Department of Neurobiology & Behavior, University of California Irvine, 2205 McGaugh Hall, Irvine, CA, 92697, USA.
Department of Anatomy & Neurobiology, University of California Irvine, 1244 Gillespie Hall, Irvine, CA, 92697, USA.
Psychopharmacology (Berl). 2021 Dec;238(12):3595-3605. doi: 10.1007/s00213-021-05976-8. Epub 2021 Sep 8.
Adolescent exposure to ∆-tetrahydrocannabinol (THC), the psychotropic constituent of cannabis, might affect brain development, and in rodent models leads to long-term behavioral and physiological alterations. Yet, the basic pharmacology of this drug in adolescent rodents, especially when ingested via ecologically relevant routes like aerosol inhalation, commonly referred to as "vaping," is still poorly characterized. Moreover, sex differences exist in THC metabolism, kinetics, and behavioral effects, but these have not been rigorously examined after vapor dosing in adolescents.
We investigated the pharmacokinetics and pharmacodynamics of aerosolized THC (30 min inhalation exposure, 25 or 100 mg/ml) in adolescent Wistar rats of both sexes.
Liquid chromatography/mass spectrometry analysis of THC and its major metabolites was conducted on blood plasma and brain tissue at 5, 30, 60, and 120 min following a 30-min aerosol dosing session. Effects on activity in a novel environment for 120 min after aerosol, and temperature, were measured in separate rats.
We found sex-dependent differences in the pharmacokinetics of THC and its active (11-OH-THC) and inactive (11-COOH-THC) metabolites in the blood and brain, along with dose- and sex-dependent effects on anxiety-like and exploratory behaviors; namely, greater 11-OH-THC levels accompanied by greater behavioral effects in females at the low dose but similar hypothermic effects in both sexes at the high dose.
These results provide a benchmark for dosing adolescent rats with aerosolized (or "vaped") THC, which could facilitate adoption by other labs of this potentially human-relevant THC exposure model to understand cannabis effects on the developing brain.
青少年接触大麻中具有致幻作用的成分 ∆-四氢大麻酚(THC)可能会影响大脑发育,在啮齿动物模型中会导致长期的行为和生理改变。然而,这种药物在青少年啮齿动物中的基本药理学特性,尤其是通过气溶胶吸入等生态相关途径(通常称为“蒸气吸入”)摄入时,仍未得到充分描述。此外,THC 在代谢、动力学和行为效应方面存在性别差异,但这些差异在青少年蒸气给药后并未得到严格检查。
我们研究了青少年 Wistar 大鼠经气溶胶(30 分钟吸入暴露,25 或 100mg/ml)给药后 THC 的药代动力学和药效学。
在气溶胶给药 30 分钟后,通过液相色谱/质谱分析对血液和脑组织中的 THC 及其主要代谢物进行分析。在另一些大鼠中,测量了气溶胶给药后 120 分钟新环境中的活动和体温。
我们发现,在血液和大脑中,THC 及其活性(11-OH-THC)和非活性(11-COOH-THC)代谢物的药代动力学存在性别依赖性差异,并且在焦虑样和探索性行为方面存在剂量和性别依赖性效应;即,在低剂量时,雌性大鼠的 11-OH-THC 水平更高,行为效应更大,但在高剂量时,两性的体温下降效应相似。
这些结果为青少年大鼠经气溶胶(或“蒸气吸入”)给予 THC 提供了一个基准,这可能会促进其他实验室采用这种潜在的人类相关 THC 暴露模型来了解大麻对发育中大脑的影响。