Sara Shirazpour, Farahnaz Taheri, Gholamreza Sepehri, Manzumeh Shamsi Meymandi, Mahla Zangiabadizadeh, Mostafa Zangiabadi, Najmeh Sadat Hosseini, Mohammad Amin Rajizadeh, Sara Sheikhi, Nazanin Sabet
{"title":"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","authors":"Sara Shirazpour, Farahnaz Taheri, Gholamreza Sepehri, Manzumeh Shamsi Meymandi, Mahla Zangiabadizadeh, Mostafa Zangiabadi, Najmeh Sadat Hosseini, Mohammad Amin Rajizadeh, Sara Sheikhi, Nazanin Sabet","doi":"10.1002/brb3.70925","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>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.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>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.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Tramadol induced significant impairments in learning and memory (<i>p</i> < 0.001). MPH, HIIT, and their combination attenuated these deficits. Tramadol and MPH increased MDA and NO levels (<i>p</i> < 0.001) and reduced TAC (<i>p</i> < 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 (<i>p</i> < 0.001) and by increasing GPx (<i>p</i> < 0.05) and TAC (<i>p</i> < 0.001).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>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.</p>\n </section>\n </div>","PeriodicalId":9081,"journal":{"name":"Brain and Behavior","volume":"15 10","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/brb3.70925","citationCount":"0","resultStr":"{\"title\":\"Ameliorative Effects of High-Intensity Interval Training (HIIT) and Methylphenidate Against Tramadol-Induced Cognitive Impairment: The Role of Hippocampal Oxidative Stress\",\"authors\":\"Sara Shirazpour, Farahnaz Taheri, Gholamreza Sepehri, Manzumeh Shamsi Meymandi, Mahla Zangiabadizadeh, Mostafa Zangiabadi, Najmeh Sadat Hosseini, Mohammad Amin Rajizadeh, Sara Sheikhi, Nazanin Sabet\",\"doi\":\"10.1002/brb3.70925\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>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.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>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.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Tramadol induced significant impairments in learning and memory (<i>p</i> < 0.001). MPH, HIIT, and their combination attenuated these deficits. Tramadol and MPH increased MDA and NO levels (<i>p</i> < 0.001) and reduced TAC (<i>p</i> < 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 (<i>p</i> < 0.001) and by increasing GPx (<i>p</i> < 0.05) and TAC (<i>p</i> < 0.001).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>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.</p>\\n </section>\\n </div>\",\"PeriodicalId\":9081,\"journal\":{\"name\":\"Brain and Behavior\",\"volume\":\"15 10\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/brb3.70925\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain and Behavior\",\"FirstCategoryId\":\"102\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/brb3.70925\",\"RegionNum\":3,\"RegionCategory\":\"心理学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain and Behavior","FirstCategoryId":"102","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/brb3.70925","RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
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.
期刊介绍:
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* [Acta Psychiatrica Scandinavica](https://publons.com/journal/1366/acta-psychiatrica-scandinavica)
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