Neuro-reparative potential of hyperbaric oxygen therapy in animal models of Alzheimer's and Parkinson's diseases: systematic review and meta-analysis.

IF 3.4 Q3 CLINICAL NEUROLOGY
Aiswarya Radhakrishnan, Debprasad Dutta, Moupali Saha, Srikant Venkatakrishnan, Akshay Kulkarni, Komal Prasad Chandrachari, Paul C Salins, Amritha Suresh
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Abstract

Introduction: This systematic review and meta-analysis explored the efficacy of Hyperbaric oxygen therapy (HBOT) in preclinical models of Alzheimer's disease (AD) and Parkinson's disease (PD).

Methods: Data were extracted as per PRISMA guidelines using specific search criteria, with bias assessed using SYRCLE guidelines. Random-effect models were used for meta-analyses of key outcomes, and forest plots were generated. Outcomes assessed included cognitive and motor performance, neuroinflammation, oxidative stress, mitochondrial function, apoptosis, and dopaminergic neuron survival.

Results: The PRISMA search yielded 8 studies (AD: 3; PD: 5) from a total of 8261 articles identified. A total of 308 animals were reported across the studies; however, 182 were included in the meta-analysis, as only animals from relevant treatment and corresponding control groups with extractable outcome data were eligible for quantitative analysis. HBOT significantly improved cognitive function (reduced escape latency, Standardized Mean Difference; SMD: -2.13), improved spatial memory, and reduced compensatory locomotor activity (decreased distance traveled, SMD: -6.94). The markers of neuroinflammation (lower TNF-α, higher IL-10), oxidative stress (SOD, MDA), mitochondrial biogenesis (SIRT1, PGC-1α, TFAM, VDAC), and anti-apoptotic markers (higher Bcl-xl, lower Bax) showed differences in post-HBO treatment. HBOT also preserved dopaminergic neurons in PD models.

Conclusions: These preclinical findings support HBOT as a potential complementary neuroprotective therapy for AD and PD, warranting further clinical validation.

高压氧治疗在阿尔茨海默病和帕金森病动物模型中的神经修复潜力:系统回顾和荟萃分析
本系统综述和荟萃分析探讨了高压氧治疗(HBOT)在阿尔茨海默病(AD)和帕金森病(PD)临床前模型中的疗效。方法:根据PRISMA指南使用特定的搜索标准提取数据,并使用sycle指南评估偏倚。随机效应模型用于关键结果的荟萃分析,并生成森林图。评估的结果包括认知和运动表现、神经炎症、氧化应激、线粒体功能、细胞凋亡和多巴胺能神经元存活。结果:PRISMA检索从共鉴定的8261篇文章中获得8篇研究(AD: 3; PD: 5)。这些研究共报告了308只动物;然而,182只动物被纳入荟萃分析,因为只有来自相关治疗和相应对照组的动物具有可提取的结局数据才有资格进行定量分析。HBOT显著改善认知功能(减少逃避潜伏期,标准化平均差,SMD: -2.13),改善空间记忆,减少代偿性运动活动(减少行走距离,SMD: -6.94)。神经炎症标志物(TNF-α降低、IL-10升高)、氧化应激(SOD、MDA)、线粒体生物发生(SIRT1、PGC-1α、TFAM、VDAC)和抗凋亡标志物(Bcl-xl升高、Bax降低)在hbo治疗后出现差异。HBOT还保留了PD模型中的多巴胺能神经元。结论:这些临床前研究结果支持HBOT作为AD和PD的潜在补充神经保护疗法,需要进一步的临床验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
35
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