Sourav Samanta, Firoz Akhter, Renhao Xue, Alexandre A Sosunov, Long Wu, Doris Chen, Ottavio Arancio, Shi Fang Yan, Shirley ShiDu Yan
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Using aged brain and novel transgenic mice overexpressing neuronal glyoxalase 1 (GLO1), we comprehensively analysed alterations in accumulation/build-up of AGEs and related metabolites in synaptic mitochondria and the association of AGE levels with mitochondrial function. We demonstrated for the first time that synaptic mitochondria are an early and major target of AGEs and the related toxic metabolite methylglyoxal (MG), a precursor of AGEs. MG/AGE-insulted synaptic mitochondria exhibit deterioration of mitochondrial and synaptic function. Such accumulation of MG/AGEs positively correlated with mitochondrial perturbation and oxidative stress in ageing brain. Importantly, clearance of AGE-related metabolites by enhancing neuronal GLO1, a key enzyme for detoxification of AGEs, reduces synaptic mitochondrial AGE accumulation and improves mitochondrial and cognitive function in ageing and AGE-challenged mice. 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引用次数: 0
摘要
线粒体和突触功能障碍是大脑衰老和认知能力下降的病理特征。突触线粒体对于满足突触传递的高能量需求至关重要。然而,人们对与年龄相关的新陈代谢变化与突触线粒体完整性之间的联系知之甚少。为此,我们研究了高级糖化终产物(AGEs)介导线粒体和突触压力的机制,并评估了消除这些有毒代谢物的策略。我们利用衰老的大脑和过表达神经元乙二醛酶 1 (GLO1) 的新型转基因小鼠,全面分析了 AGEs 和相关代谢物在突触线粒体中积累/堆积的变化,以及 AGE 水平与线粒体功能的关联。我们首次证明,突触线粒体是 AGEs 和相关毒性代谢物甲基乙二醛(MG)(AGEs 的前体)的早期和主要目标。受 MG/AGEs 影响的突触线粒体表现出线粒体和突触功能的退化。这种 MG/AGEs 的积累与衰老大脑中的线粒体扰动和氧化应激呈正相关。重要的是,通过增强神经元 GLO1(AGEs 的解毒/关键酶)来清除 AGEs 相关代谢物可减少突触线粒体 AGEs 的积累,并改善衰老和 AGE 挑战小鼠的线粒体和认知功能。此外,我们还通过记录长期电位(LTP)和测量自发发生的微型兴奋性突触后电流(mEPSCs),评估了 AGEs 对作为体外模型的活体脑片和体外培养的海马神经元突触功能的直接影响。神经元 GLO1 可完全恢复 LTP 或 mEPSC 频率的下降,从而挽救 AGE 诱导的突触可塑性和传递的缺陷。这些研究探索了突触线粒体功能障碍与大脑衰老和认知能力下降相关的年龄相关代谢变化之间的相互影响。突触线粒体特别容易受到 AGE 诱导的损伤,这凸显了突触线粒体功能障碍在与年龄相关的认知衰退中突触退化的核心重要性。因此,增强 GLO1 清除有毒代谢物的功能是减少与年龄相关的 AGEs 积累、改善线粒体功能以及学习和记忆的一种治疗方法。
Synaptic mitochondria glycation contributes to mitochondrial stress and cognitive dysfunction.
Mitochondrial and synaptic dysfunction are pathological features of brain ageing and cognitive decline. Synaptic mitochondria are vital for meeting the high energy demands of synaptic transmission. However, little is known about the link between age-related metabolic changes and the integrity of synaptic mitochondria. To this end, we investigated the mechanisms of advanced glycation end product (AGE)-mediated mitochondrial and synaptic stress and evaluated the strategies to eliminate these toxic metabolites. Using aged brain and novel transgenic mice overexpressing neuronal glyoxalase 1 (GLO1), we comprehensively analysed alterations in accumulation/build-up of AGEs and related metabolites in synaptic mitochondria and the association of AGE levels with mitochondrial function. We demonstrated for the first time that synaptic mitochondria are an early and major target of AGEs and the related toxic metabolite methylglyoxal (MG), a precursor of AGEs. MG/AGE-insulted synaptic mitochondria exhibit deterioration of mitochondrial and synaptic function. Such accumulation of MG/AGEs positively correlated with mitochondrial perturbation and oxidative stress in ageing brain. Importantly, clearance of AGE-related metabolites by enhancing neuronal GLO1, a key enzyme for detoxification of AGEs, reduces synaptic mitochondrial AGE accumulation and improves mitochondrial and cognitive function in ageing and AGE-challenged mice. Furthermore, we evaluated the direct effect of AGEs on synaptic function in hippocampal neurons in live brain slices as an ex vivo model and in vitro cultured hippocampal neurons by recording long-term potentiation (LTP) and measuring spontaneously occurring miniature excitatory postsynaptic currents (mEPSCs). Neuronal GLO1 rescues deficits in AGE-induced synaptic plasticity and transmission by full recovery of decline in LTP or frequency of mEPSC. These studies explored crosstalk between synaptic mitochondrial dysfunction and age-related metabolic changes relevant to brain ageing and cognitive decline. Synaptic mitochondria are particularly susceptible to AGE-induced damage, highlighting the central importance of synaptic mitochondrial dysfunction in synaptic degeneration in age-related cognitive decline. Thus, augmenting GLO1 function to scavenge toxic metabolites represents a therapeutic approach to reduce age-related AGE accumulation and improve mitochondrial function and learning and memory.
期刊介绍:
Brain, a journal focused on clinical neurology and translational neuroscience, has been publishing landmark papers since 1878. The journal aims to expand its scope by including studies that shed light on disease mechanisms and conducting innovative clinical trials for brain disorders. With a wide range of topics covered, the Editorial Board represents the international readership and diverse coverage of the journal. Accepted articles are promptly posted online, typically within a few weeks of acceptance. As of 2022, Brain holds an impressive impact factor of 14.5, according to the Journal Citation Reports.