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西格玛受体:最新进展与新的临床潜力

Sigma receptors: recent advances and new clinical potentials.

作者信息

Bowen W D

机构信息

Unit on Receptor Biochemistry and Pharmacology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0815, USA.

出版信息

Pharm Acta Helv. 2000 Mar;74(2-3):211-8. doi: 10.1016/s0031-6865(99)00034-5.

Abstract

Several recent advances are leading to a better understanding of sigma receptors. Here we focus on our recent findings regarding cellular functions of sigma-2 receptors and discuss their possible clinical implications. Agonists at sigma-2 receptors induced changes in cell morphology and apoptosis in various cell types. Sigma-2 receptor activation produced both transient and sustained increases in [Ca++]i, derived from different intracellular stores. These changes in [Ca++]i and cytotoxic effects are mediated by intracellular sigma-2 receptors. Sigma-2 agonists induced apoptosis in drug-resistant cancer cells, enhanced the potency of DNA damaging agents, and down-regulated expression of p-glycoprotein mRNA. Thus, sigma-2 receptor agonists may be useful in treatment of drug-resistant cancers. Sigma radioligands have been used in tumor imaging. We also discuss how sigma-2 antagonists might prevent the irreversible motor side effects of typical neuroleptics. Sigma-2 receptors may subserve a novel signalling pathway to apoptosis, involved in regulation of cell proliferation and/or viability.

摘要

最近的几项进展使人们对σ受体有了更好的理解。在此,我们重点关注我们最近关于σ-2受体细胞功能的研究发现,并讨论其可能的临床意义。σ-2受体激动剂可诱导多种细胞类型的细胞形态变化和凋亡。σ-2受体激活导致细胞内钙浓度([Ca++]i)出现短暂和持续升高,钙来源于不同的细胞内储存库。[Ca++]i的这些变化和细胞毒性作用由细胞内的σ-2受体介导。σ-2激动剂可诱导耐药癌细胞凋亡,增强DNA损伤剂的效力,并下调P-糖蛋白mRNA的表达。因此,σ-2受体激动剂可能对耐药癌症的治疗有用。σ放射性配体已用于肿瘤成像。我们还讨论了σ-2拮抗剂如何预防典型抗精神病药物不可逆的运动副作用。σ-2受体可能参与一条新的凋亡信号通路,涉及细胞增殖和/或活力的调节。

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