Cannabidiol (CBD) potentiates physiological and behavioral markers of hypothalamic-pituitary-adrenal (HPA) axis responsivity in female and male mice.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Bryan W Jenkins, Hayley A Spina, Kate Nicholson, Amy E M Newman, Jibran Y Khokhar
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引用次数: 0

Abstract

Rationale: Clinical literature indicates there may be a therapeutic use of cannabidiol (CBD) for stress-related disorders. Preclinical literature remains conflicted regarding the underlying neurobehavioral mechanisms, reporting mixed effects of CBD (increased, decreased, or no effect) on anxiety- and fear-related behaviors. Preclinical data demonstrated that CBD modulates hypothalamus-pituitary-adrenal (HPA) axis gene expression; it is unknown whether CBD changes HPA axis responsivity and how this relates to altered behavior.

Objectives: We aimed to evaluate whether acute or chronic CBD administration would alter physiological and behavioral measures of HPA axis responsivity in male or female mice.

Methods: C57BL/6 mice of both sexes were injected with vehicle or CBD (30 mg/kg, i.p.) daily for 26 days. Plasma corticosterone (CORT) levels were evaluated following dexamethasone suppression and adrenocorticotropin hormone stimulation tests after acute and chronic CBD exposure. After chronic CBD, mice were tested for anxiety-like behavior using an elevated plus maze (EPM) and associative fear learning and memory using a trace fear conditioning (FC) protocol.

Results: Compared to vehicle, CBD induced a state of HPA axis hyperactivation, an effect which was significant in males; it also normalized anxiety-like behavior in female mice classified as having HPA axis hypofunction and primed all female mice for enhanced conditioned responding. Significant sex differences were also detected: females had greater plasma CORT levels and HPA axis responsivity than males, exhibited less EPM anxiety-like behavior, and were more responsive during FC.

Conclusions: CBD potentiated physiological and behavioral markers of HPA axis function and normalized anxiety-like behavior in a sex-specific manner. This observation has implications for cannabinoid-based drug development targeting individuals with stress-related disorders involving HPA axis hypofunction pathology.

大麻二酚(CBD)增强了雌性和雄性小鼠下丘脑-垂体-肾上腺(HPA)轴反应性的生理和行为标记。
理由:临床文献表明,大麻二酚(CBD)可能用于治疗压力相关疾病。关于潜在的神经行为机制,临床前文献仍然存在冲突,报告了CBD对焦虑和恐惧相关行为的混合影响(增加,减少或没有影响)。临床前数据表明,CBD调节下丘脑-垂体-肾上腺(HPA)轴基因表达;目前尚不清楚CBD是否会改变HPA轴的反应性,以及这与改变的行为有何关系。目的:我们旨在评估急性或慢性CBD政府将是否会改变雄性或雌性小鼠HPA轴反应性的生理和行为指标。方法:对C57BL/6小鼠,雌雄同体,每日注射给药剂或CBD (30 mg/kg, i.p),连续26 d。急性和慢性CBD暴露后,在地塞米松抑制和促肾上腺皮质激素刺激试验后评估血浆皮质酮(CORT)水平。在长期使用CBD后,小鼠使用升高+迷宫(EPM)测试焦虑样行为,使用痕量恐惧条件反射(FC)协议测试联想恐惧学习和记忆。结果:与对照剂相比,CBD可诱导大鼠HPA轴过度激活,且在雄性小鼠中效果显著;它还使被归类为下丘脑轴功能障碍的雌性小鼠的焦虑样行为正常化,并为所有雌性小鼠的增强条件反应做好准备。显著的性别差异也被发现:女性的血浆CORT水平和HPA轴反应性高于男性,表现出更少的EPM焦虑样行为,并且在FC期间反应更灵敏。结论:CBD增强了HPA轴功能的生理和行为标记,并以性别特异性的方式正常化了焦虑样行为。这一观察结果对以大麻素为基础的药物开发具有压力相关疾病涉及HPA轴功能障碍病理的个体具有启示意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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