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1.
Journal of Zhejiang University. Medical sciences ; (6): 267-276, 2021.
Artigo em Inglês | WPRIM | ID: wpr-879970

RESUMO

Transient receptor potential M2 (TRPM2) ion channel is a non-selective cationic channel that can permeate calcium ions, and plays an important role in neuroinflammation, ischemic reperfusion brain injury, neurodegenerative disease, neuropathic pain, epilepsy and other neurological diseases. In ischemic reperfusion brain injury, TRPM2 mediates neuronal death by modulating the different subunits of glutamate N-methyl-D-aspartic acid receptor in response to calcium/zinc signal. In Alzheimer's disease, TRPM2 is activated by reactive oxygen species generated by β-amyloid peptide to form a malignant positive feedback loop that induces neuronal death and is involved in the pathological process of glial cells by promoting inflammatory response and oxidative stress. In epilepsy, the TRPM2-knockout alleviates epilepsy induced neuronal degeneration by inhibiting autophagy and apoptosis related proteins. The roles of TRPM2 channel in the pathogenesis of various central nervous system diseases and its potential drug development and clinical application prospects are summarized in this review.


Assuntos
Humanos , Peptídeos beta-Amiloides/metabolismo , Doenças Neurodegenerativas , Neuroglia , Canais de Cátion TRPM/genética , Canais de Potencial de Receptor Transitório
2.
Journal of Shanghai Jiaotong University(Medical Science) ; (12): 1484-1488, 2018.
Artigo em Chinês | WPRIM | ID: wpr-843551

RESUMO

As nonselective cation channels, transient receptor potential melastain 2 (TRPM2) channels are widely distributed in the brain, mainly mediate the inflow of Na+ and Ca2+, leading to cell depolarization and the increasement of intracellular concentration of Ca2+, which are involved in many physiological and pathophysiological processes. Due to increased calcium concentration or oxidative stress, channel gating is induced by either direct or indirect formation of adenosine diphosphate ribose (ADPR) that binds to a NUDT9 homology domain (NUDT9-H) in the channel. There is no specific TRPM2 antagonist so far. Considering some pathological processes are mediated by TRPM2 channels, the study and discovery of specific TRPM2 blockers might contribute to the effective treatment of many related diseases.

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