Cannabinoid Receptors in the Horse Lateral Nucleus of the Amygdala: A Potential Target for Ameliorating Pain Perception, Stress and Anxiety in Horses.
Abstract: The amygdala is composed of several nuclei, including the lateral nucleus which is the main receiving area for the input from cortical and subcortical brain regions. It mediates fear, anxiety, stress, and pain across species. Evidence suggests that the endocannabinoid system may be a promising target for modulating these processes. Cannabinoid and cannabinoid-related receptors have been identified in the amygdala of rodents, carnivores, and humans, but not in horses. This study aimed to investigate the gene expression of cannabinoid receptors 1 (CB1R) and 2 (CB2R), transient receptor potential vanilloid 1 (TRPV1), and peroxisome proliferator-activated receptor gamma (PPARγ) within the lateral nucleus of six equine amygdalae collected post mortem from an abattoir using quantitative real-time PCR, cellular distribution, and immunofluorescence. mRNA expression of CB1R and CB2R, but not TRPV1 or PPARγ, was detected. The percentage of immunoreactivity (IR) was calculated using ImageJ software. Cannabinoid receptor 1 immunoreactivity was absent in the somata but was strongly detected in the surrounding neuropil and varicosities and CB2R-IR was observed in the varicosities; TRPV1-IR showed moderate expression in the cytoplasm of somata and processes, while PPARγ-IR was weak-to-moderate in the neuronal nuclei. These findings demonstrate endocannabinoid system components in the equine amygdala and may support future studies on spp. molecules acting on these receptors.
Publication Date: 2025-08-06 PubMed ID: 40806746PubMed Central: PMC12347058DOI: 10.3390/ijms26157613Google Scholar: Lookup
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Summary
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The research article investigates the presence of cannabinoid receptors in the lateral nucleus of horse amygdalae and their potential role in influencing pain, stress, and anxiety responses in horses.
Introduction and Objective of the Research
- The study seeks to further expand the knowledge about animal neuroanatomy and neurophysiology, particularly in equines.
- The focus is on the lateral nucleus of the amygdala, one of the key nuclei associated with processing and regulating fear, anxiety, stress, and pain in several species.
- The endocannabinoid system and its related receptors have been significantly linked with the modulation of these processes in several species such as rats, carnivores, and humans. Still, its existence in horses remains unexplored.
- The primary aim of this research is to identify the expression of cannabinoid receptors 1 (CB1R) and 2 (CB2R) and other related receptors within the horse amygdala.
Methodology
- Six horse amygdalae were procured post-mortem from an abattoir for the study.
- The researchers employed quantitative real-time PCR, cellular distribution, and immunofluorescence techniques.
- They looked into the gene expression of cannabinoid receptors CB1R and CB2R, transient receptor potential vanilloid 1 (TRPV1), and peroxisome proliferator-activated receptor gamma (PPARγ).
- The extent of immunoreactivity (IR), a measure of how reactive an antigen is to an antibody, was calculated using ImageJ software.
Results
- The results showed the presence of mRNA expression of cannabinoid receptors CB1R and CB2R in the studied samples, corroborating the existence of these receptors in horses.
- However, the TRPV1 and PPARγ receptors did not exhibit any mRNA expression.
- Immunoreactivity varied across the different receptors, with differing observed reactions to antigens across the tested receptors.
- CB1R revealed strong detection in the surrounding neuropil and varicosities but was absent in the somata or cell body.
- CB2R immunoreactivity was observed in varicosities, while TRPV1 showed moderate expression in both the somata and processes. PPARγ immunoreactivity was weak-to-moderate in the neuronal nuclei.
Conclusions
- The results demonstrate the presence of endocannabinoid system components in the horse amygdala, marking an important discovery in equine anatomy and opening pathways to evaluate the potential impact on the modulation of fear, anxiety, stress, and pain in horses.
- The findings may facilitate future studies focusing on how particular molecules interact with these receptors in horses.
