Open Access

Quercetin prevents progression of disease in elastase/LPS-exposed mice by negatively regulating MMP expression

Respiratory Research201011:131

https://doi.org/10.1186/1465-9921-11-131

Received: 2 April 2010

Accepted: 28 September 2010

Published: 28 September 2010

Abstract

Background

Chronic obstructive pulmonary disease (COPD) is characterized by chronic bronchitis, emphysema and irreversible airflow limitation. These changes are thought to be due to oxidative stress and an imbalance of proteases and antiproteases. Quercetin, a plant flavonoid, is a potent antioxidant and anti-inflammatory agent. We hypothesized that quercetin reduces lung inflammation and improves lung function in elastase/lipopolysaccharide (LPS)-exposed mice which show typical features of COPD, including airways inflammation, goblet cell metaplasia, and emphysema.

Methods

Mice treated with elastase and LPS once a week for 4 weeks were subsequently administered 0.5 mg of quercetin dihydrate or 50% propylene glycol (vehicle) by gavage for 10 days. Lungs were examined for elastance, oxidative stress, inflammation, and matrix metalloproteinase (MMP) activity. Effects of quercetin on MMP transcription and activity were examined in LPS-exposed murine macrophages.

Results

Quercetin-treated, elastase/LPS-exposed mice showed improved elastic recoil and decreased alveolar chord length compared to vehicle-treated controls. Quercetin-treated mice showed decreased levels of thiobarbituric acid reactive substances, a measure of lipid peroxidation caused by oxidative stress. Quercetin also reduced lung inflammation, goblet cell metaplasia, and mRNA expression of pro-inflammatory cytokines and muc5AC. Quercetin treatment decreased the expression and activity of MMP9 and MMP12 in vivo and in vitro, while increasing expression of the histone deacetylase Sirt-1 and suppressing MMP promoter H4 acetylation. Finally, co-treatment with the Sirt-1 inhibitor sirtinol blocked the effects of quercetin on the lung phenotype.

Conclusions

Quercetin prevents progression of emphysema in elastase/LPS-treated mice by reducing oxidative stress, lung inflammation and expression of MMP9 and MMP12.

Background

Chronic obstructive pulmonary disease (COPD) is a heterogeneous disorder characterized by small airway inflammation/fibrosis, mucus plugging and emphysema. COPD is the fourth leading cause of death worldwide and the prevalence is predicted to rise in the next two decades [1].

Although the cellular and molecular mechanisms of COPD pathogenesis are not well known, oxidative stress, chronic inflammation and an imbalance of proteases and antiproteases are thought to play key roles in development and progression of the disease [1]. Therefore, a treatment with antioxidant and anti-inflammatory properties could be beneficial in preventing or slowing the progression of lung disease in COPD.

Inhalation of cigarette smoke and other environmental exposures can stimulate resident alveolar macrophages and lung epithelial cells to generate reactive oxygen species (ROS) and reactive nitric oxide species (RNS) in excess, thereby disturbing the oxidant to antioxidant balance, resulting in oxidative stress [24]. ROS and RNS stimulate the production of a number of host mediators, some of which can attract neutrophils, macrophages and other inflammatory cells to the lungs. Recruited inflammatory cells and epithelial cells produce matrix metalloproteinases (MMPs), thereby increasing protease activity in the lungs. MMPs, in turn, degrade alveolar walls, leading to enlargement of airspace and development of emphysema. In addition, chronic inflammation causes remodeling of the airways, including goblet cell metaplasia, mucus plugging and airway wall thickening.

The histone deacetylases (HDACs) are transcriptional repressors which have been implicated in the resolution of inflammation as well as the regulation of MMP expression [5]. In COPD patients, reductions in the expression of HDAC2 and HDAC5 correlate with disease severity and increased IL-8 expression [6]. Similarly, the type III HDAC Sirt1, which regulates MMP expression, was also found to be downregulated in COPD [7].

Lipopolysaccharide (LPS), a cell wall component of gram negative bacteria, is a potent inflammatory molecule and is present in appreciable amounts in cigarette smoke. It is also an active component in environmental and occupational exposures associated with the development of COPD [810]. Experimental inhalation of LPS evokes pulmonary and systemic inflammation in healthy human subjects [11, 12]. Chronic exposure of experimental animals causes emphysema, goblet cell metaplasia, and airway wall thickening. These alterations persist up to four to eight weeks following LPS administration [13, 14]. Recently, we demonstrated that mice exposed to a combination of LPS and elastase once a week for 4 weeks display COPD-like features including widespread lung inflammation, goblet cell metaplasia, increased lung volume, emphysema and decreased elastic recoil [15]. These changes persisted up to 8 weeks after cessation of exposure to elastase and LPS. These mice were also found to be more susceptible for rhinovirus infection.

