- Author:
Hao-Ran WANG
1
;
Su-Wan HU
1
;
Song ZHANG
1
;
Yu SONG
1
;
Xiao-Yi WANG
1
;
Lei WANG
1
;
Yang-Yang LI
1
;
Yu-Mei YU
1
;
He LIU
1
;
Di LIU
1
;
Hai-Lei DING
1
;
Jun-Li CAO
1
;
Hao-Ran WANG
2
;
Su-Wan HU
2
;
Song ZHANG
2
;
Yu SONG
2
;
Xiao-Yi WANG
2
;
Lei WANG
2
;
Yang-Yang LI
2
;
Yu-Mei YU
2
;
He LIU
2
;
Di LIU
2
;
Hai-Lei DING
2
;
Jun-Li CAO
2
;
Hao-Ran WANG
3
;
Song ZHANG
4
;
He LIU
5
;
Jun-Li CAO
5
Author Information
- Publication Type:Journal Article
- Keywords: Brain-derived neurotrophic factor; Chronic neuropathic pain; KCNQ; Mesocorticolimbic system; Nociception; Retigabine; Ventral tegmental area
- From: Neuroscience Bulletin 2021;37(5):597-610
- CountryChina
- Language:Chinese
- Abstract: Mesocorticolimbic dopaminergic (DA) neurons have been implicated in regulating nociception in chronic pain, yet the mechanisms are barely understood. Here, we found that chronic constructive injury (CCI) in mice increased the firing activity and decreased the KCNQ channel-mediated M-currents in ventral tegmental area (VTA) DA neurons projecting to the nucleus accumbens (NAc). Chemogenetic inhibition of the VTA-to-NAc DA neurons alleviated CCI-induced thermal nociception. Opposite changes in the firing activity and M-currents were recorded in VTA DA neurons projecting to the medial prefrontal cortex (mPFC) but did not affect nociception. In addition, intra-VTA injection of retigabine, a KCNQ opener, while reversing the changes of the VTA-to-NAc DA neurons, alleviated CCI-induced nociception, and this was abolished by injecting exogenous BDNF into the NAc. Taken together, these findings highlight a vital role of KCNQ channel-mediated modulation of mesolimbic DA activity in regulating thermal nociception in the chronic pain state.