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ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters

[Image: see text] Depression is one of the most fatal mental diseases, and there is currently a lack of efficient drugs for the treatment of depression. Emerging evidence has indicated oxidative stress as a key pathological feature of depression. We targeted reactive oxygen species (ROS) and synthes...

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Autores principales: Fu, Shengyang, Chen, Huili, Yang, Weitao, Xia, Xiaohuan, Zhao, Shu, Xu, Xiaonan, Ai, Pu, Cai, Qingyuan, Li, Xiangyu, Wang, Yi, Zhu, Jie, Zhang, Bingbo, Zheng, Jialin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185743/
https://www.ncbi.nlm.nih.gov/pubmed/35583518
http://dx.doi.org/10.1021/acs.nanolett.2c01334
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author Fu, Shengyang
Chen, Huili
Yang, Weitao
Xia, Xiaohuan
Zhao, Shu
Xu, Xiaonan
Ai, Pu
Cai, Qingyuan
Li, Xiangyu
Wang, Yi
Zhu, Jie
Zhang, Bingbo
Zheng, Jialin C.
author_facet Fu, Shengyang
Chen, Huili
Yang, Weitao
Xia, Xiaohuan
Zhao, Shu
Xu, Xiaonan
Ai, Pu
Cai, Qingyuan
Li, Xiangyu
Wang, Yi
Zhu, Jie
Zhang, Bingbo
Zheng, Jialin C.
author_sort Fu, Shengyang
collection PubMed
description [Image: see text] Depression is one of the most fatal mental diseases, and there is currently a lack of efficient drugs for the treatment of depression. Emerging evidence has indicated oxidative stress as a key pathological feature of depression. We targeted reactive oxygen species (ROS) and synthesized CeO(2)@BSA nanoclusters as a novel antidepression nanodrug via a convenient, green, and highly effective bovine serum albumin (BSA) incubation strategy. CeO(2)@BSA has ultrasmall size (2 nm) with outstanding ROS scavenging and blood-brain barrier crossing capacity, rapid metabolism, and negligible adverse effects in vitro and in vivo. CeO(2)@BSA administration alleviates depressive behaviors and depression-related pathological changes of the chronic restraint stress-induced depressive model, suggesting promising therapeutic effects of CeO(2)@BSA for the treatment of depression. Our study proved the validity by directly using nanodrugs as antidepression drugs instead of using them as a nanocarrier, which greatly expands the application of nanomaterials in depression treatment.
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spelling pubmed-91857432022-06-11 ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters Fu, Shengyang Chen, Huili Yang, Weitao Xia, Xiaohuan Zhao, Shu Xu, Xiaonan Ai, Pu Cai, Qingyuan Li, Xiangyu Wang, Yi Zhu, Jie Zhang, Bingbo Zheng, Jialin C. Nano Lett [Image: see text] Depression is one of the most fatal mental diseases, and there is currently a lack of efficient drugs for the treatment of depression. Emerging evidence has indicated oxidative stress as a key pathological feature of depression. We targeted reactive oxygen species (ROS) and synthesized CeO(2)@BSA nanoclusters as a novel antidepression nanodrug via a convenient, green, and highly effective bovine serum albumin (BSA) incubation strategy. CeO(2)@BSA has ultrasmall size (2 nm) with outstanding ROS scavenging and blood-brain barrier crossing capacity, rapid metabolism, and negligible adverse effects in vitro and in vivo. CeO(2)@BSA administration alleviates depressive behaviors and depression-related pathological changes of the chronic restraint stress-induced depressive model, suggesting promising therapeutic effects of CeO(2)@BSA for the treatment of depression. Our study proved the validity by directly using nanodrugs as antidepression drugs instead of using them as a nanocarrier, which greatly expands the application of nanomaterials in depression treatment. American Chemical Society 2022-05-18 2022-06-08 /pmc/articles/PMC9185743/ /pubmed/35583518 http://dx.doi.org/10.1021/acs.nanolett.2c01334 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Fu, Shengyang
Chen, Huili
Yang, Weitao
Xia, Xiaohuan
Zhao, Shu
Xu, Xiaonan
Ai, Pu
Cai, Qingyuan
Li, Xiangyu
Wang, Yi
Zhu, Jie
Zhang, Bingbo
Zheng, Jialin C.
ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters
title ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters
title_full ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters
title_fullStr ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters
title_full_unstemmed ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters
title_short ROS-Targeted Depression Therapy via BSA-Incubated Ceria Nanoclusters
title_sort ros-targeted depression therapy via bsa-incubated ceria nanoclusters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185743/
https://www.ncbi.nlm.nih.gov/pubmed/35583518
http://dx.doi.org/10.1021/acs.nanolett.2c01334
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