Suppr超能文献

蜈蚣毒素导致伤害感受器 TRPV1 离子通道快速脱敏。

A centipede toxin causes rapid desensitization of nociceptor TRPV1 ion channel.

机构信息

Department of Pharmacology, Qingdao University School of Pharmacy, Qingdao, Shandong, China; Department of Biophysics and Kidney Disease Center, The First Affiliated Hospital, Institute of Neuroscience, National Health Commission and Chinese Academy of Medical Sciences Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang Province, China.

Department of Biophysics and Kidney Disease Center, The First Affiliated Hospital, Institute of Neuroscience, National Health Commission and Chinese Academy of Medical Sciences Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang Province, China.

出版信息

Toxicon. 2020 Apr 30;178:41-49. doi: 10.1016/j.toxicon.2020.02.016. Epub 2020 Feb 22.

Abstract

The nociceptive transient receptor potential vanilloid 1 (TRPV1) ion channel is a polymodal receptor for multiple painful stimuli, hence actively pursued as a target for analgesic drugs. We identified a small peptide toxin RhTx2 from the Chinese red-headed centipede that strongly modulates TRPV1 activities. RhTx2, a 31-amino-acid peptide, is similar to a TRPV1-activating toxin RhTx we have previously discovered but with four extra amino acids at the N terminus. We observed that, like RhTx, RhTx2 activated TRPV1, but RhTx2 rapidly desensitized the channel upon prolonged exposure. Desensitization was achieved by reducing both the open probability and the single-channel conductance. RhTx2 is not only a tool to study the desensitization mechanism of TRPV1, but also a promising starting molecule for developing novel analgesics.

摘要

伤害性瞬时受体电位香草酸 1(TRPV1)离子通道是多种疼痛刺激的多模态受体,因此被积极用作镇痛药物的靶点。我们从中国红头蜈蚣中鉴定出一种名为 RhTx2 的小肽毒素,它强烈调节 TRPV1 的活性。RhTx2 是一种 31 个氨基酸的肽,与我们之前发现的 TRPV1 激活毒素 RhTx 相似,但 N 端有四个额外的氨基酸。我们观察到,与 RhTx 一样,RhTx2 激活 TRPV1,但 RhTx2 在长时间暴露后会迅速脱敏该通道。脱敏通过降低通道的开放概率和单通道电导来实现。RhTx2 不仅是研究 TRPV1 脱敏机制的工具,也是开发新型镇痛药的有前途的起始分子。

相似文献

1
A centipede toxin causes rapid desensitization of nociceptor TRPV1 ion channel.
Toxicon. 2020 Apr 30;178:41-49. doi: 10.1016/j.toxicon.2020.02.016. Epub 2020 Feb 22.
3
Animal Toxins Providing Insights into TRPV1 Activation Mechanism.
Toxins (Basel). 2017 Oct 16;9(10):326. doi: 10.3390/toxins9100326.
4
Different types of toxins targeting TRPV1 in pain.
Toxicon. 2013 Sep;71:66-75. doi: 10.1016/j.toxicon.2013.05.016. Epub 2013 Jun 2.
7
Design, synthesis and functional validation of peptide inhibitors based on TRPV1 ion channel agonist RhTx.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2024 Apr 25;53(2):201-207. doi: 10.3724/zdxbyxb-2023-0465.
9
Painful toxins acting at TRPV1.
Toxicon. 2008 Feb;51(2):163-73. doi: 10.1016/j.toxicon.2007.10.012. Epub 2007 Oct 26.
10
Synthesis and biological activity study of the retro-isomer of RhTx against TRPV1.
RSC Adv. 2020 Jan 10;10(4):2141-2145. doi: 10.1039/c9ra08829f. eCollection 2020 Jan 8.

引用本文的文献

1
Borneol's Pre-Clinical Analgesic Efficacy: Mediated by Receptor and Immune Mechanisms.
J Pain Res. 2025 Aug 13;18:4085-4104. doi: 10.2147/JPR.S533901. eCollection 2025.
3
Design, synthesis and functional validation of peptide inhibitors based on TRPV1 ion channel agonist RhTx.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2024 Apr 25;53(2):201-207. doi: 10.3724/zdxbyxb-2023-0465.
5
Bioactive Peptides and Proteins from Centipede Venoms.
Molecules. 2022 Jul 11;27(14):4423. doi: 10.3390/molecules27144423.
6
Centipede Venom: A Potential Source of Ion Channel Modulators.
Int J Mol Sci. 2022 Jun 26;23(13):7105. doi: 10.3390/ijms23137105.
8
Rational Design of a Modality-Specific Inhibitor of TRPM8 Channel against Oxaliplatin-Induced Cold Allodynia.
Adv Sci (Weinh). 2021 Nov;8(22):e2101717. doi: 10.1002/advs.202101717. Epub 2021 Oct 17.

本文引用的文献

1
Molecular basis for heat desensitization of TRPV1 ion channels.
Nat Commun. 2019 May 13;10(1):2134. doi: 10.1038/s41467-019-09965-6.
2
Centipede envenomation: Clinical importance and the underlying molecular mechanisms.
Toxicon. 2018 Nov;154:60-68. doi: 10.1016/j.toxicon.2018.09.008. Epub 2018 Sep 29.
3
Structural basis for the modulation of voltage-gated sodium channels by animal toxins.
Science. 2018 Oct 19;362(6412). doi: 10.1126/science.aau2596. Epub 2018 Jul 26.
5
Pain therapeutics from cone snail venoms: From Ziconotide to novel non-opioid pathways.
J Proteomics. 2019 Jan 6;190:12-20. doi: 10.1016/j.jprot.2018.05.009. Epub 2018 May 16.
7
Venom peptides as therapeutics: advances, challenges and the future of venom-peptide discovery.
Expert Rev Proteomics. 2017 Oct;14(10):931-939. doi: 10.1080/14789450.2017.1377613. Epub 2017 Sep 13.
8
A bimodal activation mechanism underlies scorpion toxin-induced pain.
Sci Adv. 2017 Aug 2;3(8):e1700810. doi: 10.1126/sciadv.1700810. eCollection 2017 Aug.
9
Understand spiciness: mechanism of TRPV1 channel activation by capsaicin.
Protein Cell. 2017 Mar;8(3):169-177. doi: 10.1007/s13238-016-0353-7. Epub 2017 Jan 2.
10
Structure of the voltage-gated calcium channel Cav1.1 complex.
Science. 2015 Dec 18;350(6267):aad2395. doi: 10.1126/science.aad2395.

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