阿托伐他汀对去卵巢大鼠硝酸甘油偏头痛病理生理的影响

Ahmet Can Hiçyılmaz, K. Akgun-Dar
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摘要

摘要目的:偏头痛是影响大多数人群的常见原发性头痛之一。然而,尽管关于偏头痛的病理生理学和各种研究的信息越来越多,但偏头痛发作的潜在机制仍未完全了解。他汀类药物具有抗氧化、抗炎、神经保护作用,可能是治疗神经退行性疾病的有效药物。在偏头痛发病机制中,有多项研究提示一氧化氮(NO)引起偏头痛发作。我们的目的是研究阿托伐他汀(AT)是他汀类药物家族的一员,对去卵巢雌性大鼠偏头痛病理生理的影响,这些大鼠使用硝酸甘油(NTG)刺激偏头痛。材料与方法:取去卵巢的成年sd雌性大鼠分为4组;控制,NTG, AT, NTG+AT。我们检测了免疫组化诱导型一氧化氮(iNOS)、内皮型一氧化氮(eNOS)、神经元型一氧化氮(nNOS)、基质金属蛋白酶-2 (MMP-2)、β-catenin在脑组织上的表达,以及生化c-fos、降钙素基因相关肽(CGRP)、β-catenin、钙结合蛋白B (S100B)、NO、总抗氧化能力(TAS)和总抗氧化能力(TOS)水平。结果:我们的结果显示,AT免疫组化提高eNOS和nNOS水平,降低iNOS。在脑匀浆中,AT降低了S100B、CGRP、c-fos、总亚硝酸盐、β-连环蛋白,但增加了TAS和TOS。MMP-2无明显变化。此外,我们的研究结果表明,AT可以通过其抗炎作用抑制星形胶质细胞的活性,对血脑屏障具有保护作用,降低偏头痛大鼠可能出现的神经退行性疾病的风险。结论:我们的研究结果表明,AT可以抑制星形胶质细胞的活性,具有抗炎作用,对血脑屏障具有保护作用,降低偏头痛大鼠可能发生的神经退行性疾病的风险。我们的研究结果将为该领域的研究提供重要的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effects of Atorvastatin on the Migraine Pathophysiology in Nitroglycerin Induced Migraine in Ovariectomized Rats
ABSTRACT Objective: Migraine is one of the common primary headaches which affects the majority of the population. However, in spite of increasing information on migraine pathophysiology and various researches, the underlying mechanisms of migraine attacks still not completely understood. Statins have antioxidant, anti-inflammatory neuroprotective effects and they might be a useful drug for curing neurodegenerative disorders. There are several studies suggesting nitric oxide (NO) causes migraine attacks in migraine pathogenesis. We aimed to investigate the effects of atorvastatin (AT) which is a member of the statin family, on migraine pathophysiology in ovariectomized female rats in which migraine was stimulated using nitroglycerine (NTG). Materials and Methods: In the study, ovariectomized adult Sprague Dawley female rats were divided into 4 groups; control, NTG, AT, NTG+AT. We examined immunohistochemically inducible nitric oxide (iNOS), endothelial nitric oxide (eNOS), neuronal nitric oxide (nNOS), matrix metalloproteinase-2 (MMP-2), β-catenin expression on brain sections and biochemically c-fos, calcitonin gene-related peptide (CGRP), β-catenin, calcium-binding protein B (S100B), NO, total antioxidant capacity (TAS) and total oxidant capacity (TOS) levels. Results: Our results showed that AT was immunohistochemically increasing eNOS and nNOS levels, and reducing iNOS. In brain homogenates AT was reducing S100B, CGRP, c-fos, total Nitrite-Nitrate, β-catenin but increasing TAS and TOS. There was no change in MMP-2. Also, our findings showed that AT could inhibit astroglial activity with its anti-inflammatory effect and showed a protective effect towards blood-brain barrier and reduced the risk of possible neurodegenerative diseases in rats with migraine. Conclusion: Our findings showed that AT could inhibit astroglial activity with its anti-inflammatory effect and showed a protective effect towards blood-brain barrier and reduced the risk of possible neurodegenerative diseases in rats with migraine. Our results will provide a significant contribution to studies in this field.
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