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利培酮和阿塞那平致敏作用及其相关 D2 受体机制的时间依赖性。

Time-dependence of risperidone and asenapine sensitization and associated D2 receptor mechanism.

机构信息

Department of Psychology, University of Nebraska-Lincoln, USA.

出版信息

Behav Brain Res. 2013 Nov 15;257:286-94. doi: 10.1016/j.bbr.2013.09.050. Epub 2013 Oct 5.

Abstract

When an antipsychotic drug is given repeatedly and intermittently, there is often a long-term increase in its behavioral efficacy, termed antipsychotic sensitization. With the passage of time, the magnitude of antipsychotic sensitization may increase or decrease based on the principle of time-dependent sensitization (TDS) or memory decay, respectively. In the present study, we examined the time-dependent feature and possible dopamine D2 receptor mechanism of sensitization induced by risperidone and asenapine in the conditioned avoidance response test. Well-trained male adult Sprague-Dawley rats were first repeatedly treated with risperidone (1.0mg/kg) or asenapine (0.2mg/kg) and tested for avoidance response daily for 5 consecutive days. Eight, 18 or 38 days after the 5th drug treatment, all rats were retested drug-free to assess the long-term impact of prior risperidone or asenapine treatment. Drug-pretreated rats had significantly lower avoidance than vehicle-pretreated ones on this test, and the group differences increased with the passage of time. In the subsequent drug challenge test at 10, 20 or 40 days after the 5th drug treatment, all rats were injected with a low dose of risperidone (0.3mg/kg) or asenapine (0.1mg/kg). Drug-pretreated rats again made significantly fewer avoidances than controls, confirming the antipsychotic sensitization effect. Finally, in the quinpirole (a D2/3 receptor agonist, 1.0mg/kg, sc)-induced hyperlocomotion test, risperidone-pretreated rats exhibited a significantly higher level of motor activity than the vehicle-pretreated ones. These findings suggest that risperidone and asenapine sensitization is long-lasting, follows the TDS principle, and is likely mediated by D2 receptor supersensitivity.

摘要

当抗精神病药物反复间歇给药时,其行为疗效通常会长期增加,这种现象被称为抗精神病药物敏感化。随着时间的推移,根据时间依赖性敏感化(TDS)或记忆衰减的原理,抗精神病药物敏感化的幅度可能会增加或减少。在本研究中,我们检查了利培酮和阿塞那平在条件性回避反应测试中诱导的敏感化的时间依赖性特征和可能的多巴胺 D2 受体机制。首先,将经过充分训练的成年雄性 Sprague-Dawley 大鼠反复用利培酮(1.0mg/kg)或阿塞那平(0.2mg/kg)处理,并在连续 5 天内每天测试回避反应。在第 5 次药物治疗后 8、18 或 38 天,所有大鼠均进行无药物测试,以评估先前利培酮或阿塞那平治疗的长期影响。与对照组相比,药物预处理组的大鼠在这项测试中的回避反应明显减少,且随着时间的推移,组间差异逐渐增大。在第 5 次药物治疗后 10、20 或 40 天进行的随后的药物挑战测试中,所有大鼠均注射低剂量利培酮(0.3mg/kg)或阿塞那平(0.1mg/kg)。与对照组相比,药物预处理组的大鼠再次出现明显较少的回避反应,证实了抗精神病药物敏感化效应。最后,在喹硫平(D2/3 受体激动剂,1.0mg/kg,sc)诱导的过度活跃测试中,利培酮预处理组大鼠的运动活性明显高于对照组。这些发现表明,利培酮和阿塞那平敏感化是持久的,遵循 TDS 原则,并且可能由 D2 受体超敏性介导。

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