State Key Lab of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Neurobiol Aging. 2011 Jan;32(1):31-41. doi: 10.1016/j.neurobiolaging.2009.07.013. Epub 2009 Oct 29.
It is widely known that exogenous formaldehyde exposure induces human cognitive impairment and animal memory loss; and recent studies show that formaldehyde at pathological levels induces Aβ deposition and misfolding of tau protein to form globular amyloid-like aggregates. Endogenous formaldehyde may be a marker for progressive senile dementia. The aim of this study was to investigate the correlation of endogenous formaldehyde in urine of senile dementia and mini mental state examination (MMSE) scores. Formaldehyde level was analyzed by high-performance liquid chromatography (with fluorescence detection) in human urine from dementia patients (n=141), patients with hypertension (n=33) or diabetes (n=16) and healthy individuals (n=38), autopsy hippocampus samples from Alzheimer's disease (AD) patients and brains of three types of AD animal model: namely, senescence accelerated mice (SAMP8), APP-transgenic mice and APP/PS1-transgenic mice. In a double-blind study, there was marked elevation of urine formaldehyde levels in patients (n=91) with dementia, and a slight increase in patients (n=50) with mild cognitive impairment. Urine formaldehyde level was inversely correlated with mini mental state examination scores (Rs=-0.441, p<0.0001). Furthermore, formaldehyde levels were significantly increased in the autopsy hippocampus from Alzheimer's patients (n=4). In SAMP8 brains the formaldehyde level was significantly increased, suggesting that the endogenous formaldehyde is related to aging in mice. The brain formaldehyde level in APP/PS1-transgenic (n=8) mice at age of 3 months and APP-transgenic (n=8) mice at age of 6 months was increased (0.56 ± 0.02 mM), respectively, as compared with their respective age-matched controls, when these two types of AD-like animals, respectively, started to form Aβ deposits and memory loss obviously. According to the level of formaldehyde in the brain of the transgenic mice, we treated normal mice with formaldehyde (0.5mM, intraperitoneal administration) and observed the memory loss of the animal in Morris water maze trial. Cognitive impairments for the senile dementia are probably related to endogenous formaldehyde levels; and the mini mental state examination scores referred to the evaluation of urine formaldehyde level in dementia patients may be used as a non-invasive method for the investigation and diagnosis of senile dementia.
众所周知,外源性甲醛暴露会导致人类认知障碍和动物记忆力丧失;最近的研究表明,病理性水平的甲醛会诱导 Aβ 沉积和 tau 蛋白错误折叠,形成球形淀粉样聚集物。内源性甲醛可能是进行性老年痴呆症的标志物。本研究旨在探讨老年痴呆症患者尿液内源性甲醛与简易精神状态检查(MMSE)评分的相关性。采用高效液相色谱法(荧光检测)分析痴呆症患者(n=141)、高血压患者(n=33)、糖尿病患者(n=16)和健康对照者(n=38)的尿液甲醛水平,分析阿尔茨海默病(AD)患者尸检海马组织样本和三种 AD 动物模型(即快速老化小鼠(SAMP8)、APP 转基因小鼠和 APP/PS1 转基因小鼠)的脑组织中甲醛水平。在一项双盲研究中,痴呆症患者(n=91)的尿液甲醛水平明显升高,轻度认知障碍患者(n=50)的尿液甲醛水平略有升高。尿液甲醛水平与简易精神状态检查评分呈负相关(Rs=-0.441,p<0.0001)。此外,阿尔茨海默病患者尸检海马组织中甲醛水平显著升高(n=4)。SAMP8 大脑中的甲醛水平显著升高,提示小鼠衰老与内源性甲醛有关。3 月龄 APP/PS1 转基因(n=8)和 6 月龄 APP 转基因(n=8)小鼠的脑内甲醛水平分别升高(0.56±0.02mM),与各自年龄匹配的对照组相比,当这两种 AD 样动物分别开始形成 Aβ 沉积和明显记忆力丧失时。根据转基因小鼠大脑中的甲醛水平,我们用甲醛(0.5mM,腹腔注射)处理正常小鼠,并观察动物在 Morris 水迷宫试验中的记忆丧失情况。老年痴呆症的认知障碍可能与内源性甲醛水平有关;痴呆症患者尿液甲醛水平的简易精神状态检查评分可作为一种非侵入性方法,用于老年痴呆症的调查和诊断。