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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Persisting cognitive deficits induced by low-dose, subchronic treatment with MK-801 in adolescent rats.
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Persisting cognitive deficits induced by low-dose, subchronic treatment with MK-801 in adolescent rats.

机译:小剂量亚慢性MK-801治疗可导致青春期大鼠持续存在认知功能障碍。

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摘要

Cognitive impairments have been proposed as a core feature of schizophrenia. Studies have shown that chronic or subchronic treatment with N-methyl-d-aspartate (NMDA) antagonists could induce cognitive deficits that resemble the symptoms of schizophrenia, yet few studies have investigated the effects of repeated NMDA blockade during adolescence on cognition. In the current study, adolescent, male rats were treated with an intraperitoneal injection of MK-801 (0.05, 0.1, and 0.2mg/kg) once daily for 14days. They were then tested 24h and 14days after drug cessation, respectively, in a series of behavioural tasks, including the object recognition task, the object-in-context recognition task and the working memory task of the Morris water maze (MWM). Results showed that object-in-context recognition and spatial working memory in the MWM were significantly impaired by repeated MK-801 treatment when animals were tested 24h after drug cessation, but object recognition was left intact. In particular, such deficits were observed 14days after drug cessation in the 0.2mg/kg group. The cognition-impairing effect of MK-801 could not be attributed to malnutrition or alterations in motor functions. Taken together, this study may provide support for establishing an animal model of cognitive deficits of schizophrenia based on low-dose, repeated treatment of MK-801 during adolescence.
机译:已经提出认知障碍是精神分裂症的核心特征。研究表明,使用N-甲基-d-天冬氨酸(NMDA)拮抗剂进行慢性或亚慢性治疗可诱发类似于精神分裂症症状的认知缺陷,但很少有研究研究青春期反复进行NMDA阻滞对认知的影响。在当前的研究中,每天一次的腹膜内注射MK-801(0.05、0.1和0.2mg / kg)治疗青春期的雄性大鼠,持续14天。然后分别在戒毒后24小时和14天对他们进行一系列行为任务的测试,包括对象识别任务,上下文对象识别任务和莫里斯水迷宫(MWM)的工作记忆任务。结果表明,在禁药后24小时对动物进行测试时,反复进行MK-801治疗会极大地损害MWM中的上下文对象识别和空间工作记忆,但对象识别仍保持不变。特别地,在0.2mg / kg的组中,戒断后第14天观察到这种缺陷。 MK-801的认知障碍作用不能归因于营养不良或运动功能改变。两者合计,这项研究可能为建立基于低剂量,MK-801青春期反复治疗的精神分裂症认知缺陷动物模型提供支持。

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