Copyright
©The Author(s) 2018.
World J Diabetes. Jun 15, 2018; 9(6): 80-91
Published online Jun 15, 2018. doi: 10.4239/wjd.v9.i6.80
Published online Jun 15, 2018. doi: 10.4239/wjd.v9.i6.80
Figure 1 Plasma biochemical change after coagonist treatment in streptozotocin-high-fat and db/db mice.
A: Body weight; B: Fasting glucose; C: HbA1c; D: Fasting insulin; E: OGTT; F: ITT; G: Plasma triglycerides; H: Plasma cholesterol; I: Plasma FGF21; J: Plasma adiponectin; K: Plasma IL-6; L: Plasma TNF-α. Results are shown as mean ± SE (n = 10) for each group and P < 0.05 considered to be statistically significant. HFSTZ: Streptozotocin-high-fat; IPGTT: Intraperitoneal glucose tolerance test; ITT: Insulin tolerance test; HbA1c: Glycosylated hemoglobin; FGF21: Fibroblast growth factor 21; IL-6: Interleukin-6; TNF-α: Tumor necrosis alfa.
- Citation: Patel VJ, Joharapurkar AA, Kshirsagar SG, Sutariya BK, Patel MS, Patel HM, Pandey DK, Bahekar RH, Jain MR. Coagonist of glucagon-like peptide-1 and glucagon receptors ameliorates kidney injury in murine models of obesity and diabetes mellitus. World J Diabetes 2018; 9(6): 80-91
- URL: https://www.wjgnet.com/1948-9358/full/v9/i6/80.htm
- DOI: https://dx.doi.org/10.4239/wjd.v9.i6.80