Compensatory Neuroprotective Response of Thioredoxin Reductase against Oxidative-Nitrosative Stress Induced by Experimental Autoimmune Encephalomyelitis in Rats: Modulation by Theta Burst Stimulation

被引:10
|
作者
Stevanovic, Ivana [1 ,2 ]
Ninkovic, Milica [1 ,2 ]
Mancic, Bojana [2 ]
Milivojevic, Marija [1 ]
Stojanovic, Ivana [3 ]
Ilic, Tihomir [2 ]
Vujovic, Maja [4 ]
Djukic, Mirjana [5 ]
机构
[1] Mil Med Acad, Inst Med Res, Belgrade 11000, Serbia
[2] Minist Def, Mil Hlth Dept, Med Fac, Belgrade 11000, Serbia
[3] Univ Nis, Fac Med, Inst Biochem, Nish 18000, Serbia
[4] Univ Nis, Fac Med, Inst Toxicol, Nish 18000, Serbia
[5] Univ Belgrade, Fac Pharm, Dept Toxicol, Belgrade 11221, Serbia
来源
MOLECULES | 2020年 / 25卷 / 17期
关键词
thioredoxin reductase; oxidative stress; nitrosative stress; theta burst stimulation; experimental autoimmune encephalomyelitis; rats; LIPID-PEROXIDATION; GLUTATHIONE; BRAIN; EXPRESSION; METABOLISM; MECHANISMS; DAMAGE; PLASMA; HEALTH; CELLS;
D O I
10.3390/molecules25173922
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
Cortical theta burst stimulation (TBS) structured as intermittent (iTBS) and continuous (cTBS) could prevent the progression of the experimental autoimmune encephalomyelitis (EAE). The interplay of brain antioxidant defense systems against free radicals (FRs) overproduction induced by EAE, as well as during iTBS or cTBS, have not been entirely investigated. This study aimed to examine whether oxidative-nitrogen stress (ONS) is one of the underlying pathophysiological mechanisms of EAE, which may be changed in terms of health improvement by iTBS or cTBS. Dark Agouti strain female rats were tested for the effects of EAE and TBS. The rats were randomly divided into the control group, rats specifically immunized for EAE and nonspecifically immuno-stimulated with Complete Freund's adjuvant. TBS or sham TBS was applied to EAE rats from 14th-24th post-immunization day. Superoxide dismutase activity, levels of superoxide anion (O-2(center dot-)), lipid peroxidation, glutathione (GSH), nicotinamide adenine dinucleotide phosphate (NADPH), and thioredoxin reductase (TrxR) activity were analyzed in rat spinal cords homogenates. The severity of EAE clinical coincided with the climax of ONS. The most critical result refers to TrxR, which immensely responded against the applied stressors of the central nervous system (CNS), including immunization and TBS. We found that the compensatory neuroprotective role of TrxR upregulation is a positive feedback mechanism that reduces the harmfulness of ONS. iTBS and cTBS both modulate the biochemical environment against ONS at a distance from the area of stimulation, alleviating symptoms of EAE. The results of our study increase the understanding of FRs' interplay and the role of Trx/TrxR in ONS-associated neuroinflammatory diseases, such as EAE. Also, our results might help the development of new ideas for designing more effective medical treatment, combining neuropsychological with noninvasive neurostimulation-neuromodulation techniques to patients living with MS.
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页数:14
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