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TRPV4 is necessary for trigeminal irritant pain and functions as a cellular formalin receptor.

Publication ,  Journal Article
Chen, Y; Kanju, P; Fang, Q; Lee, SH; Parekh, PK; Lee, W; Moore, C; Brenner, D; Gereau, RW; Wang, F; Liedtke, W
Published in: Pain
December 2014

Detection of external irritants by head nociceptor neurons has deep evolutionary roots. Irritant-induced aversive behavior is a popular pain model in laboratory animals. It is used widely in the formalin model, where formaldehyde is injected into the rodent paw, eliciting quantifiable nocifensive behavior that has a direct, tissue-injury-evoked phase, and a subsequent tonic phase caused by neural maladaptation. The formalin model has elucidated many antipain compounds and pain-modulating signaling pathways. We have adopted this model to trigeminally innervated territories in mice. In addition, we examined the involvement of TRPV4 channels in formalin-evoked trigeminal pain behavior because TRPV4 is abundantly expressed in trigeminal ganglion (TG) sensory neurons, and because we have recently defined TRPV4's role in response to airborne irritants and in a model for temporomandibular joint pain. We found TRPV4 to be important for trigeminal nocifensive behavior evoked by formalin whisker pad injections. This conclusion is supported by studies with Trpv4(-/-) mice and TRPV4-specific antagonists. Our results imply TRPV4 in MEK-ERK activation in TG sensory neurons. Furthermore, cellular studies in primary TG neurons and in heterologous TRPV4-expressing cells suggest that TRPV4 can be activated directly by formalin to gate Ca(2+). Using TRPA1-blocker and Trpa1(-/-) mice, we found that both TRP channels co-contribute to the formalin trigeminal pain response. These results imply TRPV4 as an important signaling molecule in irritation-evoked trigeminal pain. TRPV4-antagonistic therapies can therefore be envisioned as novel analgesics, possibly for specific targeting of trigeminal pain disorders, such as migraine, headaches, temporomandibular joint, facial, and dental pain, and irritation of trigeminally innervated surface epithelia.

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Published In

Pain

DOI

EISSN

1872-6623

Publication Date

December 2014

Volume

155

Issue

12

Start / End Page

2662 / 2672

Location

United States

Related Subject Headings

  • Vibrissae
  • Ubiquitin Thiolesterase
  • Trigeminal Ganglion
  • TRPV Cation Channels
  • Pyrroles
  • Pain
  • Nitriles
  • Neurons
  • Morpholines
  • Mice, Transgenic
 

Citation

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MLA
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Chen, Y., Kanju, P., Fang, Q., Lee, S. H., Parekh, P. K., Lee, W., … Liedtke, W. (2014). TRPV4 is necessary for trigeminal irritant pain and functions as a cellular formalin receptor. Pain, 155(12), 2662–2672. https://doi.org/10.1016/j.pain.2014.09.033
Chen, Yong, Patrick Kanju, Quan Fang, Suk Hee Lee, Puja K. Parekh, Whasil Lee, Carlene Moore, et al. “TRPV4 is necessary for trigeminal irritant pain and functions as a cellular formalin receptor.Pain 155, no. 12 (December 2014): 2662–72. https://doi.org/10.1016/j.pain.2014.09.033.
Chen Y, Kanju P, Fang Q, Lee SH, Parekh PK, Lee W, et al. TRPV4 is necessary for trigeminal irritant pain and functions as a cellular formalin receptor. Pain. 2014 Dec;155(12):2662–72.
Chen, Yong, et al. “TRPV4 is necessary for trigeminal irritant pain and functions as a cellular formalin receptor.Pain, vol. 155, no. 12, Dec. 2014, pp. 2662–72. Pubmed, doi:10.1016/j.pain.2014.09.033.
Chen Y, Kanju P, Fang Q, Lee SH, Parekh PK, Lee W, Moore C, Brenner D, Gereau RW, Wang F, Liedtke W. TRPV4 is necessary for trigeminal irritant pain and functions as a cellular formalin receptor. Pain. 2014 Dec;155(12):2662–2672.

Published In

Pain

DOI

EISSN

1872-6623

Publication Date

December 2014

Volume

155

Issue

12

Start / End Page

2662 / 2672

Location

United States

Related Subject Headings

  • Vibrissae
  • Ubiquitin Thiolesterase
  • Trigeminal Ganglion
  • TRPV Cation Channels
  • Pyrroles
  • Pain
  • Nitriles
  • Neurons
  • Morpholines
  • Mice, Transgenic