Localisation of cannabinoid and cannabinoid-related receptors in the equine dorsal root ganglia.


Journal

Equine veterinary journal
ISSN: 2042-3306
Titre abrégé: Equine Vet J
Pays: United States
ID NLM: 0173320

Informations de publication

Date de publication:
May 2021
Historique:
revised: 29 04 2020
received: 27 01 2020
accepted: 25 05 2020
pubmed: 12 6 2020
medline: 13 4 2021
entrez: 12 6 2020
Statut: ppublish

Résumé

Growing evidence recognises cannabinoid receptors as potential therapeutic targets for pain. Consequently, there is increasing interest in developing cannabinoid receptor agonists for treating pain. As a general rule, to better understand the actions of a drug, it would be of extreme importance to know the cellular distribution of its specific receptors. The localisation of cannabinoid receptors in the dorsal root ganglia of the horse has not yet been investigated. To localise the cellular distribution of canonical and putative cannabinoid receptors in the equine cervical dorsal root ganglia. Qualitative and quantitative immunohistochemical study. Cervical (C6-C8) dorsal root ganglia were collected from six horses (1.5 years of age) at the slaughterhouse. The tissues were fixed and processed to obtain cryosections which were used to investigate the immunoreactivity of canonical cannabinoid receptors 1 (CB1R) and 2 (CB2R), and for three putative cannabinoid-related receptors: nuclear peroxisome proliferator-activated receptor alpha (PPARα), transient receptor potential ankyrin 1 (TRPA1) and serotonin 5-HT1a receptor (5-HT1aR). The neurons showed immunoreactivity for CB1R (100%), CB2R (80% ± 13%), PPARα (100%), TRPA1 (74% ± 10%) and 5-HT1aR (84% ± 6%). The neuronal satellite glial cells showed immunoreactivity for CB2R, PPARα, TRPA1 and 5-HT1aR. The low number of horses included in the study. This study highlighted the expression of cannabinoid receptors in the sensory neurons and glial cells of the dorsal root ganglia. These findings could be of particular relevance for future functional studies assessing the effects of cannabinoids in horses to manage pain.

Sections du résumé

BACKGROUND BACKGROUND
Growing evidence recognises cannabinoid receptors as potential therapeutic targets for pain. Consequently, there is increasing interest in developing cannabinoid receptor agonists for treating pain. As a general rule, to better understand the actions of a drug, it would be of extreme importance to know the cellular distribution of its specific receptors. The localisation of cannabinoid receptors in the dorsal root ganglia of the horse has not yet been investigated.
OBJECTIVES OBJECTIVE
To localise the cellular distribution of canonical and putative cannabinoid receptors in the equine cervical dorsal root ganglia.
STUDY DESIGN METHODS
Qualitative and quantitative immunohistochemical study.
METHODS METHODS
Cervical (C6-C8) dorsal root ganglia were collected from six horses (1.5 years of age) at the slaughterhouse. The tissues were fixed and processed to obtain cryosections which were used to investigate the immunoreactivity of canonical cannabinoid receptors 1 (CB1R) and 2 (CB2R), and for three putative cannabinoid-related receptors: nuclear peroxisome proliferator-activated receptor alpha (PPARα), transient receptor potential ankyrin 1 (TRPA1) and serotonin 5-HT1a receptor (5-HT1aR).
RESULTS RESULTS
The neurons showed immunoreactivity for CB1R (100%), CB2R (80% ± 13%), PPARα (100%), TRPA1 (74% ± 10%) and 5-HT1aR (84% ± 6%). The neuronal satellite glial cells showed immunoreactivity for CB2R, PPARα, TRPA1 and 5-HT1aR.
MAIN LIMITATIONS CONCLUSIONS
The low number of horses included in the study.
CONCLUSIONS CONCLUSIONS
This study highlighted the expression of cannabinoid receptors in the sensory neurons and glial cells of the dorsal root ganglia. These findings could be of particular relevance for future functional studies assessing the effects of cannabinoids in horses to manage pain.

Identifiants

pubmed: 32524649
doi: 10.1111/evj.13305
doi:

Substances chimiques

Cannabinoids 0
Receptors, Cannabinoid 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

549-557

Subventions

Organisme : Formula Swiss AG, Switzerland

Informations de copyright

© 2020 EVJ Ltd.