Cite This Article
APA
Bombardi C, Salamanca G, Tagliavia C, Grandis A, Zamith Cunha R, Gramenzi A, De Silva M, Zannoni A, Chiocchetti R.
(2025).
Cannabinoid Receptors in the Horse Lateral Nucleus of the Amygdala: A Potential Target for Ameliorating Pain Perception, Stress and Anxiety in Horses.
Int J Mol Sci, 26(15), 7613.
https://doi.org/10.3390/ijms26157613 Publication
Researcher Affiliations
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
- Department of Translational Medicine and for Romagna, University of Ferrara, 40121 Ferrara, Italy.
- Department of Veterinary Medicine, University of Teramo, 64100 Teramo, Italy.
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
- Department of Veterinary Medicine, University of Teramo, 64100 Teramo, Italy.
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
- Department of Veterinary Medical Sciences (UNI EN ISO 9001:2008), University of Bologna, 40126 Bologna, Italy.
MeSH Terms
- Animals
- Horses
- PPAR gamma / metabolism
- PPAR gamma / genetics
- Anxiety / metabolism
- TRPV Cation Channels / metabolism
- TRPV Cation Channels / genetics
- Receptors, Cannabinoid / metabolism
- Receptors, Cannabinoid / genetics
- Pain Perception
- Receptor, Cannabinoid, CB1 / metabolism
- Receptor, Cannabinoid, CB1 / genetics
- Amygdala / metabolism
- Receptor, Cannabinoid, CB2 / metabolism
- Receptor, Cannabinoid, CB2 / genetics
- Male
- Basolateral Nuclear Complex / metabolism
Grant Funding
- No number / NBF Lanes, Milan, Italy
Conflict of Interest Statement
The authors declare no conflicts of interest.
References
This article includes 96 references
- Aggleton J.P. In: The Amygdala: A Functional Analysis. Aggleton J.P., editor. Oxford University Press; Oxford, UK: 2000.
- Bombardi C.. Neuronal Localization of the 5-HT2 Receptor Family in the Amygdaloid Complex. Front. Pharmacol. 2014;5:68.
- Salamanca G., Tagliavia C., Grandis A., Graïc J.M., Cozzi B., Bombardi C.. Distribution of Vasoactive Intestinal Peptide (VIP) Immunoreactivity in the Rat Pallial and Subpallial Amygdala and Colocalization with γ-Aminobutyric Acid (GABA). Anat. Rec. 2024;307:2891–2911.
- Pitkanen A.. Connectivity of the Rat Amygdaloid Complex. In: Aggleton J.P., editor. The Amygdala: A Functional Analysis. Oxford University Press; Oxford, UK: 2000. pp. 31–115.
- Guirado S., Real M.Á., Dávila J.C.. Distinct Immunohistochemically Defined Areas in the Medial Amygdala in the Developing and Adult Mouse. Brain Res. Bull. 2008;75:214–217.
- Rambaldi A.M., Cozzi B., Grandis A., Canova M., Mazzoni M., Bombardi C.. Distribution of Calretinin Immunoreactivity in the Lateral Nucleus of the Bottlenose Dolphin (Tursiops truncatus) Amygdala. Anat. Rec. 2017;300:2008–2016.
- Sah P., Faber E.S.L., Lopez De Armentia M., Power J.. The Amygdaloid Complex: Anatomy and Physiology. Physiol. Rev. 2003;83:803–834.
- McGaugh J.L.. The Amygdala Modulates the Consolidation of Memories of Emotionally Arousing Experiences. Annu. Rev. Neurosci. 2004;27:1–28.
- LeDoux J.. The Amygdala. Curr. Biol. 2007;17:R868–R874.
- Thompson J.M., Neugebauer V.. Amygdala Plasticity and Pain. Pain. Res. Manag. 2017;2017:8296501.
