TY - JOUR
T1 - Dimebon enhances hippocampus-dependent learning in both appetitive and inhibitory memory tasks in mice
AU - Vignisse, Julie
AU - Steinbusch, Harry W.M.
AU - Bolkunov, Alexei
AU - Nunes, Joao
AU - Santos, Ana Isabel
AU - Grandfils, Christian
AU - Bachurin, Sergei
AU - Strekalova, Tatyana
N1 - Funding Information:
We would like to thank Natalia Ivanova and Natalia Nikolaeva for their excellent technical assistance, as well as Prof. Margarida Santos Reis and Jeffrey Muskiet for their organizational help and Prof. Vladimir Grigoriev for his valuable theoretical input. This study was supported by Internationale Stichting Alzheimer Onderzoek (ISAO) grant N 09501 to T.S. (International Foundation on Alzheimer's disease research, the Netherlands), Erasmus Exchange Program of the Universities of Liege and Maastricht (to J.V.), TUL Transnational University Limburg and FP6 Nanabiopharmaceuticals and the Royal Netherlands Academy of Arts and Sciences (KNAW).
PY - 2011/3/30
Y1 - 2011/3/30
N2 - Pre-clinical and clinical studies on dimebon (dimebolin or latrepirdine) have demonstrated its use as a cognitive enhancer. Here, we show that dimebon administered to 3-month-old C57BL6N mice 15. min prior to training in both appetitive and inhibitory learning tasks via repeated (0.1. mg/kg) and acute (0.5. mg/kg) i.p. injections, respectively, increases memory scores. Acute treatment with dimebon was found to enhance inhibitory learning, as also shown in the step-down avoidance paradigm in 7-month-old mice. Bolus administration of dimebon did not affect the animals' locomotion, exploration or anxiety-like behaviour, with the exception of exploratory behaviour in older mice in the novel cage test. In a model of appetitive learning, a spatial version of the Y-maze, dimebon increased the rate of correct choices and decreased the latency of accessing a water reward after water deprivation, and increased the duration of drinking behaviour during training/testing procedures. Repeated treatment with dimebon did not alter the behaviours in other tests or water consumption. Acute treatment of water-deprived and non-water-deprived mice with dimebon also did not affect their water intake. Our data suggest that dimebon enhances hippocampus-dependent learning in both appetitive and inhibitory tasks in mice.
AB - Pre-clinical and clinical studies on dimebon (dimebolin or latrepirdine) have demonstrated its use as a cognitive enhancer. Here, we show that dimebon administered to 3-month-old C57BL6N mice 15. min prior to training in both appetitive and inhibitory learning tasks via repeated (0.1. mg/kg) and acute (0.5. mg/kg) i.p. injections, respectively, increases memory scores. Acute treatment with dimebon was found to enhance inhibitory learning, as also shown in the step-down avoidance paradigm in 7-month-old mice. Bolus administration of dimebon did not affect the animals' locomotion, exploration or anxiety-like behaviour, with the exception of exploratory behaviour in older mice in the novel cage test. In a model of appetitive learning, a spatial version of the Y-maze, dimebon increased the rate of correct choices and decreased the latency of accessing a water reward after water deprivation, and increased the duration of drinking behaviour during training/testing procedures. Repeated treatment with dimebon did not alter the behaviours in other tests or water consumption. Acute treatment of water-deprived and non-water-deprived mice with dimebon also did not affect their water intake. Our data suggest that dimebon enhances hippocampus-dependent learning in both appetitive and inhibitory tasks in mice.
KW - Alzheimer's disease
KW - Dimebon
KW - Hippocampus-dependent memory
KW - Mouse
UR - http://www.scopus.com/inward/record.url?scp=79952901355&partnerID=8YFLogxK
U2 - 10.1016/j.pnpbp.2010.12.007
DO - 10.1016/j.pnpbp.2010.12.007
M3 - Article
C2 - 21163318
AN - SCOPUS:79952901355
SN - 0278-5846
VL - 35
SP - 510
EP - 522
JO - Progress in Neuro-Psychopharmacology and Biological Psychiatry
JF - Progress in Neuro-Psychopharmacology and Biological Psychiatry
IS - 2
ER -