Inhibition of transient receptor potential vanilloid type 1 through α2 adrenergic receptors at peripheral nerve terminals relieves pain
Author:
Affiliation:
1. The United Graduate School of Veterinary Science, Yamaguchi University, Yamaguchi 753-8511, Japan
2. Laboratory of Veterinary Physiology, Faculty of Agriculture, Tottori University, Tottori 680-8553, Japan
Publisher
Japanese Society of Veterinary Science
Subject
General Veterinary
Link
https://www.jstage.jst.go.jp/article/jvms/83/10/83_21-0429/_pdf
Reference40 articles.
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2. 2. Caterina, M. J., Schumacher, M. A., Tominaga, M., Rosen, T. A., Levine, J. D. and Julius, D. 1997. The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature 389: 816–824.
3. 3. Chakraborty, S., Elvezio, V., Kaczocha, M., Rebecchi, M. and Puopolo, M. 2017. Presynaptic inhibition of transient receptor potential vanilloid type 1 (TRPV1) receptors by noradrenaline in nociceptive neurons. J. Physiol. 595: 2639–2660.
4. 4. Coderre, T. J., Katz, J., Vaccarino, A. L. and Melzack, R. 1993. Contribution of central neuroplasticity to pathological pain: review of clinical and experimental evidence. Pain 52: 259–285.
5. 5. Cortright, D. N. and Szallasi, A. 2004. Biochemical pharmacology of the vanilloid receptor TRPV1. An update. Eur. J. Biochem. 271: 1814–1819.
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