高强度间歇训练(HIIT)和哌醋甲酯对曲马多诱导的认知障碍的改善作用:海马氧化应激的作用

IF 2.7 3区 心理学 Q2 BEHAVIORAL SCIENCES
Sara Shirazpour, Farahnaz Taheri, Gholamreza Sepehri, Manzumeh Shamsi Meymandi, Mahla Zangiabadizadeh, Mostafa Zangiabadi, Najmeh Sadat Hosseini, Mohammad Amin Rajizadeh, Sara Sheikhi, Nazanin Sabet
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引用次数: 0

摘要

曲马多(TM)滥用会导致严重的认知功能障碍。本研究旨在探讨8周高强度间歇训练(HIIT)方案和哌醋甲酯(MPH)给药(单独或联合)对慢性TM给药后认知功能和海马氧化应激标志物的影响。方法将56只成年雄性大鼠(200 ~ 250 g)分为8组,分别给予曲马多(50 mg/kg,腹腔注射,第1个月5天/周,第2个月3天/周)、哌甲酯(10 mg/kg,腹腔注射,3次/周,连续60天)、HIIT(5次/周,连续8周)或生理盐水(1 mL,腹腔注射,每天60天)。采用Morris水迷宫(MWM)和被动回避测试评估学习和记忆。采用TBARS法和FRAP法分别测定海马丙二醛(MDA)、谷胱甘肽过氧化物酶(GPx)和总抗氧化能力(TAC)。用商业检测试剂盒检测海马一氧化氮(NO)水平。结果曲马多对学习和记忆的影响显著(p < 0.001)。MPH、HIIT和它们的组合可以减轻这些缺陷。曲马多和MPH增加MDA和NO水平(p < 0.001),降低TAC (p < 0.001)。相比之下,HIIT降低了这些参数,即使存在MPH。事实上,HIIT通过降低MDA和NO (p < 0.001)和增加GPx (p < 0.05)和TAC (p < 0.001)逆转了曲马多和MPH的不良影响。结论:尽管MPH和HIIT干预都显示出减轻曲马多诱导的认知缺陷的希望,但它们的作用机制似乎有很大不同。HIIT可能通过调节氧化应激发挥作用,而MPH似乎破坏了氧化应激,这表明了不同的潜在机制。需要进一步的研究来更详细地阐明这些机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ameliorative Effects of High-Intensity Interval Training (HIIT) and Methylphenidate Against Tramadol-Induced Cognitive Impairment: The Role of Hippocampal Oxidative Stress

Ameliorative Effects of High-Intensity Interval Training (HIIT) and Methylphenidate Against Tramadol-Induced Cognitive Impairment: The Role of Hippocampal Oxidative Stress

Background

Tramadol (TM) abuse results in significant cognitive dysfunction. This study aimed to investigate the impact of an 8-week high-intensity interval training (HIIT) regimen and methylphenidate (MPH) administration (alone and in combination) on cognitive function and hippocampal oxidative stress markers following chronic TM administration.

Methods

Fifty-six adult male rats (200–250 g) were divided into eight groups and received one of the following treatments: tramadol (50 mg/kg, intraperitoneally, 5 days/week for the first month and 3 days/week for the second month), methylphenidate (10 mg/kg, intraperitoneally, 3 times/week for 60 days), HIIT (five sessions/week for 8 weeks), or saline (1 mL, intraperitoneally, daily for 60 days). Learning and memory were assessed using the Morris water maze (MWM) and passive avoidance tests. Hippocampal malondialdehyde (MDA), glutathione peroxidase (GPx), and total antioxidant capacity (TAC) were measured using TBARS and FRAP methods, respectively. Hippocampal nitric oxide (NO) levels were determined with a commercial assay kit.

Results

Tramadol induced significant impairments in learning and memory (p < 0.001). MPH, HIIT, and their combination attenuated these deficits. Tramadol and MPH increased MDA and NO levels (p < 0.001) and reduced TAC (p < 0.001). In contrast, HIIT reduced these parameters, even in the presence of MPH. In fact, HIIT reversed the adverse effects of tramadol and MPH by reducing MDA and NO (p < 0.001) and by increasing GPx (p < 0.05) and TAC (p < 0.001).

Conclusion

Although both MPH and HIIT interventions show promise in mitigating tramadol-induced cognitive deficits, their mechanisms of action appear to differ significantly. HIIT likely exerts its effects by modulating oxidative stress, whereas MPH seems to disrupt it, suggesting distinct underlying mechanisms. Further studies are required to elucidate these mechanisms in greater detail.

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来源期刊
Brain and Behavior
Brain and Behavior BEHAVIORAL SCIENCES-NEUROSCIENCES
CiteScore
5.30
自引率
0.00%
发文量
352
审稿时长
14 weeks
期刊介绍: Brain and Behavior is supported by other journals published by Wiley, including a number of society-owned journals. The journals listed below support Brain and Behavior and participate in the Manuscript Transfer Program by referring articles of suitable quality and offering authors the option to have their paper, with any peer review reports, automatically transferred to Brain and Behavior. * [Acta Psychiatrica Scandinavica](https://publons.com/journal/1366/acta-psychiatrica-scandinavica) * [Addiction Biology](https://publons.com/journal/1523/addiction-biology) * [Aggressive Behavior](https://publons.com/journal/3611/aggressive-behavior) * [Brain Pathology](https://publons.com/journal/1787/brain-pathology) * [Child: Care, Health and Development](https://publons.com/journal/6111/child-care-health-and-development) * [Criminal Behaviour and Mental Health](https://publons.com/journal/3839/criminal-behaviour-and-mental-health) * [Depression and Anxiety](https://publons.com/journal/1528/depression-and-anxiety) * Developmental Neurobiology * [Developmental Science](https://publons.com/journal/1069/developmental-science) * [European Journal of Neuroscience](https://publons.com/journal/1441/european-journal-of-neuroscience) * [Genes, Brain and Behavior](https://publons.com/journal/1635/genes-brain-and-behavior) * [GLIA](https://publons.com/journal/1287/glia) * [Hippocampus](https://publons.com/journal/1056/hippocampus) * [Human Brain Mapping](https://publons.com/journal/500/human-brain-mapping) * [Journal for the Theory of Social Behaviour](https://publons.com/journal/7330/journal-for-the-theory-of-social-behaviour) * [Journal of Comparative Neurology](https://publons.com/journal/1306/journal-of-comparative-neurology) * [Journal of Neuroimaging](https://publons.com/journal/6379/journal-of-neuroimaging) * [Journal of Neuroscience Research](https://publons.com/journal/2778/journal-of-neuroscience-research) * [Journal of Organizational Behavior](https://publons.com/journal/1123/journal-of-organizational-behavior) * [Journal of the Peripheral Nervous System](https://publons.com/journal/3929/journal-of-the-peripheral-nervous-system) * [Muscle & Nerve](https://publons.com/journal/4448/muscle-and-nerve) * [Neural Pathology and Applied Neurobiology](https://publons.com/journal/2401/neuropathology-and-applied-neurobiology)
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