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雌激素缺乏型大鼠神经退行性变和记忆缺失诱导过程中的分子事件。

Molecular events during the induction of neurodegeneration and memory loss in estrogen-deficient rats.

机构信息

Biological Science Program, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

Gen Comp Endocrinol. 2013 Jan 15;181:316-23. doi: 10.1016/j.ygcen.2012.07.034. Epub 2012 Oct 1.

Abstract

This study aims to delineate the relationship among estrogen deficiency, neurodegeneration, and cognitive impairment of ovariectomized rats. Female Sprague-Dawley rats were ovariectomized and euthanized after 1-4 month periods (M(0)-M(4) groups). Blood samples were collected for the determination of serum levels of 17β-estradiol (E(2)), luteinizing hormone (LH), and follicle stimulating hormone (FSH). Five consecutive days before the euthanization, cognitive performance of the rats was examined by Morris water maze test. After euthanization, the hippocampus was collected, and expression of the genes associated with amyloid plaques (App, Adam10 and Bace1) and neurofibrillary tangles (Tau4 and Tau3) were examined by real-time PCR. Serum E(2) levels were declined following 2 weeks of ovariectomy. Conversely, serum FSH and LH levels were profoundly increased by 2 weeks of ovariectomy for approximately 4 and 22 times, respectively. Cognitive impairments, indicated by the longer latency and distance, were observed only in the M(3) and M(4) groups. The Tau4 mRNA levels were significantly increased as early as 1 month after ovariectomy (in the M(1) group; P<0.05), and tended to be increased further with the advancing time. Similarly, the Tau3 mRNA levels were increased by ovariectomy, but with the highest level in the M(1) group, and decreased thereafter. The mRNA levels of App, Adam10 and Bace1 were increased by ovariectomy, but significant differences were observed only in the M(4) group. These results indicate that estrogen deficiency can induce a sequence of events that results in the production of neurofibrillary tangles, amyloid deposition, and spatial memory deficit in rats.

摘要

本研究旨在描绘去卵巢大鼠雌激素缺乏、神经退行性变和认知障碍之间的关系。雌性 Sprague-Dawley 大鼠去卵巢,在 1-4 个月后处死(M(0)-M(4)组)。采集血样,测定血清 17β-雌二醇(E(2))、促黄体生成素(LH)和卵泡刺激素(FSH)水平。在处死前连续 5 天,通过 Morris 水迷宫试验检测大鼠的认知表现。处死大鼠后,采集海马,通过实时 PCR 检测与淀粉样斑块(App、Adam10 和 Bace1)和神经原纤维缠结(Tau4 和 Tau3)相关的基因表达。去卵巢 2 周后,血清 E(2)水平下降。相反,去卵巢 2 周后,血清 FSH 和 LH 水平分别显著增加约 4 倍和 22 倍。只有在 M(3)和 M(4)组中观察到认知障碍,表现为潜伏期和距离延长。去卵巢后 1 个月(M(1)组;P<0.05)Tau4 mRNA 水平显著增加,且随着时间的推移进一步增加。同样,Tau3 mRNA 水平也因去卵巢而增加,但在 M(1)组中水平最高,随后降低。去卵巢后 App、Adam10 和 Bace1 的 mRNA 水平增加,但仅在 M(4)组中观察到显著差异。这些结果表明,雌激素缺乏可引发一系列事件,导致大鼠产生神经原纤维缠结、淀粉样沉积和空间记忆缺陷。

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