- Millan M.J.. The Neurobiology and Control of Anxious States. Prog. Neurobiol. 2003;70:83–244.
- Neugebauer V., Li W., Bird G.C., Han J.S.. The Amygdala and Persistent Pain. Neuroscientist. 2004;10:221–234.
- Liu C.C., Shi C.-Q., Franaszczuk P.J., Crone N.E., Schretlen D., Ohara S., Lenz F.A.. Painful Laser Stimuli Induce Directed Functional Interactions within and between the Human Amygdala and Hippocampus. Neuroscience. 2011;178:208–217.
- Takeuchi T., Sugita S.. Histological Atlas and Morphological Features by Nissl Staining in the Amygdaloid Complex of the Horse, Cow and Pig. J. Equine Sci. 2007;18:13–25.
- Hall C., Randle H., Pearson G., Preshaw L., Waran N.. Assessing Equine Emotional State. Appl. Anim. Behav. Sci. 2018;205:183–193.
- Kreitzer F.R., Stella N.. The Therapeutic Potential of Novel Cannabinoid Receptors. Pharmacol. Ther. 2009;122:83–96.
- Lowin T., Pongratz G., Straub R.H.. The Synthetic Cannabinoid WIN55,212-2 Mesylate Decreases the Production of Inflammatory Mediators in Rheumatoid Arthritis Synovial Fibroblasts by Activating CB2, TRPV1, TRPA1 and yet Unidentified Receptor Targets. J. Inflamm. 2016;13:15.
- 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;96:1593–1659.
- Morales P., Hurst D.P., Reggio P.H.. Molecular Targets of the Phytocannabinoids: A Complex Picture. In: Kinghorn A.D., Falk H., Gibbons S., Kobayashi J., editors. Phytocannabinoids. Volume 103. Springer International Publishing; Cham, Switzerland: 2017. pp. 103–131. Progress in the Chemistry of Organic Natural Products.
- Mlost J., Bryk M., Starowicz K.. Cannabidiol for Pain Treatment: Focus on Pharmacology and Mechanism of Action. Int. J. Mol. Sci. 2020;21:8870.
- McDonald A.J., Mascagni F.. Localization of the CB1 Type Cannabinoid Receptor in the Rat Basolateral Amygdala: High Concentrations in a Subpopulation of Cholecystokinin-Containing Interneurons. Neuroscience. 2001;107:641–652.
- McDonald A.J.. Expression of the Type 1 Cannabinoid Receptor (CB1R) in CCK-Immunoreactive Axon Terminals in the Basolateral Amygdala of the Rhesus Monkey (Macaca mulatta). Neurosci. Lett. 2021;745:135503.
- Amaral D.G.. Anatomical Organization of the Primate Amygdaloid Complex. In: Aggleton J.P., editor. The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction. Wiley-Liss; New York, NY, USA: 1992. pp. 1–66.
- Vásquez C.E., Reberger R., Dall’Oglio A., Calcagnotto M.E., Rasia-Filho A.A.. Neuronal Types of the Human Cortical Amygdaloid Nucleus. J. Comp. Neurol. 2018;526:2776–2801.
- McDonald A.J.. Chapter 1—Functional Neuroanatomy of the Basolateral Amygdala: Neurons, Neurotransmitters, and Circuits. In: Urban J.H., Rosenkranz J.A., editors. Handbook of Behavioral Neuroscience. Volume 26. Elsevier; Amsterdam, The Netherlands: 2020. pp. 1–38. Handbook of Amygdala Structure and Function.
- McDonald A.J., Augustine J.R.. Nonpyramidal Neurons in the Primate Basolateral Amygdala: A Golgi Study in the Baboon (Papio cynocephalus) and Long-Tailed Macaque (Macaca fascicularis). J. Comp. Neurol. 2020;528:772–786.
- Degroot A.. Role of Cannabinoid Receptors in Anxiety Disorders. In: Köfalvi A., editor. Cannabinoids and the Brain. Springer US; Boston, MA, USA: 2008. pp. 559–572.
