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首页> 外文期刊>Chemical Senses >Isothiocyanates from Wasabia japonica Activate Transient Receptor Potential Ankyrin 1 Channel
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Isothiocyanates from Wasabia japonica Activate Transient Receptor Potential Ankyrin 1 Channel

机译:山葵的异硫氰酸盐激活瞬态受体电位锚蛋白1通道

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摘要

6-(Methylsulfinyl)hexyl isothiocyanate (6-MSITC) and 6-(methylthio)hexyl isothiocyanate (6-MTITC) have low pungency and are responsible for the fresh flavor of wasabi (Wasabia japonica [Miq] Matsumura). In this study, we found that these two isothiocyanates activate transient receptor potential ankyrin 1 (TRPA1), and 6-MSITC activates transient receptor potential vanilloid 1 (TRPV1), but not other transient receptor potential channels expressed in sensory neurons. Both 6-MSITC and 6-MTITCinduced intracellular Ca2+ increases in human embryonic kidney-derived 293 cells expressing mouse TRPA1 (mTRPA1) as measured by Ca2+ imaging. In whole-cell patch-clamp recordings, 6-MSITC and 6-MTITC dose-dependently activated both mTRPA1 (EC50 = 147±26 µM for 6-MSITC and 30±3 µM for 6-MTITC) and human TRPA1 (hTRPA1; EC50 = 39±4 µM for 6-MSITC and 34±3 µM for 6-MTITC). In addition, TRPA1 N-terminal cysteines, which are reported to be important for channel activation by electrophilic ligands, were involved in 6-MSITC- and 6-MTITC-evoked TRPA1 activation. These isothiocyanates also activated endogenous TRPA1 expressed in mouse dorsal root ganglion neurons and intraplantar injection of 10–30mM 6-MSITC-evoked pain-related behaviors in mice. These results indicate the following: 1) 6-MSITC and 6-MTITC activate both mTRPA1 and hTRPA1; 2) 6-MSITC activates mTRPV1; and 3) the pharmacological functions of these isothiocyanates could be derived from TRPA1 activation.
机译:6-(甲基亚磺酰基)己基异硫氰酸酯(6-MSITC)和6-(甲基硫基)己基异硫氰酸酯(6-MTITC)的辛辣度低,是芥末(Wasabia japonica [Miq] Matsumura)的新鲜风味。在这项研究中,我们发现这两个异硫氰酸盐激活瞬态受体电位锚蛋白1(TRPA1),而6-MSITC激活瞬态受体电位香草醛1(TRPV1),但不激活在感觉神经元中表达的其他瞬态受体电位通道。通过Ca 2 + 成像测量,6-MSITC和6-MTITC诱导的表达小鼠TRPA1(mTRPA1)的人胚胎肾脏衍生的293细胞内细胞内Ca 2 + 均增加。在全细胞膜片钳记录中,6-MSITC和6-MTITC剂量依赖性地激活了mTRPA1(6-MSITC的EC 50 = 147±26 µM,6-MTITC的30±3 µM )和人类TRPA1(hTRPA1; 6-MSITC的EC 50 = 39±4 µM,6-MTITC的EC 50 = 34±3 µM)。此外,据报道对于亲电配体激活通道很重要的TRPA1 N端半胱氨酸参与了6-MSITC和6-MTITC引起的TRPA1激活。这些异硫氰酸盐还激活了小鼠背根神经节神经元中表达的内源性TRPA1,以及小鼠足底注射10-30mM 6-MSITC引起的疼痛相关行为。这些结果表明:1)6-MSITC和6-MTITC激活mTRPA1和hTRPA1。 2)6-MSITC激活mTRPV1; 3)这些异硫氰酸酯的药理功能可以源自TRPA1激活。

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  • 来源
    《Chemical Senses 》 |2012年第9期| p.809-818| 共10页
  • 作者单位

    1 Division of Cell Signaling, Okazaki Institute for Integrative Bioscience (National Institute for Physiological Sciences), National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan, 2 Kinjirushi Co., Ltd., Nagoya, Aichi 454-8526, Japanand 3 Department of Physiological Sciences, The Graduate University for Advanced Studies Okazaki, Aichi 444-8585, Japan;

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