par Malaisse, Willy 
;Marynissen, Greta ;Sener, Abdullah
Référence Metabolism, clinical and experimental, 41, 8, page (814-819)
Publication Publié, 1992
;Marynissen, Greta ;Sener, Abdullah Référence Metabolism, clinical and experimental, 41, 8, page (814-819)
Publication Publié, 1992
Article révisé par les pairs
| Résumé : | Rat pancreatic islets cultured for 1 to 5 days in the presence of 20 to 80 mmol/L D-glucose accumulate glycogen in a time- and concentration-dependent manner. When the glycogen-rich islets are incubated for 6 to 10 minutes in the absence of D-glucose, the rate of glycogenolysis is grossly proportional to the glycogen content. Exogenous D-glucose (7 to 20 mmol/L) inhibits glycogenolysis. This inhibitory effect opposes the increase in glycolytic flux attributable to the utilization of exogenous glucose. Both the inhibitory effect of D-glucose on glycogenolysis and the utilization of exogenous hexose tend to be higher with α- than with β-D-glucose. In light of these findings, it is proposed that the interference of D-glucose with glycogenolysis might play a role in the paradoxical changes in insulin output and its altered anomeric specificity in response to D-glucose administration, as is often encountered in non-insulin-dependent diabetic subjects and experimental models of B-cell glucotoxicity. |
