Identification of Natural Compound Carnosol as a Novel TRPA1 Receptor Agonist

被引:13
作者
Zhai, Chenxi [1 ]
Liu, Qing [1 ]
Zhang, Yuxin [1 ]
Wang, Shifeng [1 ]
Zhang, Yanling [1 ]
Li, Shiyou [2 ]
Qiao, Yanjiang [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Pharm, Key Lab TCM Informat Engn State Adm TCM, Beijing 100102, Peoples R China
[2] Chinese Acad Sci, Beijing Inst Genom, Lab Genome Variat & Precis Biomed, Beijing 100101, Peoples R China
基金
中国国家自然科学基金;
关键词
TRPA1; canosol; anti-nociceptive; calcium mobilization; POTENTIAL ANKYRIN 1; SALVIA-OFFICINALIS; CHANNEL TRPA1; ESSENTIAL OIL; HYPERALGESIA; TRPV1; ACTIVATION; EXPRESSION; EXTRACT; ACID;
D O I
10.3390/molecules191118733
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
The transient receptor potential ankyrin 1 (TRPA1) cation channel is one of the well-known targets for pain therapy. Herbal medicine is a rich source for new drugs and potentially useful therapeutic agents. To discover novel natural TRPA1 agonists, compounds isolated from Chinese herbs were screened using a cell-based calcium mobilization assay. Out of the 158 natural compounds derived from traditional Chinese herbal medicines, carnosol was identified as a novel agonist of TRPA1 with an EC50 value of 12.46 mu M. And the agonistic effect of carnosol on TRPA1 could be blocked by A-967079, a selective TRPA1 antagonist. Furthermore, the specificity of carnosol was verified as it showed no significant effects on two other typical targets of TRP family member: TRPM8 and TRPV3. Carnosol exhibited anti-inflammatory and anti-nociceptive properties; the activation of TRPA1 might be responsible for the modulation of inflammatory nociceptive transmission. Collectively, our findings indicate that carnosol is a new anti-nociceptive agent targeting TRPA1 that can be used to explore further biological role in pain therapy.
引用
收藏
页码:18733 / 18746
页数:14
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