Cargando…

Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease

Chronic airway inflammation and airway remodeling are the major pathophysiological characteristics of chronic obstructive pulmonary disease (COPD). Resveratrol and genistein have been previously demonstrated to have anti-inflammatory and antioxidative properties. The present study aimed to measure t...

Descripción completa

Detalles Bibliográficos
Autores principales: LIU, XIAO-JU, BAO, HAI-RONG, ZENG, XIAO-LI, WEI, JUN-MING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838123/
https://www.ncbi.nlm.nih.gov/pubmed/27035424
http://dx.doi.org/10.3892/mmr.2016.5057
_version_ 1782427940076650496
author LIU, XIAO-JU
BAO, HAI-RONG
ZENG, XIAO-LI
WEI, JUN-MING
author_facet LIU, XIAO-JU
BAO, HAI-RONG
ZENG, XIAO-LI
WEI, JUN-MING
author_sort LIU, XIAO-JU
collection PubMed
description Chronic airway inflammation and airway remodeling are the major pathophysiological characteristics of chronic obstructive pulmonary disease (COPD). Resveratrol and genistein have been previously demonstrated to have anti-inflammatory and antioxidative properties. The present study aimed to measure the inhibitory effects of resveratrol and genistein on tumor necrosis factor (TNF)-α and matrix metalloproteinase (MMP)-9 concentration in patients with COPD. Lymphocytes were isolated from the blood of 34 patients with COPD and 30 healthy subjects, then randomly divided into the following four treatment groups: Control, dexamethasone (0.5 µmol/l), resveratrol (12.5 µmol/l) and genistein (25 µmol/l) groups. After 1 h of treatment, 100 µl lymphocytes were collected for nuclear factor (NF)-κB immunocytochemical staining. After 48 h treatment, the supernatant of the lymphocytes was collected for analysis of TNF-α and MMP-9 concentration levels. The percentage of lymphocytes with positive nuclear NF-κB expression was analyzed by immunocytochemical staining. The concentration levels of TNF-α and MMP-9 were measured using radioimmunoassay and enzyme-linked immunosorbent assay, respectively. The present study demonstrated that the percentage of NF-κB-positive cells, and the levels of TNF-α and MMP-9 in lymphocytes from patients with COPD patients were significantly higher compared with healthy subjects. Additionally, there were positive correlations between the percentage of NF-κB-positive cells, and the concentration levels of TNF-α and MMP-9 in patients with COPD. All three factors were significantly reduced in lymphocytes treated with resveratrol and genistein, and the inhibitory effects of resveratrol on NF-κB, TNF-α and MMP-9 were more potent than the effects of genistein. In conclusion, resveratrol and genistein may inhibit the NF-κB, TNF-α and MMP-9-associated pathways in patients with COPD. It is suggested that resveratrol and genistein may be potential drugs candidates for use in the treatment of COPD.
format Online
Article
Text
id pubmed-4838123
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-48381232016-04-21 Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease LIU, XIAO-JU BAO, HAI-RONG ZENG, XIAO-LI WEI, JUN-MING Mol Med Rep Articles Chronic airway inflammation and airway remodeling are the major pathophysiological characteristics of chronic obstructive pulmonary disease (COPD). Resveratrol and genistein have been previously demonstrated to have anti-inflammatory and antioxidative properties. The present study aimed to measure the inhibitory effects of resveratrol and genistein on tumor necrosis factor (TNF)-α and matrix metalloproteinase (MMP)-9 concentration in patients with COPD. Lymphocytes were isolated from the blood of 34 patients with COPD and 30 healthy subjects, then randomly divided into the following four treatment groups: Control, dexamethasone (0.5 µmol/l), resveratrol (12.5 µmol/l) and genistein (25 µmol/l) groups. After 1 h of treatment, 100 µl lymphocytes were collected for nuclear factor (NF)-κB immunocytochemical staining. After 48 h treatment, the supernatant of the lymphocytes was collected for analysis of TNF-α and MMP-9 concentration levels. The percentage of lymphocytes with positive nuclear NF-κB expression was analyzed by immunocytochemical staining. The concentration levels of TNF-α and MMP-9 were measured using radioimmunoassay and enzyme-linked immunosorbent assay, respectively. The present study demonstrated that the percentage of NF-κB-positive cells, and the levels of TNF-α and MMP-9 in lymphocytes from patients with COPD patients were significantly higher compared with healthy subjects. Additionally, there were positive correlations between the percentage of NF-κB-positive cells, and the concentration levels of TNF-α and MMP-9 in patients with COPD. All three factors were significantly reduced in lymphocytes treated with resveratrol and genistein, and the inhibitory effects of resveratrol on NF-κB, TNF-α and MMP-9 were more potent than the effects of genistein. In conclusion, resveratrol and genistein may inhibit the NF-κB, TNF-α and MMP-9-associated pathways in patients with COPD. It is suggested that resveratrol and genistein may be potential drugs candidates for use in the treatment of COPD. D.A. Spandidos 2016-05 2016-03-28 /pmc/articles/PMC4838123/ /pubmed/27035424 http://dx.doi.org/10.3892/mmr.2016.5057 Text en Copyright: © Liu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
LIU, XIAO-JU
BAO, HAI-RONG
ZENG, XIAO-LI
WEI, JUN-MING
Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
title Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
title_full Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
title_fullStr Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
title_full_unstemmed Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
title_short Effects of resveratrol and genistein on nuclear factor-κB, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
title_sort effects of resveratrol and genistein on nuclear factor-κb, tumor necrosis factor-α and matrix metalloproteinase-9 in patients with chronic obstructive pulmonary disease
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838123/
https://www.ncbi.nlm.nih.gov/pubmed/27035424
http://dx.doi.org/10.3892/mmr.2016.5057
work_keys_str_mv AT liuxiaoju effectsofresveratrolandgenisteinonnuclearfactorkbtumornecrosisfactoraandmatrixmetalloproteinase9inpatientswithchronicobstructivepulmonarydisease
AT baohairong effectsofresveratrolandgenisteinonnuclearfactorkbtumornecrosisfactoraandmatrixmetalloproteinase9inpatientswithchronicobstructivepulmonarydisease
AT zengxiaoli effectsofresveratrolandgenisteinonnuclearfactorkbtumornecrosisfactoraandmatrixmetalloproteinase9inpatientswithchronicobstructivepulmonarydisease
AT weijunming effectsofresveratrolandgenisteinonnuclearfactorkbtumornecrosisfactoraandmatrixmetalloproteinase9inpatientswithchronicobstructivepulmonarydisease