Wu Shaw-Wen, Fowler Daniel K, Shaffer Forrest J, Lindberg Jonathon E M, Peters James H
Department of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington (D.K.F., F.J.S., J.E.M.L., J.H.P.); and Department of Neuroscience, The Scripps Research Institute, Jupiter, Florida (S.-w.W.)
Department of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington (D.K.F., F.J.S., J.E.M.L., J.H.P.); and Department of Neuroscience, The Scripps Research Institute, Jupiter, Florida (S.-w.W.).
J Pharmacol Exp Ther. 2017 Sep;362(3):368-377. doi: 10.1124/jpet.116.239384. Epub 2017 Jun 15.
The nonselective cation channel transient receptor potential ankryn subtype family 1 (TRPA1) is expressed in neurons of dorsal root ganglia and trigeminal ganglia and also in vagal afferent neurons that innervate the lungs and gastrointestinal tract. Many TRPA1 agonists are reactive electrophilic compounds that form covalent adducts with TRPA1. Allyl isothiocyanate (AITC), the common agonist used to identify TRPA1, contains an electrophilic group that covalently binds with cysteine residues of TRPA1 and confers a structural change on the channel. There is scientific motivation to identify additional compounds that can activate TRPA1 with different mechanisms of channel gating. We provide evidence that ethyl vanillin (EVA) is a TRPA1 agonist. Using fluorescent calcium imaging and whole-cell patch-clamp electrophysiology on dissociated rat vagal afferent neurons and TRPA1-transfected COS-7 cells, we discovered that EVA activates cells also activated by AITC. Both agonists display similar current profiles and conductances. Pretreatment with A967079, a selective TRPA1 antagonist, blocks the EVA response as well as the AITC response. Furthermore, EVA does not activate vagal afferent neurons from TRPA1 knockout mice, showing selectivity for TRPA1 in this tissue. Interestingly, EVA appears to be pharmacologically different from AITC as a TRPA1 agonist. When AITC is applied before EVA, the EVA response is occluded. However, they both require intracellular oxidation to activate TRPA1. These findings suggest that EVA activates TRPA1 but via a distinct mechanism that may provide greater ease for study in native systems compared with AITC and may shed light on differential modes of TRPA1 gating by ligand types.
非选择性阳离子通道瞬时受体电位锚蛋白1型(TRPA1)在背根神经节和三叉神经节的神经元中表达,也在支配肺和胃肠道的迷走传入神经元中表达。许多TRPA1激动剂是反应性亲电化合物,可与TRPA1形成共价加合物。用于鉴定TRPA1的常见激动剂异硫氰酸烯丙酯(AITC)含有一个亲电基团,该基团与TRPA1的半胱氨酸残基共价结合并使通道发生结构变化。有科学动机去鉴定能够通过不同通道门控机制激活TRPA1的其他化合物。我们提供证据表明乙基香兰素(EVA)是一种TRPA1激动剂。通过对离体大鼠迷走传入神经元和TRPA1转染的COS-7细胞进行荧光钙成像和全细胞膜片钳电生理学研究,我们发现EVA可激活也被AITC激活的细胞。两种激动剂表现出相似的电流图谱和电导。用选择性TRPA1拮抗剂A967079预处理可阻断EVA反应以及AITC反应。此外,EVA不会激活TRPA1基因敲除小鼠的迷走传入神经元,表明在该组织中对TRPA1具有选择性。有趣的是,作为TRPA1激动剂,EVA在药理学上似乎与AITC不同。当在EVA之前应用AITC时,EVA反应被阻断。然而,它们都需要细胞内氧化来激活TRPA1。这些发现表明EVA可激活TRPA1,但通过一种独特的机制,与AITC相比,该机制可能为在天然系统中的研究提供更大的便利,并且可能揭示TRPA1通过配体类型的不同门控模式。