Evaluation of behavioural and neurochemical effects of psilocybin in mice subjected to chronic unpredictable mild stress.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Ines Erkizia-Santamaría, Igor Horrillo, Nerea Martínez-Álvarez, Daniel Pérez-Martínez, Guadalupe Rivero, Amaia M Erdozain, J Javier Meana, Jorge E Ortega
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引用次数: 0

Abstract

Depression and anxiety are disabling and high incidence mental disorders characterized by phenotypic heterogeneity. Currently available treatments show severe limitations. Thus, there is an urgent need for effective treatments in this population. In the search for novel rapid-acting antidepressants, the psychedelic psilocybin has emerged as a promising therapy in several clinical trials. However, its antidepressant mechanism of action is still not well understood. The aim of the present study was to evaluate the therapeutic potential of psilocybin in ameliorating the adverse behavioural and neurochemical consequences of chronic stress. To this end, a chronic unpredictable mild stress (CUMS) animal model was used, and psilocybin treatment was administered (two doses of 1 mg/kg, i.p., administered 7 days apart). Psilocybin reversed impairments in anhedonia and behavioural despair dimensions of depressive phenotype but not in apathy-related behaviour. Psilocybin administration was also able to exert an anxiolytic-like effect on treated animals. Physiological alterations caused by stress, indicative of a hyperactive hypothalamic-pituitary-adrenal axis (HPA), were not reversed by psilocybin. When neuroplasticity-related proteins were assessed in cerebral cortex, brain-derived neurotrophic factor (BDNF) was found to be decreased in stressed animals, and treatment did not reverse such impairment. Psilocybin administration increased the expression and function of serotonin-2A-receptor (5HT2AR) in brain cortex of control and CUMS groups. Furthermore, psilocybin treatment caused a selective increase in the expression of glucocorticoid-receptor (GR) in brain cortex of CUMS mice. In conclusion, psilocybin was able to rescue impairments in the depressive phenotype, and to induce anxiolytic-like effects. Furthermore, an enhancement in sensitivity to psilocybin-induced HTR was observed following a booster dose. Altogether, this work provides new knowledge on the putative benefit/risk actions of psilocybin and contributes to the understanding of the therapeutic mechanism of action of psychedelics.

评估裸盖菇素对慢性不可预测轻度应激小鼠的行为和神经化学作用。
抑郁和焦虑是致残和高发的精神障碍,具有表型异质性。目前可用的治疗方法显示出严重的局限性。因此,迫切需要对这一人群进行有效的治疗。在寻找新型速效抗抑郁药的过程中,迷幻药裸盖菇素在几项临床试验中成为一种很有前景的治疗方法。然而,其抗抑郁作用机制尚不清楚。本研究的目的是评估裸盖菇素在改善慢性应激的不良行为和神经化学后果方面的治疗潜力。为此,采用慢性不可预测轻度应激(CUMS)动物模型,给予裸盖菇素治疗(2次剂量,1 mg/kg, ig,间隔7天给药)。裸盖菇素逆转了抑郁表型的快感缺乏和行为绝望维度的损伤,但对冷漠相关行为没有影响。裸盖菇素也能对治疗过的动物产生类似抗焦虑的作用。应激引起的生理改变,表明下丘脑-垂体-肾上腺轴(HPA)过度活跃,裸盖菇素不能逆转。当评估大脑皮层中的神经可塑性相关蛋白时,发现应激动物的脑源性神经营养因子(BDNF)减少,治疗并不能逆转这种损伤。裸盖菇素增加了对照组和CUMS组大脑皮层5 -羟色胺- 2a受体(5HT2AR)的表达和功能。此外,裸盖菇素处理导致CUMS小鼠脑皮质糖皮质激素受体(GR)的表达选择性增加。综上所述,裸盖菇素能够挽救抑郁表型的损伤,并诱导抗焦虑样作用。此外,在加强剂量后观察到对裸盖菇素诱导的HTR的敏感性增强。综上所述,本研究为裸盖菇素的获益/风险作用提供了新的认识,并有助于理解致幻剂作用的治疗机制。
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
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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