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Lynx1 原毒素:神经元烟碱型乙酰胆碱受体的关键辅助蛋白。

Lynx1 prototoxins: critical accessory proteins of neuronal nicotinic acetylcholine receptors.

机构信息

Lehigh University, Department of Biological Sciences, 111 Research Drive, Bethlehem, PA, United States.

出版信息

Curr Opin Pharmacol. 2021 Feb;56:46-51. doi: 10.1016/j.coph.2020.09.016. Epub 2020 Nov 27.

Abstract

Nicotinic receptors of the cholinergic system are ligand-gated ion channels, responding to the excitatory neurotransmitter, acetylcholine, and the addictive component of tobacco, nicotine. They help to transduce salient information in the environment by activating specific neural circuitry in normal and disease states. While nicotinic receptors are promising neurological and neuropsychiatric disorder targets, they have fallen out of favor after several late-stage clinical failures. Targeting the complex of the nicotinic receptor, including lynx1 accessory proteins, could be the key to unlocking the intractable nAChR for therapeutic development. Lynx1 binds to the extracellular face of the nAChR and acts as a critical modulator, suppressing memory, learning, and plasticity. Lynx1 removal in animal models leads to memory and plasticity enhancements, some of which have therapeutic relevance for neuropsychiatric and neurological disease. A review of the lynx1 accessory modulator and its role in modulating neuronal nAChRs will be discussed.

摘要

胆碱能系统的烟碱受体是配体门控离子通道,对兴奋性神经递质乙酰胆碱和烟草中的成瘾成分尼古丁作出反应。它们通过在正常和疾病状态下激活特定的神经回路,帮助转换环境中的显著信息。虽然烟碱受体是有前途的神经和神经精神疾病靶点,但在几项后期临床失败后,它们已经失宠。针对烟碱受体复合物,包括 Lynx1 辅助蛋白,可能是为治疗开发解开难以捉摸的 nAChR 的关键。Lynx1 结合到 nAChR 的细胞外表面,作为关键的调节剂,抑制记忆、学习和可塑性。在动物模型中去除 Lynx1 会导致记忆和可塑性增强,其中一些与神经精神疾病和神经退行性疾病的治疗相关。将讨论 Lynx1 辅助调节剂及其在调节神经元烟碱受体中的作用的综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84b2/8771676/d1e98bf434bc/nihms-1645332-f0001.jpg

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