Quercetin is a 3,3',4',5,7-pentahydroxyflavone found in many plants. Based on its polyphenol structure, quercetin has potent antioxidant effects, combining with free radical species to form considerably less reactive phenoxy radicals [16, 17]. Quercetin also has anti-inflammatory effects, inhibiting lipid, protein tyrosine and serine/threonine kinases by its capacity to compete with the binding of ATP at the nucleotide binding site [18]. Previously, we demonstrated that quercetin inhibits TNF-α stimulated IL-8 expression at the transcriptional level in airway epithelial cells and decreases airways hyperresponsiveness in cockroach allergen-sensitized and challenged mice, a model of allergic airways disease, at a dose of 0.6 mg per day (approximately 30 mg/kg body weight) [19]. Quercetin was also shown to suppress eosinophilic inflammation in ovalbumin-sensitized and -challenged mice at a dose of 10 mg/kg body weight [20]. Further, quercetin decreases the expression of MMP9 stimulated by TNF-α in epidermal cells [21]. Based on these observations, we hypothesized that quercetin reverses oxidative stress and inhibit MMP production, perhaps by increasing the expression of the histone deacetylase Sirt-1, thereby preventing the progression of lung disease in COPD. To test this hypothesis, we treated elastase/LPS exposed mice with quercetin (10 mg/kg body weight), and examined oxidative stress, inflammation and expression of MMP9, MMP12 and SIRT-1 in the lungs. We also determined the effect of quercetin on the histone acetylation of the MMP9 and MMP12 promoters by chromatin immunoprecipitation assay.

Methods

Animals and treatment

Eight to ten weeks old C57BL/6 mice (Charles River Laboratories International Inc., Wilmington, MA) were exposed to elastase and LPS for four consecutive weeks as described previously [15]. Animals were exposed by the intranasal route to 1.2 U of porcine pancreatic elastase (Elastin Products, Owensville, MO) on day one and 7 μg (approximately 70 endotoxin units) of LPS from E. coli O26:B6 (Sigma-Aldrich, St. Louis, MO) on day four of the week for four consecutive weeks. Control mice were exposed to PBS. Seven days after the last exposure to LPS, mice were orally gavaged with 300 μl of 50% propylene glycol (vehicle) or 0.2 mg of quercetin (10 mg/kg body weight; Sigma-Aldrich, St. Louis, MO) dissolved in 50% propylene glycol, once a day for 10 days. We chose this dose of quercetin based on previous studies in which quercetin at 10 mg/kg body weight reduced airways responsiveness and lung inflammation in an allergic mouse model of asthma [19, 20]. In some experiments, mice were treated intraperitoneally with 100 μl PBS or PBS containing sirtinol (0.5 mg/kg body weight, Calbiochem, Gibbstown, NJ) along with quercetin or vehicle for 10 days. Mice were sacrificed 1 h after the last quercetin treatment. In some experiments, mice were examined 7 and 17 days after the last exposure to LPS without any treatment in order to examine the progression of emphysema after cessation of exposure to elastase/LPS. Unexposed mice treated with vehicle or quercetin (10 mg/kg body weight) were used as negative controls. All experiments described herein were approved by the Animal Care and Use Committee of the University of Michigan.

Measurement Of Lung Elasticity

Mice Were Anesthetized By Intraperitoneal Injection Of Ketamine (2.5-5 Mg/100 G Body Weight) And A Steel Cannula Was Inserted Into The Trachea And Connected To A Miniature Computerized Flexivent Ventilator (Scireq, Montreal, Quebec, Canada). Sodium Pentabarbitol (2 Mg/100 G Body Weight) Was Also Given To Provide Further Sedation And Allow Stabilization On The Ventillator. To Determine Elastic Recoil, Lungs Were Gradually Inflated To 30 Cm H2O And Pressure And Lung Volume Measured Continuously During Inflation And Deflation Of The Lungs. Static Elastance And Compliance Were Recorded By Inflating The Lungs To Full Capacity.

