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28 天每日暴露于致幻剂“死藤水”后的毒性,以及对 Wistar 大鼠大脑中单胺类神经递质和脑源性神经营养因子(BDNF)的影响。

Toxicity of ayahuasca after 28 days daily exposure and effects on monoamines and brain-derived neurotrophic factor (BDNF) in brain of Wistar rats.

机构信息

Laboratory of Toxicology, Department of Pharmacy, Faculty of Health Sciences, University of Brasilia, Brasilia, DF, Brazil.

Laboratory of Embryology and Developmental Biology, Department of Genetic and Morphology, Institute of Biology, University of Brasilia, Brasilia, DF, Brazil.

出版信息

Metab Brain Dis. 2020 Jun;35(5):739-751. doi: 10.1007/s11011-020-00547-w. Epub 2020 Feb 27.

Abstract

Ayahuasca is a hallucinogenic beverage that affects the serotonergic system and have therapeutic potential for many diseases and disorders, including depression and drug addiction. The objectives of this study were to evaluate the potential toxic effects of ayahuasca on rats after chronic exposure, and the levels of monoamines, their metabolites and the brain-derived neurotrophic factor (BDNF) in the brain. Female and male rats were treated orally for 28 days with HO (control), fluoxetine (FLX), a selective serotonin reuptake inhibitor antidepressant, or ayahuasca (Aya) at doses of 0.5X, 1X and 2X the ritualistic dose (7 to 10 animals/group). Clinical, hematological and macroscopic results showed that ayahuasca was safe to the rats. Behavior tests conducted one hour after the last treatment showed that male rats from the Aya1 group explored the open field central area less than the control group, and the number of entries in the central area compared to total locomotion was also significantly lower in this group and in the FLX group. The hippocampus was removed for BDNF analysis and the remaining brain was used for monoamine analysis by HPLC-FL. Serotonin levels were significantly higher than control only in the Aya2 female group, while a significant reduction of its metabolite 5-HIAA was observed in the FLX group. Dopamine levels were similar among the experimental groups, but the levels of its metabolite DOPAC increased significantly in the Aya1 and Aya2 groups compared to controls, especially in females, and the DOPAC/dopamine turnover was significantly higher in Aya2 group. The levels of HVA, another dopamine metabolite, did not change with the treatments compared to controls, but HVA/DOPAC ratio was significantly lower in all ayahuasca male groups. Norepinephrine was not detected in any brain sample, and the levels of its metabolite MHPG did not change significantly among the groups. BDNF levels in the hippocampus were significantly higher in the FLX and Aya2 female groups compared to controls when expressed in relation to the total brain weight. The mechanisms involved in the increase in serotonin, dopamine turnover and BDNF levels observed in ayahuasca treated animals should be further investigated in specific brain areas.

摘要

安非他命是一种致幻饮料,会影响血清素能系统,对许多疾病和障碍具有治疗潜力,包括抑郁症和药物成瘾。本研究的目的是评估慢性暴露后安非他命对大鼠的潜在毒性作用,以及大脑中单胺、其代谢物和脑源性神经营养因子 (BDNF) 的水平。雌性和雄性大鼠分别连续口服 28 天 HO(对照)、氟西汀(FLX,一种选择性 5-羟色胺再摄取抑制剂抗抑郁药)或安非他命(Aya),剂量为仪式剂量的 0.5X、1X 和 2X(每组 7-10 只动物)。临床、血液学和大体结果表明,安非他命对大鼠是安全的。最后一次治疗后 1 小时进行的行为测试显示,Aya1 组的雄性大鼠比对照组大鼠在开阔场中央区域的探索较少,且该组和 FLX 组中央区域的进入次数与总运动相比也明显较低。取出海马体进行 BDNF 分析,其余大脑用于 HPLC-FL 分析单胺。只有雌性 Aya2 组的血清素水平明显高于对照组,而 FLX 组的其代谢物 5-HIAA 水平显著降低。各组多巴胺水平相似,但 Aya1 和 Aya2 组多巴胺的代谢物 DOPAC 水平显著高于对照组,尤其是雌性,Aya2 组 DOPAC/多巴胺周转率明显更高。另一种多巴胺代谢物 HVA 的水平与对照组相比,各处理组均无变化,但所有雄性安非他命组的 HVA/DOPAC 比值明显低于对照组。任何脑样本中均未检测到去甲肾上腺素,各组间其代谢物 MHPG 水平无明显变化。与对照组相比,FLX 和 Aya2 雌性组的海马体 BDNF 水平显著升高,与大脑总重量相关时表达。在特定脑区进一步研究观察到的安非他命处理动物中血清素、多巴胺周转率和 BDNF 水平升高的相关机制。

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