Cooperative role of the glucagon-like peptide-1 receptor and 3-adrenergic-mediated signalling on fat mass reduction through the downregulation of PKA/AKT/AMPK signalling in the adipose tissue and muscle of rats

被引:47
作者
Decara, J. [1 ]
Rivera, P. [2 ]
Arrabal, S. [1 ]
Vargas, A. [1 ]
Serrano, A. [1 ]
Pavon, F. J. [1 ]
Dieguez, C. [3 ,4 ]
Nogueiras, R. [3 ,4 ]
Rodriguez de Fonseca, F. [1 ]
Suarez, J. [1 ,5 ]
机构
[1] Univ Malaga, Inst Invest Biomed Malaga, Hosp Univ Reg Malaga, UGC Salud Mental, Malaga, Spain
[2] Hosp Infantil Univ Nino Jesus, Dept Endocrinol, Fdn Invest Biomed, Madrid, Spain
[3] Univ Santiago De Compostela, Dept Physiol, Inst Invest Sanitaria, Sch Med,CIMUS, Santiago De Compostela, Spain
[4] Inst Salud Carlos III, CIBER OBN, Madrid, Spain
[5] Univ Malaga, Dept Biol Celular Genet & Fisiol, IBIMA, Fac Ciencias, Malaga, Spain
关键词
3-adrenergic receptor; adipose tissue; glucagon-like peptide-1; lipid metabolism; muscle; thermogenesis; SYMPATHETIC-NERVOUS-SYSTEM; ACTIVATED PROTEIN-KINASE; GLP-1; RECEPTOR; SKELETAL-MUSCLE; FOOD-INTAKE; BETA(3)-ADRENOCEPTOR AGONIST; GENE-EXPRESSION; ACID OXIDATION; ANTIOBESITY EFFICACY; HEPATIC STEATOSIS;
D O I
10.1111/apha.13008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
AimTo explore the cooperation of GLP-1 receptor and 3-adrenergic receptor (3-AR)-mediated signalling in the control of fat mass/feeding behaviour by studying the effects of a combined therapy composed of the GLP-1R agonist liraglutide and the 3-AR agonist CL316243. MethodsThe study included the analysis of key mechanisms regulating lipid/cholesterol metabolism, and thermogenesis in brown (BAT) and epididymal white (eWAT) adipose tissues, abdominal muscle and liver of male rats. ResultsCL316243 (1mgkg(-1)) and liraglutide (100gkg(-1)) co-administration over 6days potentiated an overall negative energy balance (reduction in food intake, body weight gain, fat/non-fat mass ratio, liver fat content, and circulating levels of non-essential fatty acids, triglycerides, very low-density lipoprotein-cholesterol and leptin). These effects were accompanied by increased plasma levels of insulin and IL6. We also observed increased gene expression of uncoupling proteins regulating thermogenesis in BAT/eWAT (Ucp1) and muscle (Ucp2/3). Expression of transcription factor and enzymes involved either in de novo lipogenesis (Chrebp, Acaca, Fasn, Scd1, Insig1, Srebp1) or in fatty acid -oxidation (Cpt1b) was enhanced in eWAT and/or muscle but decreased in BAT. Ppar and Ppar, essentials in lipid flux/storage, were decreased in BAT/eWAT but increased in the muscle and liver. Cholesterol synthesis regulators (Insig2, Srebp2, Hmgcr) were particularly over-expressed in muscle. These GLP-1R/3-AR-induced metabolic effects were associated with the downregulation of cAMP-dependent signalling pathways (PKA/AKT/AMPK). ConclusionCombined activation of GLP-1 and 3-ARs potentiate changes in peripheral pathways regulating lipid/cholesterol metabolism in a tissue-specific manner that favours a switch in energy availability/expenditure and may be useful for obesity treatment.
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页数:20
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