par Malaisse, Willy 
;Hutton, J C;Carpinelli, Angelo;Herchuelz, André ;Sener, Abdullah
Référence Diabetes (New York, N.Y.), 29, 6, page (431-437)
Publication Publié, 1980-06
;Hutton, J C;Carpinelli, Angelo;Herchuelz, André ;Sener, Abdullah Référence Diabetes (New York, N.Y.), 29, 6, page (431-437)
Publication Publié, 1980-06
Article révisé par les pairs
| Résumé : | When isolated rat pancreatic islets are exposed to L-leucine (20 mM), the rate of NH4 production is close to the summed rates of L-[1-14C] leucine decarboxylation and alpha-ketoisocarproate production, whereas the rates of acetoacetate production and L-[U-14C]-leucine oxidation are compatible with conversion of each mole of the amino acid to one mole of acetoacetate and three moles of CO2. ATP content, ATP/ADP ratio, and adenylate charge are maintained at normal values by L-leucine, whereas the NADH/NAD+ ratio (but not the NADPH/NADP+ ratio) is significantly increased. The release of insulin evoked by L-leucine is potentiated by 2-ketoisovalerate, unaffected by L-valine, and inhibited by menadione. L-leucine mimicks the effect of D-glucose on 86Rb+ and 45Ca2+ handling by the islets. However, relative to its rate of oxidation, the insulinotropic effect of L-leucine is less marked than that of D-glucose. This may be due, in part at least, to a decrease in the oxidation of endogenous nutrients. It is concluded that the metabolic, cationic, and secretory effects of L-leucine in isolated islets are not incompatible with the fuel hypothesis for insulin release. |
