4.7 Article

The Novel Analogue of Modafinil CE-158 Protects Social Memory against Interference and Triggers the Release of Dopamine in the Nucleus Accumbens of Mice

期刊

BIOMOLECULES
卷 12, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/biom12040506

关键词

cognitive enhancement; social recognition memory; retroactive interference; dopamine transport inhibitor; nucleus accumbens; microdialysis; long-term memory

资金

  1. Austrian Science Fund (FWF) [P 33534-B]

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The novel dopamine-transporter inhibitor CE-158 has been found to enhance memory in a social recognition memory task. This effect may be mediated by increased dopamine neurotransmission in the nucleus accumbens. Therefore, CE-158 may represent an interesting drug candidate for the treatment of memory complaints in individuals with cognitive impairments and dementia.
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-transporterinhibitor 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-transporterinhibitors such as CE-158 may represent interesting drug candidates for the treatment of memory complaints observed in humans with cognitive impairments and dementia.

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