Adenosine diphosphate and calcium stimulation of respiration in mitochondria from alloxan diabetic rats
โ Scribed by Rita Anne Garrick; James C. Hall
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 605 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0021-9541
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โฆ Synopsis
Abstract
Liver mitochondria from normal and alloxan diabetic rats, isolated in 0.25 M sucrose, were assayed with an oxygen electrode for ADP/O and Ca^+2^/O ratios, respiratory ratio, and respiratory control index. Mitochondria were incubated with two substrates, succinate and ฮฒโhydroxybutyrate; two types of ionic media, Na^+^ medium (Na^+^ the major monovalent cation) and K^+^ medium (K^+^ the major monovalent cation); and two respiratory stimulants, ADP (352 ฮผM) and Ca^+2^ (187 ฮผM). Significant differences between respiratory rates and ADP/O ratios were dependent upon the substrate and ionic medium employed. The results confirm previous studies which showed no alteration in ADP/O ratio but decreased State 3 respiratory rates under similar conditions of K^+^ medium with ADP stimulation in the diabetic. Furthermore, the State 3 respiration was prolonged compared to normal. Ca^+2^ stimulation was the same in normal and diabetic mitochondria in K^+^ medium. Studies in Na^+^ media revealed more significant differences in RCI's, respiratory rates, and ADP/O ratios that were substrate dependent as well as ion dependent. The results from these various studies can be accounted for by an hypothesis linking mitochondrial K^+^ interaction with alterations in the diabetic mitochondria.
๐ SIMILAR VOLUMES
The flux through branched-chain a-ketoacid dehydrogenase and the activity of the branched-chain a-ketoacid dehydrogenase complex were measured in hepatocytes isolated from fed, starved and alloxan diabetic rats. The highest rate of branched-chain a-ketoacid oxidation was found in hepatocytes isolate
Under normal conditions, glucose acutely influences pancreatic islet B, A and D cell secretion. In addition, prior exposure to glucose modulates the secretory responsiveness of these cells (priming effect). We have tested whether alloxan diabetes influences priming effects of glucose on A and D cell