Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, 1800 Denison Ave., Manhattan, KS, 66502, USA.
Department of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, 1800 Denison Ave., Manhattan, KS, 66502, USA.
Sci Rep. 2020 Jul 29;10(1):12753. doi: 10.1038/s41598-020-69768-4.
Cannabinoid production for medicinal purposes has renewed interest in utilizing byproducts of industrial hemp (IH) as a feed source for livestock. However, the presence of bioactive residues in animal tissues may pose a risk to consumers. The purpose of this study was to characterize the plasma pharmacokinetics (PK) of cannabinoids and their metabolites in cattle after a single oral exposure to IH. Eight castrated male Holstein calves received a single oral dose of 35 g of IH to achieve a target dose of 5.4 mg/kg cannabidiolic acid (CBDA). Blood samples were collected for 96 h after dosing. Plasma cannabinoid concentrations were profiled using liquid chromatography coupled with mass-spectroscopy (UPLC) and PK parameters were calculated using noncompartmental methods. The cannabinoids CBDA, tetrahydrocannabinolic acid-A (THCA-A), cannabidivarinic acid (CBDVA), and cannabichromenic acid (CBCA) were detected in all cattle after IH dosing. The geometric mean maximum concentration of CBDA of 72.7 ng/mL was observed at 14 h after administration. The geometric mean half-life of CBDA was 14.1 h. No changes in serum biochemistry analysis were observed following IH dosing compared to baseline values. These results show acidic cannabinoids, especially CBDA, are readily absorbed from the rumen and available for distribution throughout the body.
出于药用目的而生产大麻素,使人们重新产生了利用工业大麻(IH)副产物作为牲畜饲料来源的兴趣。然而,动物组织中生物活性残留物的存在可能对消费者构成风险。本研究的目的是描述牛在单次口服 IH 后大麻素及其代谢物的血浆药代动力学(PK)特征。八头去势雄性荷斯坦小牛口服 35 g IH 以达到 5.4 mg/kg 大麻二羧酸(CBDA)的目标剂量。给药后 96 小时内采集血样。使用液相色谱-质谱联用(UPLC)对血浆大麻素浓度进行分析,并使用非房室方法计算 PK 参数。在 IH 给药后,所有牛均检测到 CBDA、四氢大麻酚酸-A(THCA-A)、大麻二酚酸(CBDVA)和大麻色酸(CBCA)。给药后 14 小时观察到 CBDA 的几何平均最大浓度为 72.7ng/mL。CBDA 的几何平均半衰期为 14.1 小时。与基线值相比,IH 给药后血清生化分析没有变化。这些结果表明,酸性大麻素,尤其是 CBDA,很容易从瘤胃中吸收,并可分布到全身。