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首页> 外文期刊>St. Petersburg Polytechnic University Journal: Physics and Mathematics >Sigma-1 receptor as a potential pharmacological target for the treatment of neuropathology
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Sigma-1 receptor as a potential pharmacological target for the treatment of neuropathology

机译:Sigma-1受体作为治疗神经病理学的潜在药理靶标

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Sigma receptors are usually classified as a separate class of intracellular receptors. Among them the sigma-1 receptor has been the most studied regarding its pharmacological applications. This receptor with average or high affinity binds a wide range of chemical compounds of very different structural classes and a variety of therapeutic and pharmacological properties. The sigma-1 receptor is a trans-membrane protein placed in the endoplasmic reticulum (ER), which regulates the function of inositol-3-phosphate receptor, stabilizing the calcium signaling between ER and mitochondria. There are studies that the sigma-1 receptor is involved in the formation of many neurological and psychiatric conditions. It is assumed that the sigma-1 receptor acts as a sensor of normal calcium operation. The studies over the recent years have shown the role of the violation in calcium signaling in the pathogenesis of Alzheimer's and Huntington's diseases. In particular, changes in calcium homeostasis of the endoplasmic reticulum lead to the break of synaptic connections in the neurons. Thus, the sigma-1 receptor holds promise in application as a potential therapeutic target for the treatment of neuropathological diseases.
机译:Sigma受体通常被分类为细胞内受体的单独类别。其中,关于sigma-1受体的药理应用研究最多。这种具有中等或高亲和力的受体结合了非常不同的结构类别以及各种治疗和药理性质的多种化合物。 sigma-1受体是一种跨膜蛋白,位于内质网(ER)中,调节肌醇3-磷酸酯受体的功能,稳定ER和线粒体之间的钙信号传导。有研究表明,sigma-1受体参与许多神经和精神疾病的形成。假定sigma-1受体充当正常钙操作的传感器。近年来的研究表明,钙信号违规在阿尔茨海默氏病和亨廷顿氏病发病机理中的作用。特别地,内质网钙稳态的变化导致神经元中突触连接的中断。因此,sigma-1受体有望作为神经病理疾病的潜在治疗靶标应用。

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