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评估不宁腿综合征疑似动物模型中的周期性肢体运动。

Evaluation of periodic limb movements in a putative animal model of restless leg syndrome.

机构信息

Department of Psychobiology, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.

出版信息

Mov Disord. 2012 Mar;27(3):413-20. doi: 10.1002/mds.24058. Epub 2011 Dec 9.

Abstract

Restless leg syndrome (RLS) is a major healthcare burden with increasing prevalence. It has been demonstrated that periodic limb movements (PLM) can occur as an isolated phenomenon, but they are often associated with this syndrome and are the only symptom of this disorder that can be measured electrophysiologically. The aim of this study was to examine the sleep-wake behavior and the presence of limb movement in a rat model of RLS induced by lesioning the A11 dopaminergic nuclei with the neurotoxin 6-hydroxydopamine (6-OHDA). Rats were implanted with electrodes for electrocorticography and electromyography. Sleep recordings were monitored during light/dark periods lasting 12 hours each and were evaluated on days 7, 15, and 28 after injection of the drug or phosphate-buffered saline (PBS). A control group that did not receive any injection was also included. Wakefulness percentages were generated for 4-hour segments of the dark period, yielding the following 3 bins: 7 PM to 11 PM, 11 PM to 3 AM, and 3 PM to 7 PM. Additionally, slow wave sleep, paradoxical sleep, wakefulness, and limb movements were evaluated over the entire 12 hours of the light/dark cycle. All A11-lesioned rats exhibited an increased percentage of wakefulness during the last block of the dark period, as would be expected for an animal model of this syndrome. In addition, at all time points after lesioning, these animals presented increased frequencies of limb movement during both the light and the dark periods. These alterations were reversed by the acute administration of the dopaminergic agonist pramipexole. This animal model strengthens the notion that 6-OHDA-induced A11 lesions can be a valid animal model for RLS and PLM.

摘要

不宁腿综合征(RLS)是一种患病率不断增加的主要医疗保健负担。已经证明,周期性肢体运动(PLM)可以作为一种孤立的现象发生,但它们通常与该综合征有关,并且是唯一可以通过电生理测量来衡量的这种疾病的症状。本研究的目的是检查 A11 多巴胺能核损伤诱导的 RLS 大鼠模型中的睡眠-觉醒行为和肢体运动的存在,使用神经毒素 6-羟多巴胺(6-OHDA)。大鼠被植入用于皮层电图和肌电图的电极。在药物或磷酸盐缓冲盐水(PBS)注射后第 7、15 和 28 天,监测持续 12 小时的每个光/暗期的睡眠记录,并进行评估。还包括一个未接受任何注射的对照组。为暗期的 4 小时段生成觉醒百分比,产生以下 3 个箱:7 PM 至 11 PM、11 PM 至 3 AM 和 3 PM 至 7 PM。此外,还评估了整个 12 小时光/暗周期中的慢波睡眠、异相睡眠、觉醒和肢体运动。所有 A11 损伤的大鼠在暗期的最后一个块中表现出觉醒百分比增加,这是该综合征动物模型的预期。此外,在损伤后的所有时间点,这些动物在光期和暗期都表现出肢体运动频率增加。这些改变在急性给予多巴胺激动剂普拉克索后得到逆转。这种动物模型加强了这样一种观点,即 6-OHDA 诱导的 A11 损伤可以成为 RLS 和 PLM 的有效动物模型。

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