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首页> 外文期刊>Behavioral neuroscience >Effects of a typical and an atypical antipsychotic on the disruption of prepulse inhibition caused by corticotropin-releasing factor and by rat strain
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Effects of a typical and an atypical antipsychotic on the disruption of prepulse inhibition caused by corticotropin-releasing factor and by rat strain

机译:典型的和非典型的抗精神病药对促肾上腺皮质激素释放因子和大鼠品系引起的前冲抑制作用的破坏

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Male Wistar-Kyoto (WKY) and Brown Norway (BN) rats (11-12 weeks, n = 184) received an injection of saline, haloperidol, or clozapine, followed by an intracerebroventricular infusion of saline or corticotropin-releasing factor (CRF). Rats were tested for prepulse inhibition (PPI) of the acoustic startle response. BN rats showed less PPI than WKY rats, and neither antipsychotic alone enhanced PPI. In WKY rats, both haloperidol and clozapine attenuated the CRF-induced decrease in PPI. In CRF-treated BN rats, clozapine-enhanced PPI. A clozapine-induced decrease in startle amplitude was seen in CRF-treated BN rats but not in CRF-treated WKY rats. Although the disruption of PPI caused by exogenous CRF administration can be reversed by acute antipsychotic treatment, baseline PPI is not altered.
机译:雄性Wistar-Kyoto(WKY)和Brown Norway(BN)大鼠(11-12周,n = 184)注射了盐水,氟哌啶醇或氯氮平注射液,然后脑室内注射了盐水或促肾上腺皮质激素释放因子(CRF) 。测试了大鼠对声音惊吓反应的脉冲前抑制(PPI)。 BN大鼠显示的PPI低于WKY大鼠,单独的抗精神病药均不能增强PPI。在WKY大鼠中,氟哌啶醇和氯氮平均减弱了CRF诱导的PPI下降。在接受CRF治疗的BN大鼠中,氯氮平增强了PPI。在CRF治疗的BN大鼠中观察到了氯氮平引起的惊吓幅度降低,但在CRF治疗的WKY大鼠中未观察到。尽管通过急性抗精神病药物治疗可以逆转外源性CRF给药引起的PPI破坏,但基线PPI不会改变。

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