2014
DOI: 10.1016/j.autneu.2014.08.004
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Neurons in the nucleus tractus solitarius mediate the acupuncture analgesia in visceral pain rats

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Cited by 23 publications
(14 citation statements)
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“…Obviously, analgesia induced by different frequencies of EA occurs in distinct neural pathways. Although several investigators have determined the roles of individual cerebral nuclei or areas in EA-induced analgesia (EAA) with classical physical approaches (the stimulation and abolition of certain nerve fibres or nuclei) as well as pharmacological approaches (assessing antagonists and antibodies) [ 6 – 8 ], the neuronal circuitry underlying analgesia induced by different frequencies of EA is not yet clear.…”
Section: Introductionmentioning
confidence: 99%
“…Obviously, analgesia induced by different frequencies of EA occurs in distinct neural pathways. Although several investigators have determined the roles of individual cerebral nuclei or areas in EA-induced analgesia (EAA) with classical physical approaches (the stimulation and abolition of certain nerve fibres or nuclei) as well as pharmacological approaches (assessing antagonists and antibodies) [ 6 – 8 ], the neuronal circuitry underlying analgesia induced by different frequencies of EA is not yet clear.…”
Section: Introductionmentioning
confidence: 99%
“…Specifically, tVNS acts upon the auricular branch of the vagus nerve located medial of the tragus at the entry of the acoustic meatus (Kreuzer et al, 2012). By means of delivery of electric pulses, the stimulation of the auricular branch of the vagus nerve reaches the brain through direct projections to the nucleus of the solitary tract (NST; He et al, 2013;Liu et al, 2014;Nomura & Mizuno, 1984) and the LC (Van Bockstaele, Peoples, & Telegan, 1999). Recent neuroimaging studies confirmed the activation of this brainstem circuitry (NST and LC) following vagal stimulation (Dietrich et al, 2008;Frangos, Ellrich, & Komisaruk, 2015;Kraus et al, 2013).…”
mentioning
confidence: 99%
“…Research on the mechanism of EA for relieving GI visceral pain found that AP pretreatment markedly reduced c-fos positive neurons and GFAP expression in the NTS in model rats with GI visceral pain; these results suggest that the regulatory process of AP in visceral pain is closely related to the NTS [ 91 ]. Meanwhile, CRD can induce an excitatory response in related neurons in the NTS whereas EA stimulation poses an inhibitory effect on these neurons; these findings provide electrophysiological evidence that the NTS receives the afferent information of CRD-induced visceral pain and participates in the analgesic process of AP [ 92 , 93 ] ( Figure 1 ).…”
Section: Neurological Mechanisms Of Ea For Relieving Gi Visceral Pmentioning
confidence: 99%