Lung Histology And Morphometry

Lungs Were Perfused With 20 Mm Edta And Inflation-Fixed With 10% Buffered Formalin, And Embedded In Paraffin. Five Micron Thick Sagittal Sections Were Stained With Hematoxylin And Eosin (H & E) Or Periodic-Acid Schiff'(Pas) Reagent. Alveolar Chord Length Was Determined Using Sagittal Sections Obtained At 5 Mm Intervals Through The Length Of The Lungs, And Diameter Of The Airspaces Was Measured In Random Areas Using Nih Image J Analysis Software [15].

Bronchoalveolar Lavage (Bal)

Mice Were Euthanized And Lungs Were Lavaged With Pbs. Bal Fluid Was Centrifuged And The Supernatant Was Collected For Determination Of Mmp Levels. Total And Differential Cell Counts In Bal Fluid Were Determined As Described Previously [15, 22].

Lung Cytokine Levels

After Relevant Treatment, Mice Were Euthanized, Lungs Were Collected, Homogenized In Pbs Containing Complete Protease Inhibitors And Centrifuged (Roche, Indianapolis, In). Cytokine Protein Levels In The Lung Homogenate Supernatants Were Measured Either By Elisa (R & D Systems, Minneapolis, Mn) Or Multiplex Immunoassay (Biorad, Hercules, Ca) [15, 22].

Alveolar Macrophage Cell Culture

Murine Alveolar Macrophages (Crl-2019, American Type Culture Collection, Manassas, Va) Were Cultured In Rpmi1640 Supplemented With 10% Fetal Bovine Serum, Penicillin (100 Units/Ml), Streptomycin (100 μG/Ml), 1% Glutamine And 0.01% β-Mercaptoethanol. To Determine The Effect Of Quercetin On Mmp Expression, Cells Were Seeded In 6 Well Plates And Grown For 24 H. Cells Were Then Exposed To Cell Culture Media Containing 1 Ng/Ml Lps For 8 Hours A Day For Three Days. In Between Exposures To Lps, Cells Were Maintained In Cell Culture Media Alone. Cells Were Then Shifted To Serum-Free Media Containing Quercetin Dihydrate Or Dmso, Incubated For 24 H, And Media And Cells Were Harvested. Cells Exposed To Media Alone Instead Of Lps Were Used As Negative Controls.

Gelatin Zymography

Mmp Activity Was Determined By Gelatin Zymography As Described.[23]. Briefly, Equal Volumes Of Bal Supernatant Or Conditioned Cell Culture Media Was Incubated With Non-Reducing Sample Buffer And Subjected To Electrophoresis On 8% Polyacrylamide Gels Impregnated With 0.1% Gelatin. Gels Were Washed With 1% Triton X-100, Developed In Tris Buffer Containing 10 Mm Cacl2 And 5μM Zncl2 And Stained With 0.5% Coomassie Blue.

Measurement Of Plasma Quercetin Levels

Mice Were Sacrificed And Blood Was Collected By Cardiac Puncture In Tubes With Anticoagulant, Centrifuged And Plasma Was Collected. Levels Of Quercetin In Plasma Were Determined By Hplc As Described Previously [19].

Chromatin Immunoprecipitation (Chip) Assay

Chip Assays Were Performed With A Chip-It Kit (Active Motif, Carlsbad, Ca) Following The Manufacturer'S Instructions. Briefly, Cells Were Fixed, Lysed And Chromatin Was Subjected To Enzymatic Shearing. Chromatin Fragments Of 100-1000 Bp Were Immunoprecipitated With An Antibody To Acetylhistone H4 Antibody. Chip And Input Dna Were Purified And Subjected To Qpcr Using Primers Specific For The Nf-κB Binding Site In The Mmp9 And Mmp12 Promoters. Qpcr Conditions Were As Follows: 95°C For 15 Minutes; 95°C For 10 Seconds, 60°C For 30 Seconds, 72°C For 30 Seconds, Repeated For 50 Cycles, 72°C For 10 Minutes. The Primers Used For Qpcr Were Mmp9: Sense 5'-TTTAAACAGAAGAGGAAGGAT AGTGC-3' And Antisense 5'-CCTGATAGAGTCTTT GACTCAGCTTC-3'; Mmp12: Sense 5'-TTGCTGAATCATTTCATGGC-3' And Antisense 5'-AGTGCATAGGTATG TGAATGGG-3'.

Quantitative Pcr

Expression Of Mmp9, Mmp12, Sirt1, Inducible Nitric Oxide Synthase (Inos), Heme Oxygenase (Hmox)-1, And Muc5Ac Was Determined By Qpcr. All Pcr Reactions Were Performed In An Eppendorf Mastercycler (Westbury, Ny) And Gene Expression Was Quantified Using The Comparative Ct Method.

