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The Role of NMDA Receptor Partial Antagonist, Carbamathione, As a Therapeutic Agent for Transient Global Ischemia

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Journal Biomedicines
Date 2023 Jul 29
PMID 37509524
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Abstract

Carbamathione (Carb), an NMDA glutamate receptor partial antagonist, has potent neuroprotective functions against hypoxia- or ischemia-induced neuronal injury in cell- or animal-based stroke models. We used PC-12 cell cultures as a cell-based model and bilateral carotid artery occlusion (BCAO) for stroke. Whole-cell patch clamp recording in the mouse retinal ganglion cells was performed. Key proteins involved in apoptosis, endoplasmic reticulum (ER) stress, and heat shock proteins were analyzed using immunoblotting. Carb is effective in protecting PC12 cells against glutamate- or hypoxia-induced cell injury. Electrophysiological results show that Carb attenuates NMDA-mediated glutamate currents in the retinal ganglion cells, which results in activation of the AKT signaling pathway and increased expression of pro-cell survival biomarkers, e.g., Hsp 27, P-AKT, and Bcl2 and decreased expression of pro-cell death markers, e.g., Beclin 1, Bax, and Cleaved caspase 3, and ER stress markers, e.g., CHOP, IRE1, XBP1, ATF 4, and eIF2α. Using the BCAO animal stroke model, we found that Carb reduced the brain infarct volume and decreased levels of ER stress markers, GRP 78, CHOP, and at the behavioral level, e.g., a decrease in asymmetric turns and an increase in locomotor activity. These findings for Carb provide promising and rational strategies for stroke therapy.

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Cerebral Hypoxia-Induced Molecular Alterations and Their Impact on the Physiology of Neurons and Dendritic Spines: A Comprehensive Review.

Cui C, Jiang X, Wang Y, Li C, Lin Z, Wei Y Cell Mol Neurobiol. 2024; 44(1):58.

PMID: 39105862 PMC: 11303443. DOI: 10.1007/s10571-024-01491-4.

References
1.
Davalos A, Shuaib A, Wahlgren N . Neurotransmitters and pathophysiology of stroke: evidence for the release of glutamate and other transmitters/mediators in animals and humans. J Stroke Cerebrovasc Dis. 2007; 9(6 Pt 2):2-8. DOI: 10.1053/jscd.2000.18908. View

2.
Yenari M . Heat shock proteins and neuroprotection. Adv Exp Med Biol. 2003; 513:281-99. DOI: 10.1007/978-1-4615-0123-7_10. View

3.
Hazell A . Excitotoxic mechanisms in stroke: an update of concepts and treatment strategies. Neurochem Int. 2007; 50(7-8):941-53. DOI: 10.1016/j.neuint.2007.04.026. View

4.
Zhang L, Schallert T, Zhang Z, Jiang Q, Arniego P, Li Q . A test for detecting long-term sensorimotor dysfunction in the mouse after focal cerebral ischemia. J Neurosci Methods. 2002; 117(2):207-14. DOI: 10.1016/s0165-0270(02)00114-0. View

5.
Prentice H, Modi J, Wu J . Mechanisms of Neuronal Protection against Excitotoxicity, Endoplasmic Reticulum Stress, and Mitochondrial Dysfunction in Stroke and Neurodegenerative Diseases. Oxid Med Cell Longev. 2015; 2015:964518. PMC: 4630664. DOI: 10.1155/2015/964518. View