Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease

Abstract The present study aimed to assess whether our newly developed redox nanoparticle (RNPN) that has antioxidant potential decreases Aβ levels or prevents Aβ aggregation associated with oxidative stress. The transgenic Tg2576 Alzheimer’s disease (AD) mice were used to investigate the effect of...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Phetcharat Boonruamkaew, Pennapa Chonpathompikunlert, Long Binh Vong, Sho Sakaue, Yasushi Tomidokoro, Kazuhiro Ishii, Akira Tamaoka, Yukio Nagasaki
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/19f1d06e64ea4430ba9e11162baa235a
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:19f1d06e64ea4430ba9e11162baa235a
record_format dspace
spelling oai:doaj.org-article:19f1d06e64ea4430ba9e11162baa235a2021-12-02T16:06:11ZChronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease10.1038/s41598-017-03411-72045-2322https://doaj.org/article/19f1d06e64ea4430ba9e11162baa235a2017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-03411-7https://doaj.org/toc/2045-2322Abstract The present study aimed to assess whether our newly developed redox nanoparticle (RNPN) that has antioxidant potential decreases Aβ levels or prevents Aβ aggregation associated with oxidative stress. The transgenic Tg2576 Alzheimer’s disease (AD) mice were used to investigate the effect of chronic ad libitum drinking of RNPN solution for 6 months, including memory and learning functions, antioxidant activity, and amyloid plaque aggregation. The results showed that RNPN-treated mice had significantly attenuated cognitive deficits of both spatial and non-spatial memories, reduced oxidative stress of lipid peroxide, and DNA oxidation. RNPN treatment increased the percent inhibition of superoxide anion and glutathione peroxidase activity, neuronal densities in the cortex and hippocampus, decreased Aβ(1-40), Aβ(1-42) and gamma (γ)-secretase levels, and reduced Aβ plaque observed using immunohistochemistry analysis and thioflavin S staining. Our results suggest that RNPN may be a promising candidate for AD therapy because of its antioxidant properties and reduction in Aβ aggregation, thereby suppressing its adverse side effect.Phetcharat BoonruamkaewPennapa ChonpathompikunlertLong Binh VongSho SakaueYasushi TomidokoroKazuhiro IshiiAkira TamaokaYukio NagasakiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Phetcharat Boonruamkaew
Pennapa Chonpathompikunlert
Long Binh Vong
Sho Sakaue
Yasushi Tomidokoro
Kazuhiro Ishii
Akira Tamaoka
Yukio Nagasaki
Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease
description Abstract The present study aimed to assess whether our newly developed redox nanoparticle (RNPN) that has antioxidant potential decreases Aβ levels or prevents Aβ aggregation associated with oxidative stress. The transgenic Tg2576 Alzheimer’s disease (AD) mice were used to investigate the effect of chronic ad libitum drinking of RNPN solution for 6 months, including memory and learning functions, antioxidant activity, and amyloid plaque aggregation. The results showed that RNPN-treated mice had significantly attenuated cognitive deficits of both spatial and non-spatial memories, reduced oxidative stress of lipid peroxide, and DNA oxidation. RNPN treatment increased the percent inhibition of superoxide anion and glutathione peroxidase activity, neuronal densities in the cortex and hippocampus, decreased Aβ(1-40), Aβ(1-42) and gamma (γ)-secretase levels, and reduced Aβ plaque observed using immunohistochemistry analysis and thioflavin S staining. Our results suggest that RNPN may be a promising candidate for AD therapy because of its antioxidant properties and reduction in Aβ aggregation, thereby suppressing its adverse side effect.
format article
author Phetcharat Boonruamkaew
Pennapa Chonpathompikunlert
Long Binh Vong
Sho Sakaue
Yasushi Tomidokoro
Kazuhiro Ishii
Akira Tamaoka
Yukio Nagasaki
author_facet Phetcharat Boonruamkaew
Pennapa Chonpathompikunlert
Long Binh Vong
Sho Sakaue
Yasushi Tomidokoro
Kazuhiro Ishii
Akira Tamaoka
Yukio Nagasaki
author_sort Phetcharat Boonruamkaew
title Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease
title_short Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease
title_full Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease
title_fullStr Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease
title_full_unstemmed Chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in Tg2576 mouse model of Alzheimer’s disease
title_sort chronic treatment with a smart antioxidative nanoparticle for inhibition of amyloid plaque propagation in tg2576 mouse model of alzheimer’s disease
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/19f1d06e64ea4430ba9e11162baa235a
work_keys_str_mv AT phetcharatboonruamkaew chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT pennapachonpathompikunlert chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT longbinhvong chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT shosakaue chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT yasushitomidokoro chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT kazuhiroishii chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT akiratamaoka chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
AT yukionagasaki chronictreatmentwithasmartantioxidativenanoparticleforinhibitionofamyloidplaquepropagationintg2576mousemodelofalzheimersdisease
_version_ 1718385072945496064