The novel mechanism of recombinant human ciliary neurotrophic factor on the anti-diabetes activity

被引:15
作者
Liu, Qing-Shan
Gao, Mei
Zhu, Shen-Yin
Lie, Shao-Jing
Zhang, Li
Wang, Qiu-Juan
Du, Guan-Hua
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Materia Medica, Beijing 100050, Peoples R China
[2] China Pharmaceut Univ, Nanjing, Peoples R China
[3] Chongqing Univ Med Sci, Chongqing, Peoples R China
关键词
D O I
10.1111/j.1742-7843.2007.00092.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In a previous study, the ciliary neurotrophic factor (CNTF) were demonstrated to lead to weight-loss partly by up-regulating the energy metabolism and the expression of uncoupling protein-1, mitochondrial transcription factor A and nuclear respiratory factor-1 in adipose tissues or muscle. To investigate the up-stream regulators of the expression, recombinant human CNTF (rhCNTF) (0.1, 0.3 and 0.9 mg/kg/day subcutaneously) were administered to KK-Ay mice for 30 days, resulting in reduction of perirenal fat mass, serum free fatty acids and islet triacylglycerol; furthermore, the values of oral glucose tolerance test were found improved. In brown adipose tissues, the gene expressions of peroxisome proliferator-activated receptor a (PPAR alpha) and peroxisome proliferator-activated receptor coactivator-1 a (PGC-1 alpha) were found to be upregulated by rhCNTF. To the best of our knowledge, the changes of gene expression of PPARa and PGC-1 alpha represent new insights into the mechanisms of anti-diabetes by rhCNTF. In addition, the activity of mitochondrial complexII was found to be increased by rhCNTF Stimulation of PPARa, PGC-1 alpha, uncoupling protein-1 and enhanced activity of mitochondrial complex II may be associated with the effects of anti-diabetes. The present study indicates new mechanisms of the activity and mechanisms on anti-diabetes of rhCNTF, which may be a novel anti-diabetes reagent partly acting by enhancing energy metabolism.
引用
收藏
页码:78 / 84
页数:7
相关论文
共 29 条
[1]   PGC-l-related coactivator, a novel, serum-inducible coactivator of nuclear respiratory factor 1-dependent transcription in mammalian cells [J].
Andersson, U ;
Scarpulla, RC .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (11) :3738-3749
[2]   Skeletal muscle overexpression of nuclear respiratory factor 1 increases glucose transport capacity [J].
Baar, K ;
Song, Z ;
Semenkovich, CF ;
Jones, TE ;
Han, DH ;
Nolte, LA ;
Ojuka, EO ;
Chen, M ;
Holloszy, JO .
FASEB JOURNAL, 2003, 17 (12) :1666-1673
[3]   Peroxisome proliferator-activated receptor (PPAR)-α agonism prevents the onset of type 2 diabetes in Zucker diabetic fatty rats:: A comparison with PPARγ agonism [J].
Bergeron, Raynald ;
Yao, Jun ;
Woods, John W. ;
Zycband, Emanuel I. ;
Liu, Cherrie ;
Li, Zhihua ;
Adams, Alan ;
Berger, Joel P. ;
Zhang, Bei B. ;
Moller, David E. ;
Doebber, Thomas W. .
ENDOCRINOLOGY, 2006, 147 (09) :4252-4262
[4]   Ciliary neurotrophic factor AX15 alters energy homeostasis, decreases body weight, and improves metabolic control in diet-induced obese and UCP1-DTA mice [J].
Blüher, S ;
Moschos, S ;
Bullen, J ;
Kokkotou, E ;
Maratos-Flier, E ;
Wiegand, SJ ;
Sleemann, MW ;
Mantzoros, CS .
DIABETES, 2004, 53 (11) :2787-2796
[5]   Free fatty acids in obesity and type 2 diabetes:: defining their role in the development of insulin resistance and β-cell dysfunction [J].
Boden, G ;
Shulman, GI .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2002, 32 :14-23
[6]  
Chaldakov George N, 2003, Med Sci Monit, V9, pHY19
[7]   Peroxisome proliferator-activated receptor δ activates fatty acid oxidation in cultured neonatal and adult cardiomyocytes [J].
Cheng, LH ;
Ding, GL ;
Qin, QH ;
Xiao, Y ;
Woods, D ;
Chen, YQE ;
Yang, QL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 313 (02) :277-286
[8]   EGb 761 protects liver mitochondria against injury induced by in vitro anoxia/reoxygenation [J].
Du, GH ;
Willet, K ;
Mouithys-Mickalad, A ;
Sluse-Goffart, CM ;
Droy-Lefaix, MT ;
Sluse, FE .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (5-6) :596-604
[9]   Role of NADH shuttle system in glucose-induced activation of mitochondrial metabolism and insulin secretion [J].
Eto, K ;
Tsubamoto, Y ;
Terauchi, Y ;
Sugiyama, T ;
Kishimoto, T ;
Takahashi, N ;
Yamauchi, N ;
Kubota, N ;
Murayama, S ;
Aizawa, S ;
Akanuma, Y ;
Aizawa, S ;
Kasai, H ;
Yazaki, Y ;
Kadowaki, T .
SCIENCE, 1999, 283 (5404) :981-985
[10]   Hypothyroid phenotype is contributed by mitochondrial complex I inactivation due to translocated neuronal nitric-oxide synthase [J].
Franco, MC ;
Arciuch, VGA ;
Peralta, JG ;
Galli, S ;
Levisman, D ;
López, LM ;
Romorini, L ;
Poderoso, JJ ;
Carreras, MC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (08) :4779-4786