Muscle-specific overexpression of AdipoR1 or AdipoR2 gives rise to common and discrete local effects whilst AdipoR2 promotes additional systemic effects

• DOI: 10.1038/srep41792
• Publication Date: 2017-02-01T10:19:38Z
• Authors: Sahar Keshvari; Darren C. Henstridge; Choaping Ng; Mark A. Febbraio; Jonathan P. White...
• Keywords: obesity; 670; Gene Expression; Mice, Obese; adiponectin receptor 1; Diet, High-Fat; Article; Mice; 03 medical and health sciences; blood; Genes, Reporter; lipid metabolism; 616; C741 Medical Biochemistry; Animals; animal; genetics; Obesity; Muscle, Skeletal; mouse; Inflammation; 2. Zero hunger; 0303 health sciences; Multidisciplinary; adiponectin; antibody specificity; C130 Cell Biology; Lipid Metabolism; adipose tissue; Adipose Tissue; inflammation; Organ Specificity; 1000 General; gene expression; Adiponectin; Receptors, Adiponectin; adiponectin receptor; metabolism; lipid diet; B120 Physiology; Signal Transduction

AbstractHypoadiponectinemia and adiponectin resistance are implicated in the aetiology of obesity-related cardiometabolic disorders, hence represent a potential therapeutic axis. Here we characterised the effects of in vivo electrotransfer-mediated overexpression of the adiponectin receptors, AdipoR1 or AdipoR2, into tibialis anterior muscle (TAM) of lean or obese mice. In lean mice, TAM-specific overexpression of AdipoR1 (TAMR1) or AdipoR2 (TAMR2) increased phosphorylation of AMPK, AKT and ERK and expression of the insulin responsive glucose transporter glut4. In contrast, only TAMR2 increased pparα and a target gene acox1. These effects were decreased in obese mice despite no reduction in circulating adiponectin levels. TAMR2 also increased expression of adipoQ in TAM of lean and obese mice. Furthermore, in obese mice TAMR2 promoted systemic effects including; decreased weight gain; reduced epididymal fat mass and inflammation; increased epididymal adipoQ expression; increased circulating adiponectin. Collectively, these results demonstrate that AdipoR1 and AdipoR2 exhibit overlapping and distinct effects in skeletal muscle consistent with enhanced adiponectin sensitivity but these appear insufficient to ameliorate established obesity-induced adiponectin resistance. We also identify systemic effects upon TAMR2 in obese mice and postulate these are mediated by altered myokine production. Further studies are warranted to investigate this possibility which may reveal novel therapeutic approaches.