An update on the development of drugs for neuropsychiatric disorders:: focusing on the σ1 receptor ligand

被引:86
作者
Hayashi, Teruo [1 ]
Su, Tsung-Ping [1 ]
机构
[1] NIDA, IRP, NIH, Cellular Pathobiol Unit,Dev Plast Sect,Cellular N, Baltimore, MD 21224 USA
关键词
Alzheimer's disease; antidepressant; antipsychotic; depression; endoplasmic reticulum; neurodegenerative disorder; neurotrophic factor; sigma receptor; sigma(1) receptor; stroke;
D O I
10.1517/14728222.12.1.45
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The a, receptor is an intracellular molecule that shares no homology with any mammalian proteins. sigma(1) receptors normally localize at the endoplasmic reticulum and regulate a variety of signal transductions including intracellular Ca2+ dynamics and neurotrophic factor signaling. In the brain, sigma(1) receptors are known to regulate the activity of diverse ion channels via protein-protein interactions. Accumulated evidences strongly indicate that the activation/upregulation of sigma(1) receptors promotes the neuronal differentiation as well as a robust antiapoptotic action. In animals, sigma(1) receptor agonists exhibit an antidepressant-like action. Furthermore, the agonists enhanced neuronal survival eventhough they were administered several hours after a brain ischemia. Thus, primary clinical targets of sigma(1) receptor ligands are proposed to include stroke, neurodegenerative disorders and depression. Ligands for the sigma(1) receptor may constitute a new class of therapeutic drugs targeting an endoplasmic reticular protein.
引用
收藏
页码:45 / 58
页数:14
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