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TRP 通道在痛觉传递中的相互作用:治疗机会。

TRP Channel Cooperation for Nociception: Therapeutic Opportunities.

机构信息

Center for Clinical Pharmacology, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000 Leuven, Belgium.

Laboratory of Endometrium, Endometriosis and Reproductive Medicine, Department of Development and Regeneration, KU Leuven, 3000 Leuven, Belgium.

出版信息

Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:655-677. doi: 10.1146/annurev-pharmtox-010919-023238. Epub 2020 Sep 25.


DOI:10.1146/annurev-pharmtox-010919-023238
PMID:32976736
Abstract

Chronic pain treatment remains a sore challenge, and in our aging society, the number of patients reporting inadequate pain relief continues to grow. Current treatment options all have their drawbacks, including limited efficacy and the propensity of abuse and addiction; the latter is exemplified by the ongoing opioid crisis. Extensive research in the last few decades has focused on mechanisms underlying chronic pain states, thereby producing attractive opportunities for novel, effective and safe pharmaceutical interventions. Members of the transient receptor potential (TRP) ion channel family represent innovative targets to tackle pain sensation at the root. Three TRP channels, TRPV1, TRPM3, and TRPA1, are of particular interest, as they were identified as sensors of chemical- and heat-induced pain in nociceptor neurons. This review summarizes the knowledge regarding TRP channel-based pain therapies, including the bumpy road of the clinical development of TRPV1 antagonists, the current status of TRPA1 antagonists, and the future potential of targeting TRPM3.

摘要

慢性疼痛治疗仍然是一个棘手的挑战,在我们这个老龄化的社会中,报告疼痛缓解不足的患者人数持续增加。目前的治疗选择都有其缺点,包括疗效有限以及滥用和成瘾的倾向;后者的例子就是持续的阿片类药物危机。在过去几十年中,大量研究集中在慢性疼痛状态的机制上,从而为新型、有效和安全的药物干预提供了有吸引力的机会。瞬时受体电位 (TRP) 离子通道家族的成员代表了从根本上解决疼痛感觉的创新靶点。TRPV1、TRPM3 和 TRPA1 这三种 TRP 通道特别引人关注,因为它们被确定为伤害感受器神经元中化学和热诱导疼痛的传感器。这篇综述总结了基于 TRP 通道的疼痛治疗的知识,包括 TRPV1 拮抗剂临床开发的坎坷道路、TRPA1 拮抗剂的现状以及靶向 TRPM3 的未来潜力。

相似文献

[1]
TRP Channel Cooperation for Nociception: Therapeutic Opportunities.

Annu Rev Pharmacol Toxicol. 2021-1-6

[2]
TRP Channels in Nociception and Pathological Pain.

Adv Exp Med Biol. 2018

[3]
Targeting TRP channels for pain relief: A review of current evidence from bench to bedside.

Curr Opin Pharmacol. 2024-4

[4]
Targeting TRP channels for pain relief.

Eur J Pharmacol. 2013-3-14

[5]
Targeting nociceptive transient receptor potential channels to treat chronic pain: current state of the field.

Br J Pharmacol. 2017-11-6

[6]
Transient receptor potential channels in the context of nociception and pain - recent insights into TRPM3 properties and function.

Biol Chem. 2019-6-26

[7]
[Activation and regulation of nociceptive transient receptor potential (TRP) channels, TRPV1 and TRPA1].

Yakugaku Zasshi. 2010-3

[8]
Sensory TRP channels: the key transducers of nociception and pain.

Prog Mol Biol Transl Sci. 2015

[9]
The role of TRP ion channels in migraine and headache.

Neurosci Lett. 2022-1-18

[10]
Therapeutic targeting of TRP channels--the TR(i)P to pain relief.

Curr Top Med Chem. 2011

引用本文的文献

[1]
Decoding Pain: Next-Generation In Vitro Systems for Mechanistic Insights and Drug Discovery.

FASEB J. 2025-8-31

[2]
Insights into ion channels to identify drug target for neuropathic pain management.

Inflammopharmacology. 2025-8-12

[3]
Pathophysiology of Endometriosis: Insights from Immunohistochemical Analysis of Ectopic and Eutopic Tissues.

Int J Mol Sci. 2025-6-22

[4]
Neuronal ion channel modulation by Drimys winteri compounds: Opening a new chemical space to neuropharmacology.

Neural Regen Res. 2026-4-1

[5]
Inhibition of TRPM3 by Primidone Provides a Potential Therapeutic Method for Adenomyosis Management.

Drug Des Devel Ther. 2025-4-2

[6]
Dual targeting carbonic anhydrase inhibitors as promising therapeutic approach: a structural overview.

Front Mol Biosci. 2025-2-3

[7]
Exploring the role of ubiquitination modifications in migraine headaches.

Front Immunol. 2025-1-31

[8]
Slick potassium channels limit TRPM3-mediated activation of sensory neurons.

Front Pharmacol. 2024-12-18

[9]
Muscarinic acetylcholine type 1 receptor antagonism activates TRPM3 to augment mitochondrial function and drive axonal repair in adult sensory neurons.

Mol Metab. 2025-2

[10]
The role of TRPV1 in chronic prostatitis: a review.

Front Pharmacol. 2024-9-19

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