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猪黏膜来源的硫酸乙酰肝素促进 APP/PS1 小鼠的淀粉样β清除,并减轻阿尔茨海默病病理。

Heparan sulfate from porcine mucosa promotes amyloid-beta clearance in APP/PS1 mice and alleviates Alzheimer's pathology.

机构信息

Key Laboratory of Chemical Biology (Ministry of Education), Institute of Biochemical and Biotechnological Drugs, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, Shandong, China.

Key Laboratory of Chemical Biology (Ministry of Education), Institute of Biochemical and Biotechnological Drugs, School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, Shandong, China; NMPA Key Laboratory for Quality Research and Evaluation of Carbohydrate-based Medicine, National Glycoengineering Research Center, Shandong University, Jinan 250012, Shandong, China; Shandong Provincial Key Laboratory of Carbohydrate Chemistry and Glycobiology, Shandong University, Jinan 250012, China.

出版信息

Carbohydr Polym. 2022 Jun 1;285:119205. doi: 10.1016/j.carbpol.2022.119205. Epub 2022 Feb 7.

Abstract

Alzheimer's disease (AD) is a neurodegenerative disease characterized by memory loss and cognitive impairments. Amyloid-β (Aβ) deposition and neurotoxicity play important roles in AD. It has been widely reported that heparan sulfate (HS) proteoglycans play a nonnegligible role in the release, uptake and misfolding of Aβ, resulting in the discovery of HS as a therapeutic drug for AD. In this manuscript, HS from porcine mucosa could promote Aβ fibrosis and improve the cognitive defects of APPswe/PS1ΔE9 mice. Furthermore, HS enhanced the phagocytosis of neutrophils to clear Aβ from peripheral circulation, reduced peripheral Aβ flow to the brain and increased Aβ efflux from the brain. Therefore, the deposition of Aβ plaques in the brain was decreased. In addition, HS alleviated neutrophil infiltration and reduced neuroinflammation. Conclusively, HS is a promising neuroprotective candidate for AD treatment.

摘要

阿尔茨海默病(AD)是一种以记忆丧失和认知障碍为特征的神经退行性疾病。淀粉样蛋白-β(Aβ)沉积和神经毒性在 AD 中起着重要作用。有广泛报道称,硫酸乙酰肝素(HS)蛋白聚糖在 Aβ 的释放、摄取和错误折叠中发挥着不可忽视的作用,这导致 HS 被发现为 AD 的一种治疗药物。在本手稿中,来自猪黏膜的 HS 可促进 Aβ 纤维化,并改善 APPswe/PS1ΔE9 小鼠的认知缺陷。此外,HS 增强了中性粒细胞的吞噬作用,以清除外周循环中的 Aβ,减少外周 Aβ 向大脑的流动,并增加 Aβ 从大脑的流出。因此,大脑中 Aβ 斑块的沉积减少了。此外,HS 减轻了中性粒细胞浸润并减少了神经炎症。总之,HS 是一种很有前途的 AD 治疗神经保护候选药物。

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