| First Author | Eto K | Year | 1999 |
| Journal | Science | Volume | 283 |
| Issue | 5404 | Pages | 981-5 |
| PubMed ID | 9974390 | Mgi Jnum | J:75839 |
| Mgi Id | MGI:2177914 | Doi | 10.1126/science.283.5404.981 |
| Citation | Eto K, et al. (1999) Role of NADH shuttle system in glucose-induced activation of mitochondrial metabolism and insulin secretion. Science 283(5404):981-5 |
| abstractText | Glucose metabolism in glycolysis and in mitochondria is pivotal to glucose-induced insulin secretion from pancreatic beta cells. One or more factors derived from glycolysis other than pyruvate appear to be required for the generation of mitochondrial signals that lead to insulin secretion. The electrons of the glycolysis-derived reduced form of nicotinamide adenine dinucleotide (NADH) are transferred to mitochondria through the NADH shuttle system. By abolishing the NADH shuttle function, glucose-induced increases in NADH autofluorescence, mitochondrial membrane potential, and adenosine triphosphate content were reduced and glucose-induced insulin secretion was abrogated. The NADH shuttle evidently couples glycolysis with activation of mitochondrial energy metabolism to trigger insulin secretion. |
