The contextual fear conditioning deficit presented by spontaneously hypertensive rats (SHR) is not improved by mood stabilizers

被引:19
作者
Calzavara, Mariana Bendlin [1 ,2 ]
Medrano, Wladimir Agostini [2 ]
Levin, Raquel [1 ,2 ]
Libanio, Tania Cristina [1 ,2 ]
Ribeiro, Rosana de Alencar [2 ]
Abilio, Vanessa Costhek [1 ,2 ]
机构
[1] Univ Fed Sao Paulo, Dept Psychiat, LiNC, BR-04039032 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Dept Pharmacol, BR-04039032 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bipolar disorder; Contextual fear conditioning; Lamotrigine; Lithium; Schizophrenia; SHR; SEROTONIN REUPTAKE INHIBITOR; INDUCED OXIDATIVE STRESS; ANIMAL-MODEL; ANTICONVULSANT DRUGS; ANTIEPILEPTIC DRUGS; MEMORY PERFORMANCE; BIPOLAR DEPRESSION; WISTAR-KYOTO; LAMOTRIGINE; LITHIUM;
D O I
10.1016/j.pnpbp.2011.06.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: We have recently reported that spontaneously hypertensive rats (SHR) present a contextual fear conditioning (CFC) deficit. This deficit is improved by antipsychotic drugs, potentiated by proschizophrenia manipulations and not altered by acute administration of carbamazepine, lamotrigine and valproic acid. Nevertheless, the effects of lithium a classical mood stabilizer or repeated treatment with these drugs were not evaluated. The main aim of the present study was to extend our previous work by investigating a possible beneficial effect of acute and/or chronic treatments with lithium or lamotrigine on the acquisition deficit of CFC presented by SHR. Methods: Rats were submitted to CFC task after an acute treatment with lithium and/or a repeated treatment with lithium and lamotrigine. Results: Our data revealed that the CFC deficit presented by SHR is not improved by acute or repeated treatment with lithium. Repeated lamotrigine treatment potentiated the deficit presented by SHR and impaired CFC in control animals (Wistar Rats). Conclusions: These data reinforce the absence of beneficial effects of mood stabilizers on the emotional context processing impairment modeled by SHR. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1607 / 1611
页数:5
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