Western Blotting

Nuclear Proteins Were Resolved By 7.5% Sds-Polyacrylamine Gel Electrophoresis, Proteins Transferred To Nitrocellulose Membrane And Probed With Antibody To Sirt1 And β-Actin (Santa Cruz Biotechnology, Santa Cruz, Ca). Specific Bands Were Quantified By Densitometry Using Nih Imagej And Expressed As A Ratio Of Sirt1/B-Actin Which Is Normalized To Untreated Control Mice.

Lipid Peroxidation

The Amount Of Lipid Peroxidation Products In The Lungs Was Assayed As Thiobarburtic Acid Reacting Substances (Tbars) (Cell Biolabs, San Diego, Ca) Following Manufacturer'S Instructions.

Statistical Analysis

Statistical Analysis Of Significance Was Calculated By One-Way Analysis Of Variance Followed By Tukey'S Post Hoc Test, Anova On Ranks With Dunn'S Post Hoc Analysis Or By Mann-Whitney Test As Appropriate. Results Represent Mean ± Sd Or Sem, Or Range Of Data With Median.

Results

Effect of quercetin on elastase/LPS-induced emphysema

As observed previously [15], mice at seven days after the four-week exposure to elastase/LPS showed an upward and leftward shift compared to control mice, demonstrative of reduced elastic recoil (Figure 1A). Because mice receiving quercetin or vehicle for 10 days were studied a total of 17 days after the last exposure to elastase/LPS, we also measured the lung function of untreated mice at this time point. The volume-pressure curve was shifted further to the left, indicating further progression of emphysema after cessation of exposure to elastase/LPS. This shift may be due to persistence of oxidative stress and MMP activity even after cessation of exposure to elastase/LPS. This situation is analogous to the further progression of emphysema in COPD patients even after cessation of smoking [24].
Figure 1

Quercetin partially improves lung function in elastase-LPS exposed mice. Mice were anesthetized and pressure-volume relationships, compliance and elastance were measured using flexivent system. Chord length was determined by morphometry. Seven days after the last exposure to elastase/LPS, untreated mice showed a leftward and upward shift in the pressure-volume (PV)-loop (A) compared to PBS-exposed vehicle treated mice, indicative of a loss of elastic recoil. Seventeen days after the last exposure to elastase/LPS, this curve shifted further, indicating progression in the loss of elastic recoil. Quercetin treatment for 10 days prevented progression in loss of elastic recoil in elastase/LPS-exposed mice but had no effect on PBS-exposed mice (B). Each of these mice was examined 17 days after the last elastase/LPS treatment. Elastase/LPS-exposed mice treated with quercetin also showed increased elastance (C), decreased compliance (D) and decreased alveolar chord length (E) compared to vehicle treated mice. Representative PV curves from 5 to 6 mice from each group are shown in A and B. Data in C, D and E represent mean and SD calculated from 6 animals per group (*different from PBS group, p≤0.05 one-way ANOVA; † different from vehicle treated mice, p≤0.05 Mann-Whitney test).

Next, we examined the lung function of mice treated with quercetin (0.2 mg) or vehicle for 10 days starting one week after the four-week course of elastase/LPS-treatment. Compared to vehicle, mice receiving quercetin showed a rightward and downward shift in their volume-pressure curve (Figure 1B). Shifts in the pressure-volume loops were accompanied by appropriate changes in elastance and compliance (Figures 1C and 1D). Finally, compared to vehicle, quercetin treatment was associated with a reduction in alveolar chord length (Figure 1E). However, quercetin treatment did not completely reverse the emphysematous changes caused by elastase/LPS. Quercetin treatment did not affect any of these measurements in the lungs of mice exposed to PBS. Together, these data suggest that quercetin treatment prevented further progression of emphysema after elastase/LPS treatment rather than stimulating the regeneration of degraded alveoli.

