NMDAR and JNK Activation in the Spinal Trigeminal Nucleus Caudalis Contributes to Masseter Hyperalgesia Induced by Stress

• Published in: Frontiers in cellular neuroscience Vol. 13; p. 495
• Main Authors: Lin, Wenqing, Zhao, Yajuan, Cheng, Baixiang, Zhao, Haidan, Miao, Li, Li, Qiang, Chen, Yongjin, Zhang, Min
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 14.11.2019; Frontiers Media S.A
• Subjects: Animals; Antagonists; Astrocytes; Body weight gain; c-Jun N- terminal kinase; Catheters; Cell signaling; Cellular Neuroscience; chronic masseter pain; Dizocilpine; Experiments; Glutamic acid receptors; Guanylate cyclase; Hyperalgesia; Hypotheses; intercellular communication; Kinases; Masseter muscle; N-methyl-D-aspartate receptor; N-Methyl-D-aspartic acid receptors; Neurons; Neurosciences; Nitric-oxide synthase; Oral diseases; Pain; Pain perception; Phosphorylation; psychological stress; Spinal cord; Spinal trigeminal nucleus; spinal trigeminal nucleus caudalis; Studies; United States > US; China; chronic masseter pain; N-methyl-D-aspartate receptor; intercellular communication; spinal trigeminal nucleus caudalis; c-Jun N- terminal kinase; psychological stress
• ISSN: 1662-5102; 1662-5102
• DOI: 10.3389/fncel.2019.00495

It is commonly accepted that psychological stress is closely associated with the occurrence and development of chronic orofacial pain. However, the pathogenesis underlying this process has not been fully elucidated. In the present study, we explored the role of N-methyl-D-aspartate receptors (NMDARs) and Jun N-terminal kinase (JNK) mediated intercellular communication between neurons and astrocytes in the spinal trigeminal nucleus caudalis (Vc) in the induction of masseter hyperalgesia by psychological stress in rats. We found that subjecting rats to 14 days of restraint stress (8 h/d) caused a significant decrease in body weight gain, behavioral changes and marked masseter hyperalgesia in the rats. We also found that exposure to restraint stress for 14 days caused the expression of pJNK in astrocytes in the Vc to significantly increase, and intrathecally infusing a JNK inhibitor significantly prevented restraint stress-induced masseter hyperalgesia in the rats. In addition, after exposure to restraint stress for 14 days, the stressed group exhibited a noticeably increased expression level of pNR2B in neurons in the Vc. Then, we intrathecally injected MK-801 (an NMDAR inhibitor) and ifenprodil (a selective NR2B subunit antagonist) and observed that the two types of inhibitors not only alleviated masseter hyperalgesia but also significantly inhibited the phosphorylation of JNK in the Vc after restraint stress; this indicates that the effect of NMDAR antagonists may influence the activation of astrocytic JNK. Furthermore, inhibitors of neuronal nitric oxide synthase (nNOS) activation and guanylate cyclase (GC) inhibitor could not only inhibit the expression of pJNK in the Vc, but also effectively alleviate masseter hyperalgesia induced by restraint stress. Taken together, our results suggest that NMDAR activation could increase JNK phosphorylation in astrocytes after restraint stress, which may depend on the nNOS-GC pathway. The intercellular communication between neurons and astrocytes in the Vc may play a key role in the induction of masseter muscle hyperalgesia by psychological stress in rats.