312 related articles for article (PubMed ID: 9974390)
1. Role of NADH shuttle system in glucose-induced activation of mitochondrial metabolism and insulin secretion.
Eto K; Tsubamoto Y; Terauchi Y; Sugiyama T; Kishimoto T; Takahashi N; Yamauchi N; Kubota N; Murayama S; Aizawa T; Akanuma Y; Aizawa S; Kasai H; Yazaki Y; Kadowaki T
Science; 1999 Feb; 283(5404):981-5. PubMed ID: 9974390
[TBL] [Abstract][Full Text] [Related]
2. [Role of the NADH shuttle system in glucose-induced insulin secretion].
Eto K; Kadowaki T
Nihon Rinsho; 1999 Mar; 57(3):503-14. PubMed ID: 10199125
[TBL] [Abstract][Full Text] [Related]
3. Silencing of the mitochondrial NADH shuttle component aspartate-glutamate carrier AGC1/Aralar1 in INS-1E cells and rat islets.
Casimir M; Rubi B; Frigerio F; Chaffard G; Maechler P
Biochem J; 2009 Dec; 424(3):459-66. PubMed ID: 19764902
[TBL] [Abstract][Full Text] [Related]
4. Pancreatic islet beta-cells transiently metabolize pyruvate.
Rocheleau JV; Head WS; Nicholson WE; Powers AC; Piston DW
J Biol Chem; 2002 Aug; 277(34):30914-20. PubMed ID: 12070148
[TBL] [Abstract][Full Text] [Related]
5. NADH shuttle system regulates K(ATP) channel-dependent pathway and steps distal to cytosolic Ca(2+) concentration elevation in glucose-induced insulin secretion.
Eto K; Suga S; Wakui M; Tsubamoto Y; Terauchi Y; Taka J; Aizawa S; Noda M; Kimura S; Kasai H; Kadowaki T
J Biol Chem; 1999 Sep; 274(36):25386-92. PubMed ID: 10464266
[TBL] [Abstract][Full Text] [Related]
6. [Role of NADH shuttle system in glucose-stimulated insulin secretion].
Eto K; Kadowaki T
Nihon Rinsho; 2002 Jul; 60 Suppl 7():190-207. PubMed ID: 12238047
[No Abstract] [Full Text] [Related]
7. The malate-aspartate NADH shuttle member Aralar1 determines glucose metabolic fate, mitochondrial activity, and insulin secretion in beta cells.
Rubi B; del Arco A; Bartley C; Satrustegui J; Maechler P
J Biol Chem; 2004 Dec; 279(53):55659-66. PubMed ID: 15494407
[TBL] [Abstract][Full Text] [Related]
8. What couples glycolysis to mitochondrial signal generation in glucose-stimulated insulin secretion?
Ishihara H; Wollheim CB
IUBMB Life; 2000 May; 49(5):391-5. PubMed ID: 10902570
[TBL] [Abstract][Full Text] [Related]
9. The oscillatory behavior of pancreatic islets from mice with mitochondrial glycerol-3-phosphate dehydrogenase knockout.
Ravier MA; Eto K; Jonkers FC; Nenquin M; Kadowaki T; Henquin JC
J Biol Chem; 2000 Jan; 275(3):1587-93. PubMed ID: 10636849
[TBL] [Abstract][Full Text] [Related]
10. Histochemical evidence for pathways insulin cells use to oxidize glycolysis-derived NADH.
MacDonald MJ; Kelley PC; Laclau M
Metabolism; 2002 Mar; 51(3):318-21. PubMed ID: 11887167
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial metabolism sets the maximal limit of fuel-stimulated insulin secretion in a model pancreatic beta cell: a survey of four fuel secretagogues.
Antinozzi PA; Ishihara H; Newgard CB; Wollheim CB
J Biol Chem; 2002 Apr; 277(14):11746-55. PubMed ID: 11821387
[TBL] [Abstract][Full Text] [Related]
12. Role of NADH shuttles in glucose-induced insulin secretion from fetal beta-cells.
Tan C; Tuch BE; Tu J; Brown SA
Diabetes; 2002 Oct; 51(10):2989-96. PubMed ID: 12351438
[TBL] [Abstract][Full Text] [Related]
13. Acute metabolic amplification of insulin secretion in mouse islets is mediated by mitochondrial export of metabolites, but not by mitochondrial energy generation.
Panten U; Willenborg M; Schumacher K; Hamada A; Ghaly H; Rustenbeck I
Metabolism; 2013 Oct; 62(10):1375-86. PubMed ID: 23790612
[TBL] [Abstract][Full Text] [Related]
14. Overexpression of mitochondrial FAD-linked glycerol-3-phosphate dehydrogenase does not correct glucose-stimulated insulin secretion from diabetic GK rat pancreatic islets.
Ueda K; Tanizawa Y; Ishihara H; Kizuki N; Ohta Y; Matsutani A; Oka Y
Diabetologia; 1998 Jun; 41(6):649-53. PubMed ID: 9662045
[TBL] [Abstract][Full Text] [Related]
15. Chronic exposure to beta-hydroxybutyrate inhibits glucose-induced insulin release from pancreatic islets by decreasing NADH contents.
Takehiro M; Fujimoto S; Shimodahira M; Shimono D; Mukai E; Nabe K; Radu RG; Kominato R; Aramaki Y; Seino Y; Yamada Y
Am J Physiol Endocrinol Metab; 2005 Feb; 288(2):E372-80. PubMed ID: 15479955
[TBL] [Abstract][Full Text] [Related]
16. Quantitative NAD(P)H/flavoprotein autofluorescence imaging reveals metabolic mechanisms of pancreatic islet pyruvate response.
Rocheleau JV; Head WS; Piston DW
J Biol Chem; 2004 Jul; 279(30):31780-7. PubMed ID: 15148320
[TBL] [Abstract][Full Text] [Related]
17. Dependence on NADH produced during glycolysis for beta-cell glucose signaling.
Dukes ID; McIntyre MS; Mertz RJ; Philipson LH; Roe MW; Spencer B; Worley JF
J Biol Chem; 1994 Apr; 269(15):10979-82. PubMed ID: 8157622
[TBL] [Abstract][Full Text] [Related]
18. alpha-Glycerophosphate shuttle in a clonal beta-cell line.
Meglasson MD; Smith KM; Nelson D; Erecinska M
Am J Physiol; 1989 Jan; 256(1 Pt 1):E173-8. PubMed ID: 2643340
[TBL] [Abstract][Full Text] [Related]
19. Mouse lacking NAD+-linked glycerol phosphate dehydrogenase has normal pancreatic beta cell function but abnormal metabolite pattern in skeletal muscle.
MacDonald MJ; Marshall LK
Arch Biochem Biophys; 2000 Dec; 384(1):143-53. PubMed ID: 11147825
[TBL] [Abstract][Full Text] [Related]
20. Direct Stimulation of Islet Insulin Secretion by Glycolytic and Mitochondrial Metabolites in KCl-Depolarized Islets.
Pizarro-Delgado J; Deeney JT; Corkey BE; Tamarit-Rodriguez J
PLoS One; 2016; 11(11):e0166111. PubMed ID: 27851770
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