Quercetin decreases oxidative stress in elastase/LPS-exposed mice

To determine the mechanism by which quercetin prevents progression of emphysema in elastase/LPS-treated mice, we examined the effects of quercetin on indices of lung oxidative stress and inflammation. Elastase/LPS-exposed mice were treated with 0.2 mg of quercetin for 10 days and lung levels of TBARS, iNOS mRNA and Hmox-1 mRNA determined. Compared to unexposed mice either treated with vehicle or quercetin, elastase/LPS-exposed mice treated with vehicle showed significantly increased levels of TBARS and iNos, and decreased levels of Hmox-1 mRNA. The ratio of iNos/Hmox-1 was increased (Figures 2A to 2D). In contrast, elastase/LPS exposed mice treated with 0.2 mg of quercetin for 10 days showed significantly reduced TBARS, increased Hmox-1 mRNA and decreased iNos/Hmox-1 compared to vehicle treated controls. These results indicate that exposure of mice to elastase/LPS increases oxidative stress, and that treatment with quercetin reverses this effect.
Figure 2

Quercetin treatment reduces TBARS and increasesHmox-1expression in elastase/LPS exposed mice. Mice exposed to PBS or elastase/LPS were orally gavaged with 0.2 mg of quercetin or vehicle daily for 10 days and sacrificed on the last day of quercetin treatment. A to D. Elastase/LPS exposed mice show increased levels of TBARS, increased iNOS mRNA levels, decreased Hmox-1 mRNA and increased ratio of iNOS/Hmox-1 compared to PBS exposed mice treated with either vehicle or quercetin. Quercetin treatment reduces TBARS, increases Hmox-1 mRNA and decreases ratio of iNOS/Hmox-1 in elastase/LPS-exposed mice. Data represent mean and SEM (n = 10-14, *different from PBS/vehicle and PBS/quercetin group, p≤0.05; † different from vehicle treated elastase/LPS-exposed mice, p≤0.05 one-way ANOVA).

Quercetin treatment reduces lung inflammation in elastase/LPS-exposed mice

Lung cytokine levels, histology, total and differential cells counts in the BAL, and expression of the mucin gene Muc5AC were determined to test whether quercetin treatment reduces inflammation in elastase/LPS exposed mice. As previously noted, elastase/LPS-exposed mice showed increased protein expression of the chemokines KC/CXCL-1, MIP-2/CXCL-2 and MCP-1/CCL2 and pro-inflammatory cytokines IL-1β, IL-12p40 and MIP-1β (Figure 3). Compared to vehicle, quercetin treatment significantly decreased the levels of all chemokines and pro-inflammatory cytokines examined. PBS-exposed mice treated with quercetin showed similar levels of all cytokines measured compared to mice treated with vehicle (data not shown).
Figure 3

Quercetin treatment decreases chemokine and cytokine levels in elastase/LPS exposed mice. Mice exposed to elastase/LPS were orally gavaged with vehicle or quercetin as described. A to F. Elastase/LPS exposed mice show increased levels of KC, MIP2, MCP-1, IL-1β, IL-12p40 and MIP-1β compared to control naïve mice. Quercetin treatment reduces all the examined cytokines and chemokines. Data represent mean and SEM (n = 10, *different from PBS/vehicle group, p≤0.05; † different from vehicle-treated elastase/LPS exposed mice, p≤0.05 one-way ANOVA).

Evaluation of H & E-stained lung sections showed wide-spread lung inflammation and emphysema in elastase/LPS exposed mice as observed previously (Figure 4A). Quercetin-treated elastase/LPS exposed mice showed an overall reduction in lung inflammation compared to vehicle treated mice (Figure 4C). Immunostaining of lung sections with anti-MUC5AC antibody showed intense signals in the airway epithelium of elastase/LPS-exposed mice treated with vehicle but not mice treated with quercetin (Figures 4B and 4D). Consistent with the histologic changes, elastase/LPS-exposed mice showed increased total cell counts, macrophages and neutrophils compared to PBS-exposed mice, and each of these variables was significantly reduced by quercetin (Figure 4E). We also observed decreased mRNA expression of Muc5AC in quercetin-treated, elastase/LPS-exposed mice compared to vehicle-treated mice (Figure 4F).
Figure 4

Quercetin treatment reduces lung inflammation and reverses goblet cell metaplasia. Lung sections from elastase/LPS exposed mice were stained with H & E or immunostained with an antibody to Muc5AC. A and B. Mice treated with vehicle show mild-to-moderate wide-spread lung inflammation, emphysema and goblet cell metaplasia. C and D. Mice treated with quercetin show less emphysema with very mild inflammation and a complete reduction in MUC5AC producing goblet cells. Asterisks in A and C represent emphysema. Arrows in B indicate MUC5AC- producing goblet cells. Images are representative of 6 mice per group. E. Examination of BAL fluid reveals increased numbers of total cells, macrophages and neutrophils in elastase/LPS treated mice, which were almost completely reversed by quercetin treatment. F. qPCR analysis of total lung RNA shows increased Muc5AC transcript levels in elastase/LPS-exposed mice, and this was reduced in quercetin treated mice. Data represent mean and SEM (n = 10, *different from PBS/vehicle group, p≤0.05; † different from vehicle treated elastase/LPS exposed mice, p≤0.05 one-way ANOVA).