- Zamith Cunha R., Zannoni A., Salamanca G., De Silva M., Rinnovati R., Gramenzi A., Forni M., Chiocchetti R.. Expression of Cannabinoid (CB1 and CB2) and Cannabinoid-Related Receptors (TRPV1, GPR55, and PPARα) in the Synovial Membrane of the Horse Metacarpophalangeal Joint. Front. Vet. Sci. 2023;10:1045030.
- Zamith Cunha R., Semprini A., Salamanca G., Gobbo F., Morini M., Pickles K.J., Roberts V., Chiocchetti R.. Expression of Cannabinoid Receptors in the Trigeminal Ganglion of the Horse. Int. J. Mol. Sci. 2023;24:15949.
- Galiazzo G., De Silva M., Giancola F., Rinnovati R., Peli A., Chiocchetti R.. Cellular Distribution of Cannabinoid-related Receptors TRPV1, PPAR-gamma, GPR55 and GPR3 in the Equine Cervical Dorsal Root Ganglia. Equine Vet. J. 2022;54:788–798.
- Chiocchetti R., Rinnovati R., Tagliavia C., Stanzani A., Galiazzo G., Giancola F., Silva M.D., Capodanno Y., Spadari A.. Localisation of Cannabinoid and Cannabinoid-Related Receptors in the Equine Dorsal Root Ganglia. Equine Vet. J. 2021;53:549–557.
- Katona I., Rancz E.A., Acsády L., Ledent C., Mackie K., Hájos N., Freund T.F.. Distribution of CB1 Cannabinoid Receptors in the Amygdala and Their Role in the Control of GABAergic Transmission. J. Neurosci. 2001;21:9506–9518.
- Fitzgerald M.L., Mackie K., Pickel V.M.. Ultrastructural Localization of Cannabinoid CB1 and mGluR5 Receptors in the Prefrontal Cortex and Amygdala. J. Comp. Neurol. 2019;527:2730–2741.
- Glass M., Faull R.L.M., Dragunow M.. Cannabinoid Receptors in the Human Brain: A Detailed Anatomical and Quantitative Autoradiographic Study in the Fetal, Neonatal and Adult Human Brain. Neuroscience. 1997;77:299–318.
- Wang X., Dow-Edwards D., Keller E., Hurd Y.L.. Preferential Limbic Expression of the Cannabinoid Receptor mRNA in the Human Fetal Brain. Neuroscience. 2003;118:681–694.
- Zhu L., Zheng D., Li R., Shen C.-J., Cai R., Lyu C., Tang B., Sun H., Wang X., Ding Y.. Induction of Anxiety-Like Phenotypes by Knockdown of Cannabinoid Type-1 Receptors in the Amygdala of Marmosets. Neurosci. Bull. 2023;39:1669–1682.
- 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.
- Gong J.-P., Onaivi E.S., Ishiguro H., Liu Q.-R., Tagliaferro P.A., Brusco A., Uhl G.R.. Cannabinoid CB2 Receptors: Immunohistochemical Localization in Rat Brain. Brain Res. 2006;1071:10–23.
- Roberts J.C., Davis J.B., Benham C.D.. [3H]Resiniferatoxin Autoradiography in the CNS of Wild-Type and TRPV1 Null Mice Defines TRPV1 (VR-1) Protein Distribution. Brain Res. 2004;995:176–183.
- Mezey É., Tóth Z.E., Cortright D.N., Arzubi M.K., Krause J.E., Elde R., Guo A., Blumberg P.M., Szallasi A.. Distribution of mRNA for Vanilloid Receptor Subtype 1 (VR1), and VR1-like Immunoreactivity, in the Central Nervous System of the Rat and Human. Proc. Nat. Acad. Sci. USA. 2000;97:3655–3660.
