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多奈哌齐改善 5xFAD 小鼠的淀粉样β病理但不改善 tau 病理。

Donepezil ameliorates Aβ pathology but not tau pathology in 5xFAD mice.

机构信息

Department of Neural Development and Disease, Korea Brain Research Institute (KBRI), 61, Cheomdan-ro, Dong-gu, 41068, Daegu, Republic of Korea.

Department of Brain Sciences, Daegu Gyeongbuk Institute of Science & Technology, 42988, Daegu, Korea.

出版信息

Mol Brain. 2022 Jul 18;15(1):63. doi: 10.1186/s13041-022-00948-1.

Abstract

The cholinesterase inhibitor donepezil is used to improve Aβ pathology and cognitive function in patients with Alzheimer's disease (AD). However, the impact of donepezil on tau pathology is unclear. Thus, we examined the effects of donepezil on Aβ and tau pathology in 5xFAD mice (a model of AD) in this study. We found that intraperitoneal injection of donepezil (1 mg/kg, i.p.) exhibited significant reductions in Aβ plaque number in the cortex and hippocampal DG region. In addition, donepezil treatment (1 mg/kg, i.p.) reduced Aβ-mediated microglial and, to a lesser extent, astrocytic activation in 5xFAD mice. However, neither intraperitoneal/oral injection of donepezil nor oral injection of rivastigmine altered tau phosphorylation at Thr212/Ser214 (AT100), Thr396, and Thr231 in 5xFAD mice. Surprisingly, we observed that intraperitoneal/oral injection of donepezil treatment significantly increased tau phosphorylation at Thr212 in 5xFAD mice. Taken together, these data suggest that intraperitoneal injection of donepezil suppresses Aβ pathology but not tau pathology in 5xFAD mice.

摘要

胆碱酯酶抑制剂多奈哌齐用于改善阿尔茨海默病(AD)患者的 Aβ 病理学和认知功能。然而,多奈哌齐对 tau 病理学的影响尚不清楚。因此,本研究在 5xFAD 小鼠(AD 模型)中研究了多奈哌齐对 Aβ 和 tau 病理学的影响。我们发现,腹腔内注射多奈哌齐(1mg/kg,ip)可显著减少皮质和海马 DG 区的 Aβ 斑块数量。此外,多奈哌齐治疗(1mg/kg,ip)可减少 5xFAD 小鼠中 Aβ 介导的小胶质细胞激活,在一定程度上减少星形胶质细胞激活。然而,无论腹腔内/口服给予多奈哌齐还是口服给予利斯的明,都不能改变 5xFAD 小鼠中 tau 的 Thr212/Ser214(AT100)、Thr396 和 Thr231 磷酸化。令人惊讶的是,我们观察到腹腔内/口服给予多奈哌齐治疗可显著增加 5xFAD 小鼠中 tau 的 Thr212 磷酸化。总之,这些数据表明,腹腔内注射多奈哌齐可抑制 5xFAD 小鼠的 Aβ 病理学,但不能抑制 tau 病理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f23f/9290238/59d6bcbab265/13041_2022_948_Fig1_HTML.jpg

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