Adolescent THC impacts on mPFC dopamine-mediated cognitive processes in male and female rats.

IF 3.5 3区 医学 Q2 NEUROSCIENCES Psychopharmacology Pub Date : 2024-08-27 DOI:10.1007/s00213-024-06676-9
Maricela X Martinez, Vanessa Alizo Vera, Christina M Ruiz, Stan B Floresco, Stephen V Mahler
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Abstract

Rationale: Adolescent cannabis use is linked to later-life changes in cognition, learning, and memory. Rodent experimental studies suggest Δ9-tetrahydrocannabinol (THC) influences development of circuits underlying these processes, especially in the prefrontal cortex, which matures during adolescence.

Objective: We determined how 14 daily THC injections (5 mg/kg) during adolescence persistently impacts medial prefrontal cortex (mPFC) dopamine-dependent cognition.

Methods: In adult Long Evans rats treated as adolescents with THC (AdoTHC), we quantify performance on two mPFC dopamine-dependent reward-based tasks-strategy set shifting and probabilistic discounting. We also determined how acute dopamine augmentation with amphetamine (0, 0.25, 0.5 mg/kg), or specific chemogenetic stimulation of ventral tegmental area (VTA) dopamine neurons and their projections to mPFC impact probabilistic discounting.

Results: AdoTHC sex-dependently impacts acquisition of cue-guided instrumental reward seeking, but has minimal effects on set-shifting or probabilistic discounting in either sex. When we challenged dopamine circuits acutely with amphetamine during probabilistic discounting, we found reduced discounting of improbable reward options, with AdoTHC rats being more sensitive to these effects than controls. In contrast, neither acute chemogenetic stimulation of VTA dopamine neurons nor pathway-specific chemogenetic stimulation of their projection to mPFC impacted probabilistic discounting in control rats, although stimulation of this cortical dopamine projection slightly disrupted choices in AdoTHC rats.

Conclusions: These studies confirm a marked specificity in the cognitive processes impacted by AdoTHC exposure. They also suggest that some persistent AdoTHC effects may alter amphetamine-induced cognitive changes in a manner independent of VTA dopamine neurons or their projections to mPFC.

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青春期 THC 对雄性和雌性大鼠多巴胺介导的 mPFC 认知过程的影响。
理由青少年吸食大麻与日后认知、学习和记忆方面的变化有关。啮齿类动物实验研究表明,Δ9-四氢大麻酚(THC)会影响这些过程的基础回路的发育,尤其是在青春期发育成熟的前额叶皮层:我们确定了在青春期每天注射 14 次 THC(5 毫克/千克)如何持续影响内侧前额叶皮层(mPFC)多巴胺依赖性认知:我们对成年长伊文大鼠在青春期接受 THC(AdoTHC)治疗后的表现进行了量化,这两项任务是基于多巴胺依赖性的奖赏任务--策略集转移和概率贴现。我们还确定了使用苯丙胺(0、0.25、0.5 毫克/千克)进行急性多巴胺增强或对腹侧被盖区(VTA)多巴胺神经元及其向 mPFC 的投射进行特定化学刺激对概率折扣的影响:结果:AdoTHC对线索引导的工具性奖赏寻求的获得具有性别依赖性影响,但对两种性别的集合转移或概率折扣的影响都很小。当我们在概率折现过程中用苯丙胺对多巴胺回路进行急性挑战时,我们发现大鼠对不可能的奖赏选项的折现减少了,与对照组相比,AdoTHC大鼠对这些影响更加敏感。与此相反,对VTA多巴胺神经元的急性化学刺激或对其投射到mPFC的通路特异性化学刺激都不会影响对照组大鼠的概率折现,尽管对这一皮质多巴胺投射的刺激会轻微干扰AdoTHC大鼠的选择:这些研究证实,暴露于 AdoTHC 影响的认知过程具有明显的特异性。结论:这些研究证实了暴露于 AdoTHC 对认知过程的影响具有明显的特异性,同时也表明 AdoTHC 的某些持续作用可能会以独立于 VTA 多巴胺神经元或其向 mPFC 投射的方式改变苯丙胺引起的认知变化。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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