PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21470398-7 2011 High extracellular potassium and 10 mM tolbutamide abrogated the inhibition of insulin secretion by GA. Glyceraldehyde, dihydroxyacetone, methylpyruvate, GLP-1, and forskolin, an activator of adenylate cyclase, did not abrogate the inhibition. Glyceraldehyde 104-118 insulin Homo sapiens 79-86 14675555-5 2004 If glucose metabolism through the glycolytic pathway is impaired, as in insulin resistance, there will be a build-up of glyceraldehyde, glyceraldehyde-3-phosphate and dihydroxyacetone phosphate with further metabolism to methylglyoxal, a highly reactive ketoaldehyde. Glyceraldehyde 120-134 insulin Homo sapiens 72-79 9972287-2 1998 Glucose, mannose, fructose, glyceraldehyde and dihydroxyacetone all at 8 mM, significantly enhanced the release of insulin elicited by basal concentrations of these carbohydrates (2 mM). Glyceraldehyde 28-42 insulin Homo sapiens 115-122 9224548-3 1997 Two K(+)-ATP channel openers (diazoxide and BPDZ44) inhibited; while a K(+)-ATP channel blocker (tolbutamide) and metabolizable sugars (glucose, glyceraldehyde) significantly stimulated the output of insulin. Glyceraldehyde 145-159 insulin Homo sapiens 200-207 7646447-0 1995 The stimulation of insulin secretion by D-glyceraldehyde correlates with its rate of oxidation in islet cells. Glyceraldehyde 40-56 insulin Homo sapiens 19-26 7646447-1 1995 D-Glyceraldehyde"s capacity to mimic the effect of D-glucose on insulin secretion has not yet been sufficiently substantiated. Glyceraldehyde 0-16 insulin Homo sapiens 64-71 7646447-7 1995 The ratio of the maximum insulin responses D-glyceraldehyde and D-glucose (57%) correlated with the ratio of their respective maximum rates of oxidation (68%). Glyceraldehyde 43-59 insulin Homo sapiens 25-32 7646447-10 1995 The lower potency of D-glyceraldehyde as an insulin secretagogue than D-glucose is determined by the lower capacity of islets to oxidize the triose compared with the hexose. Glyceraldehyde 21-37 insulin Homo sapiens 44-51 8412503-3 1993 However, glyceraldehyde highly attenuated the insulin-secretory response of pancreatic islets to alpha-D-glucose compared with that to beta-D-glucose. Glyceraldehyde 9-23 insulin Homo sapiens 46-53 1596516-7 1992 The carbohydrate insulin secretagogues mannose and D-glyceraldehyde have also been found to induce islet PGE2 release, but the non-secretagogue carbohydrates L-glucose and lactate do not. Glyceraldehyde 51-67 insulin Homo sapiens 17-24 1347743-1 1992 This study examines the effects of donor age on exogenous somatostatin inhibition of insulin secretion stimulated by 10 mM D-glyceraldehyde and by 20 mM beta-D-glucose in isolated perfused rat pancreas. Glyceraldehyde 123-139 insulin Homo sapiens 85-92 1347743-2 1992 Both 6 and 30 nM synthetic somatostatin-14 affect both glyceraldehyde- and glucose-stimulated insulin secretion to a greater degree in pancreases from old animals (24-27 months) than in those from young (2-5 months). Glyceraldehyde 55-69 insulin Homo sapiens 94-101 2245873-6 1990 Because glyceraldehyde, which enters metabolism at the triose phosphates in the glycolytic pathway, is a potent insulin secretagogue but pyruvate, which is metabolized in the mitochondrion, is not an insulin secretagogue, the proximal signal for glucose-induced insulin release originates with an interaction between the central part of the glycolytic pathway and mitochondrial metabolism. Glyceraldehyde 8-22 insulin Homo sapiens 112-119 2186702-7 1990 The effects of glyceraldehyde suggest that glucose signals the first phase of insulin release by an agonist-like mechanism that originates in the cytosol and requires minimal energy. Glyceraldehyde 15-29 insulin Homo sapiens 78-85 2699445-8 1989 Exposing the cells to 1 mM or 2 mM butyrate for two days, resulted in a 50% increase in cellular insulin content at the expense of a partial (1 mM) or complete (2 mM) loss of stimulated insulin release in response to glyceraldehyde or serine. Glyceraldehyde 217-231 insulin Homo sapiens 186-193 2539042-2 1989 Glyceraldehyde has been known to be an insulin secretagogue for more than 15 years. Glyceraldehyde 0-14 insulin Homo sapiens 39-46 2539042-7 1989 These data suggest that besides stimulating insulin release in islets via its entering metabolism by phosphorylation to glyceraldehyde phosphate in the triokinase reaction, glyceraldehyde could be phosphorylated by Pi in the glyceraldehyde phosphate dehydrogenase reaction to form glycerate 1-phosphate which is probably unmetabolizable in islets. Glyceraldehyde 120-134 insulin Homo sapiens 44-51 2452099-0 1988 Single-channel Ba2+ currents in insulin-secreting cells are activated by glyceraldehyde stimulation. Glyceraldehyde 73-87 insulin Homo sapiens 32-39 2452099-4 1988 Glyceraldehyde, a substance evoking insulin secretion from the RINm5F cells, enhances the voltage-activated Ca2+ channel opening by increasing the mean open time and decreasing the longer of the two mean shut times and also decreases the voltage threshold for channel opening. Glyceraldehyde 0-14 insulin Homo sapiens 36-43 2830753-3 1987 Glyceraldehyde stimulated insulin release in a concentration dependent manner, maximum stimulation occurring at 20 mmol/l. Glyceraldehyde 0-14 insulin Homo sapiens 26-33 25582325-1 2015 BACKGROUND: We have previously shown that serum levels of glyceraldehyde-derived advanced glycation end products (Gly-AGEs) are elevated under oxidative stress and/or diabetic conditions and associated with insulin resistance, endothelial dysfunction and vascular inflammation in humans. Glyceraldehyde 58-72 insulin Homo sapiens 207-214