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Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet
Obesity causes adipocyte hypertrophy, which leads to cell death. Consequently, macrophages and lymphocytes infiltrate into the adipose tissue and elevate pro-inflammatory cytokine production through TLR activation. This study aimed to determine the efficacy of soybean extract, which was elicited by...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Polish Society of Experimental and Clinical Immunology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526585/ https://www.ncbi.nlm.nih.gov/pubmed/31114431 http://dx.doi.org/10.5114/ceji.2019.84010 |
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author | Nur’aini, Farida D. Rahayu, Sri Rifa’i, Muhaimin |
author_facet | Nur’aini, Farida D. Rahayu, Sri Rifa’i, Muhaimin |
author_sort | Nur’aini, Farida D. |
collection | PubMed |
description | Obesity causes adipocyte hypertrophy, which leads to cell death. Consequently, macrophages and lymphocytes infiltrate into the adipose tissue and elevate pro-inflammatory cytokine production through TLR activation. This study aimed to determine the efficacy of soybean extract, which was elicited by Saccharomyces cerevisiae and light, as an anti-inflammatory agent in mice with a high-fat and -fructose diet (HFFD). The elicited soybean extract (ESE) was administered orally to mice for four weeks after being given an HFFD for 20 weeks. Three different doses were used: (1) low-dose (78 mg/kg BW); (2) normal dose (104 mg/kg BW); and (3) high dose (130 mg/kg BW). HFFD mice model treated with simvastatin 2.8 mg/kg BW considered as drug control. After 24 weeks, the lymphocytes were isolated and the relative number of CD4(+)TLR3(+) T, CD4(+)TLR4(+) T, CD4(+)TNF-α(+) T, and CD4(+)IFN-γ(+) T cells were analysed using flow cytometry. The results showed that the HFFD mouse model had an increased number of CD4(+)TLR3(+) T, CD4(+)TLR4(+) T, CD4(+)TNF-α(+) T, and CD4(+)IFN-γ(+) T cells. ESE administration decreased the relative number of CD4(+)TLR3(+) T, CD4(+)TLR4(+) T, CD4(+)TNF-α(+) T, and CD4(+)IFN-γ(+) T cells. The normal dose of ESE is the most effective dose in suppressing inflammation compared to positive controls. ESE 104 mg/kg BW can be considered as an alternative herbal medicine that may suppress inflammation in HFFD mice. |
format | Online Article Text |
id | pubmed-6526585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Polish Society of Experimental and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65265852019-05-21 Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet Nur’aini, Farida D. Rahayu, Sri Rifa’i, Muhaimin Cent Eur J Immunol Experimental Immunology Obesity causes adipocyte hypertrophy, which leads to cell death. Consequently, macrophages and lymphocytes infiltrate into the adipose tissue and elevate pro-inflammatory cytokine production through TLR activation. This study aimed to determine the efficacy of soybean extract, which was elicited by Saccharomyces cerevisiae and light, as an anti-inflammatory agent in mice with a high-fat and -fructose diet (HFFD). The elicited soybean extract (ESE) was administered orally to mice for four weeks after being given an HFFD for 20 weeks. Three different doses were used: (1) low-dose (78 mg/kg BW); (2) normal dose (104 mg/kg BW); and (3) high dose (130 mg/kg BW). HFFD mice model treated with simvastatin 2.8 mg/kg BW considered as drug control. After 24 weeks, the lymphocytes were isolated and the relative number of CD4(+)TLR3(+) T, CD4(+)TLR4(+) T, CD4(+)TNF-α(+) T, and CD4(+)IFN-γ(+) T cells were analysed using flow cytometry. The results showed that the HFFD mouse model had an increased number of CD4(+)TLR3(+) T, CD4(+)TLR4(+) T, CD4(+)TNF-α(+) T, and CD4(+)IFN-γ(+) T cells. ESE administration decreased the relative number of CD4(+)TLR3(+) T, CD4(+)TLR4(+) T, CD4(+)TNF-α(+) T, and CD4(+)IFN-γ(+) T cells. The normal dose of ESE is the most effective dose in suppressing inflammation compared to positive controls. ESE 104 mg/kg BW can be considered as an alternative herbal medicine that may suppress inflammation in HFFD mice. Polish Society of Experimental and Clinical Immunology 2019-04-15 2019 /pmc/articles/PMC6526585/ /pubmed/31114431 http://dx.doi.org/10.5114/ceji.2019.84010 Text en Copyright: © 2019 Polish Society of Experimental and Clinical Immunology http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Experimental Immunology Nur’aini, Farida D. Rahayu, Sri Rifa’i, Muhaimin Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet |
title | Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet |
title_full | Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet |
title_fullStr | Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet |
title_full_unstemmed | Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet |
title_short | Anti-inflammatory activity of elicited soybean (Glycine max) extract on Balb/C mice (Mus musculus) with high-fat and -fructose diet |
title_sort | anti-inflammatory activity of elicited soybean (glycine max) extract on balb/c mice (mus musculus) with high-fat and -fructose diet |
topic | Experimental Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526585/ https://www.ncbi.nlm.nih.gov/pubmed/31114431 http://dx.doi.org/10.5114/ceji.2019.84010 |
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