Oligomycin sensitivity of mitochondrial F1F0-ATPase in diabetes-prone BHE/Cdb rats

被引:14
|
作者
Kim, SB [1 ]
Berdanier, CD [1 ]
机构
[1] Univ Georgia, Dept Foods & Nutr, Athens, GA 30602 USA
关键词
oxidative phosphorylation; mitochondria; diabetes;
D O I
10.1152/ajpendo.1999.277.4.E702
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oligomycin sensitivity of mitochondrial F1F0-ATPase in diabetes-prone BHE/Cdb rats. BHE/Cdb and Sprague-Dawley rats differ in their mitochondrial DNA sequence for the ATPase 6 ("subunit a") gene. Base substitutions in this sequence result in the substitution of asparagine for aspartate at position 101 and the substitution of serine for leucine at position 129. Differences in sensitivity to oligomycin were observed. When the isolated F1F0-ATPase complex was studied and ATPase activity was assessed, that which was isolated from the BHE/Cdb rats was less sensitive to oligomycin inhibition than that which was isolated from the Sprague-Dawley rats. In contrast, when oxygen consumption was measured [oxygen phosphorylation (OXPHOS)] and a dose-response curve was generated with isolated mitochondria from these two strains, there was a shift to the left for the BHE/Cdb rat mitochondria. These mitochondria were more sensitive to oligomycin inhibition of OXPHOS than were mitochondria isolated from Sprague-Dawley rats. The OXPHOS results are consistent with those from human fibroblasts having either a normal or mutated ATPase 6 gene.
引用
收藏
页码:E702 / E707
页数:6
相关论文
共 50 条
  • [1] Modifiers of the oligomycin sensitivity of the mitochondrial F1F0-ATPase
    Pagliarani, Alessandra
    Nesci, Salvatore
    Ventrella, Vittoria
    MITOCHONDRION, 2013, 13 (04) : 312 - 319
  • [2] DEFECTS IN HEPATIC MITOCHONDRIAL F1F0ATPASE OF BHE/CDB RATS
    BAK, SBK
    BERDANIER, CD
    FASEB JOURNAL, 1995, 9 (04): : A749 - A749
  • [3] A point mutation in the mitochondrial DNA of diabetes-prone BHE/cdb rats
    Mathews, CE
    McGraw, RA
    Berdanier, CD
    FASEB JOURNAL, 1995, 9 (15): : 1638 - 1642
  • [4] A POINT MUTATION IN THE MITOCHONDRIAL-DNA OF DIABETES-PRONE BHE/CDB RATS
    MATHEWS, CE
    MCGRAW, RA
    BERDANIER, CD
    FASEB JOURNAL, 1995, 9 (04): : A749 - A749
  • [5] Mitochondrial mutations decrease mitochondrial respiration and ATP production in diabetes-prone BHE Cdb rats
    Mathews, CE
    Kim, SB
    Everts, HB
    Berdanier, CD
    DIABETES, 1999, 48 : A451 - A451
  • [6] Thiol oxidation is crucial in the desensitization of the mitochondrial F1F0-ATPase to oligomycin and other macrolide antibiotics
    Nesci, Salvatore
    Ventrella, Vittoria
    Trombetti, Fabiana
    Pirini, Maurizio
    Pagliarani, Alessandra
    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2014, 1840 (06): : 1882 - 1891
  • [7] Further studies of diabetes-prone BHE/Cdb rats: Increased sensitivity to calcium ion suppression of oxidative phosphorylation
    Kim, SB
    Berdanier, CD
    JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1999, 10 (01): : 31 - 36
  • [8] The IF1 inhibitor protein of the mitochondrial F1F0-ATPase
    Green, DW
    Grover, GJ
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2000, 1458 (2-3): : 343 - 355
  • [9] Attenuation of circadian rhythms of food intake and respiration in aging diabetes-prone BHE/Cdb rats
    Mathews, CE
    Wickwire, K
    Flatt, WP
    Berdanier, CD
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 279 (01) : R230 - R238
  • [10] Effects of chromium and copper depletion on lymphocyte reactivity to mitogens in diabetes-prone BHE/cdb rats
    Rhee, YS
    Burnham, K
    Stoecker, BJ
    Lucas, E
    NUTRITION, 2004, 20 (03) : 274 - 279