Quercetin treatment inhibits MMP9 and MMP12 activity and increases Sirt1 expression

Increased MMP levels are thought to play a role in the development and/or progression of emphysema in COPD patients [2527]. Consistant with this, lungs of elastase/LPS exposed mice showed increased mRNA and activity levels of MMP9 and MMP12 compared to vehicle treated PBS-exposed mice (Figure 5A-C). Lung MMP levels did not change in quercetin treated PBS-exposed mice (data not shown). Quercetin treatment significantly decreased the mRNA and activity levels of both MMP9 and MMP12 in elastase/LPS-exposed mice.
Figure 5

Quercetin treatment decreases levels of MMP9 and MMP12 and increases expression of SIRT1 in elastase/LPS-exposed mice. mRNA expression of Mmp9, Mmp12, and Sirt1 was measured by qPCR. MMP activity was determined by gelatin zymography. Sirt1 protein level was measured in the lung homogenates by Western blot analysis. A and B. Quercetin treated elastase/LPS exposed mice show significantly reduced Mmp9 and Mmp12 mRNA levels compared to mice treated with vehicle. C Quercetin treatment completely reduces MMP9 and MMP12 activities in elastase/LPS exposed mice. D and E. Quercetin increases Sirt1 mRNA and protein levels in elastase/LPS exposed mice. F. Ratio of Sirt1 protein/β-actin normalized to control mice calculated from 6 mice per group. Data represent mean and SEM (n = 10, *different from PBS/vehicle group, p≤0.05; † different from vehicle-treated, elastase/LPS-exposed mice, p≤0.05 one-way ANOVA). Images in C and E are representative of 4 to 6 animals per group.

MMP9 transcription is negatively regulated by a histone deacetylase, SIRT1 (2). We examined whether reductions in Mmp9 and Mmp12 mRNA levels were associated with increases in SIRT1 expression in quercetin-treated, elastase/LPS-exposed mice. Vehicle-treated elastase/LPS-exposed mice showed an 83.2% reduction in mRNA expression of Sirt1 compared to mice unexposed to elastase/LPS (Figure 5D). Similarly, we observed 53% reduction in protein levels of Sirt1 in the lungs of vehicle-treated, elastase/LPS-exposed mice (Figure 5E and 5F). Quercetin treatment of elastase/LPS exposed mice increased both Sirt1 mRNA and protein levels. These results suggest that quercetin may suppress MMP9 and MMP12 expression by increasing Sirt1 levels.

A Sirt1 inhibitor blocks the protective effect of quercetin

To determine the contribution of Sirt1 expression to the observed effects of quercetin on lung phenotype, elastase/LPS exposed mice were treated with polyethylene glycol or quercetin along with sirtinol, an inhibitor of Sirt1 activity [28]. As observed earlier, compared to vehicle-treated elastase/LPS-exposed mice, lungs of quercetin-treated mice showed reduced mRNA expression of MMP9 and MMP12 (Figure 6A and 6B) and improved elastic recoil as indicated by leftward and downward shift in pressure-volume loops, decreased static compliance and increased static elastance (Figure 6C and 6E). In contrast, mice treated with quercetin along with sirtinol showed a similar level of MMP mRNA expression as vehicle treated elastase/LPS mice. Sirtinol treatment also blocked the improvements of elastic recoil, static compliance and static elastance induced by quercetin. These results are consistent with the notion that quercetin exerts its effects by increasing Sirt1 levels, which negatively regulate MMP expression.
Figure 6

Inhibition of Sirt1 activity in quercetin-treated mice attenuates querecetin-induced changes in MMP expression and emphysema progression. Elastase/LPS-exposed mice were treated with vehicle or quercetin along with sirtinol or PBS. A and B. Mice treated with quercetin and sirtinol did not show reduced MMP9 or MMP12 mRNA expression. Results represent range of data with median (n = 4-6, *different from all other groups, p≤0.05; ANOVA on ranks). C-E. Sirtinol also inhibited quercetin's effects on elastic recoil (C), compliance (D) and elastance (E). Data represent mean and SEM (n = 4-6, *different from all other groups, p≤0.05; one-way ANOVA). C. Representative of 4-6 animals per group.

