Web11 apr. 2024 · Background: Insulin resistance (IR) is a major contributing factor to the pathogenesis of metabolic syndrome and type 2 diabetes mellitus (T2D). Adipocyte metabolism is known to play a crucial role in IR. Therefore, the aims of this study were to identify metabolism-related proteins that could be used as potential biomarkers of IR and … WebBy comparing transcript levels of 3 insulin secreting MIN6 cell sublines with strong glucose-responsiveness and 3 with mildly reduced responsiveness, we identified 630 differentially expressed genes. Using our recently developed system based on recombinase-mediated cassette exchange, we conducted large-scale generation of stable clones …
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WebInhibition of Insulin Secretion Induces Golgi Morphological Changes. DOI. IWAMOTO TATSUYA Department of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine Department of Pathological Cell Biology, Medical Research Institute, Tokyo Medical and Dental ... Web7 apr. 2024 · The particular fraction can stimulate insulin secretion in glucose-responsive MIN6 clonal beta-cells and improve glucose uptake (approximately 1.5-fold) in L6-GLUT4myc myoblast cells. UD fraction probably has cyclical peptides that facilitate glucose uptake ( Domola, Vu, Robson-Doucette, Sweeney, & Wheeler, 2010 ). rowlands pharmacy charminster bournemouth
(PDF) Extracellular Vesicles in Immune System Regulation and …
WebIn cultured MIN6 cells, which produce and secret insulin, HZL treatment restored insulin secretion through inhibiting the expression of TXNIP and lowering intracellular calcium concentration. These observations mechanistically linked the beneficial effects of HZL with the regulation on cellular redox status and mitochondrial function. WebGlucose stimulated insulin release (GSIR) results (Figure 7b) showed that the recovered MIN6 spheroids exhibited glucose stimulated insulin secretion. Notably, cell spheroids recovered from initial packing density of 10 7 cells/mL showed higher amount of insulin secretion, potentially due to their smaller spheroid diameters. Webassayed glucose-stimulated insulin secretion in rodent islets and the insulinoma cell line MIN6. Insulin release from MIN6 cells and rodent islets was significantly inhibited by the PI indinavir with IC 50 values of 1.1 and 2.1 mol/l, respectively. The uptake of 2-deoxyglucose in MIN6 cells was similarly inhibited (IC 50 of 2.0 mol/ rowlands pharmacy caversham