Center for Neuroscience and Cell Biology (CNC), University of Coimbra, 3004-504 Coimbra, Portugal.
Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3004-504 Coimbra, Portugal.
Int J Mol Sci. 2021 Jan 5;22(1):461. doi: 10.3390/ijms22010461.
The lack of effective disease-modifying therapeutics to tackle Alzheimer's disease (AD) is unsettling considering the actual prevalence of this devastating neurodegenerative disorder worldwide. Intermittent hypoxic conditioning (IHC) is a powerful non-pharmacological procedure known to enhance brain resilience. In this context, the aim of the present study was to investigate the potential long-term protective impact of IHC against AD-related phenotype, putting a special focus on cognition and mitochondrial bioenergetics and dynamics. For this purpose, six-month-old male triple transgenic AD mice (3×Tg-AD) were submitted to an IHC protocol for two weeks and the behavioral assessment was performed at 8.5 months of age, while the sacrifice of mice occurred at nine months of age and their brains were removed for the remaining analyses. Interestingly, IHC was able to prevent anxiety-like behavior and memory and learning deficits and significantly reduced brain cortical levels of amyloid-β (Aβ) in 3×Tg-AD mice. Concerning brain energy metabolism, IHC caused a significant increase in brain cortical levels of glucose and a robust improvement of the mitochondrial bioenergetic profile in 3×Tg-AD mice, as mirrored by the significant increase in mitochondrial membrane potential (ΔΨm) and respiratory control ratio (RCR). Notably, the improvement of mitochondrial bioenergetics seems to result from an adaptative coordination of the distinct but intertwined aspects of the mitochondrial quality control axis. Particularly, our results indicate that IHC favors mitochondrial fusion and promotes mitochondrial biogenesis and transport and mitophagy in the brain cortex of 3×Tg-AD mice. Lastly, IHC also induced a marked reduction in synaptosomal-associated protein 25 kDa (SNAP-25) levels and a significant increase in both glutamate and GABA levels in the brain cortex of 3×Tg-AD mice, suggesting a remodeling of the synaptic microenvironment. Overall, these results demonstrate the effectiveness of the IHC paradigm in forestalling the AD-related phenotype in the 3×Tg-AD mouse model, offering new insights to AD therapy and forcing a rethink concerning the potential value of non-pharmacological interventions in clinical practice.
间歇性低氧训练(IHC)是一种强大的非药物干预手段,已知其可增强大脑的抗逆性。在这种情况下,本研究旨在探究 IHC 对 AD 相关表型的潜在长期保护作用,特别关注认知功能和线粒体生物能学和动力学。为此,将 6 月龄的三转基因 AD 小鼠(3×Tg-AD)进行为期两周的 IHC 处理,并在 8.5 月龄时进行行为评估,然后在 9 月龄时处死小鼠,取出其大脑进行其余分析。有趣的是,IHC 可预防焦虑样行为和记忆与学习缺陷,并显著降低 3×Tg-AD 小鼠大脑皮质中的淀粉样蛋白-β(Aβ)水平。关于大脑能量代谢,IHC 可使大脑皮质中的葡萄糖水平显著升高,并显著改善 3×Tg-AD 小鼠的线粒体生物能学特征,表现为线粒体膜电位(ΔΨm)和呼吸控制比(RCR)的显著增加。值得注意的是,线粒体生物能学的改善似乎源自于对线粒体质量控制轴不同但相互交织的方面进行适应性协调的结果。具体而言,我们的结果表明,IHC 有利于线粒体融合,并促进线粒体生物发生、转运和自噬。最后,IHC 还可降低突触相关蛋白 25 kDa(SNAP-25)水平,并增加 3×Tg-AD 小鼠大脑皮质中的谷氨酸和 GABA 水平,提示突触微环境发生重塑。总之,这些结果表明 IHC 范式可有效预防 3×Tg-AD 小鼠模型中的 AD 相关表型,为 AD 治疗提供新的见解,并迫使人们重新思考非药物干预在临床实践中的潜在价值。