抗精神病配体对Sigma I受体占用的验证:分子视角

N. LathaL, Gyananath Garimella, Anjaneyalu Kasa, Z. Pudukulathan
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引用次数: 2

摘要

Sigma-1受体是一类独特的受体,广泛表达于中枢神经系统,参与各种神经递质的调节,在各种组织的肿瘤细胞系中经常过表达,如黑色素瘤、乳腺癌、小肺癌和前列腺癌。因此,sigma配体在体内和体外都显示出抗癌活性。在本研究中,我们试图从分子角度验证sigma-1受体并研究其抗精神病配体的相互作用。将单层生长的C6细胞(大鼠胶质瘤)暴露于氟哌啶醇(sigma-1拮抗剂)和其他抗精神病配体中,MTT法测定氟哌啶醇、配体1、配体2和配体3的相对细胞毒性分别为42.79%、18.96%、24.95%和22.72%。通过DNA阶梯研究发现,抗精神病配体通过sigma-1受体调节精神病。
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Validation of Sigma I Receptor Occupancy with Antipsychotic Ligands: A Molecular Perspective
Sigma-1 receptors are unique and distinct class of receptors widely expressed in the central nervous system with involvement in regulation of various neutransmitters and are often over expressed in tumor cell lines of various tissues, such as melanoma, breast cancer, small lung carcinoma and prostate cancer. Accordingly, sigma ligands display anticancer activity in- vivo and in-vitro. In the present study, an attempt has been made to validate sigma-1receptor and study its antipsychotic ligand interactions in a molecular perspective. C6 cells (rat glioma)  grown in monolayers were exposed to haloperidol (sigma-1 antagonist) and other anti-psychotic ligands and their relative cytotoxicity was determined by MTT assay to be 42.79 %, 18.96 %, 24.95 and 22.72% for haloperidol, ligand 1, ligand 2 and ligand 3 respectively. Occupancy of sigma receptors with ligands through DNA laddering studies reveal the antipsychotic ligands modulate psychosis via sigma-1receptor.
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