Wang Tongxin Charlotte, Wakshlag Joseph J, Jager Mason C, Schwark Wayne S, Trottier Nathalie L, Chevalier Jacqueline M, Pearson Garett, Cercone Marta
Department of Animal Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, NY.
Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY.
Am J Vet Res. 2025 Jan 9;86(3). doi: 10.2460/ajvr.24.08.0235. Print 2025 Mar 1.
To compare the pharmacokinetics of cannabidiol (CBD) and cannabidiolic acid (CBDA) in horses and to evaluate the safety of their chronic administration.
CBD- and CBDA-rich oil (1 mg/kg) were administered orally twice daily to 7 adult horses over 6 weeks in a randomized, crossover design with a 2-week washout period. A 12-hour pharmacokinetic analysis was conducted on day 1 of each 6-week trial, followed by the measurement of peak and trough concentrations at weeks 1, 2, 4, and 6. The cannabinoids safety was assessed via daily physical examination, periodic bloodwork, and liver biopsy at the beginning and end of the study.
12-hour pharmacokinetics revealed a higher maximum serum concentration (103 vs 12 ng/mL) and greater area under the curve (259 vs 62 ng·h/mL) for CBDA when compared to CBD. Cannabidiolic acid nadir and peak serum levels over time ranged from 46 to 122 ng/mL, which was higher than CBD (12 to 38 ng/mL). Complete blood count and serum chemistry revealed no clinically relevant changes with either CBD or CBDA. No significant abnormalities were detected on liver ultrasonographic and histopathologic evaluation on day 0 and after both phases of the study.
A dose of either 1 mg/kg of CBD or CBDA administered long term appears safe; however, CBDA serum concentrations suggest superior absorption/retention.
Chronic cannabinoid supplementation in horses is safe. Considering the higher absorption of CBDA, its use is recommended to evaluate the therapeutic efficacy of this common hemp derived cannabinoid.
比较大麻二酚(CBD)和大麻二酚酸(CBDA)在马匹体内的药代动力学,并评估长期给药的安全性。
采用随机交叉设计,在6周内每天给7匹成年马口服富含CBD和CBDA的油(1mg/kg),每日两次,洗脱期为2周。在每个6周试验的第1天进行12小时药代动力学分析,随后在第1、2、4和6周测量峰浓度和谷浓度。通过每日体格检查、定期血液检查以及在研究开始和结束时进行肝活检来评估大麻素的安全性。
12小时药代动力学显示,与CBD相比,CBDA的最高血清浓度更高(103对12ng/mL),曲线下面积更大(259对62ng·h/mL)。随着时间的推移,CBDA的最低血清水平和峰值血清水平在46至122ng/mL之间,高于CBD(12至38ng/mL)。全血细胞计数和血清化学检查显示,CBD或CBDA均未引起临床相关变化。在研究第0天以及两个阶段结束后,肝脏超声检查和组织病理学评估均未发现明显异常。
长期给予1mg/kg的CBD或CBDA似乎是安全的;然而,CBDA的血清浓度表明其吸收/保留效果更佳。
长期补充大麻素对马匹是安全的。考虑到CBDA的吸收更高,建议使用CBDA来评估这种常见的源自大麻的大麻素的治疗效果。