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Nanonized black soybean enhances immune response in senescence-accelerated mice
Soy isoflavones may have applications in cancer prevention and anti-inflammation, therefore this study was conducted to investigate the effect of dietary supplementation with black soybean on the immune response in the senescence-accelerated-prone mice (SAMP8) and -resistant mice (SAMPR1, as control...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720740/ https://www.ncbi.nlm.nih.gov/pubmed/19421368 |
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author | Chan, Yin-Ching Wu, Chia-Chuan Chan, Kung-Chi Lin, Yo-Giao Liao, Jiunn-Wang Wang, Ming-Fu Chang, Yung-Ho Jeng, Kee-Ching |
author_facet | Chan, Yin-Ching Wu, Chia-Chuan Chan, Kung-Chi Lin, Yo-Giao Liao, Jiunn-Wang Wang, Ming-Fu Chang, Yung-Ho Jeng, Kee-Ching |
author_sort | Chan, Yin-Ching |
collection | PubMed |
description | Soy isoflavones may have applications in cancer prevention and anti-inflammation, therefore this study was conducted to investigate the effect of dietary supplementation with black soybean on the immune response in the senescence-accelerated-prone mice (SAMP8) and -resistant mice (SAMPR1, as controls). The mechanism of isoflavones was also investigated. Six-month-old male SAMP8 and SAMR1 mice were divided into the control groups and experimental groups supplemented with nanonized (Nano-soy) or microparticled (Micro-soy) black soybeans (n = 8/group), respectively for 12 weeks. Human peripheral blood mononuclear cells (PBMC) and murine splenocytes were stimulated with mitogens and cytokines were determined by reverse transcriptase-polymerase chain reaction and/or ELISA. The results showed that body weight, food intake, and relative weights of organs did not differ among the SAMP8 control and experimental groups. Isoflavone (daidzin and genistin) intake was higher in the Nano-soy group than the Micro-soy group. The lymphoproliferation and production of interleukin-2 (IL-2) and interferon-gamma (IFN-γ) in the Nano-soy group had a significantly higher (P < 0.05) than those in the control and Micro-soy groups. The Nano-soy supplemented mice reached these cytokine levels similar to SAMR1 mice. This result was consistent with the in vitro data that daidzein (a metabolite of daidzin), at a concentration of 10 μM, increased IL-2, IL-4, and IFN-γ production from phytohemagglutinin-stimulated PBMC (P < 0.05). However at higher concentrations (> 50 μM), daidzein only reduced IL-10 and IFN-γ levels, whereas genistein reduced levels of the IL-2, IL-4, IL-10, IFN-γ mRNA and protein and these results suggest that the Nano-soy supplementation improved immune response in SAMP8 mice which may be attributable to higher daidzin content in the black soybean preparation. |
format | Text |
id | pubmed-2720740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27207402009-08-31 Nanonized black soybean enhances immune response in senescence-accelerated mice Chan, Yin-Ching Wu, Chia-Chuan Chan, Kung-Chi Lin, Yo-Giao Liao, Jiunn-Wang Wang, Ming-Fu Chang, Yung-Ho Jeng, Kee-Ching Int J Nanomedicine Original Research Soy isoflavones may have applications in cancer prevention and anti-inflammation, therefore this study was conducted to investigate the effect of dietary supplementation with black soybean on the immune response in the senescence-accelerated-prone mice (SAMP8) and -resistant mice (SAMPR1, as controls). The mechanism of isoflavones was also investigated. Six-month-old male SAMP8 and SAMR1 mice were divided into the control groups and experimental groups supplemented with nanonized (Nano-soy) or microparticled (Micro-soy) black soybeans (n = 8/group), respectively for 12 weeks. Human peripheral blood mononuclear cells (PBMC) and murine splenocytes were stimulated with mitogens and cytokines were determined by reverse transcriptase-polymerase chain reaction and/or ELISA. The results showed that body weight, food intake, and relative weights of organs did not differ among the SAMP8 control and experimental groups. Isoflavone (daidzin and genistin) intake was higher in the Nano-soy group than the Micro-soy group. The lymphoproliferation and production of interleukin-2 (IL-2) and interferon-gamma (IFN-γ) in the Nano-soy group had a significantly higher (P < 0.05) than those in the control and Micro-soy groups. The Nano-soy supplemented mice reached these cytokine levels similar to SAMR1 mice. This result was consistent with the in vitro data that daidzein (a metabolite of daidzin), at a concentration of 10 μM, increased IL-2, IL-4, and IFN-γ production from phytohemagglutinin-stimulated PBMC (P < 0.05). However at higher concentrations (> 50 μM), daidzein only reduced IL-10 and IFN-γ levels, whereas genistein reduced levels of the IL-2, IL-4, IL-10, IFN-γ mRNA and protein and these results suggest that the Nano-soy supplementation improved immune response in SAMP8 mice which may be attributable to higher daidzin content in the black soybean preparation. Dove Medical Press 2009 2009-04-01 /pmc/articles/PMC2720740/ /pubmed/19421368 Text en © 2009 Dove Medical Press Limited. All rights reserved |
spellingShingle | Original Research Chan, Yin-Ching Wu, Chia-Chuan Chan, Kung-Chi Lin, Yo-Giao Liao, Jiunn-Wang Wang, Ming-Fu Chang, Yung-Ho Jeng, Kee-Ching Nanonized black soybean enhances immune response in senescence-accelerated mice |
title | Nanonized black soybean enhances immune response in senescence-accelerated mice |
title_full | Nanonized black soybean enhances immune response in senescence-accelerated mice |
title_fullStr | Nanonized black soybean enhances immune response in senescence-accelerated mice |
title_full_unstemmed | Nanonized black soybean enhances immune response in senescence-accelerated mice |
title_short | Nanonized black soybean enhances immune response in senescence-accelerated mice |
title_sort | nanonized black soybean enhances immune response in senescence-accelerated mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720740/ https://www.ncbi.nlm.nih.gov/pubmed/19421368 |
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