Bailey Matthew R, Williamson Cait, Mezias Chris, Winiger Vanessa, Silver Rae, Balsam Peter D, Simpson Eleanor H
Department of Psychology, Columbia University, New York, NY, USA.
Columbia University, Mail Code 5501, 1190 Amsterdam Avenue Room 406, Schermerhorn Hall, New York, NY, 10027, USA.
Psychopharmacology (Berl). 2016 Feb;233(4):615-24. doi: 10.1007/s00213-015-4135-3. Epub 2015 Nov 11.
Impaired goal-directed motivation represents a debilitating class of symptoms common to psychological disorders including schizophrenia and some affective disorders. Despite the known negative impact of impaired motivation, there are currently no effective pharmacological interventions to treat these symptoms.
Here, we evaluate the effectiveness of the serotonin 2C (5-HT2C) receptor selective ligand, SB242084, as a potential pharmacological intervention for enhancing goal-directed motivation in mice. The studies were designed to identify not only efficacy but also the specific motivational processes that were affected by the drug treatment.
We tested subjects following treatment with SB242084 (0.75 mg/kg) in several operant lever pressing assays including the following: a progressive ratio (PR) schedule of reinforcement, an effort-based choice task, a progressive hold down task (PHD), and various food intake tests.
Acute SB242084 treatment leads to an increase in instrumental behavior. Using a battery of behavioral tasks, we demonstrate that the major effect of SB242084 is an increase in the amount of responses and duration of effort that subjects will make for food rewards. This enhancement of behavior is not the result of non-specific hyperactivity or arousal nor is it due to changes in food consumption.
Because of this specificity of action, we suggest that the 5-HT2C receptor warrants further attention as a novel therapeutic target for treating pathological impairments in goal-directed motivation.
目标导向动机受损是包括精神分裂症和一些情感障碍在内的心理障碍常见的一类使人衰弱的症状。尽管已知动机受损有负面影响,但目前尚无有效的药物干预措施来治疗这些症状。
在此,我们评估5-羟色胺2C(5-HT2C)受体选择性配体SB242084作为增强小鼠目标导向动机的潜在药物干预措施的有效性。这些研究旨在不仅确定疗效,还确定受药物治疗影响的特定动机过程。
我们在几种操作性杠杆按压试验中对接受SB242084(0.75毫克/千克)治疗的受试者进行了测试,包括以下试验:渐进比率(PR)强化程序、基于努力的选择任务、渐进按压任务(PHD)以及各种食物摄入测试。
急性SB242084治疗导致工具性行为增加。通过一系列行为任务,我们证明SB242084的主要作用是增加受试者为获得食物奖励而做出的反应量和努力持续时间。行为的这种增强不是非特异性多动或唤醒的结果,也不是食物消耗变化所致。
由于这种作用的特异性,我们建议5-HT2C受体作为治疗目标导向动机病理性损害的新治疗靶点值得进一步关注。