Références

Krames ES. The dorsal root ganglion in chronic pain and as a target for neuromodulation: a review. Neuromodulation. 2015;18:24-32.
Esposito MF, Malayil R, Hanes M, Deer T. Unique characteristics of the dorsal root ganglion as a target for neuromodulation. Pain Med. 2019;20:S23-S30.
Hanani M. Satellite glial cells in sensory ganglia: from form to function. Brain Res Rev. 2005;48:457-76.
Ji RR, Berta T, Nedergaard M. Glia and pain: is chronic pain a gliopathy? Pain. 2013;154(Suppl 1):S10-28.
Hogan QH. Labat lecture: the primary sensory neuron: where it is, what it does, and why it matters. Reg Anesth Pain Med. 2010;35:306-11.
Calignano A, La Rana G, Giuffrida A, Piomelli D. Control of pain initiation by endogenous cannabinoids. Nature. 1998;394:277-81.
Ligresti A, De Petrocellis L, Di Marzo V. From phytocannabinoids to cannabinoid receptors and endocannabinoids: pleiotropic physiological and pathological roles through complex pharmacology. Physiol Rev. 2016;96:1593-659.
Pergolizzi JV Jr, Lequang JA, Taylor R Jr, Raffa RB, Colucci D. NEMA Research Group. The role of cannabinoids in pain control: the good, the bad, and the ugly. Minerva Anestesiol. 2018;84:955-69.
Yanes JA, McKinnell ZE, Reid MA, Busler JN, Michel JS, Pangelinan MM, et al. Effects of cannabinoid administration for pain: A meta-analysis and meta-regression. Exp Clin Psychopharmacol. 2019;27:370-82.
Kogan L, Schoenfeld-Tacher R, Hellyer P, Rishniw M. US Veterinarians' Knowledge, Experience, and Perception Regarding the Use of Cannabidiol for Canine Medical Conditions. Front Vet Sci. 2019;5:338.
Ellis KL, Contino EK. Case Report: Treatment using cannabidiol in a horse with mechanical allodynia. Equine vet Educ 2021;33:e79-e82.
Williamson EM, Liu X, Izzo AA. Trends in use, pharmacology and clinical applications of emerging herbal nutraceuticals. Br J Pharmacol. 2020;177:1227-40
Mechoulam R, Peters M, Murillo-Rodriguez E, Hanus LO. Cannabidiol-recent advances. Chem Biodivers. 2007;4:1678-92.
Pertwee RG. The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: delta9-tetrahydrocannabinol, cannabidiol and delta9-tetrahydrocannabivarin. Br J Pharmacol. 2008;153:199-215.
Morales P, Hurst DP, Reggio PH. Molecular targets of the phytocannabinoids: a complex picture. Prog Chem Org Nat Prod. 2017;103:103-31.
Ahluwalia J, Urban L, Capogna M, Bevan S, Nagy I. Cannabinoid 1 receptors are expressed in nociceptive primary sensory neurons. Neuroscience. 2000;100:685-8.
Svízenská IH, Brázda V, Klusáková I, Dubový P. Bilateral changes of cannabinoid receptor type 2 protein and mRNA in the dorsal root ganglia of a rat neuropathic pain model. J Histochem Cytochem. 2013;61:529-47.
Freundt-Revilla J, Kegler K, Baumgärtner W, Tipold A. Spatial distribution of cannabinoid receptor type 1 (CB1) in normal canine central and peripheral nervous system. PLoS One. 2017;12:e0181064.
Chiocchetti R, Galiazzo G, Tagliavia C, Stanzani A, Giancola F, Menchetti M, et al. Cellular distribution of canonical and putative cannabinoid receptors in canine cervical dorsal root ganglia. Front Vet Sci. 2019;6:313.
Russo D, Bombardi C, Castellani G, Chiocchetti R. Characterization of spinal ganglion neurons in horse (Equus caballus). A morphometric, neurochemical and tracing study. Neuroscience. 2011;176:53-71.
Giancola F, Rambaldi AM, Bianco F, Iusco S, Romagnoli N, Tagliavia C, et al. Localization of the 5-hydroxytryptamine 4 receptor in equine enteric neurons and extrinsic sensory fibers. Neurogastroenterol Motil. 2017;29: https://doi.org/10.1111/nmo.13045
Wager-Miller J, Westenbroek R, Mackie K. Dimerization of G protein-coupled receptors: CB1 cannabinoid receptors as an example. Chem Phys Lipids. 2002;121:83-9.
Anand U, Otto WR, Sanchez-Herrera D, Facer P, Yiangou Y, Korchev Y, et al. Cannabinoid receptor CB2 localisation and agonist-mediated inhibition of capsaicin responses in human sensory neurons. Pain. 2008a;138:667-80.
Sánchez-Aparicio P, Florán B, Rodríguez Velázquez D, Ibancovichi JA, Varela Guerrero JA, Recillas S. Cannabinoids CB2 receptors, one new promising drug target for chronic and degenerative pain conditions in equine veterinary patients. J Equine Vet Science. 2020;85:102880.
