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Diallyl sulfides in garlic activate both TRPA1 and TRPV1
Authors:Kanako Koizumi  Masataka Narukawa  Yuji Iitsuka  Taiichiro Seki  Tatsuo Watanabe
Institution:a Graduate School of Nutritional and Environmental Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan
b Global COE Program, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan
c Department of Applied Life Sciences, Nihon University Graduate School of Bioresource Sciences, 1866 Kameino, Fujisawa, Kanagawa 252-8510, Japan
Abstract:We searched for novel agonists of TRP receptors especially for TRPA1 and TRPV1 in foods. We focused attention on garlic compounds, diallyl sulfide (DAS), diallyl disulfide (DADS), and diallyl trisulfide (DATS). In TRPA1 or TRPV1 heterogeneously expressed CHO cells, all of those compounds increased Ca2+]i in concentration-dependent manner. The EC50 values of DADS and DATS were similar to that of allyl isothiocyanate (AITC) and that of DAS was 170-fold larger than that of AITC. Maximum responses of these sulfides were equal to that of AITC. The EC50 values of these compounds for TRPV1 were around 100 μM against that of capsaicin (CAP), 25.6 nM and maximum responses of garlic compounds were half to that of CAP. The Ca2+ responses were significantly suppressed by co-application of antagonist. We conclude that DAS, DADS, and DATS are agonist of both TRPA1 and TRPV1 but with high affinity for TRPA1.
Keywords:TRP  transient receptor potential  TRPA1  transient receptor potential cation channel  subfamily A  member 1  TRPV1  transient receptor potential cation channel  subfamily V  member 1  DAS  diallyl sulfide  DADS  diallyl disulfide  DATS  diallyl trisulfide  AITC  allyl isothiocyanate  CAP  capsaicin  CNA  cinnamaldehyde  CPZ  capsazepine  [Ca2+]i  intracellular Ca2+ concentration
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