Turovskaya Maria V, Zinchenko Valery P
Institute of Cell Biophysics of the Russian Academy of Sciences, Federal Research Center "Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences", 142290 Pushchino, Russia.
Int J Mol Sci. 2025 Aug 18;26(16):7966. doi: 10.3390/ijms26167966.
Using in vitro models of hypoxia, episodes of short-term hypoxia/reoxygenation, and ischemia-like conditions, we were able to establish different sensitivities of hippocampal neurons to their damaging factors. Using a combination of fluorescence microscopy and immunocytochemistry methods, it was possible to show that GABAergic neurons are the most vulnerable to the damaging effects of hypoxia and ischemia-like conditions, as they have a special metabolism, which is characterized by increased production of reactive oxygen species and nitric oxide. It was shown that long-term hypoxia causes the death of GABAergic neurons due to the induction of a global [Ca] increase, whereas pyramidal neurons are resistant to 30-min hypoxia. Episodes of short-term hypoxia/reoxygenation activate the phenomenon of hypoxic preconditioning in glutamatergic neurons, while this endogenous protective mechanism is absent in GABAergic neurons. Selective activation of PI3K and PKG, combined with NOS inhibition, potentiates the preconditioning effect of hypoxia/reoxygenation in glutamatergic neurons and partially activates this neuroprotective mechanism in GABAergic neurons, as indicated by diminished post-hypoxic NMDA-induced Ca transients. These findings suggest that pharmacological intervention can protect GABAergic neuronal populations. The expression of parvalbumin, calbindin, or calretinin in the cytosol of GABAergic neurons contributes to the suppression of the global [Ca] increase during hypoxia/reoxygenation episodes, which correlates with their survival even in the absence of the hypoxic preconditioning phenomenon. Additionally, all three studied calcium-binding proteins showed potential high efficiency in maintaining the bioenergetics of GABAergic neurons during ischemia-like conditions, limiting ROS production by mitochondria and in the cytosol, and reducing nitric oxide formation. In this case, parvalbumin showed the greatest efficiency.
利用缺氧的体外模型、短期缺氧/复氧发作以及类缺血条件,我们能够确定海马神经元对其损伤因素具有不同的敏感性。通过结合荧光显微镜和免疫细胞化学方法,有可能表明γ-氨基丁酸能(GABAergic)神经元对缺氧和类缺血条件的损伤作用最为敏感,因为它们具有特殊的代谢,其特征是活性氧和一氧化氮的产生增加。结果表明,长期缺氧由于诱导全局[Ca]升高而导致GABAergic神经元死亡,而锥体神经元对30分钟的缺氧具有抗性。短期缺氧/复氧发作激活了谷氨酸能神经元中的缺氧预处理现象,而GABAergic神经元中不存在这种内源性保护机制。PI3K和PKG的选择性激活,结合一氧化氮合酶抑制,增强了谷氨酸能神经元中缺氧/复氧的预处理效应,并在GABAergic神经元中部分激活了这种神经保护机制,缺氧后NMDA诱导的Ca瞬变减少表明了这一点。这些发现表明,药物干预可以保护GABAergic神经元群体。GABAergic神经元胞质中小白蛋白、钙结合蛋白或钙视网膜蛋白的表达有助于抑制缺氧/复氧发作期间全局[Ca]的升高,这与其即使在没有缺氧预处理现象的情况下仍能存活相关。此外,所有三种研究的钙结合蛋白在类缺血条件下维持GABAergic神经元的生物能量学、限制线粒体和胞质中活性氧的产生以及减少一氧化氮的形成方面都显示出潜在的高效率。在这种情况下,小白蛋白显示出最大的效率。