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Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation

We investigated the neuroprotective effects of deca nano-graphene oxide (daNGO) against reactive oxygen species (ROS) and inflammation in the human neuroblastoma cell line SH-SY5Y and in the 6-hydroxydopamine (6-OHDA) induced Parkinsonian rat model. An MTT assay was performed to measure cell viabili...

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Autores principales: Kim, Hee-Yeong, Yoon, Hyung Ho, Seong, Hanyu, Seo, Dong Kwang, Choi, Soon Won, Ryu, Jaechul, Kang, Kyung-Sun, Jeon, Sang Ryong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068341/
https://www.ncbi.nlm.nih.gov/pubmed/36443003
http://dx.doi.org/10.5483/BMBRep.2022-0137
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author Kim, Hee-Yeong
Yoon, Hyung Ho
Seong, Hanyu
Seo, Dong Kwang
Choi, Soon Won
Ryu, Jaechul
Kang, Kyung-Sun
Jeon, Sang Ryong
author_facet Kim, Hee-Yeong
Yoon, Hyung Ho
Seong, Hanyu
Seo, Dong Kwang
Choi, Soon Won
Ryu, Jaechul
Kang, Kyung-Sun
Jeon, Sang Ryong
author_sort Kim, Hee-Yeong
collection PubMed
description We investigated the neuroprotective effects of deca nano-graphene oxide (daNGO) against reactive oxygen species (ROS) and inflammation in the human neuroblastoma cell line SH-SY5Y and in the 6-hydroxydopamine (6-OHDA) induced Parkinsonian rat model. An MTT assay was performed to measure cell viability in vitro in the presence of 6-OHDA and/or daNGO. The intracellular ROS level was quantified using 2’,7’-dichlorofluorescein diacetate. daNGO showed neuroprotective effects against 6-OHDA-induced toxicity and also displayed ROS scavenging properties. We then tested the protective effects of daNGO against 6-OHDA induced toxicity in a rat model. Stepping tests showed that the akinesia symptoms were improved in the daNGO group compared to the control group. Moreover, in an apomorphine-induced rotation test, the number of net contralateral rotations was decreased in the daNGO group compared to the control group. By immunofluorescent staining, the animals in the daNGO group had more tyrosine hydroxylase-positive cells than the controls. By anti-Iba1 staining, 6-OHDA induced microglial activation showed a significantly decrease in the daNGO group, indicating that the neuroprotective effects of graphene resulted from anti-inflammation. In conclusion, nano-graphene oxide has neuroprotective effects against the neurotoxin induced by 6-OHDA on dopaminergic neurons.
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spelling pubmed-100683412023-04-04 Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation Kim, Hee-Yeong Yoon, Hyung Ho Seong, Hanyu Seo, Dong Kwang Choi, Soon Won Ryu, Jaechul Kang, Kyung-Sun Jeon, Sang Ryong BMB Rep Article We investigated the neuroprotective effects of deca nano-graphene oxide (daNGO) against reactive oxygen species (ROS) and inflammation in the human neuroblastoma cell line SH-SY5Y and in the 6-hydroxydopamine (6-OHDA) induced Parkinsonian rat model. An MTT assay was performed to measure cell viability in vitro in the presence of 6-OHDA and/or daNGO. The intracellular ROS level was quantified using 2’,7’-dichlorofluorescein diacetate. daNGO showed neuroprotective effects against 6-OHDA-induced toxicity and also displayed ROS scavenging properties. We then tested the protective effects of daNGO against 6-OHDA induced toxicity in a rat model. Stepping tests showed that the akinesia symptoms were improved in the daNGO group compared to the control group. Moreover, in an apomorphine-induced rotation test, the number of net contralateral rotations was decreased in the daNGO group compared to the control group. By immunofluorescent staining, the animals in the daNGO group had more tyrosine hydroxylase-positive cells than the controls. By anti-Iba1 staining, 6-OHDA induced microglial activation showed a significantly decrease in the daNGO group, indicating that the neuroprotective effects of graphene resulted from anti-inflammation. In conclusion, nano-graphene oxide has neuroprotective effects against the neurotoxin induced by 6-OHDA on dopaminergic neurons. Korean Society for Biochemistry and Molecular Biology 2023-03-31 2023-02-02 /pmc/articles/PMC10068341/ /pubmed/36443003 http://dx.doi.org/10.5483/BMBRep.2022-0137 Text en Copyright © 2023 by the The Korean Society for Biochemistry and Molecular Biology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Kim, Hee-Yeong
Yoon, Hyung Ho
Seong, Hanyu
Seo, Dong Kwang
Choi, Soon Won
Ryu, Jaechul
Kang, Kyung-Sun
Jeon, Sang Ryong
Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
title Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
title_full Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
title_fullStr Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
title_full_unstemmed Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
title_short Preventive effects of nano-graphene oxide against Parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
title_sort preventive effects of nano-graphene oxide against parkinson’s disease via reactive oxygen species scavenging and anti-inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068341/
https://www.ncbi.nlm.nih.gov/pubmed/36443003
http://dx.doi.org/10.5483/BMBRep.2022-0137
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