- Hempel B., Crissman M., Pari S., Klein B., Bi G.-H., Alton H., Xi Z.-X.. PPARα and PPARγ Are Expressed in Midbrain Dopamine Neurons and Modulate Dopamine- and Cannabinoid-Mediated Behavior in Mice. Mol. Psychiatry. 2023;28:4203–4214.
- Domi E., Uhrig S., Soverchia L., Spanagel R., Hansson A.C., Barbier E., Heilig M., Ciccocioppo R., Ubaldi M.. Genetic Deletion of Neuronal PPARγ Enhances the Emotional Response to Acute Stress and Exacerbates Anxiety: An Effect Reversed by Rescue of Amygdala PPARγ Function. J. Neurosci. 2016;36:12611–12623.
- Girella A., Di Bartolomeo M., Dainese E., Buzzelli V., Trezza V., D’Addario C.. Fatty Acid Amide Hydrolase and Cannabinoid Receptor Type 1 Genes Regulation Is Modulated by Social Isolation in Rats. Neurochem. Res. 2024;49:1278–1290.
- De Sa Nogueira D., Bourdy R., Alcala-Vida R., Filliol D., Andry V., Goumon Y., Zwiller J., Romieu P., Merienne K., Olmstead M.C.. Hippocampal Cannabinoid 1 Receptors Are Modulated Following Cocaine Self-Administration in Male Rats. Mol. Neurobiol. 2022;59:1896–1911.
- Schwerdtfeger J., Krause A., Kalbe C., Mazzuoli-Weber G., Eggert A., Puppe B., Kuhla B., Röttgen V.. Endocannabinoid Administration Affects Taste Preference and the Expression of Cannabinoid and Opioid Receptors in the Amygdala of Early Lactating Cows. Sci. Rep. 2023;13:4967.
- Biscaia M., Marín S., Fernández B., Marco E.M., Rubio M., Guaza C., Ambrosio E., Viveros M.P.. Chronic Treatment with CP 55,940 during the Peri-Adolescent Period Differentially Affects the Behavioural Responses of Male and Female Rats in Adulthood. Psychopharmacology. 2003;170:301–308.
- Urigüen L., Pérez-Rial S., Ledent C., Palomo T., Manzanares J.. Impaired Action of Anxiolytic Drugs in Mice Deficient in Cannabinoid CB1 Receptors. Neuropharmacology. 2004;46:966–973.
- Pertwee R.G.. Pharmacology of Cannabinoid CB1 and CB2 Receptors. Pharmacol. Ther. 1997;74:129–180.
- Rakhshan F., Day T.A., Blakely R.D., Barker E.L.. Carrier-Mediated Uptake of the Endogenous Cannabinoid Anandamide in RBL-2H3 Cells. J. Pharmacol. Exp. Ther. 2000;292:960–967.
- Gunduz-Cinar O.. The Endocannabinoid System in the Amygdala and Modulation of Fear. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2021;105:110116.
- Gunduz-Cinar O., Castillo L.I., Xia M., Leer E.V., Brockway E.T., Pollack G.A., Yasmin F., Bukalo O., Limoges A., Oreizi-Esfahani S.. A Cortico-Amygdala Neural Substrate for Endocannabinoid Modulation of Fear Extinction. Neuron. 2023;111:3053–3067.e10.
- Adhikari A.. Endocannabinoids Modulate Fear Extinction Controlled by a Cortical-Amygdala Projection. Neuron. 2023;111:2948–2950.
- Patel S., Cravatt B.F., Hillard C.J.. Synergistic Interactions between Cannabinoids and Environmental Stress in the Activation of the Central Amygdala. Neuropsychopharmacology. 2005;30:497–507.
- Marsicano G., Wotjak C.T., Azad S.C., Bisogno T., Rammes G., Cascio M.G., Hermann H., Tang J., Hofmann C., Zieglgänsberger W.. The Endogenous Cannabinoid System Controls Extinction of Aversive Memories. Nature. 2002;418:530–534.
