Department of Neurobiology and Behavior, University of California, Irvine, CA, 92697, USA.
Department of Anatomy and Neurobiology, University of California, Irvine, CA, 92697, USA.
Neuropsychopharmacology. 2021 Apr;46(5):959-969. doi: 10.1038/s41386-020-00839-w. Epub 2020 Sep 14.
Δ-tetrahydrocannabinol (THC) is the intoxicating constituent of cannabis and is responsible for the drug's reinforcing effects. Retrospective human studies suggest that cannabis use during adolescence is linked to long-term negative psychological outcomes, but in such studies it is difficult to distinguish the effects of THC from those of coexisting factors. Therefore, translationally relevant animal models are required to properly investigate THC effects in adolescents. However, though the relevance of these studies depends upon human-relevant dosing, surprisingly little is known about THC pharmacology and its effects on behavior and brain activity in adolescent rodents-especially in females. Here, we conducted a systematic investigation of THC pharmacokinetics, metabolism and distribution in blood and brain, and of THC effects upon behavior and neural activity in adolescent Long Evans rats of both sexes. We administered THC during an early-middle adolescent window (postnatal days 27-45) in which the brain may be particularly sensitive to developmental perturbation by THC. We determined the pharmacokinetic profile of THC and its main first-pass metabolites (11-hydroxy-THC and 11-nor-9-carboxy-THC) in blood and brain following acute injection (0.5 or 5 mg/kg, intraperitoneal). We also evaluated THC effects on behavioral assays of anxiety, locomotion, and place conditioning, as well as c-Fos expression in 14 brain regions. Confirming previous work, we find marked sex differences in THC metabolism, including a female-specific elevation in the bioactive metabolite 11-hydroxy-THC. Furthermore, we find dose-dependent and sex-dependent effects on behavior, neural activity, and functional connectivity across multiple nodes of brain stress and reward networks. Our findings are relevant for interpreting results of rat adolescent THC exposure studies, and may lend new insights into how THC impacts the brain in a sex-dependent manner.
Δ-四氢大麻酚(THC)是大麻中的致醉成分,负责大麻的强化作用。回顾性人类研究表明,青少年时期使用大麻与长期的负面心理后果有关,但在这些研究中,很难区分 THC 的作用与共存因素的作用。因此,需要转化相关的动物模型来正确研究青少年时期的 THC 作用。然而,尽管这些研究的相关性取决于与人类相关的剂量,但令人惊讶的是,人们对 THC 的药理学及其对青少年啮齿动物行为和大脑活动的影响知之甚少——尤其是在雌性动物中。在这里,我们对 THC 在血液和大脑中的药代动力学、代谢和分布,以及 THC 对青春期长爪沙鼠(无论雌雄)行为和神经活动的影响进行了系统研究。我们在大脑可能特别容易受到 THC 发育干扰的早期到中期青少年期(出生后第 27-45 天)期间给予 THC。我们在急性注射(0.5 或 5mg/kg,腹腔内)后确定了 THC 及其主要的首次通过代谢物(11-羟基-THC 和 11-去甲-9-羧酸-THC)在血液和大脑中的药代动力学特征。我们还评估了 THC 对焦虑、运动和位置条件作用行为测试以及 14 个脑区中 c-Fos 表达的影响。证实了以前的工作,我们发现 THC 代谢存在明显的性别差异,包括生物活性代谢物 11-羟基-THC 的女性特异性升高。此外,我们发现行为、神经活动和多个脑应激和奖励网络节点的功能连接存在剂量依赖性和性别依赖性影响。我们的发现对于解释大鼠青春期 THC 暴露研究的结果具有重要意义,并可能为 THC 以性别依赖方式影响大脑的方式提供新的见解。