1. Academic Validation
  2. Modulation of NR1 receptor by CaMKIIα plays an important role in chronic itch development in mice

Modulation of NR1 receptor by CaMKIIα plays an important role in chronic itch development in mice

  • Brain Res Bull. 2020 May;158:66-76. doi: 10.1016/j.brainresbull.2020.02.011.
Nan-Qi Li 1 Yang Tang 1 Si-Ting Huang 1 Xue-Ting Liu 2 Li-Ping Zeng 2 Hui Li 3 Li Wan 4
Affiliations

Affiliations

  • 1 Department of Pain Management, The State Key Clinical Specialty in Pain Medicine, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, 510260, P.R. China.
  • 2 Guangdong Provincial Key Laboratory of Allergy & Clinic Immunology, Sino-French Hoffmann Institute, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, 510260, P.R. China.
  • 3 Department of Anatomy, Histology and Embryology & K. K. Leung Brain Research Centre, The Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China.
  • 4 Department of Pain Management, The State Key Clinical Specialty in Pain Medicine, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, 510260, P.R. China. Electronic address: wanli5000cn@163.com.
Abstract

Intractable scratching is the characteristic of chronic itch, which represents a great challenge in clinical practice. However, the mechanism underlying chronic itch development is largely unknown. In the present study, we investigated the role of NMDA Receptor in acute itch and in development of chronic itch. A mouse model was developed by painting DNFB to induce allergic contact dermatitis (ACD). We found that the expression of pNR1, which is a subunit of NMDA Receptor, was significantly increased in the dorsal root ganglion in the DNFB model. The DNFB-evoked spontaneous scratching was blocked by the NMDA antagonist D-AP-5, the calcium-calmodulin-dependent protein kinase (CaMK) inhibitor KN-93, a CaMKIIα siRNA and the PKC Inhibitor LY317615. Moreover, activation of PKC did not reverse the CaMKIIα knockdown-induced decrease in scratching, suggesting that PKC functions upstream of CaMKIIα. Thus, our study indicates that modulation of NR1 receptor by CaMKIIα plays an important role in the development of chronic itch.

Keywords

CaMKIIα; Central sensitization; GRP; Itch; NMDA.

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