Calcium Signaling Laboratory, National Neuroscience Institute, 308433, Singapore.
Department of Pharmaceutical Life Sciences, Faculty of Pharmacy, Universiti Teknologi MARA (UiTM), Puncak Alam, 42300, Selangor, Malaysia; Centre for Drug Research, Universiti Sains Malaysia, 11800 Penang, Malaysia.
Neurobiol Dis. 2024 Feb;191:106408. doi: 10.1016/j.nbd.2024.106408. Epub 2024 Jan 9.
Excitotoxicity arises from unusually excessive activation of excitatory amino acid receptors such as glutamate receptors. Following an energy crisis, excitotoxicity is a major cause for neuronal death in neurological disorders. Many glutamate antagonists have been examined for their efficacy in mitigating excitotoxicity, but failed to generate beneficial outcome due to their side effects on healthy neurons where glutamate receptors are also blocked. In this study, we found that during chronic hypoxia there is upregulation and activation of a nonselective cation channel TRPM4 that contributes to the depolarized neuronal membrane potential and enhanced glutamate-induced calcium entry. TRPM4 is involved in modulating neuronal membrane excitability and calcium signaling, with a complex and multifaceted role in the brain. Here, we inhibited TRPM4 using a newly developed blocking antibody M4P, which could repolarize the resting membrane potential and ameliorate calcium influx upon glutamate stimulation. Importantly, M4P did not affect the functions of healthy neurons as the activity of TRPM4 channel is not upregulated under normoxia. Using a rat model of chronic hypoxia with both common carotid arteries occluded, we found that M4P treatment could reduce apoptosis in the neurons within the hippocampus, attenuate long-term potentiation impairment and improve the functions of learning and memory in this rat model. With specificity to hypoxic neurons, TRPM4 blocking antibody can be a novel way of controlling excitotoxicity with minimal side effects that are common among direct blockers of glutamate receptors.
兴奋性毒性是由于兴奋性氨基酸受体(如谷氨酸受体)异常过度激活引起的。在能量危机后,兴奋性毒性是神经紊乱中神经元死亡的主要原因。许多谷氨酸拮抗剂已被研究用于减轻兴奋性毒性的功效,但由于它们对健康神经元的副作用(谷氨酸受体也被阻断)而未能产生有益的结果。在这项研究中,我们发现,在慢性缺氧期间,一种非选择性阳离子通道 TRPM4 的表达和激活上调,这有助于去极化神经元膜电位和增强谷氨酸诱导的钙内流。TRPM4 参与调节神经元膜兴奋性和钙信号转导,在大脑中具有复杂而多方面的作用。在这里,我们使用一种新开发的阻断抗体 M4P 抑制 TRPM4,该抗体可以使静息膜电位复极化,并改善谷氨酸刺激时的钙内流。重要的是,M4P 不会影响健康神经元的功能,因为在正常氧条件下,TRPM4 通道的活性不会上调。在使用双侧颈总动脉阻塞的慢性缺氧大鼠模型中,我们发现 M4P 治疗可以减少海马内神经元的凋亡,减轻长时程增强损伤,并改善该大鼠模型的学习和记忆功能。由于 TRPM4 阻断抗体具有对缺氧神经元的特异性,因此它可以成为一种控制兴奋性毒性的新方法,副作用最小,而直接阻断谷氨酸受体的方法通常会产生副作用。