Division of Behavioral Biology, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Johns Hopkins Bayview Research Campus, Behavioral Biology Research Center, 5510 Nathan Shock Drive, Suite 3000, Baltimore, MD, 21224, USA.
Psychopharmacology (Berl). 2022 May;239(5):1397-1408. doi: 10.1007/s00213-021-05995-5. Epub 2021 Oct 15.
The legalization of medicinal use of Cannabis sativa in most US states and the removal of hemp from the Drug Enforcement Agency (DEA) controlled substances act has resulted in a proliferation of products containing Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD) for oral consumption (e.g., edibles, oils, and tinctures) that are being used for recreational and medicinal purposes.
This study examined the effects of cannabinoids THC and CBD when administered orally on measures of pain sensitivity, body temperature, locomotor activity, and catalepsy (i.e., cannabinoid tetrad) in male and female Sprague Dawley rats.
Rats (N = 24, 6 per sex/drug group) were administered THC (1-20 mg/kg), CBD (3-30 mg/kg), or sesame oil via oral gavage. Thermal and mechanical pain sensitivity (tail flick assay, von Frey test), rectal measurements for body temperature, locomotor activity, and the bar-test of catalepsy were completed. A separate group of rats (N = 8/4 per sex) was administered morphine (5-20 mg/kg; intraperitoneal, IP) and evaluated for pain sensitivity as a positive control.
We observed classic tetrad effects of antinociception, hypothermia, hyper- and hypolocomotion, and catalepsy after oral administration of THC that were long lasting (> 7 h). CBD modestly increased mechanical pain sensitivity and produced sex-dependent effects on body temperature and locomotor activity.
Oral THC and CBD produced long lasting effects that differed in magnitude and time course when compared with other routes of administration. Examination of cannabinoid effects administered via different routes of administration, species, and in both males and females is critical to enhance translation.
在美国大多数州,医用大麻合法化以及将大麻从毒品管制局(DEA)管制物质法案中移除,导致含有 Δ9-四氢大麻酚(THC)和大麻二酚(CBD)的口服产品(例如,可食用食品、油和酊剂)大量出现,这些产品被用于娱乐和医疗目的。
本研究检测了口服给予大麻素 THC 和 CBD 对雄性和雌性 Sprague Dawley 大鼠的疼痛敏感性、体温、运动活动和僵住(即大麻素四联症)的影响。
大鼠(N = 24,每组 6 只,雄性和雌性/药物组)给予 THC(1-20mg/kg)、CBD(3-30mg/kg)或芝麻油经口服灌胃。完成了热和机械疼痛敏感性(尾巴拍打试验,von Frey 试验)、直肠体温测量、运动活动以及棒试验的僵住评估。一组单独的大鼠(每组 8/4 只,雄性和雌性)给予吗啡(5-20mg/kg;腹腔内,IP),并作为阳性对照评估疼痛敏感性。
我们观察到口服给予 THC 后出现了镇痛、体温降低、运动过度和运动不足以及僵住的经典四联症效应,这些效应持续时间较长(> 7 小时)。CBD 适度增加了机械疼痛敏感性,并对体温和运动活动产生了性别依赖性影响。
口服给予 THC 和 CBD 产生了持久的效应,与其他给药途径相比,其程度和时程不同。检查通过不同给药途径、物种以及雄性和雌性给予的大麻素效应对于提高转化至关重要。