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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Neonatal lesions of the ventral hippocampus in rats lead to prefrontal cognitive deficits at two maturational stages.
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Neonatal lesions of the ventral hippocampus in rats lead to prefrontal cognitive deficits at two maturational stages.

机译:大鼠腹侧海马的新生儿损伤在两个成熟阶段导致前额叶认知功能障碍。

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This experiment assessed the effect of neonatal ventral hippocampus lesions in rats, a heuristic approach to model schizophrenia, on continuous delayed alternation and conditional discrimination learning performance before and after complete cerebral maturation. Delays (0, 5, 15, and 30 s) were introduced in the tasks to help dissociate between a hippocampal and a prefrontal cortex dysfunction. At postnatal day (PND) 6 or 7, rats received bilateral microinjections of ibotenic acid or phosphate-buffered saline in the ventral hippocampus. From PND 26 to PND 35, rats were tested on the alternation task in a T-maze; from PND 47 to PND 85, the same rats were tested in the discrimination task where a stimulus and a response location had to be paired. Deficits in ventral hippocampus-lesioned rats were observed in both tasks whether a delay was introduced before a response or not. Impaired performance regardless of delay length, combined with high rates of perseverative errors, suggested a post-lesional prefrontal cortex dysfunction which persisted from the juvenile stage into adulthood. Premature cognitive impairments could not be predicted on the basis of the neurodevelopmental animal model of schizophrenia. Nevertheless, they appear consistent with accounts of premorbidly compromised memory, both immediate and delayed, in subgroups of schizophrenia patients.
机译:该实验评估了大鼠新生腹侧海马损伤(一种启发式的精神分裂症治疗方法)对大脑完全成熟前后持续延迟交替和条件歧视学习表现的影响。在任务中引入了延迟(0、5、15和30 s),以帮助分离海马和前额叶皮质功能障碍。在出生后第6天或第7天,大鼠在腹侧海马接受了双微注射的异丁烯酸或磷酸盐缓冲盐水。从PND 26到PND 35,在T型迷宫中测试了老鼠的交替任务;从PND 47到PND 85,在区分任务中测试了同一只老鼠,其中必须将刺激和反应位置配对。无论是否在反应之前引入延迟,在两项任务中均观察到腹侧海马损伤大鼠的缺陷。无论延迟时间长短,性能受损,再加上顽固性错误的发生率高,提示病变后前额叶皮质功能障碍从少年阶段一直持续到成年。无法根据精神分裂症的神经发育动物模型预测过早的认知障碍。然而,它们似乎与精神分裂症患者亚组中病态受损的记忆(即刻和延迟)一致。

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