Department of Pharmacology and Toxicology, Institute of Pharmacy and Center for Molecular Biosciences Innsbruck, University of Innsbruck, 6020 Innsbruck, Austria.
AG Neuroendokrinologie und Verhalten, Institut für Biochemie und Zellbiologie, Otto-von-Guericke-Universität Magdeburg, 39120 Magdeburg, Germany.
Biomolecules. 2022 Mar 27;12(4):506. doi: 10.3390/biom12040506.
Previous studies have shown that atypical dopamine-transporter-inhibitors such as modafinil and its analogues modify behavioral and cognitive functions in rodents. Here, we tested potential promnestic effects of the novel, more dopamine-transporter selective modafinil analogue CE-158 in the social discrimination memory task in male mice. Systemic administration of CE-158 1 h before the social learning event prevented the impairment of social-recognition memory following retroactive interference 3 h after the learning session of a juvenile conspecific. This effect was dose-dependent, as mice treated with 10 mg/kg, but not with 1 mg/kg CE-158, were able to discriminate between the novel and familiar conspecific despite the presentation of an interference stimulus, both 3 h and 6 h post learning. However, when 10 mg/kg of the drug was administered after learning, CE-158 failed to prevent social memory from interference. Paralleling these behavioral effects, the systemic administration of 10 mg/kg CE-158 caused a rapid and sustained elevation of extracellular dopamine in the nucleus accumbens, a brain area where dopaminergic signaling plays a key role in learning and memory function, of freely moving mice, while 1 mg/kg was not sufficient for altering dopamine levels. Taken together, our findings suggest promnestic effects of the novel dopamine-transporter-inhibitor CE-158 in a social recognition memory test that may be in part mediated via increased dopamine-neurotransmission in the nucleus accumbens. Thus, selective-dopamine-transporter-inhibitors such as CE-158 may represent interesting drug candidates for the treatment of memory complaints observed in humans with cognitive impairments and dementia.
先前的研究表明,非典型多巴胺转运体抑制剂,如莫达非尼及其类似物,可改变啮齿动物的行为和认知功能。在这里,我们测试了新型、更具多巴胺转运体选择性的莫达非尼类似物 CE-158 在雄性小鼠社交辨别记忆任务中的潜在促智作用。在社交学习事件前 1 小时系统给予 CE-158,可防止在学习后 3 小时进行少年同型物的逆行干扰后,社交识别记忆受损。这种作用呈剂量依赖性,因为用 10mg/kg 的 CE-158 处理的小鼠,而不是用 1mg/kg 的 CE-158 处理的小鼠,尽管在学习后 3 小时和 6 小时呈现干扰刺激,也能够辨别新颖和熟悉的同型物。然而,当在学习后给予 10mg/kg 的药物时,CE-158 不能防止社交记忆受到干扰。与这些行为效应平行的是,在自由活动的小鼠中,系统给予 10mg/kg 的 CE-158 可快速而持续地增加伏隔核中的细胞外多巴胺,而 1mg/kg 的 CE-158 不足以改变多巴胺水平。总之,我们的发现表明,新型多巴胺转运体抑制剂 CE-158 在社交识别记忆测试中具有促智作用,这可能部分是通过增加伏隔核中的多巴胺神经传递来介导的。因此,选择性多巴胺转运体抑制剂,如 CE-158,可能代表了具有认知障碍和痴呆症的人类记忆障碍治疗的有趣候选药物。