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Title: Ketone bodies and islet function: sup 86 Rb handling and metabolic data

Journal Article · · American Journal of Physiology; (USA)
OSTI ID:6873856

The metabolism of ketone bodies was investigated in rat pancreatic islets incubated in the absence or presence of D-glucose. The generation of {sup 14}CO{sub 2} from 3-{sup 14}C-labeled ketone bodies, the interconversion of D-(-)-beta-hydroxybutyrate and acetoacetate (AcAc), the reciprocal effects of ketone bodies and D-glucose on their respective catabolism, and the influence of these exogenous nutrients on the output of {sup 14}CO{sub 2} from islets preincubated with either L-(U-{sup 14}C)glutamine or (U-{sup 14}C)palmitate provided an estimation of the nutrient-induced changes in O2 uptake that was in fair agreement with the observed modifications of islet respiration. There was a close correlation between such changes and the corresponding values for insulin output. Because the stimulation of insulin release by ketone bodies also coincided with a decrease in 86Rb outflow from prelabeled islets, these findings suggest that the insulinotropic action of ketone bodies is causally linked to their catabolism through an increase in ATP generation rate and a subsequent decrease in K+ conductance. A complementary participation of changes in mitochondrial redox state to stimulus-secretion coupling is considered, however, in the light of comparisons between the effects of D-(-)-beta-hydroxybutyrate and AcAc, respectively, on mitochondrial NADH generation, 45Ca net uptake, and D-(6-{sup 14}C)glucose oxidation.

OSTI ID:
6873856
Journal Information:
American Journal of Physiology; (USA), Vol. 259; ISSN 0002-9513
Country of Publication:
United States
Language:
English

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