Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats
Back to article page
OriginalPaper|Updated:2021-08-27
|
Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats
Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats
中国结合医学杂志(英文版)2007年13卷第1期 页码:41-45
Affiliations:
Institute of Integrative Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology,Wuhan,China
Author bio:
Funds:
Supported by the National Natural Science Foundation of P. R. China (No. 30371816) and Specialized Research Fund for the Doctoral Program of Higher Education (No. 20030487008)
Chen, G., Lu, Fe., Jin, D. et al. Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats., Chin. J Integ. Med. 13, 41–45 (2007). https://doi.org/10.1007/s11655-007-0041-9
Chen Guang, Lu Fu-er, Jin Dan, et al. Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats[J]. Chinese Journal of Integrative Medicine, 2007,13(1):41-45.
Chen, G., Lu, Fe., Jin, D. et al. Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats., Chin. J Integ. Med. 13, 41–45 (2007). https://doi.org/10.1007/s11655-007-0041-9DOI:
Chen Guang, Lu Fu-er, Jin Dan, et al. Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats[J]. Chinese Journal of Integrative Medicine, 2007,13(1):41-45. DOI: 10.1007/s11655-007-0041-9.
Effect of Huanglian Jiedu Decoction (黄连解毒汤) on glucose transporter 4 expression in adipose and skeletal muscle tissues of insulin resistant rats
摘要
To investigate the effects of Huanglian Jiedu Decoction (黄连解毒汤
HLJDD) on glucose transporter 4 (GLUT4) protein expressions in insulin-resistant murine target tissues. The experimental male Wistar rats were established into insulin resistant models by injecting streptozotocin (STZ 30 mg/kg) via caudal vein and feeding them with high fat high caloric diet
and randomly divided into the model group
the aspirin group and the HLJDD group. Besides
a normal group was set up for control. Changes of body weight (BW)
levels of serum fasting blood glucose (FBG)
serum fasting insulin (FINS) and oral glucose tolerance test (OGTT) were routinely determined. The expression of GLUT4 protein in adipose and skeletal muscle tissues before and after insulin stimulation was determined with Western blot. In the HLJDD group after treatment
BW and FBG got decreased
OGTT improved
and the expression and translocation of GLUT4 protein elevated obviously
either before or after insulin stimulation
as compared with those in the model group
showing significant differences respectively. The mechanism of improving insulin resistance by HLJDD is probably associated with its effect in elevating GLUT4 protein expression and translocation in adipose and skeletal muscle tissues of insulin resistant rats.
Abstract
To investigate the effects of Huanglian Jiedu Decoction (黄连解毒汤
HLJDD) on glucose transporter 4 (GLUT4) protein expressions in insulin-resistant murine target tissues. The experimental male Wistar rats were established into insulin resistant models by injecting streptozotocin (STZ 30 mg/kg) via caudal vein and feeding them with high fat high caloric diet
and randomly divided into the model group
the aspirin group and the HLJDD group. Besides
a normal group was set up for control. Changes of body weight (BW)
levels of serum fasting blood glucose (FBG)
serum fasting insulin (FINS) and oral glucose tolerance test (OGTT) were routinely determined. The expression of GLUT4 protein in adipose and skeletal muscle tissues before and after insulin stimulation was determined with Western blot. In the HLJDD group after treatment
BW and FBG got decreased
OGTT improved
and the expression and translocation of GLUT4 protein elevated obviously
either before or after insulin stimulation
as compared with those in the model group
showing significant differences respectively. The mechanism of improving insulin resistance by HLJDD is probably associated with its effect in elevating GLUT4 protein expression and translocation in adipose and skeletal muscle tissues of insulin resistant rats.
Mueckler M, Caruso C, Baldwin SA, et al. Sequence and structure of a human glucose transporter. Science 1985; 229: 941–945.
Bryant NJ, Govers R, James DE. Regulated transport of the glucose transporter GLUT4. Nat Rev Mol Cell Biol 2002; 3: 267–277.
Leng SH, Lu FE, Tu QN, et al. Effects of Huanglian Jiedu Decoction on blood glucose and lipids metabolisms in type II diabetic rats. Chin J Basic Med Tradit Chin Med 2003; 9(4): 43–45.
Leng SH, Lu FE, et al. Therapeutic effects of berberine in impaired glucose tolerance rats and its influence on insulin secretion. Acta Pharmacol Sin 2004; 25: 496–502.
