Atractylodin Produces Antinociceptive Effect through a Long-Lasting TRPA1 Channel Activation

被引:9
作者
Kanda, Hirosato [1 ,2 ,3 ]
Yang, Yanjing [1 ,4 ]
Duan, Shaoqi [1 ]
Kogure, Yoko [1 ]
Wang, Shenglan [1 ,5 ]
Iwaoka, Emiko [1 ]
Ishikawa, Miku [1 ]
Takeda, Saki [1 ]
Sonoda, Hidemi [1 ]
Mizuta, Kyoka [1 ]
Aoki, Shunji [1 ]
Yamamoto, Satoshi [1 ]
Noguchi, Koichi [2 ]
Dai, Yi [1 ,2 ,3 ]
机构
[1] Hyogo Univ Hlth Sci, Sch Pharm, Dept Pharm, Kobe, Hyogo 6508530, Japan
[2] Hyogo Coll Med, Dept Anat & Neurosci, Nishinomiya, Hyogo 6638501, Japan
[3] Hyogo Coll Med, Chinese Med Confucius Inst, Tradit Med Res Ctr, Nishinomiya, Hyogo 6638501, Japan
[4] Shenyang Med Coll, Dept Pathophysiol, Shenyang 110034, Peoples R China
[5] Beijing Univ Chinese Med, Sch Acupuncture Moxibust & Tuina, Beijing 100029, Peoples R China
关键词
atractylodin; transient receptor potential ankyrin-1 (TRPA1); pain; dorsal root ganglion; QX-314;
D O I
10.3390/ijms22073614
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atractylodin (ATR) is a bioactive component found in dried rhizomes of Atractylodes lancea (AL) De Candolle. Although AL has accumulated empirical evidence for the treatment of pain, the molecular mechanism underlying the anti-pain effect of ATR remains unclear. In this study, we found that ATR increases transient receptor potential ankyrin-1 (TRPA1) single-channel activity in hTRPA1 expressing HEK293 cells. A bath application of ATR produced a long-lasting calcium response, and the response was completely diminished in the dorsal root ganglion neurons of TRPA1 knockout mice. Intraplantar injection of ATR evoked moderate and prolonged nociceptive behavior compared to the injection of allyl isothiocyanate (AITC). Systemic application of ATR inhibited AITC-induced nociceptive responses in a dose-dependent manner. Co-application of ATR and QX-314 increased the noxious heat threshold compared with AITC in vivo. Collectively, we concluded that ATR is a unique agonist of TRPA1 channels, which produces long-lasting channel activation. Our results indicated ATR-mediated anti-nociceptive effect through the desensitization of TRPA1-expressing nociceptors.
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页数:12
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