Measurement of quercetin levels in plasma

Chromatographic analysis of plasma obtained from mice treated with 0.2 mg quercetin for 10 days revealed a major peak which corresponded to quercetin aglycone and other minor peaks as we observed previously [19]. Quantification of the major peak indicated a mean plasma quercetin level of 0.131 ± 0.038 μM in mice treated with quercetin. This level was significantly higher than the quercetin level observed in vehicle-treated mice (0.004 ± 0.0019 μM).

Quercetin inhibits transcription of MMP 9 and MMP12 in alveolar macrophages in vitro

Sirt1, a histone deacetylase, negatively regulates MMP9 transcription by deacetylating histone H4 in the promoter region NF-κB binding site [7]. To determine whether quercetin increases H4 deacetylation at this site, we employed an in vitro cell culture system. Murine alveolar macrophages exposed to low levels of LPS for three days showed increased Mmp9 and Mmp12 mRNA levels, with a concomitant decrease in Sirt1 expression (Figure 7A-C). We also observed increased MMP9 activity (Figure 7D) and decreased SIRT1 protein expression (Figure 7E and 7F) in LPS-treated alveolar macrophages. Consistent with these in vivo results, in vitro quercetin treatment of alveolar macrophages significantly decreased LPS-induced mRNA expression of Mmp9 and Mmp12 as well as MMP9 activity, while increasing mRNA and protein expression of Sirt1. Next, we examined whether quercetin increases histone deacetylation of the MMP9 and MMP12 promoter NF-κB binding sites by ChIP assay. Histone H4 acetylation at the MMP9 and MMP12 promoter NF-κB binding sites was increased in LPS-exposed alveolar macrophages compared to media-treated controls, and this was completely inhibited by treatment with quercetin (Figures 7G and 7H). These results suggest that quercetin inhibits H4-acetylation of MMP promoters by increasing Sirt-1 expression, thereby regulating MMP expression at the transcriptional level.
Figure 7

Quercetin decreases MMP9 and MMP12 and increases Sirt1 in LPS-treated alveolar macrophages. Mouse alveolar macrophages were treated with LPS (1 ng/ml) for 3 days and treated with DMSO (vehicle) or 25 µM quercetin for 16 h. A and B. LPS treatment induced mRNA expression of MMP9 and MMP12 which are partially reversed by quercetin. C and E. Quercetin increases Sirt1 mRNA and protein expression. D. MMP9 activity in LPS-exposed was abrogated by quercetin treatment. E. A representative Western blot showing Sirt1 and β-actin expression. F. Ratio of Sirt1 protein/β-actin normalized to untreated cells calculated from 3 independent experiments. G and H. Quercetin decreased LPS-induced histone H4 acetylation at the NF-κB binding sites in the promoter regions of both Mmp9 and Mmp12. Zymogram and immunoblot images are representative of three independent experiments. Data represent mean and SEM calculated from 3 independent experiments performed in duplicates or triplicates (*different from macrophages exposed to media in the absence of quercetin, p≤0.05; †different from LPS-exposed macrophages which are not treated with quercetin, p≤0.05 one-way ANOVA).

Discussion

We demonstrate that oral administration of quercetin, a major flavonoid in the human diet, significantly decreases oxidative stress and inflammation in the lungs of elastase/LPS-treated mice, which show features typical of COPD. Quercetin also decreases MMP9 and MMP12 levels by increasing expression of the type III protein deacetylase Sirt-1, a negative regulator of MMP transcription both in vivo and in vitro. Further, quercetin improves lung elasticity and compliance in elastase/LPS treated mice by preventing progression of emphysema.

In this study, mice were exposed to elastase and LPS, rather than cigarette smoke, the primary trigger of COPD in industrialized nations. This published murine model system [15] produces structural and functional features that are more pronounced and more typical of human COPD than can be achieved in wild type mice by even prolonged exposures to tobacco-smoke alone. These changes include not only pulmonary emphysema, loss of lung elastic recoil, hyperinflation, but also diffuse lung inflammation, goblet cell metaplasia, airway remodeling and markedly increased numbers of neutrophils, T and B lymphocytes, monocytes and immature macrophages in the airways and alveoli [15]. By contrast, mice exposed to cigarette smoke develop pulmonary emphysema and accumulation of alveolar macrophages, but fail to demonstrate chronic bronchitis or goblet cell metaplasia [29]. Importantly, in our model system, these morphological and inflammatory changes were accompanied by increases in lung IL-1β, IL-6, TNF-α, and MIP-2/CXCL2, markers of oxidative stress, MMP expression and reduction in Sirt1 levels, as seen in humans with COPD [3032]. Moreover, LPS is a significant constituent of cigarette smoke [9, 10]. Therefore, we believe that elastase/LPS-exposed mice are suitable for examining the therapeutic effects of quercetin or other potential drug candidates.

