Suppr超能文献

酸敏感离子通道(ASIC)1a慢脱敏(快速耐受性)的调节

Modulation of Slow Desensitization (Tachyphylaxis) of Acid-Sensing Ion Channel (ASIC)1a.

作者信息

Komarova Margarita S, Bukharev Andrey R, Potapieva Natalia N, Tikhonov Denis B

机构信息

Laboratory of Biophysics of Synaptic Processes, I.M Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia.

出版信息

Cell Mol Neurobiol. 2023 Mar;43(2):771-783. doi: 10.1007/s10571-022-01207-6. Epub 2022 Feb 24.

Abstract

Among the proton-activated channels of the ASIC family, ASIC1a exhibits a specific tachyphylaxis phenomenon in the form of a progressive decrease in the response amplitude during a series of activations. This process is well known, but its mechanism is poorly understood. Here, we demonstrated a partial reversibility of this effect using long-term whole-cell recording of CHO cells transfected with rASIC1a cDNA. Thus, tachyphylaxis represents a slow desensitization of ASIC1a. Prolonged acidifications provided the same recovery from slow desensitization as short acidifications of the same frequency. Slow desensitization and steady-state desensitization are independent processes although the latter attenuates the development of the former. We found that drugs which facilitate ASIC1a activation (e.g., amitriptyline) cause an enhancement of slow desensitization, while inhibition of ASIC1a by 9-aminoacridine attenuates this process. Overall, for a broad variety of exposures, including increased calcium concentration, different pH conditions, and modulating drugs, we found a correlation between their effects on ASIC1a response amplitude and the development of slow desensitization. Thus, our results demonstrate that slow desensitization occurs only when ASIC1a is in the open state.

摘要

在酸敏感离子通道(ASIC)家族的质子激活通道中,ASIC1a在一系列激活过程中表现出一种特殊的快速脱敏现象,即反应幅度逐渐降低。这个过程是众所周知的,但其机制却知之甚少。在这里,我们通过对转染了rASIC1a cDNA的CHO细胞进行长期全细胞记录,证明了这种效应的部分可逆性。因此,快速脱敏代表了ASIC1a的缓慢脱敏。长时间酸化与相同频率的短时间酸化一样,能使缓慢脱敏恢复。缓慢脱敏和稳态脱敏是相互独立的过程,尽管后者会减弱前者的发展。我们发现,促进ASIC1a激活的药物(如阿米替林)会增强缓慢脱敏,而9-氨基吖啶对ASIC1a的抑制作用则会减弱这一过程。总体而言,对于包括钙浓度增加、不同pH条件和调节药物在内的多种暴露情况,我们发现它们对ASIC1a反应幅度的影响与缓慢脱敏的发展之间存在相关性。因此,我们的结果表明,缓慢脱敏仅在ASIC1a处于开放状态时发生。

相似文献

9
Heteroarylguanidines as Allosteric Modulators of ASIC1a and ASIC3 Channels.杂芳基胍类作为 ASIC1a 和 ASIC3 通道的别构调节剂。
ACS Chem Neurosci. 2018 Jun 20;9(6):1357-1365. doi: 10.1021/acschemneuro.7b00529. Epub 2018 Mar 30.

本文引用的文献

5
Structure and Pharmacology of Voltage-Gated Sodium and Calcium Channels.电压门控钠离子和钙离子通道的结构与药理学
Annu Rev Pharmacol Toxicol. 2020 Jan 6;60:133-154. doi: 10.1146/annurev-pharmtox-010818-021757. Epub 2019 Sep 19.
10
Modulation of Proton-Gated Channels by Antidepressants.抗抑郁药对质子门控通道的调制作用。
ACS Chem Neurosci. 2019 Mar 20;10(3):1636-1648. doi: 10.1021/acschemneuro.8b00560. Epub 2018 Dec 5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验