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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9185743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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