Thymoquinone Induces Mitochondrial Damage and Death of Cerebellar Granule Neurons

被引:9
|
作者
Stelmashook, E. V. [1 ]
Chetverikov, N. S. [2 ]
Golyshev, S. A. [3 ]
Genrikhs, E. E. [1 ]
Isaev, N. K. [1 ,2 ]
机构
[1] Res Ctr Neurol, Moscow 125367, Russia
[2] Lomonosov Moscow State Univ, Fac Biol, Moscow 119234, Russia
[3] Lomonosov Moscow State Univ, Belozersky Inst Phys Chem Biol, Moscow 119991, Russia
关键词
thymoquinone; mitochondria; cerebellar granule neurons; N-acetyl-L-cysteine; ISCHEMIA-REPERFUSION INJURY; ACETYL-L-CYSTEINE; OXIDATIVE STRESS; NIGELLA-SATIVA; LIPID-PEROXIDATION; DOWN-REGULATION; RAT; APOPTOSIS; TOXICITY; CELLS;
D O I
10.1134/S0006297920020078
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thymoquinone (TQ) exhibits a wide spectrum of biological activities. Most studies on the neurotoxic action of TQ have been carried out in cancer cell lines. Here, we studied the toxic effect of TQ in primary neuronal cultures in vitro. Incubation with 0.04-0.05 mM TQ for 24 h induced the death of cultured cerebellar granule neurons (CGNs) in a dose dependent manner. Neuronal death was preceded by an increase in the reactive oxygen species (ROS) generation, as demonstrated using CellROX Green and MitoSOX Red. Confocal and electron microscopy showed that incubation with 0.05 mM TQ for 5 h induced changes in the intracellular localization of mitochondria and mitochondria hypertrophy and cell swelling. The antioxidant N-acetyl-L-cysteine (2 mM) protected CGNs from the toxic action of TQ. Taken together, these facts suggest that TQ is toxic for normal neurons, while ROS-induced changes in the mitochondria can be one of the major causes of the TQ-induced neuronal damage and death.
引用
收藏
页码:205 / 212
页数:8
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