Operation of the Permeability Transition Pore in Rat Heart Mitochondria in Aging

被引:1
|
作者
Odinokova, I., V [1 ]
Baburina, Yu L. [1 ]
Kruglov, A. G. [1 ]
Santalova, I. M. [1 ]
Azarashvili, T. S. [1 ]
Krestinina, O., V [1 ]
机构
[1] Russian Acad Sci, Inst Theoret & Expt Biophys, Ul Inst Skaya 3, Pushchino 142290, Moscow Oblast, Russia
来源
BIOLOGICHESKIE MEMBRANY | 2018年 / 35卷 / 01期
关键词
rat heart mitochondria; mitochondrial permeability transition pore; aging; oxidative stress; AGE-RELATED-CHANGES; 2'; 3'-CYCLIC NUCLEOTIDE 3'-PHOSPHODIESTERASE; MYELIN BASIC-PROTEIN; BRAIN MITOCHONDRIA; SUPEROXIDE FLASHES; COMPLEX-I; BENZODIAZEPINE-RECEPTOR; CELL-DEATH; GENERATION; SITES;
D O I
10.7868/S023347551801005X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The functioning of the mitochondria] permeability transition pore (mPTP) is involved in the mechanism of programmed cell death and mitochondria] dysfunction observed with aging. In this work, the functional state of heart mitochondria isolated from young (mature and 2-3-month old) and old (20-22-month old) rats under the conditions of mPTP opening was studied. In mitochondria of old rats, the rate of absorption of Ca2+ and TPP+ decreased by 40 and 42%, respectively, the threshold concentration of Ca2+ decreased by 20%, and the swelling rate of mitochondria from old animals was by 40% higher than that of mitochondria from young ones. In the heart mitochondria of old animals, the content and production of reactive oxygen species (ROS) varied, the superoxide anion content was increased, and the level of hydroperoxide (H2O2) increased at a threshold calcium concentration. Electron microscopy revealed a decrease in the number of cristae in mitochondria of the rat heart during aging. To study the potential role of proteins modulating the mPTP functioning, the content of 2',3' -cyclonucleotide-3'-phosphodiesterase (CN Pase) and translocator protein (TSPO) in heart mitochondria of rats from different ages was measured. A significant age-related decrease in the level of CNPase and an increase in the amount of TSPO was detected. The role of these proteins in the mitochondrial dysfunction observed during aging is discussed.
引用
收藏
页码:42 / 51
页数:10
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