- Azad S.C., Monory K., Marsicano G., Cravatt B.F., Lutz B., Zieglgänsberger W., Rammes G.. Circuitry for Associative Plasticity in the Amygdala Involves Endocannabinoid Signaling. J. Neurosci. 2004;24:9953–9961.
- Rea K., Olango W.M., Harhen B., Kerr D.M., Galligan R., Fitzgerald S., Moore M., Roche M., Finn D.P.. Evidence for a Role of GABAergic and Glutamatergic Signalling in the Basolateral Amygdala in Endocannabinoid-Mediated Fear-Conditioned Analgesia in Rats. Pain. 2013;154:576–585.
- Rubino T., Sala M., Viganò D., Braida D., Castiglioni C., Limonta V., Guidali C., Realini N., Parolaro D.. Cellular Mechanisms Underlying the Anxiolytic Effect of Low Doses of Peripheral Delta9-Tetrahydrocannabinol in Rats. Neuropsychopharmacology. 2007;32:2036–2045.
- Onaivi E.S., Ishiguro H., Gong J.-P., Patel S., Perchuk A., Meozzi P.A., Myers L., Mora Z., Tagliaferro P., Gardner E.. Discovery of the Presence and Functional Expression of Cannabinoid CB2 Receptors in Brain. Ann. N. Y. Acad. Sci. 2006;1074:514–536.
- Cabral G.A., Raborn E.S., Griffin L., Dennis J., Marciano-Cabral F.. CB2 Receptors in the Brain: Role in Central Immune Function. Br. J. Pharmacol. 2008;153:240–251.
- Brusco A., Tagliaferro P., Saez T., Onaivi E.S.. Postsynaptic Localization of CB2 Cannabinoid Receptors in the Rat Hippocampus. Synapse. 2008;62:944–949.
- Roche M., Finn D.P.. Brain CB2 Receptors: Implications for Neuropsychiatric Disorders. Pharmaceuticals. 2010;3:2517–2553.
- Atwood B.K., Mackie K.. CB2: A Cannabinoid Receptor with an Identity Crisis. Br. J. Pharmacol. 2010;160:467–479.
- Bahi A., Al Mansouri S., Al Memari E., Al Ameri M., Nurulain S.M., Ojha S.. β-Caryophyllene, a CB2 Receptor Agonist Produces Multiple Behavioral Changes Relevant to Anxiety and Depression in Mice. Physiol. Behav. 2014;135:119–124.
- Ramikie T.S., Patel S.. Endocannabinoid Signaling in the Amygdala: Anatomy, Synaptic Signaling, Behavior, and Adaptations to Stress. Neuroscience. 2012;204:38–52.
- García-Gutiérrez M.S., Manzanares J.. Overexpression of CB2 Cannabinoid Receptors Decreased Vulnerability to Anxiety and Impaired Anxiolytic Action of Alprazolam in Mice. J. Psychopharmacol. 2011;25:111–120.
- Manning B.H., Martin W.J., Meng I.D.. The Rodent Amygdala Contributes to the Production of Cannabinoid-Induced Antinociception. Neuroscience. 2003;120:1157–1170.
- Argue K.J., VanRyzin J.W., Falvo D.J., Whitaker A.R., Yu S.J., McCarthy M.M.. Activation of Both CB1 and CB2 Endocannabinoid Receptors Is Critical for Masculinization of the Developing Medial Amygdala and Juvenile Social Play Behavior. eNeuro. 2017;4:e0344.
- Segev A., Akirav I.. Cannabinoids and Glucocorticoids in the Basolateral Amygdala Modulate Hippocampal–Accumbens Plasticity After Stress. Neuropsychopharmacology. 2016;41:1066–1079.
- Zschenderlein C., Gebhardt C., von Bohlen und Halbach O., Kulisch C., Albrecht D.. Capsaicin-Induced Changes in LTP in the Lateral Amygdala Are Mediated by TRPV1. PLoS ONE. 2011;6:e16116.
