Pharmacokinetics of Sativex® in Dogs: Towards a Potential Cannabinoid-Based Therapy for Canine Disorders

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dc.contributor.authorFernández Trapero, María
dc.contributor.authorPérez Díaz, Carmen
dc.contributor.authorEspejo Porras, Francisco
dc.contributor.authorLago Femia, Eva de
dc.contributor.authorFernández Ruiz, Javier
dc.date.accessioned2023-06-17T09:00:55Z
dc.date.available2023-06-17T09:00:55Z
dc.date.issued2020-02-11
dc.description.abstractThe phytocannabinoid-based medicine Sativex® is currently marketed for the treatment of spasticity and pain in multiple sclerosis patients and is being investigated for other central and peripheral pathological conditions. It may also serve in Veterinary Medicine for the treatment of domestic animals, in particular for dogs affected by different pathologies, including human-like pathological conditions. With the purpose of assessing different dosing paradigms for using Sativex in Veterinary Medicine, we investigated its pharmacokinetics when administered to naïve dogs via sublingual delivery. In the single dose arm of the study, adult Beagle dogs were treated with 3 consecutive sprays of Sativex, and blood samples were collected at 12 intervals up to 24 h later. In the multiple dose arm of the study, Beagle dogs received 3 sprays daily for 14 days, and blood samples were collected for 24 h post final dose. Blood was used to obtain plasma samples and to determine the levels of cannabidiol (CBD), ∆9-tetrahydrocannabinol (∆9-THC) and its metabolite 11-hydroxy-∆9-THC. Maximal plasma concentrations of both ∆9-THC (Cmax = 18.5 ng/mL) and CBD (Cmax = 10.5 ng/mL) were achieved 2 h after administration in the single dose condition and at 1 h in the multiple dose treatment (∆9-THC: Cmax = 24.5 ng/mL; CBD: Cmax = 15.2 ng/mL). 11-hydroxy-∆9-THC, which is mainly formed in the liver from ∆9-THC, was almost undetected, which is consistent with the use of sublingual delivery. A potential progressive accumulation of both CBD and ∆9-THC was detected following repeated exposure, with maximum plasma concentrations for both cannabinoids being achieved following multiple dose. Neurological status, body temperature, respiratory rate and some hemodynamic parameters were also recorded in both conditions, but in general, no changes were observed. In conclusion, this study demonstrates that single or multiple dose sublingual administration of Sativex to naïve dogs results in the expected pharmacokinetic profile, with maximal levels of phytocannabinoids detected at 1–2 h and suggested progressive accumulation after the multiple dose treatment.
dc.description.departmentSección Deptal. de Bioquímica y Biología Molecular (Medicina)
dc.description.departmentDepto. de Medicina y Cirugía Animal
dc.description.facultyFac. de Medicina
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.sponsorshipComunidad de Madrid
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/64483
dc.identifier.doi10.3390/biom10020279
dc.identifier.issn2218-273X
dc.identifier.officialurlhttps://doi.org/10.3390/biom10020279
dc.identifier.relatedurlhttps://www.mdpi.com/2218-273X/10/2/279
dc.identifier.urihttps://hdl.handle.net/20.500.14352/7928
dc.issue.number2
dc.journal.titleBiomolecules
dc.language.isoeng
dc.page.initial279
dc.publisherMDPI
dc.relation.projectID(SAF2012-39173, SAF2015-68580-C2-1-R and RTI2018-098885-B-100)
dc.relation.projectIDCANNAB-CM (S2010/BMD-2308)
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordpharmacokinetics
dc.subject.keywordsublingual delivery
dc.subject.keywordSativex®
dc.subject.keywordcannabidiol
dc.subject.keyword∆9-tetrahydrocannabinol
dc.subject.keywordnaïve dogs
dc.subject.ucmAnimales de compañía
dc.subject.ucmPatología veterinaria
dc.subject.unesco3109.07 Patología
dc.titlePharmacokinetics of Sativex® in Dogs: Towards a Potential Cannabinoid-Based Therapy for Canine Disorders
dc.typejournal article
dc.volume.number10
dspace.entity.typePublication
relation.isAuthorOfPublication70d75adf-0216-4101-8ca9-f042ff991f44
relation.isAuthorOfPublication33cdaaf5-0e2e-42f9-afda-d1a34e5273ee
relation.isAuthorOfPublication.latestForDiscovery70d75adf-0216-4101-8ca9-f042ff991f44
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