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利血平给药后大鼠神经化学和认知损伤的时程发展。

Temporal development of neurochemical and cognitive impairments following reserpine administration in rats.

机构信息

Graduate Program of Developmental and Cellular Biology, Center of Biological Sciences, Federal University of Santa Catarina, Florianópolis, SC, 88040-900, Brazil; Graduate Program of Neuroscience, Center of Biological Sciences, Federal University of Santa Catarina, Florianópolis, SC, 88040-900, Brazil.

Graduate Program of Pharmacology, Center of Biological Sciences, Federal University of Santa Catarina, Florianópolis, SC, 88040-900, Brazil.

出版信息

Behav Brain Res. 2020 Apr 6;383:112517. doi: 10.1016/j.bbr.2020.112517. Epub 2020 Jan 30.

Abstract

The systemic administration of low reserpine (RES) doses (0.1-1.0 mg/kg) has been proposed as a valuable rat model for the study of non-motor symptoms of Parkinson's disease (PD). Here, we investigated the temporal-dependent effects of RES (1 mg/kg, s.c.) on short-term memory and locomotion, as well as, the levels of dopamine, serotonin and its metabolites in the striatum, hippocampus and prefrontal cortex at 3, 24 or 72 h after RES administration. RES administrations resulted in social and object recognition memory impairment and increased dopamine turnover in the striatum, without changes in the rat spontaneous locomotor activity, 3 h after RES administration. Altogether, these results provide new insights for the use of RES administration as an experimental design for the study of PD non-motor symptoms in rats.

摘要

低利血平(RES)剂量(0.1-1.0 mg/kg)的系统给药已被提议作为研究帕金森病(PD)非运动症状的有价值的大鼠模型。在这里,我们研究了 RES(1 mg/kg,sc)在 RES 给药后 3、24 或 72 小时对短期记忆和运动以及纹状体、海马和前额叶皮质中多巴胺、血清素及其代谢物水平的时间依赖性影响。RES 给药导致社会和物体识别记忆障碍,并增加纹状体中的多巴胺周转率,而在 RES 给药后 3 小时,大鼠自发运动活动没有变化。总之,这些结果为 RES 给药作为研究大鼠 PD 非运动症状的实验设计提供了新的见解。

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