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Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice
Alzheimer’s disease (AD) is the most common form of dementia among older people. Although soluble amyloid species are recognized triggers of the disease, no therapeutic approach is able to stop it. 6-(Methylsulfinyl)hexyl isothiocyanate (6-MSITC) is a major bioactive compound in Wasabia japonica, wh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073905/ https://www.ncbi.nlm.nih.gov/pubmed/30021941 http://dx.doi.org/10.3390/ijms19072083 |
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author | Morroni, Fabiana Sita, Giulia Graziosi, Agnese Turrini, Eleonora Fimognari, Carmela Tarozzi, Andrea Hrelia, Patrizia |
author_facet | Morroni, Fabiana Sita, Giulia Graziosi, Agnese Turrini, Eleonora Fimognari, Carmela Tarozzi, Andrea Hrelia, Patrizia |
author_sort | Morroni, Fabiana |
collection | PubMed |
description | Alzheimer’s disease (AD) is the most common form of dementia among older people. Although soluble amyloid species are recognized triggers of the disease, no therapeutic approach is able to stop it. 6-(Methylsulfinyl)hexyl isothiocyanate (6-MSITC) is a major bioactive compound in Wasabia japonica, which is a typical Japanese pungent spice. Recently, in vivo and in vitro studies demonstrated that 6-MSITC has several biological properties. The aim of the present study was to investigate the neuroprotective activity of 6-MSITC in a murine AD model, induced by intracerebroventricular injection of β-amyloid oligomers (Aβ(1-42)O). The treatment with 6-MSITC started 1 h after the surgery for the next 10 days. Behavioral analysis showed that 6-MSITC ameliorated Aβ(1-42)O-induced memory impairments. The decrease of glutathione levels and increase of reactive oxygen species in hippocampal tissues following Aβ(1-42)O injection were reduced by 6-MSITC. Moreover, activation of caspases, increase of inflammatory factors, and phosphorylation of ERK and GSK3 were inhibited by 6-MSITC. These results highlighted an interesting neuroprotective activity of 6-MSITC, which was able to restore a physiological oxidative status, interfere positively with Nrf2-pathway, decrease apoptosis and neuroinflammation and contribute to behavioral recovery. Taken together, these findings demonstrated that 6-MSITC could be a promising complement for AD therapy. |
format | Online Article Text |
id | pubmed-6073905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60739052018-08-13 Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice Morroni, Fabiana Sita, Giulia Graziosi, Agnese Turrini, Eleonora Fimognari, Carmela Tarozzi, Andrea Hrelia, Patrizia Int J Mol Sci Article Alzheimer’s disease (AD) is the most common form of dementia among older people. Although soluble amyloid species are recognized triggers of the disease, no therapeutic approach is able to stop it. 6-(Methylsulfinyl)hexyl isothiocyanate (6-MSITC) is a major bioactive compound in Wasabia japonica, which is a typical Japanese pungent spice. Recently, in vivo and in vitro studies demonstrated that 6-MSITC has several biological properties. The aim of the present study was to investigate the neuroprotective activity of 6-MSITC in a murine AD model, induced by intracerebroventricular injection of β-amyloid oligomers (Aβ(1-42)O). The treatment with 6-MSITC started 1 h after the surgery for the next 10 days. Behavioral analysis showed that 6-MSITC ameliorated Aβ(1-42)O-induced memory impairments. The decrease of glutathione levels and increase of reactive oxygen species in hippocampal tissues following Aβ(1-42)O injection were reduced by 6-MSITC. Moreover, activation of caspases, increase of inflammatory factors, and phosphorylation of ERK and GSK3 were inhibited by 6-MSITC. These results highlighted an interesting neuroprotective activity of 6-MSITC, which was able to restore a physiological oxidative status, interfere positively with Nrf2-pathway, decrease apoptosis and neuroinflammation and contribute to behavioral recovery. Taken together, these findings demonstrated that 6-MSITC could be a promising complement for AD therapy. MDPI 2018-07-18 /pmc/articles/PMC6073905/ /pubmed/30021941 http://dx.doi.org/10.3390/ijms19072083 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Morroni, Fabiana Sita, Giulia Graziosi, Agnese Turrini, Eleonora Fimognari, Carmela Tarozzi, Andrea Hrelia, Patrizia Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice |
title | Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice |
title_full | Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice |
title_fullStr | Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice |
title_full_unstemmed | Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice |
title_short | Protective Effects of 6-(Methylsulfinyl)hexyl Isothiocyanate on Aβ(1-42)-Induced Cognitive Deficit, Oxidative Stress, Inflammation, and Apoptosis in Mice |
title_sort | protective effects of 6-(methylsulfinyl)hexyl isothiocyanate on aβ(1-42)-induced cognitive deficit, oxidative stress, inflammation, and apoptosis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073905/ https://www.ncbi.nlm.nih.gov/pubmed/30021941 http://dx.doi.org/10.3390/ijms19072083 |
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