1. Academic Validation
  2. X-ray induces mechanical and heat allodynia in mouse via TRPA1 and TRPV1 activation

X-ray induces mechanical and heat allodynia in mouse via TRPA1 and TRPV1 activation

  • Mol Pain. 2019 Jan-Dec;15:1744806919849201. doi: 10.1177/1744806919849201.
Su Cun-Jin 1 2 Xu Jian-Hao 3 Liu Xu 2 Zhao Feng-Lun 1 Pan Jie 1 Shi Ai-Ming 1 Hu Duan-Min 4 Yu Yun-Li 5 Liu Tong 2 6 Zhang Yu-Song 3
Affiliations

Affiliations

  • 1 1 Department of Pharmacy, The Second Affiliated Hospital of Soochow University, Suzhou, China.
  • 2 2 Institute of Neuroscience, Soochow University, Suzhou, China.
  • 3 3 Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
  • 4 4 Department of Gastroenterology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
  • 5 5 Department of Clinical Pharmacology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
  • 6 6 College of Life Sciences, Yanan University, Yanan, China.
Abstract

Radiotherapy-related pain is a common adverse reaction with a high incidence among Cancer patients undergoing radiotherapy and remarkably reduces the quality of life. However, the mechanisms of ionizing radiation-induced pain are largely unknown. In this study, mice were treated with 20 Gy X-ray to establish ionizing radiation-induced pain model. X-ray evoked a prolonged mechanical, heat, and cold allodynia in mice. Transient receptor potential vanilloid 1 and transient receptor potential ankyrin 1 were significantly upregulated in lumbar dorsal root ganglion. The mechanical and heat allodynia could be transiently reverted by intrathecal injection of transient receptor potential vanilloid 1 antagonist capsazepine and transient receptor potential ankyrin 1 antagonist HC-030031. Additionally, the phosphorylated extracellular regulated protein kinases (ERK) and Jun NH2-terminal Kinase (JNK) in pain neural pathway were induced by X-ray treatment. Our findings indicated that activation of transient receptor potential ankyrin 1 and transient receptor potential vanilloid 1 is essential for the development of X-ray-induced allodynia. Furthermore, our findings suggest that targeting on transient receptor potential vanilloid 1 and transient receptor potential ankyrin 1 may be promising prevention strategies for X-ray-induced allodynia in clinical practice.

Keywords

X-ray; dorsal root ganglion; pain; radiation; transient receptor potential ankyrin 1; transient receptor potential vanilloid 1.

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