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