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10.4239/wjd.v9.i6.80

http://scihub22266oqcxt.onion/10.4239/wjd.v9.i6.80
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C6033704!6033704!29988851
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suck abstract from ncbi


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pmid29988851      World+J+Diabetes 2018 ; 9 (6): 80-91
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  • Coagonist of glucagon-like peptide-1 and glucagon receptors ameliorates kidney injury in murine models of obesity and diabetes mellitus #MMPMID29988851
  • Patel VJ; Joharapurkar AA; Kshirsagar SG; Sutariya BK; Patel MS; Patel HM; Pandey DK; Bahekar RH; Jain MR
  • World J Diabetes 2018[Jun]; 9 (6): 80-91 PMID29988851show ga
  • AIM: To investigate the role of glucagon-like peptide-1 (GLP-1)/glucagon receptors coagonist on renal dysfunction associated with diabetes and obesity. METHODS: Chronic high-fat diet fed C57BL/6J mice, streptozotocin-treated high-fat diet fed C57BL/6J mice and diabetic C57BLKS/J db/db mice were used as models of diabetes-induced renal dysfunction. The streptozotocin-treated high-fat diet fed mice and db/db mice were treated with the GLP-1 and glucagon receptors coagonist (Aib2 C24 Chimera2, 150 ?g/kg, sc) for twelve weeks, while in chronic high-fat diet fed mice, coagonist (Aib2 C24 Chimera2, 150 ?g/kg, sc) treatment was continued for forty weeks. Kidney function, histology, fibrosis, inflammation, and plasma biochemistry were assessed at the end of the treatment. RESULTS: Coagonist treatment decreased body weight, plasma lipids, insulin resistance, creatinine, blood urea nitrogen, urinary albumin excretion rate and renal lipids. In kidney, expression of lipogenic genes (SREBP-1C, FAS, and SCD-1) was decreased, and expression of genes involved in ?-oxidation (CPT-1 and PPAR-?) was increased due to coagonist treatment. In plasma, coagonist treatment increased adiponectin and FGF21 and decreased IL-6 and TNF-?. Coagonist treatment reduced expression of inflammatory (TNF-?, MCP-1, and MMP-9) and pro-fibrotic (TGF-?, COL1A1, and ?-SMA) genes and also improved histological derangement in renal tissue. CONCLUSION: Coagonist of GLP-1 and glucagon receptors alleviated diabetes and obesity-induced renal dysfunction by reducing glucose intolerance, obesity, and hyperlipidemia.
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