Unraveling psilocybin's therapeutic potential: behavioral and neuroplasticity insights in Wistar-Kyoto and Wistar male rat models of treatment-resistant depression.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2025-07-01 Epub Date: 2024-07-04 DOI:10.1007/s00213-024-06644-3
Magdalena Kolasa, Agnieszka Nikiforuk, Agata Korlatowicz, Joanna Solich, Agnieszka Potasiewicz, Marta Dziedzicka-Wasylewska, Ryszard Bugno, Adam Hogendorf, Andrzej Bojarski, Agata Faron-Górecka
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引用次数: 0

Abstract

Rationale: Our study aimed to unravel the unknown mechanisms behind the exceptional efficacy of Psilocybin (PSI) in treating treatment-resistant depression (TRD). Focusing on Wistar-Kyoto (WKY) rats with a TRD phenotype and Wistar (WIS) rats as a normative comparison, we investigated behavioral and neuroplasticity-related responses to PSI, striving to shed light on the distinctive features of its antidepressant effects.

Objectives: We set out to assess the behavioral impact of acute and prolonged PSI administration on WKY and WIS rats, employing Novel Object Recognition (NORT), Social Interaction (SI), and Forced Swimming Test (FST). Our secondary objectives involved exploring strain-specific alterations in neuroplasticity-related parameters, including brain-derived neurotrophic factor (BDNF) and activity-regulated cytoskeleton-associated protein (Arc).

Methods: Conducting post-acute and extended assessments after a single PSI administration, we applied behavioral tests and biochemical analyses to measure serum BDNF levels and neuroplasticity-related parameters in the prefrontal cortex. Statistical analyses were deployed to discern significant differences between the rat strains and assess the impact of PSI on behavioral and biochemical outcomes.

Results: Our findings uncovered significant behavioral disparities between WKY and WIS rats, indicating passive behavior and social withdrawal in the former. PSI demonstrated pronounced pro-social and antidepressant effects in both strains, each with its distinctive temporal trajectory. Notably, we identified strain-specific variations in BDNF-related signaling and observed the modulation of Arc expression in WKY rats.

Conclusions: Our study delineated mood-related behavioral nuances between WKY and WIS rat strains, underscoring the antidepressant and pro-social properties of PSI in both groups. The distinct temporal patterns of observed changes and the identified strain-specific neuroplasticity alterations provide valuable insights into the TRD phenotype and the mechanisms underpinning the efficacy of PSI.

Abstract Image

揭示迷幻药的治疗潜力:Wistar-Kyoto 和 Wistar 雄性大鼠耐药性抑郁症模型的行为和神经可塑性研究。
理论依据:我们的研究旨在揭示迷幻药(Psilocybin,PSI)在治疗难治性抑郁症(TRD)方面的特殊疗效背后的未知机制。我们以具有 TRD 表型的 Wistar-Kyoto (WKY) 大鼠和作为标准对比的 Wistar (WIS) 大鼠为研究对象,调查了它们对 PSI 的行为和神经可塑性相关反应,试图揭示 PSI 抗抑郁作用的独特之处:我们采用新颖物体识别(NORT)、社会交往(SI)和强迫游泳测试(FST)评估了急性和长期 PSI 给药对 WKY 和 WIS 大鼠行为的影响。我们的次要目标是探索神经可塑性相关参数(包括脑源性神经营养因子(BDNF)和活动调节细胞骨架相关蛋白(Arc))的品系特异性改变:在单次 PSI 给药后进行急性期后评估和扩展评估,我们采用行为测试和生化分析来测量血清 BDNF 水平和前额叶皮层的神经可塑性相关参数。通过统计分析,我们发现了大鼠品系间的显著差异,并评估了 PSI 对行为和生化结果的影响:结果:我们的研究结果发现,WKY 和 WIS 大鼠之间存在明显的行为差异,前者表现出被动行为和社会退缩。PSI 对这两个品系的大鼠都有明显的促进社交和抗抑郁作用,而且每种作用都有其独特的时间轨迹。值得注意的是,我们发现了 BDNF 相关信号传导的品系特异性变化,并观察到 Arc 表达在 WKY 大鼠中的调节作用:我们的研究描述了 WKY 和 WIS 大鼠品系之间与情绪相关的行为细微差别,强调了 PSI 在这两个群体中的抗抑郁和促进社会属性。观察到的变化的不同时间模式和已确定的品系特异性神经可塑性改变为了解 TRD 表型和 PSI 的疗效机制提供了宝贵的见解。
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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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