Lu FE, He MK, Wang KF, Leng SH. Effects and mechanisms of berberine on hyperlipidemic and insulin resistant rats. Proceedings China Association Sci Technol 2004; 1(1): 141–144.
Tremblay F, Lavigne C, Jacques H, et al. Dietary cod protein restores insulin-induces activation of phosphatidylinositol 3-kinase/AKT and GLUT4 translocation to the T-tubules in skeletal muscle of high-fat-fed obese rats. Diabetes 2003; 52: 29–37.
Wu HY, Jiang XQ, Chen XQ. Study on extraction process for Huanglianjiedu capsules. Chin Tradit Patent Med 1998; 20(11): 1–3.
Yuan M, Konstantopoulos N, Lee J, et al. Reversal of obesity-and diet-induced insulin resistance with salicylates or targeted disruption of IKKβ. Science 2001; 293: 1673–1677.
Klip A, Ramlal T, Young DA, et al. Insulin-induced translocation of glucose transporters in rat hindlimb muscles. FEBS Lett 1987; 224: 224–230.
Harrison SA, Buxton JM, Clancy BM, et al. Evidence that erythroid-type glucose transporter intrinsic activity is modulated by cadmium treatment of mouse 3T3-L1 cells. J Biol Chem 1991; 266: 19438–19449.
Lazar MA. How obesity causes diabetes: not a tall tale. Science 2005; 307: 373–375.
Lu FE, Wang ZM, Guo AQ. Exploration on the hypothesis of treating diabetes mellitus with the detoxification principle of traditional Chinese medicine. Chin J Basic Med Tradit Chin Med 2002; 8(5): 335–337.
Ye AL, Lu FE, Xu LJ. et al. Effects of Huanglian Jiedu Decoction on IRS-1 expression and tyrosine phosphorylation level in skeletal muscles of the rats with insulin resistanc. J Tradit Chin Med 2005;46(9): 695–697.
Somwar R, Kim DY, Sweeney G, et al. GLUT4 Translocation precedes the stimulation of glucose uptake by insulin in muscle cells: potential activation of GLUT4 via p38 mitogen-activated protein kinase. Biochem J 2001; 359(Pt 3): 639–649.
Pascoe WS, Jenkins AB, Kusunoki M, et al. Insulin action and determinants of glycaemia in a rat model of type 2 (non-insulin-dependent) diabetes mellitus. Diabetologia 1992; 35: 208–215.
Kraegen EW, Clark PW, Jenkins AB, et al. Development of muscle insulin resistance after liver insulin resistance in high-fat-fed rats. Diabetes 1991; 40: 1397–1403.
Reed MJ, Meszaros K, Entes LJ, et al. A new rat model of type 2 diabetes: the fat-fed, streptozotocin-treated rat. Metabolism 2000;49: 1390–1394.
Pascoe WS, Storlien LH. Inducement by fat feeding of basal hyperglycemia in rats with abnormal beta-cell function. Model for study of etiology and pathogenesis of NIDDM. Diabetes 1990; 39: 226–233.
Hundal RS, Petersen KF, Mayerson AB, et al. Mechanism by which high-dose aspirin improves glucose metabolism in type 2 diabetes. J Clin Invest 2002;109: 1321–1326.
Furtado LM, Poon V, Klip A. GLUT4 activation: thoughts on possible mechanisms. Acta Physiol Scand 2003;178: 287–296.
Kandror KV. A long search for Glut4 activation. Sci STKE 2003; 2003: pe5.
Ping-tang Recipe (平糖方) improves insulin resistance and attenuates hepatic steatosis in high-fat diet-induced obese rats
Puerarin improve insulin resistance of adipocyte through activating Cb1 binding protein path
Effects of Bushen Tongmai Recipe (补肾通脉方) on protein kinase Bα expression in polycystic ovary rats with insulin resistance
Preliminary comparative study on the effect of different chinese drugs for strengthening Pi (脾) in antagonizing diet induced obesity
Study on insulin resistance and genetic polymorphisms in essential hypertension patients of two different kinds of TCM constitution
相关作者
暂无数据
相关机构
Xiamen Diabetes Institute
Department of Internal Medicine, the First Affiliated Hospital of Xiamen University
Post-Graduate School, Fujian University of Traditional Chinese Medicine
Pharmaceutical College of Harbin Commercial University
Institute of Integrated Traditional and Western Medicine, Affiliated to Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology