Sosa-Higareda Mariana, Guzman David Sanchez-Migallon, Knych Heather, Lyubimov Alex, Zakharov Alexander, Gomez Beatriz, Beaufrère Hugues
William T. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, CA.
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California-Davis, Davis, CA.
Am J Vet Res. 2023 Feb 21;84(4). doi: 10.2460/ajvr.22.11.0197. Print 2023 Apr 1.
To determine the pharmacokinetics of 8 cannabinoids and 5 metabolites after oral administration of single and multiple doses of a cannabidiol (CBD)-cannabidiolic acid (CBDA)-rich hemp extract to orange-winged Amazon parrots (Amazona amazonica) as well as to evaluate the extract's adverse effects.
12 birds.
Based on pilot studies, a single-dose study based on 30/32.5 mg/kg of cannabidiol/cannabidiolic acid of a hemp extract was administered orally to 8 fasted parrots, and 10 blood samples were collected over 24 hours after administration. After a 4-week washout period, the hemp extract was administered orally to 7 birds at the previous dose every 12 hours for 7 days, and blood samples were collected at the previous time points. Cannabidiol, Δ9-tetrahydrocannabinol, cannabinol, cannabichromene, cannabigerol, cannabidiolic acid, cannabigerolic acid, Δ9-tetrahydrocannabinolic acid, and 5 specific metabolites were measured by liquid chromatography-tandem/mass-spectrometry, and pharmacokinetic parameters were calculated. Adverse effects and changes in the plasma biochemistry and lipid panels were evaluated.
Pharmacokinetic parameters for cannabidiol, cannabidiolic acid, Δ9-tetrahydrocannabinol, Δ9-tetrahydrocannabinolic acid, and the metabolite 11-hydroxy-9-tetrahydrocannabinol were established. For the multiple-dose study, cannabidiol/cannabidiolic acid mean Cmax was 337.4/602.1 ng/mL with a tmax of 30 minutes and a terminal half-life of 8.6/6.29 hours, respectively. No adverse effects were detected during the multidose study. The predominant metabolite was 11-hydroxy-9-tetrahydrocannabinol.
Twice daily oral administration of the hemp extract based on 30 mg/kg/32.5 mg/kg of cannabidiol/cannabidiolic acid was well tolerated and maintained plasma concentrations considered to be therapeutic in dogs with osteoarthritis. Findings suggest different cannabinoid metabolism from mammals.
确定单剂量和多剂量口服富含大麻二酚(CBD)-大麻二酚酸(CBDA)的大麻提取物后,8种大麻素和5种代谢物在橙翅亚马逊鹦鹉(Amazona amazonica)体内的药代动力学,并评估该提取物的不良反应。
12只鸟。
基于前期研究,将30/32.5mg/kg大麻提取物的大麻二酚/大麻二酚酸单剂量口服给予8只禁食的鹦鹉,并在给药后24小时内采集10份血样。在4周的洗脱期后,将大麻提取物以先前剂量每12小时口服给予7只鸟,持续7天,并在先前的时间点采集血样。通过液相色谱-串联/质谱法测量大麻二酚、Δ9-四氢大麻酚、大麻酚、大麻色烯、大麻萜酚、大麻二酚酸、大麻萜酚酸、Δ9-四氢大麻酚酸和5种特定代谢物,并计算药代动力学参数。评估不良反应以及血浆生化指标和血脂指标的变化。
确定了大麻二酚、大麻二酚酸、Δ9-四氢大麻酚、Δ9-四氢大麻酚酸和代谢物11-羟基-9-四氢大麻酚的药代动力学参数。对于多剂量研究,大麻二酚/大麻二酚酸的平均Cmax为337.4/602.1ng/mL,tmax为30分钟,终末半衰期分别为8.6/6.29小时。在多剂量研究期间未检测到不良反应。主要代谢物为11-羟基-9-四氢大麻酚。
基于30mg/kg/32.5mg/kg大麻二酚/大麻二酚酸的大麻提取物每日口服两次,耐受性良好,并维持了被认为对骨关节炎犬具有治疗作用的血浆浓度。研究结果表明其大麻素代谢与哺乳动物不同。