{"title":"Evaluating the Therapeutic Effects of Oxytocin on Animal Model of Alzheimer's Disease: A Systematic Review.","authors":"Ensieh Shafigh, Giti Sadeghi, Negar Abbasi Jamat, Fatemeh Hassanpour, Moslem Solhirad, Leila Karimi-Zandi","doi":"10.2174/0115672050386593250521064527","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Alzheimer's Disease (AD) is the most prevalent progressive neurodegenerative disorder, leading to significant cognitive decline and dementia. Oxytocin (OXT), a peptide hormone synthesized in the hypothalamus, has emerged as a critical player in cognitive functioning. Notably, alterations in OXT levels have been reported in individuals with Alzheimer's disease.</p><p><strong>Methods: </strong>This systematic review aims to synthesize existing literature from databases such as PubMed, Scopus, and Web of Science, focusing on the therapeutic potential of OXT in AD treatment. Two independent individuals conducted the screening procedure for all articles.</p><p><strong>Results: </strong>Our screening revealed that studies investigating OXT therapy primarily involve animal models. These studies consistently demonstrate that, OXT administration mitigates various memory deficits in animal models of AD. These improvements are linked to mechanisms such as reduced microglial-driven inflammation and decreased amyloid-beta (Aβ) deposition, but changes in plaque load do not always correspond directly to cognitive improvement.</p><p><strong>Discussion: </strong>While these findings are promising and oxytocin could be a potential therapeutic candidate for AD, the evidence is limited to animal studies. There is a lack of robust human data, making it difficult to draw firm conclusions about oxytocin's efficacy in people with AD. Ongoing and future clinical trials will be crucial to determine whether these preclinical benefits translate to humans.</p><p><strong>Conclusion: </strong>Despite the limited number of studies examining the effects of OXT on AD and the inherent challenges in conducting such research, the available evidence from animal studies suggests promising results. These findings can serve as a valuable foundation for future human and complementary studies aimed at exploring oxytocin's therapeutic potential in treating AD.</p>","PeriodicalId":94309,"journal":{"name":"Current Alzheimer research","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Alzheimer research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115672050386593250521064527","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Alzheimer's Disease (AD) is the most prevalent progressive neurodegenerative disorder, leading to significant cognitive decline and dementia. Oxytocin (OXT), a peptide hormone synthesized in the hypothalamus, has emerged as a critical player in cognitive functioning. Notably, alterations in OXT levels have been reported in individuals with Alzheimer's disease.
Methods: This systematic review aims to synthesize existing literature from databases such as PubMed, Scopus, and Web of Science, focusing on the therapeutic potential of OXT in AD treatment. Two independent individuals conducted the screening procedure for all articles.
Results: Our screening revealed that studies investigating OXT therapy primarily involve animal models. These studies consistently demonstrate that, OXT administration mitigates various memory deficits in animal models of AD. These improvements are linked to mechanisms such as reduced microglial-driven inflammation and decreased amyloid-beta (Aβ) deposition, but changes in plaque load do not always correspond directly to cognitive improvement.
Discussion: While these findings are promising and oxytocin could be a potential therapeutic candidate for AD, the evidence is limited to animal studies. There is a lack of robust human data, making it difficult to draw firm conclusions about oxytocin's efficacy in people with AD. Ongoing and future clinical trials will be crucial to determine whether these preclinical benefits translate to humans.
Conclusion: Despite the limited number of studies examining the effects of OXT on AD and the inherent challenges in conducting such research, the available evidence from animal studies suggests promising results. These findings can serve as a valuable foundation for future human and complementary studies aimed at exploring oxytocin's therapeutic potential in treating AD.
阿尔茨海默病(AD)是最常见的进行性神经退行性疾病,导致显著的认知能力下降和痴呆。催产素(OXT)是一种在下丘脑合成的肽激素,在认知功能中起着至关重要的作用。值得注意的是,在阿尔茨海默病患者中有OXT水平改变的报道。方法:本系统综述旨在综合PubMed、Scopus、Web of Science等数据库的现有文献,重点关注OXT在AD治疗中的治疗潜力。两名独立人员对所有文章进行了筛选。结果:我们的筛选显示,研究氧化氧疗法的研究主要涉及动物模型。这些研究一致表明,OXT可以减轻AD动物模型中的各种记忆缺陷。这些改善与小胶质细胞驱动的炎症减少和β淀粉样蛋白(Aβ)沉积减少等机制有关,但斑块负荷的变化并不总是与认知改善直接对应。讨论:虽然这些发现是有希望的,催产素可能是一种潜在的治疗AD的候选药物,但证据仅限于动物研究。由于缺乏可靠的人体数据,因此很难得出催产素对阿尔茨海默病患者疗效的确切结论。正在进行的和未来的临床试验将是确定这些临床前益处是否转化为人类的关键。结论:尽管检验OXT对AD影响的研究数量有限,而且开展此类研究存在固有挑战,但从动物研究中获得的现有证据显示出有希望的结果。这些发现可以为未来的人类和补充性研究提供有价值的基础,旨在探索催产素治疗AD的治疗潜力。