Department of Biochemistry, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre (UKM-MC), Kuala Lumpur 56000, Malaysia.
Nutrients. 2023 Jan 19;15(3):524. doi: 10.3390/nu15030524.
This scoping review aimed to summarise the effects of the ketone body β-hydroxybutyrate. The review details the revealed pathways and functional properties following its intervention in the context of neurodegenerative diseases. In this study, 5 research publications that met the inclusion and exclusion criteria were shortlisted. Following the intervention, we discovered a tendency of reduced inflammatory status in microglia, as evidenced by lower levels of pro-inflammatory mediators produced, reduced microgliosis in afflicted tissues, and enhanced cognitive functions in neurodegenerative models. We found that there is a significant overlap in the mechanism of action of β-hydroxybutyrate (BHB) via activation of the G-protein-Coupled Receptor 109A (GPR109a) receptor and deactivation of the inflammasome complex. Furthermore, although comparing outcomes can be challenging due to the heterogeneity in the study model, the results we have assembled here were consistent, giving us confidence in the intervention's efficacy. We also discussed new studies where BHB is involved in various roles in regulating inflammation in microglia, allowing for fresh therapeutic targets against neurodegeneration. This brief review provides evidence to support the huge potential of BHB in the treatment of neurodegenerative illnesses.
这篇范围界定综述旨在总结酮体β-羟丁酸的作用。该综述详细介绍了在神经退行性疾病背景下,其干预后所揭示的途径和功能特性。在这项研究中,有 5 篇符合纳入和排除标准的研究被选入。干预后,我们发现小胶质细胞炎症状态有下降的趋势,表现为产生的促炎介质水平降低、受累组织中的小胶质细胞增生减少以及神经退行性模型中的认知功能增强。我们发现,β-羟丁酸(BHB)通过激活 G 蛋白偶联受体 109A(GPR109a)受体和失活炎症小体复合物发挥作用的机制有很大的重叠。此外,尽管由于研究模型的异质性,比较结果具有挑战性,但我们在这里汇集的结果是一致的,这使我们对干预的疗效有信心。我们还讨论了新的研究,其中 BHB 参与调节小胶质细胞炎症的各种作用,为针对神经退行性变的新治疗靶点提供了依据。这篇简短的综述提供了证据,支持 BHB 在治疗神经退行性疾病方面具有巨大的潜力。