{"title":"烟酰胺腺嘌呤二核苷酸前体在临床前啮齿动物模型中治疗认知疾病的潜力的系统综述。","authors":"Musaab Abdulrazzaq Qader, Leila Hosseini, Nasrin Abolhasanpour, Farnaz Oghbaei, Leila Maghsoumi-Norouzabad, Hanieh Salehi-Pourmehr, Fatemeh Fattahi, Reza Naghdi Sadeh","doi":"10.1186/s12868-025-00937-9","DOIUrl":null,"url":null,"abstract":"<p><p>This systematic review sought to assess the impact of nicotinamide adenine dinucleotide (NAD<sup>+</sup>) precursors on cognitive impairments in several diseases in rat/mouse models. Accumulating evidence suggests that inflammation, apoptosis, oxidative stress responses, and mitochondrial dysfunction are potential factors of cognitive deficits in aging, Alzheimer's disease (AD), diabetes, traumatic brain injury (TBI), vascular dementia (VAD), and schizophrenia. NAD<sup>+</sup> precursors have received increased interest due to their unique molecular structure targets antioxidant and inflammatory pathways and mitochondrial function. The PubMed, Scopus, Google Scholar, Embase, and Web of Science databases were searched through May 30, 2024. Studies investigating the effect of NAD<sup>+</sup> precursors on cognitive impairments in rodent models were included. Two reviewers independently extracted and evaluated the data. The PRISMA guidelines for reporting systematic reviews were followed. Thirty preclinical studies were included in the review. Studies have revealed that treatment with NAD<sup>+</sup> rescues cognitive deficits by inhibiting inflammation, oxidative stress, and apoptosis and improving mitochondrial function. Preclinical evidence has demonstrated that treatment with NAD<sup>+</sup> precursors may be more effective in learning and memory recovery in AD, TBI, diabetes, aging, VAD, and schizophrenia. The outcomes of this investigation may lead to additional studies on the use of NAD<sup>+</sup> precursors for treating human cognitive decline.</p>","PeriodicalId":9031,"journal":{"name":"BMC Neuroscience","volume":"26 1","pages":"17"},"PeriodicalIF":2.3000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11877801/pdf/","citationCount":"0","resultStr":"{\"title\":\"A systematic review of the therapeutic potential of nicotinamide adenine dinucleotide precursors for cognitive diseases in preclinical rodent models.\",\"authors\":\"Musaab Abdulrazzaq Qader, Leila Hosseini, Nasrin Abolhasanpour, Farnaz Oghbaei, Leila Maghsoumi-Norouzabad, Hanieh Salehi-Pourmehr, Fatemeh Fattahi, Reza Naghdi Sadeh\",\"doi\":\"10.1186/s12868-025-00937-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This systematic review sought to assess the impact of nicotinamide adenine dinucleotide (NAD<sup>+</sup>) precursors on cognitive impairments in several diseases in rat/mouse models. Accumulating evidence suggests that inflammation, apoptosis, oxidative stress responses, and mitochondrial dysfunction are potential factors of cognitive deficits in aging, Alzheimer's disease (AD), diabetes, traumatic brain injury (TBI), vascular dementia (VAD), and schizophrenia. NAD<sup>+</sup> precursors have received increased interest due to their unique molecular structure targets antioxidant and inflammatory pathways and mitochondrial function. The PubMed, Scopus, Google Scholar, Embase, and Web of Science databases were searched through May 30, 2024. Studies investigating the effect of NAD<sup>+</sup> precursors on cognitive impairments in rodent models were included. Two reviewers independently extracted and evaluated the data. The PRISMA guidelines for reporting systematic reviews were followed. Thirty preclinical studies were included in the review. Studies have revealed that treatment with NAD<sup>+</sup> rescues cognitive deficits by inhibiting inflammation, oxidative stress, and apoptosis and improving mitochondrial function. Preclinical evidence has demonstrated that treatment with NAD<sup>+</sup> precursors may be more effective in learning and memory recovery in AD, TBI, diabetes, aging, VAD, and schizophrenia. The outcomes of this investigation may lead to additional studies on the use of NAD<sup>+</sup> precursors for treating human cognitive decline.</p>\",\"PeriodicalId\":9031,\"journal\":{\"name\":\"BMC Neuroscience\",\"volume\":\"26 1\",\"pages\":\"17\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-03-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11877801/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s12868-025-00937-9\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12868-025-00937-9","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
本系统综述旨在评估烟酰胺腺嘌呤二核苷酸(NAD+)前体对几种疾病大鼠/小鼠模型认知障碍的影响。越来越多的证据表明,炎症、细胞凋亡、氧化应激反应和线粒体功能障碍是衰老、阿尔茨海默病(AD)、糖尿病、创伤性脑损伤(TBI)、血管性痴呆(VAD)和精神分裂症等认知缺陷的潜在因素。NAD+前体由于其独特的分子结构靶向抗氧化和炎症途径以及线粒体功能而受到越来越多的关注。PubMed, Scopus, b谷歌Scholar, Embase和Web of Science数据库被检索到2024年5月30日。包括研究NAD+前体对啮齿动物模型认知障碍的影响。两名审稿人独立提取和评估数据。遵循PRISMA报告系统审查的指导方针。30项临床前研究被纳入综述。研究表明,NAD+治疗通过抑制炎症、氧化应激、细胞凋亡和改善线粒体功能来拯救认知缺陷。临床前证据表明,使用NAD+前体治疗AD、TBI、糖尿病、衰老、VAD和精神分裂症的学习和记忆恢复可能更有效。这项研究的结果可能会导致更多关于使用NAD+前体治疗人类认知衰退的研究。
A systematic review of the therapeutic potential of nicotinamide adenine dinucleotide precursors for cognitive diseases in preclinical rodent models.
This systematic review sought to assess the impact of nicotinamide adenine dinucleotide (NAD+) precursors on cognitive impairments in several diseases in rat/mouse models. Accumulating evidence suggests that inflammation, apoptosis, oxidative stress responses, and mitochondrial dysfunction are potential factors of cognitive deficits in aging, Alzheimer's disease (AD), diabetes, traumatic brain injury (TBI), vascular dementia (VAD), and schizophrenia. NAD+ precursors have received increased interest due to their unique molecular structure targets antioxidant and inflammatory pathways and mitochondrial function. The PubMed, Scopus, Google Scholar, Embase, and Web of Science databases were searched through May 30, 2024. Studies investigating the effect of NAD+ precursors on cognitive impairments in rodent models were included. Two reviewers independently extracted and evaluated the data. The PRISMA guidelines for reporting systematic reviews were followed. Thirty preclinical studies were included in the review. Studies have revealed that treatment with NAD+ rescues cognitive deficits by inhibiting inflammation, oxidative stress, and apoptosis and improving mitochondrial function. Preclinical evidence has demonstrated that treatment with NAD+ precursors may be more effective in learning and memory recovery in AD, TBI, diabetes, aging, VAD, and schizophrenia. The outcomes of this investigation may lead to additional studies on the use of NAD+ precursors for treating human cognitive decline.
期刊介绍:
BMC Neuroscience is an open access, peer-reviewed journal that considers articles on all aspects of neuroscience, welcoming studies that provide insight into the molecular, cellular, developmental, genetic and genomic, systems, network, cognitive and behavioral aspects of nervous system function in both health and disease. Both experimental and theoretical studies are within scope, as are studies that describe methodological approaches to monitoring or manipulating nervous system function.