Issemann I, Green S. Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators. Nature. 1990;347:645-50.
Lo Verme J, Fu J, Astarita G, La Rana G, Russo R, Calignano A, et al. The nuclear receptor peroxisome proliferator-activated receptor-alpha mediates the antiinflammatory actions of palmitoylethanolamide. Mol Pharmacol. 2005;67:15-9.
O'Sullivan SE. Cannabinoids go nuclear: evidence for activation of peroxisome proliferator-activated receptors. Br J Pharmacol. 2007;152:576-82.
Burstein S. PPAR-gamma: a nuclear receptor with affinity for cannabinoids. Life Sci. 2005;77:1674-84.
LoVerme J, Russo R, La Rana G, Fu J, Farthing J, Mattace-Raso G, et al. Rapid broad-spectrum analgesia through activation of peroxisome proliferator-activated receptor-alpha. J Pharmacol Exp Ther. 2006;319:1051-61.
Ho WSV, Kelly MEM. Cannabinoids in the cardiovascular system. Adv Pharmacol. 2017;80:329-66.
Benyó Z, Ruisanchez É, Leszl-Ishiguro M, Sándor P, Pacher P. Endocannabinoids in cerebrovascular regulation. Am J Physiol Heart Circ Physiol. 2016;310:785-801.
Brierley SM, Hughes PA, Page AJ, Kwan KY, Martin CM, O'Donnell TA, et al. The ion channel TRPA1 is required for normal mechanosensation and is modulated by algesic stimuli. Gastroenterology. 2009;137:2084-2095.e3.
McNamara CR, Mandel-Brehm J, Bautista DM, Siemens J, Deranian KL, Zhao M, et al. TRPA1 mediates formalin-induced pain. Proc Natl Acad Sci USA. 2007;104:13525-30.
Wang XL, Cui LW, Liu Z, Gao YM, Wang S, Li H, et al. Effects of TRPA1 activation and inhibition on TRPA1 and CGRP expression in dorsal root ganglion neurons. Neural Regen Res. 2019;14:140-8.
Akopian AN, Ruparel NB, Jeske NA, Hargreaves KM. Transient receptor potential TRPA1 channel desensitization in sensory neurons is agonist dependent and regulated by TRPV1-directed internalization. J. Physiol. London. 2007;583:175-93.
Anand U, Otto WR, Facer P, Zebda N, Selmer I, Gunthorpe MJ, et al. TRPA1 receptor localisation in the human peripheral nervous system and functional studies in cultured human and rat sensory neurons. Neurosci Lett. 2008b;438:221-7.
De Petrocellis L, Vellani V, Schiano-Moriello A, Marini P, Magherini PC, Orlando P, et al. Plant-derived cannabinoids modulate the activity of transient receptor potential channels of ankyrin type-1 and melastatin type-8. J Pharmacol Exp Ther. 2008;325:1007-15.
Richardson BP. Serotonin and nociception. Ann NY Acad Sci. 1990;600:511-9.
Liu Z, Zhuang D, Lunderberg T, Yu L. Involvement of 5-hydroxytryptamine(1A) receptors in the descending anti- nociceptive pathway from periaqueductal gray to the spinal dorsal horn in intact rats, rats with nerve injury and rats with inflammation. Neuroscience. 2002;112:399-407.
Haleem DJ. Serotonin-1A receptor dependent modulation of pain and reward for improving therapy of chronic pain. Pharmacol Res. 2018;134:212-9.
Todorovic S, Anderson EG. Serotonin preferentially hyperpolarizes capsaicin-sensitive C type sensory neurons by activating 5-HT1A receptors. Brain Res. 1992;585:212-8.
Yoder EJ, Tamir H, Ellisman MH. Serotonin receptors expressed by myelinating Schwann cells in rat sciatic nerve. Brain Res. 1997;753:299-308.
Capano A, Weaver R, Burkman E. Evaluation of the effects of CBD hemp extract on opioid use and quality of life indicators in chronic pain patients: a prospective cohort study. Postgrad Med. 2019;1-6: https://doi.org/10.1080/00325481.2019.1685298

Auteurs

Roberto Chiocchetti (R)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Riccardo Rinnovati (R)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Claudio Tagliavia (C)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Agnese Stanzani (A)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Giorgia Galiazzo (G)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Fiorella Giancola (F)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Margherita De Silva (M)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Ylenia Capodanno (Y)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

Alessandro Spadari (A)

Department of Veterinary Medical Sciences (UNI EN ISO), University of Bologna, Ozzano dell'Emilia, Italy.

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