Amelioration of recognition memory impairment associated with iron loading or aging by the type 4-specific phosphodiesterase inhibitor rolipram in rats

被引:47
作者
de Lima, M. N. [1 ]
Presti-Torres, J. [1 ]
Garcia, V. A. [1 ]
Guimaraes, M. R. [1 ]
Scalco, F. S. [1 ]
Roesler, R. [2 ,3 ]
Schroder, N. [1 ]
机构
[1] Pontificia Catholic Univ, Neurobiol & Dev Biol Lab, Fac Biosci, BR-90619900 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Basic Hlth Sci, Dept Pharmacol, Cellular & Mol Neuropharmacol Res Grp, BR-90046900 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Canc Res Lab, Acad Hosp, Res Ctr, BR-90035003 Porto Alegre, RS, Brazil
关键词
Iron; Rolipram; Phosphodiesterase type 4 inhibitors; Aging; Memory dysfunction; Memory consolidation;
D O I
10.1016/j.neuropharm.2008.06.025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Increasing evidence indicates that iron deposition in the brain might play a role in cognitive dysfunction associated with neurodegenerative disorders and aging. Previous studies have not examined whether iron-induced memory deficits can be attenuated by acute treatments with memory-enhancing agents. Phosphodiesterase type 4 (PDE4) inhibitors such as rolipram (ROL) ameliorate memory impairments in several rodent models of amnesia and have been proposed as candidate cognitive-enhancing drugs. Here we show that a single posttraining systemic injection of ROL dose-dependently attenuates the impairment of memory for novel object recognition (NOR) in rats given neonatal iron loading, a model of iron-induced cognitive impairment. Posttraining administration of ROL also recovered NOR deficits associated with aging in rats. These findings provide the first evidence that stimulation of an intracellular second messenger signaling pathway can attenuate iron-induced memory impairment, and support the view that PDE4 inhibitors might ameliorate cognitive dysfunction associated with aging and neurodegenerative disorders. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:788 / 792
页数:5
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