu Yan;Yong Zhang;Juan-Juan Zhang;Li-Chao Zhang;Lian-Kun Sun.International Journal of Molecular Sciences.2017, 7
[19]  
Non-alcoholic fatty liver disease: A sign of systemic disease.[J].Isabella Reccia;Jayant Kumar;Cherif Akladios;Francesco Virdis;Madhava Pai;Nagy Habib;Duncan Spalding.Metabolism.2017,
[20]   Liraglutide ameliorates non-alcoholic fatty liver disease by enhancing mitochondrial architecture and promoting autophagy through the SIRT1/SIRT3-FOXO3a pathway [J].
Tong, Wenxin ;
Ju, Liping ;
Qiu, Miaoyan ;
Xie, Qihai ;
Chen, Ying ;
Shen, Weili ;
Sun, Weihong ;
Wang, Weiqing ;
Tian, Jingyan .
HEPATOLOGY RESEARCH, 2016, 46 (09) :933-943