Suppr超能文献

大麻二酚激活迷走传入神经元需要 TRPA1。

Cannabidiol activation of vagal afferent neurons requires TRPA1.

机构信息

Department of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington.

出版信息

J Neurophysiol. 2020 Nov 1;124(5):1388-1398. doi: 10.1152/jn.00128.2020. Epub 2020 Sep 23.

Abstract

Vagal afferent neurons abundantly express excitatory transient receptor potential (TRP) channels, which strongly influence afferent signaling. Cannabinoids have been identified as direct agonists of TRP channels, including TRPA1 and TRPV1, suggesting that exogenous cannabinoids may influence vagal signaling via TRP channel activation. The diverse therapeutic effects of electrical vagus nerve stimulation also result from administration of the nonpsychotropic cannabinoid, cannabidiol (CBD); however, the direct effects of CBD on vagal afferent signaling remain unknown. We investigated actions of CBD on vagal afferent neurons, using calcium imaging and electrophysiology. CBD produced strong excitatory effects in neurons expressing TRPA1. CBD responses were prevented by removal of bath calcium, ruthenium red, and the TRPA1 antagonist A967079, but not the TRPV1 antagonist SB366791, suggesting an essential role for TRPA1. These pharmacological experiments were confirmed using genetic knockouts where TRPA1 KO mice lacked CBD responses, whereas TRPV1 knockout (KO) mice exhibited CBD-induced activation. We also characterized CBD-provoked inward currents at resting potentials in vagal afferents expressing TRPA1 that were absent in TRPA1 KO mice, but persisted in TRPV1 KO mice. CBD also inhibited voltage-activated sodium conductances in A-fiber, but not in C-fiber afferents. To simulate adaptation, resulting from chronic cannabis use, we administered cannabis extract vapor daily for 3 wk. Cannabis exposure reduced the magnitude of CBD responses, likely due to a loss of TRPA1 signaling. Together, these findings detail a novel excitatory action of CBD at vagal afferent neurons, which requires TRPA1 and may contribute to the vagal mimetic effects of CBD and adaptation following chronic cannabis use. CBD usage has increased with its legalization. The clinical efficacy of CBD has been demonstrated for conditions including some forms of epilepsy, depression, and anxiety that are also treatable by vagus nerve stimulation. We found CBD exhibited direct excitatory effects on vagal afferent neurons that required TRPA1, were augmented by TRPV1, and attenuated following chronic cannabis vapor exposure. These effects may contribute to vagal mimetic effects of CBD and adaptation after chronic cannabis use.

摘要

迷走神经传入神经元丰富地表达兴奋性瞬时受体电位 (TRP) 通道,强烈影响传入信号。大麻素已被鉴定为 TRP 通道的直接激动剂,包括 TRPA1 和 TRPV1,这表明外源性大麻素可能通过 TRP 通道激活影响迷走神经信号。电迷走神经刺激的多种治疗效果也源于非精神活性大麻素大麻二酚 (CBD) 的给药;然而,CBD 对迷走神经传入信号的直接影响尚不清楚。我们使用钙成像和电生理学研究了 CBD 对迷走神经传入神经元的作用。CBD 在表达 TRPA1 的神经元中产生强烈的兴奋作用。用浴钙去除、钌红和 TRPA1 拮抗剂 A967079 预处理可阻止 CBD 反应,但 TRPV1 拮抗剂 SB366791 则不行,表明 TRPA1 起关键作用。这些药理学实验用 TRPA1 KO 小鼠进行了验证,TRPA1 KO 小鼠缺乏 CBD 反应,而 TRPV1 KO 小鼠则表现出 CBD 诱导的激活。我们还在表达 TRPA1 的迷走神经传入纤维中表征了 CBD 诱导的静息电位内向电流,在 TRPA1 KO 小鼠中不存在这种电流,但在 TRPV1 KO 小鼠中仍然存在。CBD 还抑制 A 纤维中的电压激活钠电流,但不抑制 C 纤维传入纤维中的钠电流。为了模拟慢性大麻使用引起的适应,我们每天给予大麻提取物蒸气 3 周。大麻暴露降低了 CBD 反应的幅度,可能是由于 TRPA1 信号的丧失。总之,这些发现详细描述了 CBD 在迷走神经传入神经元上的新型兴奋作用,该作用需要 TRPA1,可能有助于 CBD 的迷走神经模拟作用和慢性大麻使用后的适应。随着大麻合法化,CBD 的使用量有所增加。CBD 对包括某些类型癫痫、抑郁和焦虑在内的疾病的临床疗效已得到证实,这些疾病也可以通过迷走神经刺激来治疗。我们发现 CBD 对迷走神经传入神经元表现出直接的兴奋作用,需要 TRPA1,被 TRPV1 增强,并在慢性大麻蒸气暴露后减弱。这些作用可能有助于 CBD 的迷走神经模拟作用和慢性大麻使用后的适应。

相似文献

1
Cannabidiol activation of vagal afferent neurons requires TRPA1.大麻二酚激活迷走传入神经元需要 TRPA1。
J Neurophysiol. 2020 Nov 1;124(5):1388-1398. doi: 10.1152/jn.00128.2020. Epub 2020 Sep 23.

引用本文的文献

本文引用的文献

2
Inhibitory effects of cannabidiol on voltage-dependent sodium currents.大麻二酚对电压依赖性钠离子电流的抑制作用。
J Biol Chem. 2018 Oct 26;293(43):16546-16558. doi: 10.1074/jbc.RA118.004929. Epub 2018 Sep 14.
5
Effects of Δ9-THC and cannabidiol vapor inhalation in male and female rats.Δ9-THC 和大麻二酚蒸气吸入对雌雄大鼠的影响。
Psychopharmacology (Berl). 2018 Sep;235(9):2541-2557. doi: 10.1007/s00213-018-4946-0. Epub 2018 Jun 16.
6
A TRP channel trio mediates acute noxious heat sensing.一种 TRP 通道三联体介导急性有害热感觉。
Nature. 2018 Mar 29;555(7698):662-666. doi: 10.1038/nature26137. Epub 2018 Mar 14.
10
Molecular Pharmacology of Phytocannabinoids.植物大麻素的分子药理学
Prog Chem Org Nat Prod. 2017;103:61-101. doi: 10.1007/978-3-319-45541-9_3.

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