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

神经保护 多巴胺能 高压氧 医学 神经炎症 氧化应激 帕金森病 疾病 线粒体生物发生 神经科学 动物研究 动物模型 认知 药理学 生物信息学 人体研究 麻醉 系统回顾
作者
Aiswarya Radhakrishnan,Debprasad Dutta,Moupali Saha,Srikant Venkatakrishnan,Akshay Kulkarni,Komal Prasad Chandrachari,Paul C. Salins,Amritha Suresh
出处
期刊:Neurodegenerative disease management [Future Medicine]
卷期号:: 1-9
标识
DOI:10.1080/17582024.2026.2665357
摘要

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.
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