首页> 外文期刊>Neurochemical research >Castration attenuates myelin repair following lysolecithin induced demyelination in rat optic chiasm: an evaluation using visual evoked potential, marker genes expression and myelin staining.
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Castration attenuates myelin repair following lysolecithin induced demyelination in rat optic chiasm: an evaluation using visual evoked potential, marker genes expression and myelin staining.

机译:去势后减弱溶血卵磷脂诱导的大鼠视神经干脱髓鞘后髓鞘的修复:使用视觉诱发电位,标记基因表达和髓鞘染色的评估。

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摘要

Multiple sclerosis (MS) is a demyelinating disease that affects the central nervous system. MS is the most common neurological disorder in young adults with a greater incidence among females. Male gonadal hormones have a protective effect on neural system development and myelin maturation. In this study, we investigate the effect of castration on lysolecithin-induced demyelination and remyelination processes using visual evoked potentials, in addition to measuring the expressions of Olig2, MBP, Nogo-A and GFAP mRNAs as oligodendrocyte or astrocyte markers; and histological assessments by myelin-specific staining. We observed more expanded demyelination with delayed repair process in castrated rats. Expression levels of the aforementioned marker genes confirmed histological and electrophysiological observations. Our results showed a pivotal role for endogenous male hormones in the context of demyelinating insults. It may also account for the different prognosis of MS between male and female genders and provide new insights for therapeutic treatments.
机译:多发性硬化症(MS)是一种影响中枢神经系统的脱髓鞘疾病。 MS是年轻人中最常见的神经系统疾病,在女性中发病率更高。男性性腺激素对神经系统发育和髓鞘成熟具有保护作用。在这项研究中,我们用视觉诱发电位研究了去势对溶血卵磷脂诱导的脱髓鞘和再髓鞘化过程的影响,此外还测量了Olig2,MBP,Nogo-A和GFAP mRNA作为少突胶质细胞或星形胶质细胞标记的表达。和髓鞘特异性染色的组织学评估。我们观察到cast割大鼠的脱髓鞘扩大,但修复过程延迟。上述标记基因的表达水平证实了组织学和电生理学观察。我们的研究结果显示,在脱髓鞘损伤的背景下,内源性雄性激素具有关键作用。它也可能解释了男性和女性之间MS的不同预后,并为治疗方法提供了新的见解。

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