| Autor: |
Gokulakrishnan K; Department of Neurochemistry, National Institute of Mental Health and Neurosciences (NIMHANS), Hosur Road, Bengaluru, 560029, India. gokulmdrf@gmail.com.; Department of Research Biochemistry, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India. gokulmdrf@gmail.com., Pandey GK; Department of Research Biochemistry, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India.; Department of Genetics, School of Medicine, University of North Carolina, Chapel Hill, 27514, USA., Sathishkumar C; Department of Cell and Molecular Biology, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India., Sundararajan S; Department of Vascular Biology, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India., Durairaj P; Department of Cell and Molecular Biology, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India.; Department of Medical and Health Sciences (MHS), SRM Medical College Hospital & Research Centre, SRM Institute of Science and Technology (SRMIST), Kattankulathur, Chennai, 603203, India., Manickam N; Department of Vascular Biology, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India., Mohan V; Department of Research Biochemistry, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India., Balasubramanyam M; Department of Cell and Molecular Biology, Madras Diabetes Research Foundation, Gopalapuram, Chennai, 600086, India.; Department of Medical and Health Sciences (MHS), SRM Medical College Hospital & Research Centre, SRM Institute of Science and Technology (SRMIST), Kattankulathur, Chennai, 603203, India. |
| Abstrakt: |
A role of Retinol Binding Protein-4 (RBP4) in insulin resistance is widely studied. However, there is paucity of information on its receptor viz., Stimulated by Retinoic Acid-6 (STRA6) with insulin resistance. To address this, we investigated the regulation of RBP4/STRA6 expression in 3T3-L1 adipocytes exposed to glucolipotoxicity (GLT) and in visceral adipose tissue (VAT) from high fat diet (HFD) fed insulin-resistant rats. 3T3-L1 adipocytes were subjected to GLT and other experimental maneuvers with and without vildagliptin or metformin. Real-time PCR and western-blot experiments were performed to analyze RBP4, STRA6, PPARγ gene and protein expression. Adipored staining and glucose uptake assay were performed to evaluate lipid and glucose metabolism. Oral glucose tolerance test (OGTT) and Insulin Tolerance Test (ITT) were performed to determine the extent of insulin resistance in HFD fed male Wistar rats. Total serum RBP4 was measured by quantitative sandwich enzyme-linked immunosorbent assay kit. Adipocytes under GLT exhibited significantly increased RBP4/STRA6 expressions and decreased insulin sensitivity/glucose uptake. Vildagliptin and metformin not only restored the above but also decreased the expression of IL-6, NFκB, SOCS-3 along with lipid accumulation. Furthermore, HFD fed rats exhibited significantly increased serum levels of RBP4 along with VAT expression of RBP4, STRA6, PPARγ, IL-6. These molecules were significantly altered by the vildagliptin/ metformin treatment. We conclude that RBP4/STRA6 pathway is primarily involved in mediating inflammation and insulin resistance in adipocytes and visceral adipose tissues under glucolipotoxicity and in insulin resistant rats. |
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