Cannabidiol microinjection into the nucleus accumbens attenuated nociceptive behaviors in an animal model of tonic pain

2021 ◽  
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Author(s):  
Yasaman Razavi ◽  
Mina Rashvand ◽  
Asrin Sharifi ◽  
Amir Haghparast ◽  
Fariborz Keyhanfar ◽  
...  
Neurosurgery ◽  
2011 ◽  
Vol 69 (6) ◽  
pp. 1281-1290 ◽  
Author(s):  
Steven M. Falowski ◽  
Ashwini Sharan ◽  
Beverly A. S. Reyes ◽  
Carl Sikkema ◽  
Patricia Szot ◽  
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Pain ◽  
1984 ◽  
Vol 18 (3) ◽  
pp. 287-297 ◽  
Author(s):  
Kazuhisa Okuda ◽  
Hiroshi Nakahama ◽  
Hiroyoshi Miyakawa ◽  
Keisetsu Shima
Keyword(s):  

2021 ◽  
Vol 22 (16) ◽  
pp. 8421
Author(s):  
Jaisan Islam ◽  
Elina KC ◽  
Soochong Kim ◽  
Hyong Kyu Kim ◽  
Young Seok Park

The nucleus accumbens core (NAcc) is an important component of brain reward circuitry, but studies have revealed its involvement in pain circuitry also. However, its effect on trigeminal neuralgia (TN) and the mechanism underlying it are yet to be fully understood. Therefore, this study aimed to examine the outcomes of optogenetic stimulation of NAcc GABAergic neurons in an animal model of TN. Animals were allocated into TN, sham, and control groups. TN was generated by infraorbital nerve constriction and the optogenetic virus was injected into the NAcc. In vivo extracellular recordings were acquired from the ventral posteromedial nucleus of the thalamus. Alterations of behavioral responses during stimulation “ON” and “OFF” conditions were evaluated. In vivo microdialysis was performed in the NAcc of TN and sham animals. During optogenetic stimulation, electrophysiological recordings revealed a reduction of both tonic and burst firing activity in TN animals, and significantly improved behavioral responses were observed as well. Microdialysis coupled with liquid chromatography/tandem mass spectrometry analysis revealed significant alterations in extracellular concentration levels of GABA, glutamate, acetylcholine, dopamine, and citrulline in NAcc upon optic stimulation. In fine, our results suggested that NAcc stimulation could modulate the transmission of trigeminal pain signals in the TN animal model.


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