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丹蛭降糖胶囊改善肥胖大鼠骨骼肌胰岛素抵抗机制的初步研究 被引量:6

A Pilot Study on Mechanisms of Danzhi Jiangtang Capsule in Improvement of Skeletal Insulin Resistance in Obese Rats
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摘要 目的:探讨丹蛭降糖胶囊对高脂饮食诱导的肥胖大鼠骨骼肌脂联素(APN),脂联素受体结合蛋白(APPL1)及葡萄糖转运蛋白4(GLUT4)表达的影响。方法:雄性SD大鼠随机分为普通饮食组(NC组)、单纯高脂饮食组(HF组)、高脂饮食+丹蛭降糖胶囊组(FD组,470 mg·kg-1·d-1)、高脂饮食+吡格列酮组(PIO组,10 mg·kg-1·d-1)、高脂饮食+丹蛭降糖胶囊联合吡格列酮组(FD/PIO组,丹蛭降糖胶囊470 mg·kg-1·d-1+吡格列酮10 mg·kg-1·d-1),ig给药4周。NC组继续普通饲料喂养,给予蒸馏水ig。应用全自动生化分析仪测定骨骼肌甘油三酯(TG)含量;免疫组化及Western blot检测APN,APPL1,GLUT4在骨骼肌组织中的定位以及蛋白表达。结果:1HF组骨骼肌内TG含量显著高于NC组(P<0.01)。相较于HF组,各干预组大鼠骨骼肌TG含量均明显下降(P<0.05)。2免疫组化以及Western blot检测结果显示,HF组APN,APPL1,GLUT4表达较NC组明显降低(P<0.05);各干预组APN,APPL1,GLUT4表达均较HF组明显增加(P<0.05)。3相关分析发现,大鼠骨骼肌TG含量与HOMA-IR呈正相关(r=0.63,P<0.01),与APN,APPL1,GLUT4蛋白均呈负相关(r分别为-0.57,-0.51,-0.62,均P<0.01);HOMA-IR与APN,APPL1,GLUT4蛋白均呈负相关(r分别为-0.49,-0.44,-0.52,均P<0.05,P<0.01)。结论:丹蛭降糖胶囊可减轻骨骼肌脂质沉积,上调骨骼肌组织中的APN,APPL1,GLUT4表达,从而改善骨骼肌胰岛素抵抗。 Objective: To investigate the effect of Danzhi Jiangtang capsule on protein expression of adiponectin( APN),adaptor protein containing PH domain,PTB domain and leucine zipper motif1( APPL1) and glucose transporter 4( GLUT4) in skeletal muscle in obese rats fed with high-fat diet. Method: Male SpragueDawley rats were randomly divided into basal diet group( NC group),untreated high-fat diet group( HF group),high-fat diet plus Danzhi Jiangtang capsule( FD group,470 mg·kg^-1·d^-1,high-fat diet plus pioglitazone( PIO group,10 mg·kg^-1·d^-1,high-fat diet plus Danzhi Jiangtang capsule and pioglitazone( FD/PIO group,470 mg·kg^-1·d^-1or Danzhi Jiangtang capsule plus 10 mg·kg^-1·d^-1or pioglitazone). These treatment drugs were added to the animals by intragastric administration for 4 weeks. The animals in NC group continued to be given the basal diet and distilled water by intragastric administration. The contents of triglyceride in skeletal muscle were measured by automatic biochemical analyzer, and protein expression of APN, APPL1 and GLUT4 were determined by immunohistochemistry and Western blot analysis,respectively. Result: 1The contents of triglyceride in skeletal muscle were significantly higher in HF group than in NC group( P〈 0.01). Compared with HF group,The contents of triglyceride in skeletal muscle in each intervention group were reduced significantly( P〈 0.05). 2Immunohistochemistry and Western blot analysis revealed that protein expression of APN,APPL1 and GLUT4 in skeletal muscle in HF group were signicantly lower than in NC group( P〈 0.05). Compared with HF group,The APN,APPL1 and GLUT4 expression in skeletal muscle in each intervention group were increased significantly( P〈 0.05). 3Pearson correlation analysis showed that the contents of triglyceride in skeletal muscle were positive correlated with HOMA-IR( r = 0. 63,P〈 0.01). By contrast,the contents of triglyceride in skeletal muscle were negative correlated with protein expression of APN, APPL1 and GLUT4( r =- 0. 57,- 0. 51,- 0. 62,respectively,all P〈 0.01). In addition,HOMA-IR was negative correlated with protein expression of APN,APPL1 and GLUT4( r =- 0. 57,- 0. 51,- 0. 62, respectively,all P〈 0.05,P〈 0.01). Conclusion:Danzhi Jiangtang capsule can upregulate the expression of APN,APPL1 and GLUT4 in skeletal muscle of obese rats,reduce lipid deposition in skeletal muscle,thus improve skeletal insulin resistance.
出处 《中国实验方剂学杂志》 CAS 北大核心 2014年第22期151-156,共6页 Chinese Journal of Experimental Traditional Medical Formulae
基金 国家中医临床研究基地专项课题(JDZX2012005)
关键词 肥胖 骨骼肌 脂联素 脂联素受体结合蛋白 丹蛭降糖胶囊 obese skeletal muscle adiponectin adaptor protein containing PH domain PTB domain and leucine zipper motif1 Danzhi Jiangtang capsule
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  • 1方朝晖,章小平.中医药改善2型糖尿病胰岛素抵抗研究思路与方法[J].中国中医药信息杂志,2003,10(12):71-73. 被引量:15
  • 2李光伟,Step.,L.检测人群胰岛素敏感性的一项新指数[J].中华内科杂志,1993,32(10):656-660. 被引量:2126
  • 3Shulman G I.Cellular mechanisms of insulin resistance[ J ].J Clin Invest,2000,106:171-176.
  • 4Dawson R Jr,Annau Z. A behavioral assessment of arcuate nucleus damage after a single injection of monosodium glutamate. Neurobehav Toxocol Teratol,1983,5(4):399-406
  • 5Bunyan J, Murrell EA,Shah PP.The induction of obesity in rodents by means of monosodium glutamate.Br J Nutr, 1976,35(1):25-39
  • 6Nakai T, Tamai T,Takai H, et al.Decreased ketonaemia in the monosodium glutamate-induced obese rats.Life Sci, 1986,38(22):2009-13
  • 7Ochi M,Fukuhara K,Sawaa T, et al.Development of the enididymal adipose tissue in monosodium glutamate induced obese mice. J Nutr Sci Vitaminol,1988,34(3):317-326.
  • 8Betram MA,Estornell E,Barber T, et al.Nitrogen metabolism in obesity induced by monosodium glutamate in rats.Int J Obes, 1992,16(8):555-564
  • 9Caputo FA, Ali SF, Wolff GL, et al. Neonatal MSG reduces hypothalamic DA,β-endorphin and delays gain in genetically obese mice.Pharmacol Biochem Behav,1996,53(2):425-432
  • 10Hirota AE. Monosodium glutamate (MSG)-obese rats develop glucose intolerance and insulin resistance to peripheral glucose uptake. Braz J Med Biol Res,1997,30(5):671-674

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