SLC6神经递质转运抑制的药理机制。

Q3 Neuroscience
Dipanjana Bandyopadhyay, Smruti Ranjan Nayak, Aravind Penmatsa
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引用次数: 0

摘要

溶质载体6家族成员包括神经递质钠同向转运体,这些转运体主要参与突触空间释放的神经递质的再摄取。该家族包括参与生物胺和氨基酸神经递质摄取的结构相关转运蛋白,是几种抑制剂治疗抑郁症、疼痛、成瘾、癫痫发作和焦虑等疾病的已知治疗靶点。NSS转运体的抑制可以通过竞争性抑制或针对转运体多种构象状态的不同位点的变构抑制来起作用。本章探讨了针对这类转运蛋白的多种抑制剂所观察到的不同抑制策略,以及抑制策略改进的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological Mechanisms of SLC6 Neurotransmitter Transporter Inhibition.

Solute carrier 6 family members comprise of neurotransmitter sodium symporters that are the transporters primarily involved in the reuptake of released neurotransmitters from the synaptic space. The family includes structurally related transporters involved in biogenic amine and amino acid neurotransmitter uptake and is a well-known therapeutic target for several classes of inhibitors for the treatment of ailments ranging from depression, pain, addiction, seizures and anxiety. Inhibition of NSS transporters can work either through competitive inhibition or through allosteric inhibition at diverse sites that target multiple conformational states of the transporters. This chapter explores the diverse inhibition strategies observed with numerous inhibitors that target this class of transporters and potential for improvements in inhibition strategies.

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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
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0.00%
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