Wang Tongxin Charlotte, Wakshlag Joseph J, Lyubimov Alex, Zakharov Alexander, Gomez Beatriz, Schwark Wayne, Trottier Nathalie L
Department of Animal Science, Cornell University, Ithaca, NY, United States.
Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, United States.
Front Vet Sci. 2025 Aug 12;12:1639846. doi: 10.3389/fvets.2025.1639846. eCollection 2025.
The rapidly expanding market for therapeutic cannabinoid products has intensified research on their safety and efficacy in pets. Full-spectrum hemp extracts contain compounds such as terpenoids and flavonoids that may act synergistically via the "entourage effect," yet their application in companion animals remains underexplored. This study assessed the pharmacokinetics and safety of isolated and full-spectrum cannabinoids in dogs.
Eight healthy adult Beagle dogs (four males and four females) were randomly assigned to a 4 × 4 Latin square design (two dogs per kennel, same sex), consisting of four experimental periods and four treatments: CBD isolate (1 mg/kg), CBDA isolate (1 mg/kg), CBDA full spectrum (FS) (1 mg/kg), and a combined CBD/CBDA FS (1 mg/kg). Treatments were administered twice daily (every 12 h). In the morning, dogs received their assigned treatment following their daily ration of dry kibble and were immediately offered 122 grams of wet food. Each experimental period lasted 1 week and was followed by a three-week washout period.
No adverse events were associated with any treatment. CBDA showed higher Cmax and AUC than CBD in both isolate and FS forms ( < 0.001). CBDA in CBD/CBDA FS had a shorter Tmax compared to CBD ( = 0.019). Mean residence time and elimination half-life did not differ among treatments.
CBDA demonstrated superior absorption compared to CBD. No evidence supported enhanced absorption from full-spectrum products, suggesting the "entourage effect" may involve receptor-level interactions rather than absorption. All treatments were well tolerated, with normal CBC and chemistry results, indicating that administering CBD or CBDA, either as isolates or in full-spectrum extracts, at 1 mg/kg every 12 h for 1 week is safe in healthy adult dogs. This is the first comprehensive comparison of full-spectrum, isolate, and acidic cannabinoid forms in dogs.
治疗性大麻素产品市场的迅速扩张,强化了对其在宠物身上安全性和有效性的研究。全谱大麻提取物含有萜类化合物和黄酮类化合物等成分,这些成分可能通过“整体效应”产生协同作用,但其在伴侣动物中的应用仍未得到充分探索。本研究评估了分离型和全谱大麻素在犬类中的药代动力学和安全性。
八只健康成年比格犬(四只雄性和四只雌性)被随机分配到4×4拉丁方设计(每个犬舍两只狗,性别相同),包括四个实验期和四种处理:CBD分离物(1毫克/千克)、CBDA分离物(1毫克/千克)、CBDA全谱(FS)(1毫克/千克)以及CBD/CBDA全谱组合(1毫克/千克)。处理每天给药两次(每12小时一次)。早晨,犬在食用每日定量干粮后接受指定处理,并立即提供122克湿粮。每个实验期持续1周,随后是为期三周的洗脱期。
所有处理均未出现不良事件。CBDA在分离型和全谱形式中均显示出比CBD更高的Cmax和AUC(<0.001)。CBD/CBDA全谱中的CBDA与CBD相比,Tmax更短(=0.019)。各处理之间的平均驻留时间和消除半衰期没有差异。
与CBD相比,CBDA表现出更好的吸收。没有证据支持全谱产品具有增强吸收的作用,这表明“整体效应”可能涉及受体水平的相互作用而非吸收。所有处理耐受性良好,血常规和生化结果正常,表明以1毫克/千克的剂量每12小时给健康成年犬施用CBD或CBDA,持续1周是安全的。这是首次对犬类中全谱、分离型和酸性大麻素形式进行的全面比较。