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Neurobehavioral effects of lithium in the rat: Investigation of the effect/concentration relationships and the contribution of the poisoning pattern

机译:大鼠锂的神经麻烦效应:对效应/浓度关系的研究与中毒模式的贡献

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Severity of lithium poisoning depends on the ingested dose, previous treatment duration and renal function. No animal study has investigated neurobehavioral differences in relation to the lithium poisoning pattern observed in humans, while differences in lithium pharmacokinetics have been reported in lithium-pretreated rats mimicking chronic poisonings with enhanced brain accumulation in rats with renal failure. Our objectives were: 1)-to investigate lithium-related effects in overdose on locomotor activity, anxiety-like behavior, spatial recognition memory and anhedonia in the rat; 2)-to model the relationships between lithium-induced effects on locomotion and plasma, erythrocyte, cerebrospinal fluid and brain concentrations previously obtained according to the poisoning pattern. Open-field, elevated plus-maze, Y-maze and sucrose consumption tests were used. In acutely lithium-poisoned rats, we observed horizontal (p < 0.001) and vertical hypolocomotion (p < 0.0001), increased anxiety-like behavior (p < 0.05) and impaired memory (p < 0.01) but no altered hedonic status. Horizontal (p < 0.01) and vertical (p < 0.001) hypolocomotion peaked more markedly 24 h after lithium injection and was more prolonged in acute-on-chronically vs. acutely lithium-poisoned rats. Hypolocomotion in chronically lithium-poisoned rats with impaired renal function did not differ from acutely poisoned rats 24 h after the last injection. Interestingly, hypolocomotion/concentration relationships best fitted a sigmoidal Emax model in acute poisoning and a linear regression model linked to brain lithium in acute-on-chronic poisoning. In conclusion, lithium overdose alters rat behavior and consistently induces hypolocomotion which is more marked and prolonged in repeatedly lithium-treated rats. Our data suggest that differences between poisoning patterns regarding lithium-induced hypolocomotion are better explained by the duration of lithium exposure than by its brain accumulation.
机译:锂中毒的严重程度取决于摄入剂量,先前治疗持续时间和肾功能。没有动物研究已经研究了与人类观察到的锂中毒模式的神经麻烦差异,而锂药代动力学的差异已经报道锂预处理大鼠,模仿慢性中毒,肾功能衰竭大鼠脑积累增强。我们的目标是:1) - 调查对机车活动过量的锂相关效果,焦虑的行为,焦虑的行为,样式识别记忆和大鼠的厌氧血症; 2) - 根据中毒模式模拟锂诱导锂诱导效果之间的关系,红细胞,脑脊液和脑浓度的关系。采用开放式,高架加迷宫,Y型迷宫和蔗糖消耗试验。在急性锂中毒大鼠中,我们观察到水平(P <0.001)和垂直低速度(P <0.0001),增加焦虑的行为(P <0.05)和内存受损(P <0.01)但没有改变的蜂窝状况。水平(P <0.01)和垂直(P <0.001)锂注射后更明显达到峰值峰值,在急性锂锂中毒大鼠中更延长。肾功能受损的较长锂中毒大鼠中的低调率与最后一次注射后24小时没有与急性中毒大鼠不同。有趣的是,低压运动/浓缩关系最能拟合急性中毒的乙状体emax模型和与急性对慢性中毒中的脑锂相关的线性回归模型。总之,锂过量改变了大鼠的行为,一致地诱导更严重并延长在反复锂处理的大鼠中的低调率。我们的数据表明,在锂曝光的持续时间比其脑积累的持续时间更好地解释了关于锂诱导的低气旋的中毒模式之间的差异。

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