Neuro-protective effects of carbamazepine on sleep patterns and head and body shakes in kainic acid-treated rats

被引:6
作者
Alfaro-Rodriguez, Alfonso [1 ]
Gonzalez-Pina, Rigoberto [2 ]
Arch-Tirado, Emilio [3 ]
Carrasco-Portugal, Miriam [4 ]
Perez-Guille, Beatriz [5 ]
Eugenia Soriano-Rosales, Rosa [5 ]
Padilla-Martin, Krystell [1 ]
Uribe-Escamilla, Rebeca [1 ]
Labra-Ruiz, Norma [5 ]
机构
[1] Inst Nacl Rehabil, Lab Neuroquim, Dept Neurofisiol, Mexico City 14389, DF, Mexico
[2] Inst Nacl Rehabil, Lab Neuroplasticidad, Dept Neurofisiol, Mexico City 14389, DF, Mexico
[3] Inst Nacl Rehabil, Lab Bioacust, Dept Neurofisiol, Mexico City 14389, DF, Mexico
[4] Inst Nacl Enfermedades Resp, Unidad Invest, Mexico City, DF, Mexico
[5] Inst Nacl Pediat, Mexico City, DF, Mexico
关键词
Carbamazepine; Kainic acid; Sleep; Head and body shakes; 5-HT; Rat; CYCLE OSCILLATION; INDUCED SEIZURES; KINDLING MODEL; DORSAL RAPHE; BRAIN; SEROTONIN; PHENYTOIN; DOPAMINE; AMYGDALA; 5-HYDROXYTRYPTAMINE;
D O I
10.1016/j.cbi.2009.04.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this work was to analyze the effect of carbamazepine (CBZ) on sleep patterns and on "head and body shakes" and to determine the role of serotonin (5-HT) in a model of kainic-induced seizures. Thirty male Wistar rats (280-300g) were used for polygraphic sleep recording. After a basal recording. the rats were allocated into three groups: kainic acid-treated animals (KA; 10 mg/kg; n = 10), carbamazepine-treated animals (CBZ; 30 mg/kg; n = 10) and animals injected with KA 30 min after pretreatment with CBZ (CBZ + KA; n = 10). Polygraphic recordings were performed for 10 h for 3 days, with the exception of the CBZ group, which were observed for I day. In order to measure the head and body shakes that occurred over that time, a behavioral assessment was performed in two additional groups of KA (n = 10) and CBZ + KA (n = 10) animals. After 10 h of behavioral assessment, the rats were sacrificed, and the levels of 5-HT and 5-hydroxy-indol-acetic acid (5-HIAA) were analyzed. We compared these findings with the results from a group of rats without pharmacological intervention (n = 10). All of the recordings were performed from 08:00 to 18:00 h. Data analysis: the electrographic parameters, head and body shake counting and monoamine concentrations were analyzed by an ANOVA test. Differences of *p <= 0.01 and *p <= 0.001 were considered statistically significant. Our results showed that CBZ exerted a protective effect on sleep pattern alterations induced by KA, which when administered alone caused a complete inhibition of sleep for the first 10 h after administration. Although there was a reduction in the amount of sleep after the administration of KA in CBZ-pretreated animals, sleep inhibition was incomplete. In addition, CBZ decreased the frequency of head and body shakes by 60% as compared to KA. The 5-HT and 5-HIAA levels in the pons were increased in the KA and KA+CBZ groups. Our conclusion is that in addition to decreasing seizure intensity, CBZ facilitates the partial recovery of sleep. These results suggest that CBZ provides neuro-protective effects on sleep and against seizures. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:376 / 382
页数:7
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