2012
DOI: 10.1016/j.pbb.2012.06.005
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5-HT induces temporomandibular joint nociception in rats through the local release of inflammatory mediators and activation of local β adrenoceptors

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Cited by 19 publications
(13 citation statements)
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“…In patients with myofascial TMD, it has been claimed that there is also reduced blood circulation locally [2,32], leading to the inhibition of the reuptake of the algesic substances, which further strengthens the theory that myofascial TMD patients have higher 5-HT levels. The higher levels of 5-HT may indicate that TMD is caused by inflammatory mediators, as it has been reported that 5-HT induces temporomandibular joint nociception by the local release of sympathetic amines and prostaglandins [33].…”
Section: Discussionmentioning
confidence: 99%
“…In patients with myofascial TMD, it has been claimed that there is also reduced blood circulation locally [2,32], leading to the inhibition of the reuptake of the algesic substances, which further strengthens the theory that myofascial TMD patients have higher 5-HT levels. The higher levels of 5-HT may indicate that TMD is caused by inflammatory mediators, as it has been reported that 5-HT induces temporomandibular joint nociception by the local release of sympathetic amines and prostaglandins [33].…”
Section: Discussionmentioning
confidence: 99%
“…In TMJ inflammatory pain models, local sympathomimetic amines contribute to the inflammatory TMJ hyperalgesia by activating β 2 -adrenoceptors, 25 27 since β 2 -adrenoceptor antagonist or the depletion of NE in the sympathetic terminals can reverse this effect. 25 , 26 These results suggest that inflammation may sensitize nociceptors to NE and/or increase the release of the sympathetic amines. Furthermore, there is a study showing that α 1 -adrenoceptor upregulation in the dorsal root ganglion (DRG) after spinal nerve ligation may play an important role in the development of adrenergic sensitivity in injured sensory neurons.…”
Section: Possible Sympathetic Mechanisms In Orofacial Painmentioning
confidence: 93%
“…Capsaicin, as a derivative from red pepper, binds to transient receptor potential cation channel subfamily V member 1 (TRPV1) to activate sensory terminals and stimulate burning pain after injection (Ribeiro et al, 2020). The nociception induced by serotonin is realized in a rather indirect way on primary neurons via the activation of sympathomimetic amines and the synthesis of prostaglandin (Ribeiro et al, 2020;Oliveira-Fusaro et al, 2012). Zymosan, a polysaccharide derived from yeast cell walls, could induce severe and erosive arthritis and severe pain once injected (do Val et al, 2014).…”
Section: Bioactive Compounds In Preclinical Studiesmentioning
confidence: 99%