Analgesic activities of the mixed opioid and NPFF receptors agonist DN-9 in a mouse model of formalin-induced orofacial inflammatory pain

• Published in: Peptides (New York, N.Y. : 1980) Vol. 110; pp. 30 - 39
• Main Authors: Zhang, Ting, Zhao, Weidong, Zhang, Mengna, Xu, Biao, Shi, Xuerui, Zhang, Qinqin, Guo, Yuanyuan, Xiao, Jian, Chen, Dan, Zheng, Ting, Fang, Quan
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2018
• Subjects: c-Fos; ERK; Orofacial formalin model; Pain; Temporomandibular joint; Whisker pad; NTI; Whisker pad; NPFF; BN-9; Temporomandibular joint; c-Fos; S.E.M; nor-BNI; TG; Pain; ANOVA; DN-9; β-FNA; Orofacial formalin model; i.c.v; ED50; ERK
• ISSN: 0196-9781; 1873-5169
• DOI: 10.1016/j.peptides.2018.10.010

•DN-9 attenuated orofacial formalin pain via mu- and kappa-opioid receptors.•NPFF system is not involved in the orofacial formalin pain.•DN-9 inhibited the neuronal activation in trigeminal ganglion.•DN-9 inhibited the expression of p-ERK in trigeminal ganglion. Orofacial pain is one of the most common pain conditions and compromises the quality of life of the sufferer. Several studies have shown that opioid agonists produced significant analgesia in the orofacial pain, and combination of opioids with drugs belonging to other classes induced synergism in the orofacial pain. However, combination therapy of different analgesic drugs improves the risk of drug-drug interactions. Against this background, we sought to investigate the analgesic effects of the multi-functional opioid peptide DN-9, a mixed opioid and NPFF receptors agonist that produced robust analgesia in acute and inflammatory pain models, on formalin-induced orofacial pain. Our results showed that formalin injection caused significant spontaneous pain behaviors and increased the expressions of the mu-opioid receptor, c-Fos and phosphorylated extracellular signal-regulated kinase (p-ERK1/2) in the ipsilateral trigeminal ganglion (TG). In mice pretreated with DN-9, there was a significant reduction in nociceptive behaviors, which was selectively mediated by the mu- and kappa-opioid receptors, independently of the NPFF system. Four hours after formalin injection, the level of c-Fos immunoreactivity in the ipsilateral TG neurons was much lower in mice pretreated with DN-9 or morphine. In addition, DN-9 exhibited a significant inhibition in the expression of p-ERK1/2, which was reversed by the selective antagonists of the mu- and kappa-opioid receptors. In conclusion, our present results demonstrate that central administration of DN-9 produces potential antinociceptive effects via the mu- and kappa-opioid receptors, independently of the NPFF system, and this antinociceptive action is tightly linked with the intracellular ERK activation in TG neurons.