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一种用于近红外驱动氢释放以抑制阿尔茨海默病治疗中tau蛋白病的仿生上转换纳米反应器。

A biomimetic upconversion nanoreactors for near-infrared driven H release to inhibit tauopathy in Alzheimer's disease therapy.

作者信息

Zhang Qin, Li Chuanqi, Yin Bohan, Yan Jiaxiang, Gu Yutian, Huang Yingying, Chen Jiareng, Lao Xinyue, Hao Jianhua, Yi Changqing, Zhou Yi, Cheung James Chung Wai, Wong Siu Hong Dexter, Yang Mo

机构信息

Department of Biomedical Engineering, The Hong Kong Polytechnic University, 999077, Hong Kong, China.

The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen, 518000, China.

出版信息

Bioact Mater. 2024 Aug 30;42:165-177. doi: 10.1016/j.bioactmat.2024.08.029. eCollection 2024 Dec.

Abstract

Abnormal hyperphosphorylation of tau protein is a principal pathological hallmark in the onset of neurodegenerative disorders, such as Alzheimer's disease (AD), which can be induced by an excess of reactive oxygen species (ROS). As an antioxidant, hydrogen gas (H) has the potential to mitigate AD by scavenging highly harmful ROS such as •OH. However, conventional administration methods of H face significant challenges in controlling H release on demand and fail to achieve effective accumulation at lesion sites. Herein, we report artificial nanoreactors that mimic natural photosynthesis to realize near-infrared (NIR) light-driven photocatalytic H evolution in situ. The nanoreactors are constructed by biocompatible crosslinked vesicles (CVs) encapsulating ascorbic acid and two photosensitizers, chlorophyll (Chl) and indoline dye (Ind). In addition, platinum nanoparticles (Pt NPs) serve as photocatalysts and upconversion nanoparticles (UCNP) act as light-harvesting antennas in the nanoreacting system, and both attach to the surface of CVs. Under NIR irradiation, the nanoreactors release H in situ to scavenge local excess ROS and attenuate tau hyperphosphorylation in the AD mice model. Such NIR-triggered nanoreactors provide a proof-of-concept design for the great potential of hydrogen therapy against AD.

摘要

tau蛋白的异常过度磷酸化是神经退行性疾病(如阿尔茨海默病(AD))发病的主要病理标志,其可由过量的活性氧(ROS)诱导产生。作为一种抗氧化剂,氢气(H₂)有潜力通过清除高度有害的ROS(如•OH)来减轻AD症状。然而,传统的H₂给药方法在按需控制H₂释放方面面临重大挑战,并且无法在病变部位实现有效富集。在此,我们报道了一种人工纳米反应器,其模仿自然光合作用以实现近红外(NIR)光驱动的原位光催化产氢。该纳米反应器由包裹抗坏血酸以及两种光敏剂(叶绿素(Chl)和吲哚啉染料(Ind))的生物相容性交联囊泡(CVs)构建而成。此外,铂纳米颗粒(Pt NPs)作为光催化剂,上转换纳米颗粒(UCNP)在纳米反应体系中充当光捕获天线,二者均附着于CVs表面。在近红外辐射下,纳米反应器原位释放H₂以清除局部过量的ROS,并减轻AD小鼠模型中的tau过度磷酸化。这种近红外触发的纳米反应器为氢疗法治疗AD的巨大潜力提供了概念验证设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa1e/11402069/fbf4d7c90072/ga1.jpg

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