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瞬时受体电位香草酸亚型1(TRPV1)受体在疼痛下行调制中的作用。

Role of TRPV1 receptors in descending modulation of pain.

作者信息

Palazzo Enza, Rossi Francesco, Maione Sabatino

机构信息

Department of Experimental Medicine, Section of Pharmacology "L. Donatelli", Faculty of Medicine and Surgery, Second University of Naples, Via Costantinopoli 16, 80138 Naples, Italy.

出版信息

Mol Cell Endocrinol. 2008 Apr 16;286(1-2 Suppl 1):S79-83. doi: 10.1016/j.mce.2008.01.013. Epub 2008 Feb 2.

Abstract

Transient receptor potential vanilloid type 1 (TRPV1) receptor is a ligand-gated non-selective cation channel activated by heat (>43 degrees C), low pH and endogenous lipid molecules such as anandamide, N-arachidonoyl-dopamine, N-acyl-dopamines and products of lipoxygenases (12- and 15-(S)-HPETE) termed endovanilloids. Apart from peripheral primary afferent neurons and dorsal root ganglia, TRPV1 receptor is expressed throughout the brain. Recent evidence shows that TRPV1 receptor stimulation by endocannabinoids or by capsaicin within the periaqueductal grey (PAG) leads to analgesia and this effect is associated with glutamate increase and the activation of OFF cell population in the rostral ventromedial medulla (RVM). Activation of the antinociceptive descending pathway via TPRV1 receptor stimulation in the PAG may be a novel strategy for producing analgesia. This review will summarize the more recent insights into the role of TRPV1 receptor within the antinociceptive descending pathway and its possible exploitation as a target for novel pain-killer agents.

摘要

瞬时受体电位香草酸亚型1(TRPV1)受体是一种配体门控的非选择性阳离子通道,可被热(>43摄氏度)、低pH值以及内源性脂质分子(如花生四烯乙醇胺、N-花生四烯酰多巴胺、N-酰基多巴胺和脂氧合酶产物(12-和15-(S)-氢过氧化二十碳四烯酸),即内源性香草酸)激活。除了外周初级传入神经元和背根神经节外,TRPV1受体在整个大脑中均有表达。最近的证据表明,内源性大麻素或辣椒素在导水管周围灰质(PAG)内刺激TRPV1受体可导致镇痛,这种效应与谷氨酸增加以及延髓头端腹内侧(RVM)中OFF细胞群的激活有关。通过在PAG中刺激TPRV1受体来激活抗伤害感受下行通路可能是产生镇痛作用的一种新策略。本综述将总结关于TRPV1受体在抗伤害感受下行通路中的作用及其作为新型止痛药靶点的可能应用的最新见解。

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