灵霉素
抗抑郁药
致幻剂
氯胺酮
麦角酸二乙酰胺
药理学
心理学
萧条(经济学)
NMDA受体
抑郁症动物模型
医学
麻醉
神经科学
单胺类神经递质
三环类抗抑郁药
开阔地
精神科
内科学
血清素
受体
焦虑
经济
宏观经济学
作者
Meghan Hibicke,Alexus N Landry,Hannah M. Kramer,Zoe K. Talman,Charles D. Nichols
标识
DOI:10.1021/acschemneuro.9b00493
摘要
Psilocybin shows efficacy to alleviate depression in human clinical trials for six or more months after only one or two treatments. Another hallucinogenic drug, esketamine, has recently been U.S. Food and Drug Administration (FDA)-approved as a rapid-acting antidepressant. The mechanistic basis for the antidepressant effects of psilocybin and ketamine appear to be conserved. The efficacy of these two medications has not, however, been directly compared either clinically or preclinically. Further, whether or not a profound subjective existential experience is necessary for psilocybin to have antidepressant effects is unknown. To address these questions, we tested psilocybin, lysergic acid diethylamide (LSD), and ketamine in a rat model for depression. As in humans, a single administration of psilocybin or LSD produced persistent antidepressant-like effects in our model. In contrast, ketamine produced only a transient antidepressant-like effect. Our results indicate that classic psychedelics may have therapeutic efficacy that is more persistent than that of ketamine, and also suggest that a subjective existential experience may not be necessary for therapeutic effects.
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