Sommer S, Danysz W, Russ H, Valastro B, Flik G, Hauber W
Institute of Biology, Department of Animal Physiology,University of Stuttgart,D-70550 Stuttgart,Germany.
Merz Pharmaceuticals GmbH,D-60318, Frankfurt am Main,Germany.
Int J Neuropsychopharmacol. 2014 Dec;17(12):2045-56. doi: 10.1017/S1461145714000996. Epub 2014 Jun 25.
Drugs that are able to shift effort-related decision making in intact rats towards high-effort response options are largely unknown. Here, we examined the effects of two candidate drugs, MRZ-9547 and its l-enantiomer MRZ-9546 on progressive ratio (PR) responding using two different tasks, a standard PR task that involves increasing ratio requirements and a PR/chow feeding choice task in which animals can lever press for preferred food pellets under a PR schedule or approach freely available less preferred lab chow. Furthermore, we assessed the mechanisms of action of both drugs using in vitro-assay methods and in vivo-microdialysis. Results reveal that MRZ-9547 is a selective dopamine transporter (DAT) inhibitor that moderately stimulated striatal dopamine release. MRZ-9546 was a much less potent DAT inhibitor. Furthermore, MRZ-9547 dose dependently increased the tendency to work for food reinforcement both in the standard PR task and the PR/chow feeding choice task, MRZ-9546 was considerably less active. Relative to MRZ-9547, other DAT-interfering drugs had only moderate (methylphenidate) or marginal (modafinil, d-amphetamine) stimulant effects on PR responding in either task. Collectively, our data demonstrate that the DAT inhibitor MRZ-9547 can markedly stimulate PR responding and shift effort-related decision making in intact rats towards high-effort response options. An analysis of effort-related decision making in rodents could provide an animal model for motivational dysfunctions related to effort expenditure such as fatigue, e.g. in Parkinson's disease or major depression. Our findings suggest that DAT inhibitors such as MRZ-9547 could be potentially useful for treating energy-related symptoms in neurological or neuropsychiatric disorders.
能够使正常大鼠与努力相关的决策转向高努力反应选项的药物在很大程度上尚不清楚。在这里,我们使用两种不同的任务,即涉及增加比率要求的标准渐进比率(PR)任务和PR/食物喂养选择任务,研究了两种候选药物MRZ - 9547及其左旋对映体MRZ - 9546对PR反应的影响。在PR/食物喂养选择任务中,动物可以在PR时间表下按压杠杆以获取偏好的食物颗粒,或者自由接近不太偏好的现成实验室食物。此外,我们使用体外测定方法和体内微透析评估了这两种药物的作用机制。结果显示,MRZ - 9547是一种选择性多巴胺转运体(DAT)抑制剂,可适度刺激纹状体多巴胺释放。MRZ - 9546是一种效力低得多的DAT抑制剂。此外,MRZ - 9547在标准PR任务和PR/食物喂养选择任务中均剂量依赖性地增加了为获得食物强化而工作的倾向,MRZ - 9546的活性则低得多。相对于MRZ - 9547,其他干扰DAT的药物在任一任务中对PR反应仅具有中等(哌甲酯)或轻微(莫达非尼、右旋苯丙胺)的刺激作用。总体而言,我们的数据表明,DAT抑制剂MRZ - 9547可显著刺激PR反应,并使正常大鼠与努力相关的决策转向高努力反应选项。对啮齿动物与努力相关的决策进行分析可为与努力消耗相关的动机功能障碍(如疲劳,例如在帕金森病或重度抑郁症中)提供动物模型。我们的研究结果表明,像MRZ - 9547这样的DAT抑制剂可能对治疗神经或神经精神疾病中与能量相关的症状有潜在作用。