Author
Listed:
- Xi Zhou
(Hunan Normal University)
- Tingbin Ma
(Huazhong University of Science and Technology (HUST))
- Luyao Yang
(Huazhong University of Science and Technology (HUST))
- Shuijiao Peng
(Hunan Normal University)
- Lulu Li
(Huazhong University of Science and Technology (HUST))
- Zhouquan Wang
(Hunan Normal University)
- Zhen Xiao
(Hunan Normal University)
- Qingfeng Zhang
(Hunan Normal University)
- Li Wang
(Hunan Normal University)
- Yazhou Huang
(Hunan Normal University)
- Minzhi Chen
(Hunan Normal University)
- Songping Liang
(Hunan Normal University)
- Xianwei Zhang
(Tongji Hospital of HUST)
- Jing Yu Liu
(Huazhong University of Science and Technology (HUST)
Chinese Academy of Sciences)
- Zhonghua Liu
(Hunan Normal University)
Abstract
The sodium channels Nav1.7, Nav1.8 and Nav1.9 are critical for pain perception in peripheral nociceptors. Loss of function of Nav1.7 leads to congenital insensitivity to pain in humans. Here we show that the spider peptide toxin called HpTx1, first identified as an inhibitor of Kv4.2, restores nociception in Nav1.7 knockout (Nav1.7-KO) mice by enhancing the excitability of dorsal root ganglion neurons. HpTx1 inhibits Nav1.7 and activates Nav1.9 but does not affect Nav1.8. This toxin produces pain in wild-type (WT) and Nav1.7-KO mice, and attenuates nociception in Nav1.9-KO mice, but has no effect in Nav1.8-KO mice. These data indicate that HpTx1-induced hypersensitivity is mediated by Nav1.9 activation and offers pharmacological insight into the relationship of the three Nav channels in pain signalling.
Suggested Citation
Xi Zhou & Tingbin Ma & Luyao Yang & Shuijiao Peng & Lulu Li & Zhouquan Wang & Zhen Xiao & Qingfeng Zhang & Li Wang & Yazhou Huang & Minzhi Chen & Songping Liang & Xianwei Zhang & Jing Yu Liu & Zhonghu, 2020.
"Spider venom-derived peptide induces hyperalgesia in Nav1.7 knockout mice by activating Nav1.9 channels,"
Nature Communications, Nature, vol. 11(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16210-y
DOI: 10.1038/s41467-020-16210-y
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