- Marsch R., Foeller E., Rammes G., Bunck M., Kössl M., Holsboer F., Zieglgänsberger W., Landgraf R., Lutz B., Wotjak C.T.. Reduced Anxiety, Conditioned Fear, and Hippocampal Long-Term Potentiation in Transient Receptor Potential Vanilloid Type 1 Receptor-Deficient Mice. J. Neurosci. 2007;27:832–839.
- Santos C.J.P.A., Stern C.A.J., Bertoglio L.J.. Attenuation of Anxiety-Related Behaviour after the Antagonism of Transient Receptor Potential Vanilloid Type 1 Channels in the Rat Ventral Hippocampus. Behav. Pharmacol. 2008;19:357.
- Marsicano G., Kuner R.. Anatomical Distribution of Receptors, Ligands and Enzymes in the Brain and in the Spinal Cord: Circuitries and Neurochemistry. In: Köfalvi A., editor. Cannabinoids and the Brain. Springer US; Boston, MA, USA: 2008. pp. 161–201.
- Kirkedal C., Wegener G., Moreira F., Joca S.R.L., Liebenberg N.. A Dual Inhibitor of FAAH and TRPV1 Channels Shows Dose-Dependent Effect on Depression-like Behaviour in Rats. Acta Neuropsychiatr. 2017;29:324–329.
- Frias B., Merighi A.. Capsaicin, Nociception and Pain. Molecules. 2016;21:797.
- Nagy I., White J.P.M., Paule C.C., Maze M., Urban L.. Functional Molecular Biology of the TRPV1 Ion Channel. In: Köfalvi A., editor. Cannabinoids and the Brain. Springer US; Boston, MA, USA: 2008. pp. 101–130.
- Xiao Y., Chen X., Zhang P.-A., Xu Q., Zheng H., Xu G.-Y.. TRPV1-Mediated Presynaptic Transmission in Basolateral Amygdala Contributes to Visceral Hypersensitivity in Adult Rats with Neonatal Maternal Deprivation. Sci. Rep. 2016;6:29026.
- Edwards J.G.. TRPV1 in the Central Nervous System: Synaptic Plasticity, Function, and Pharmacological Implications. Prog. Drug Res. 2014;68:77–104.
- Zolezzi J.M., Santos M.J., Bastías-Candia S., Pinto C., Godoy J.A., Inestrosa N.C.. PPARs in the Central Nervous System: Roles in Neurodegeneration and Neuroinflammation. Biol. Rev. 2017;92:2046–2069.
- Cristiano L., Bernardo A., Cerù M.P.. Peroxisome Proliferator-Activated Receptors (PPARs) and Peroxisomes in Rat Cortical and Cerebellar Astrocytes. J. Neurocytol. 2001;30:671–683.
- Moreno S., Farioli-Vecchioli S., Cerù M.P.. Immunolocalization of Peroxisome Proliferator-Activated Receptors and Retinoid X Receptors in the Adult Rat CNS. Neuroscience. 2004;123:131–145.
- Warden A., Truitt J., Merriman M., Ponomareva O., Jameson K., Ferguson L.B., Mayfield R.D., Harris R.A.. Localization of PPAR Isotypes in the Adult Mouse and Human Brain. Sci. Rep. 2016;6:27618.
- Swanson C.R., Emborg M.E.. Expression of Peroxisome Proliferator-Activated Receptor-γ in the Substantia Nigra of Hemiparkinsonian Nonhuman Primates. Neurol. Res. 2014;36:634–646.
- Bernardo A., Levi G., Minghetti L.. Role of the Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ) and Its Natural Ligand 15-Deoxy-Δ12,14-Prostaglandin J2 in the Regulation of Microglial Functions. Eur. J. Neurosci. 2000;12:2215–2223.
