Vaporized Delta-9-tetrahydrocannabinol Inhalation in Female Sprague Dawley Rats: A Pharmacokinetic and Behavioral Assessment

Author:

Penman Samantha L.1,Berthold Erin C.2,Mihalkovic Abrianna1,Hammond Nikki1,McCurdy Christopher R.234,Blum Kenneth56,Eiden Rina D.7,Sharma Abhisheak23,Thanos Panayotis K.18

Affiliation:

1. Behavioral Neuropharmacology and Neuroimaging Laboratory on Addictions (BNNLA), Clinical Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA

2. Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, FL, USA

3. Translational Drug Development Core, Clinical and Translational Science Institute, University of Florida, Gainesville, FL, USA

4. Department of Medicinal Chemistry, University of Florida, Gainesville, FL, USA

5. Division of Addiction Research & Education, Center for Mental Health & Sports, Exercise and Global Mental Health, Western University Health Sciences, Pomona, CA 91766, USA

6. Department of Psychiatry, School of Medicine, University of Vermont, Burlington, VT 05405, USA

7. Department of Psychology, Pennsylvania State University, State College, PA, USA

8. Department of Psychology, University at Buffalo, Buffalo, NY, USA

Abstract

Background: Delta-9-tetrahydrocannabinol (THC) is the main psychoactive component of cannabis. Historically, rodent studies examining the effects of THC have used intraperitoneal injection as the route of administration, heavily focusing on male subjects. However, human cannabis use is often through inhalation rather than injection. Objective: We sought to characterize the pharmacokinetic and phenotypic profile of acutely inhaled THC in female rats, compared to intraperitoneal injection, to identify any differences in exposure of THC between routes of administration. Methods: Adult female rats were administered THC via inhalation or intraperitoneal injection. Serum samples from multiple time points were analyzed for THC and metabolites 11-hydroxy-delta-9-tetrahydrocannabinol and 11-nor-9-carboxy-delta-9-tetrahydrocannabinol using ultra-performance liquid chromatography-tandem mass spectrometry. Rats were similarly treated for locomotor activity analysis. Results: Rats treated with 2 mg/kg THC intraperitoneally reached a maximum serum THC concentration of 107.7 ± 21.9 ng/mL. Multiple THC inhalation doses were also examined (0.25 mL of 40 or 160 mg/mL THC), achieving maximum concentrations of 43.3 ± 7.2 and 71.6 ± 22.5 ng/mL THC in serum, respectively. Significantly reduced vertical locomotor activity was observed in the lower inhaled dose of THC and the intraperitoneal injected THC dose compared to vehicle treatment. Conclusion: This study established a simple rodent model of inhaled THC, demonstrating the pharmacokinetic and locomotor profile of acute THC inhalation, compared to an i.p. injected THC dose in female subjects. These results will help support future inhalation THC rat research which is especially important when researching behavior and neurochemical effects of inhaled THC as a model of human cannabis use.

Funder

NIDA, National Institute on Drug Abuse

NIH National Center for Advancing Translational Sciences

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmacology

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