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首页> 外文期刊>Brain research bulletin >Effects of olanzapine, fluoxetine and olanzapine/fluoxetine on creatine kinase activity in rat brain.
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Effects of olanzapine, fluoxetine and olanzapine/fluoxetine on creatine kinase activity in rat brain.

机译:奥氮平,氟西汀和奥氮平/氟西汀对大鼠脑中肌酸激酶活性的影响。

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Recently, a fixed combination of the atypical antipsychotic olanzapine and the serotonin selective reuptake inhibitor (SSRI) fluoxetine has been approved in the US for the treatment of bipolar I depression. In this work, we evaluated the effect of acute and chronic administration of fluoxetine, olanzapine and the combination of fluoxetine/olanzapine on creatine kinase (CK) activity in the brain of rats. For acute treatment, adult male Wistar rats received one single injection of olanzapine (3 or 6 mg/kg) and/or fluoxetine (12.5 or 25mg/kg). For chronic treatment, adult male Wistar rats received daily injections of olanzapine (3 or 6 mg/kg) and/or fluoxetine (12.5 or 25mg/kg) for 28 days. In the present study we observed that acute administration of OLZ inhibited CK activity in cerebellum and prefrontal cortex. The acute administration of FLX inhibited creatine kinase in cerebellum, prefrontal cortex, hippocampus, striatum and cerebral cortex. In the chronic treatment, when the animals were killed 2h after the last injection a decrease in creatine kinase activity after FLX administration, alone or in combination with OLZ, in cerebellum, prefrontal cortex, hippocampus, striatum and cerebral cortex of rats occurred. However, when the animals were killed 24h after the last injection, we found no alterations in the enzyme. Although it is difficult to extrapolate our findings to the human condition, the inhibition of creatine kinase activity by these drugs may be associated to the occurrence of some side effects of OLZ and FLX.
机译:最近,非典型抗精神病药物奥氮平和5-羟色胺选择性再摄取抑制剂(SSRI)氟西汀的固定组合已在美国被批准用于治疗双相性I型抑郁症。在这项工作中,我们评估了氟西汀,奥氮平的急性和慢性给药以及氟西汀/奥氮平的组合对大鼠脑中肌酸激酶(CK)活性的影响。为了进行急性治疗,成年雄性Wistar大鼠接受单次注射的奥氮平(3或6 mg / kg)和/或氟西汀(12.5或25mg / kg)。对于慢性治疗,成年雄性Wistar大鼠每天接受奥氮平(3或6 mg / kg)和/或氟西汀(12.5或25mg / kg)注射28天。在本研究中,我们观察到OLZ的急性给药抑制了小脑和前额叶皮层的CK活性。 FLX的急性给药抑制了小脑,前额叶皮层,海马,纹状体和大脑皮层中的肌酸激酶。在慢性治疗中,当最后一次注射后2h处死动物时,单独或与OLZ组合使用FLX后,大鼠小脑,前额叶皮层,海马,纹状体和大脑皮层中的肌酸激酶活性降低。但是,当最后一次注射后24h处死动物时,我们发现酶没有变化。尽管很难将我们的发现推论到人类疾病中,但是这些药物对肌酸激酶活性的抑制作用可能与OLZ和FLX的某些副作用有关。

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