- Roth A.D., Leisewitz A.V., Jung J.E., Cassina P., Barbeito L., Inestrosa N.C., Bronfman M.. PPAR Gamma Activators Induce Growth Arrest and Process Extension in B12 Oligodendrocyte-like Cells and Terminal Differentiation of Cultured Oligodendrocytes. J. Neurosci. Res. 2003;72:425–435.
- Gemma C., Stellwagen H., Fister M., Coultrap S.J., Mesches M.H., Browning M.D., Bickford P.C.. Rosiglitazone Improves Contextual Fear Conditioning in Aged Rats. Neuroreport. 2004;15:2255–2259.
- Gaspar J.C., Okine B.N., Dinneen D., Roche M., Finn D.P.. Effects of Intra-BLA Administration of PPAR Antagonists on Formalin-Evoked Nociceptive Behaviour, Fear-Conditioned Analgesia, and Conditioned Fear in the Presence or Absence of Nociceptive Tone in Rats. Molecules. 2022;27:2021.
- Evers D.L., Fowler C.B., Cunningham B.R., Mason J.T., O’Leary T.J.. The Effect of Formaldehyde Fixation on RNA. J. Mol. Diagn. 2011;13:282–288.
- Jones W., Greytak S., Odeh H., Guan P., Powers J., Bavarva J., Moore H.M.. Deleterious Effects of Formalin-Fixation and Delays to Fixation on RNA and miRNA-Seq Profiles. Sci. Rep. 2019;9:6980.
- Zannoni A., Bombardi C., Dondi F., Morini M., Forni M., Chiocchetti R., Spadari A., Romagnoli N.. Proteinase-Activated Receptor 2 Expression in the Intestinal Tract of the Horse. Res. Vet. Sci. 2014;96:464–471.
- Galiazzo G., Tagliavia C., Giancola F., Rinnovati R., Sadeghinezhad J., Bombardi C., Grandis A., Pietra M., Chiocchetti R.. Localisation of Cannabinoid and Cannabinoid-Related Receptors in the Horse Ileum. J. Equine Vet. Sci. 2021;104:103688.
- Kupczyk P., Rykala M., Serek P., Pawlak A., Slowikowski B., Holysz M., Chodaczek G., Madej J.P., Ziolkowski P., Niedzwiedz A.. The Cannabinoid Receptors System in Horses: Tissue Distribution and Cellular Identification in Skin. J. Vet. Intern. Med. 2022;36:1508–1524.
- Zamith Cunha R., Felisardo L.L., Salamanca G., Marchioni G.G., Neto O.I., Chiocchetti R.. The Use of Cannabidiol as a Novel Treatment for Oral Stereotypic Behaviour (Crib-Biting) in a Horse. Vet. Anim. Sci. 2023;19:100289.
- Turner S., Knych H.K., Adams A.A.. The Effects of Cannabidiol on Immune Function and Health Parameters in Senior Horses. Vet. Immunol. Immunopathol. 2023;257:110549.
- Ellis K.L., Contino E.K.. Treatment Using Cannabidiol in a Horse with Mechanical Allodynia. Eq. Vet. Ed. 2021;33:e79–e82.
- Aragona F., Tabbì M., Gugliandolo E., Giannetto C., D’Angelo F., Fazio F., Interlandi C.. Role of Cannabidiolic Acid or the Combination of Cannabigerol/Cannabidiol in Pain Modulation and Welfare Improvement in Horses with Chronic Osteoarthritis. Front. Vet. Sci. 2024;11:1496473.
- Interlandi C., Tabbì M., Di Pietro S., D’Angelo F., Costa G.L., Arfuso F., Giudice E., Licata P., Macrì D., Crupi R.. Improved Quality of Life and Pain Relief in Mature Horses with Osteoarthritis after Oral Transmucosal Cannabidiol Oil Administration as Part of an Analgesic Regimen. Front. Vet. Sci. 2024;11:1341396.
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