Sex Difference in Oxidative Stress Parameters in Spinal Cord of Rats with Experimental Autoimmune Encephalomyelitis: Relation to Neurological Deficit

被引:0
作者
Mirjana Dimitrijević
Jelena Kotur-Stevuljević
Zorica Stojić-Vukanić
Ivana Vujnović
Ivan Pilipović
Mirjana Nacka-Aleksić
Gordana Leposavić
机构
[1] University of Belgrade,Department of Immunology, Institute for Biological Research “Siniša Stanković”
[2] University of Belgrade,Department for Medical Biochemistry, Faculty of Pharmacy
[3] University of Belgrade,Department of Microbiology and Immunology, Faculty of Pharmacy
[4] Institute of Virology,Immunology Research Centre “Branislav Janković”
[5] Vaccines and Sera “Torlak”,Department of Physiology, Faculty of Pharmacy
[6] University of Belgrade,undefined
来源
Neurochemical Research | 2017年 / 42卷
关键词
Experimental autoimmune encephalomyelitis; Sex differences; Multiple sclerosis; Oxidative stress; Spinal cord; Rat;
D O I
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学科分类号
摘要
The study examined (a) whether there is sex difference in spinal cord and plasma oxidative stress profiles in Dark Agouti rats immunised for experimental autoimmune encephalomyelitis (EAE), the principal experimental model of multiple sclerosis, and (b) whether there is correlation between the oxidative stress in spinal cord and neurological deficit. Regardless of rat sex, with the disease development xanthine oxidase (XO) activity and inducible nitric oxide synthase (iNOS) mRNA expression increased in spinal cord, whereas glutathione levels decreased. This was accompanied by the rise in spinal cord malondialdehyde level. On the other hand, with EAE development superoxide dismutase (SOD) activity decreased, while O2− concentration increased only in spinal cord of male rats. Consequently, SOD activity was lower, whereas O2− concentration was higher in spinal cord of male rats with clinically manifested EAE. XO activity and iNOS mRNA expression were also elevated in their spinal cord. Consistently, in the effector phase of EAE the concentration of advanced oxidation protein product (AOPP) was higher in spinal cord of male rats, which exhibit more severe neurological deficit than their female counterparts. In as much as data obtained in the experimental models could be translated to humans, the findings may be relevant for designing sex-specific antioxidant therapeutic strategies. Furthermore, the study indicated that the increased pro-oxidant–antioxidant balance in plasma may be an early indicator of EAE development. Moreover, it showed that plasma AOPP level may indicate not only actual activity of the disease, but also serve to predict severity of its course.
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页码:481 / 492
页数:11
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共 335 条
[11]  
Nacka-Aleksić M(2001)Regulation of antioxidant enzyme activities in male and female rat macrophages by sex steroids Braz J Med Biol Res 34 683-687
[12]  
Djikić J(2004)Gender differences in superoxide generation in microvessels of hypertensive rats: role of NAD(P)H-oxidase Cardiovasc Res 61 22-29
[13]  
Pilipović I(2000)Effect of bilateral ovariectomy and ovarian steroid hormones on the antioxidant systems and plasma malondialdehyde levels in Wistar rats Endocr Res 26 97-107
[14]  
Stojić-Vukanić Z(2013)Xanthine oxidase mediates axonal and myelin loss in a murine model of multiple sclerosis PloS One 8 e71329-2085
[15]  
Kosec D(2002)Xanthine oxidoreductase activity in human liver disease Am J Gastroenterol 97 2079-1111
[16]  
Bufan B(2005)A new automated colorimetric method for measuring total oxidant status Clin Biochem 38 1103-285
[17]  
Arsenović-Ranin N(2004)A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation Clin Biochem 37 277-254
[18]  
Dimitrijević M(2007)A novel assay for the evaluation of the prooxidant-antioxidant balance, before and after antioxidant vitamin administration in type II diabetes patients Clin Biochem 40 248-198
[19]  
Leposavić G(2015)Oxidative stress and paraoxonase 1 status in acute ischemic stroke patients Atherosclerosis 241 192-169
[20]  
Constantinescu CS(1974)Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite Pharmacology 11 151-35