Epidemiologic studies of COPD patients have suggested an association of polyphenol intake with improved symptoms, as assessed by cough, sputum production, breathlessness and improved lung function, as measured by FEV1 [3335]. Several in vitro and in vivo studies also have showed a direct impact of polyphenols in reducing oxidative stress and inflammation. For instance, resveratrol, a component of red wine, decreased inflammatory cytokine production from macrophages isolated from COPD patients [36] and induced synthesis of reduced glutathione by activating NF-E2-related factor (Nrf)-2, a key antioxidant transcription factor in human lung epithelial cells [37]. Curcumin, another well-studied polyphenol, has also been reported to inhibit activation of NF-κB in vitro and inflammation in vivo and restore glucocorticoid efficacy in response to oxidative stress by upregulation of HDAC2 activity in macrophages [3840]. Curcumin also increased synthesis of Nrf2-dependent phase II antioxidant enzymes in elastase and cigarette smoke- exposed mice [41]. Quercetin, which is a potent antioxidant and possesses anti-inflammatory properties, decreased lung oxidative stress, inflammation, and prevented progression of emphysema in elastase/LPS-exposed mice.

TBARS, products of lipid peroxidation and an index of oxidative stress caused by reactive oxygen species, have been shown to be increased in COPD patients [30]. In addition, the number of HMOX-1 expressing alveolar macrophages is markedly decreased in patients with severe COPD, while iNOS expression is increased in alveolar and bronchial epithelial cells [42]. Increased staining for the nitration marker nitrotyrosine in iNOS positive cells was observed in induced sputum from patients with moderate stable COPD compared to nonsmokers [43]. Finally, overexpression of HMOX-1 in mouse lungs was shown to suppress elastase-induced emphysema by attenuating neutrophilic inflammation [44]. In the present study, quercetin treatment of elastase/LPS-exposed mice increased the expression of Hmox-1 and tended to decrease the expression of iNOS. Consistent with our observation, quercetin was noted to inhibit iNOS expression and NO production in LPS and interferon-γ-treated mouse BV-2 microglial cells, and this was associated with elevated expression of Hmox-1 [4547]. Together, these data suggest that quercetin may inhibit chemokine and pro-inflammatory cytokine production in elastase/LPS exposed mice not only by scavenging the free radicals, but also by increasing the expression of Hmox-1, which suppresses iNOS expression [48].

In our study, quercetin treatment of elastase/LPS-exposed mice was accompanied by significant decreases in the levels of neutrophil attracting C-X-C chemokines KC and MIP-2, monocyte and macrophage chemoattractant MCP-1 and pro-inflammatory cytokines including IL-1β, IL12p40 and MIP-1β. In addition to its antioxidant effects, quercetin may attenuate lung inflammation by inhibition of protein and lipid kinases involved in inflammatory cytokine and chemokine production. Quercetin has inhibitory effects on phosphatidylinositol 3-kinase, AMP-activated kinase, casein kinase 2, p90 ribosomal protein S6 kinase, p70 ribosomal S6 kinase [49], protein kinase C [50], epidermal growth factor receptor tyrosine kinase [51] and IκB kinase [52]. Indeed, the design of the synthetic PI 3-kinase inhibitor LY294002 was based on the structure of quercetin [53].

Another important finding of this study was that quercetin inhibited MMP expression in elastase/LPS treated mice. MMP expression is increased in COPD patients and plays a critical role in development and progression of emphysema. MMP also increases mucin production, leading to airway obstruction [5458]. Further, levels of Sirt1, a type III histone deacetylase which negatively regulates MMP9 transcription [7], were reported to be downregulated in patients with severe COPD but not in healthy smokers, suggesting a role for endogenous oxidative stress from activated neutrophils and macrophages in the reduction of Sirt1 [7]. Further, treatment of cigarette smoke-exposed mice with Sirt1 activator blocked MMP9 expression and pulmonary neutrophilic inflammation. In the present study, we found that elastase/LPS treatment increased expression and activity of MMP9 and MMP12. Interestingly, we also found decreased levels of the protein deacetylase Sirt1 in these mice. Quercetin treatment decreased MMP9 and MMP12 levels in elastase/LPS-exposed mice, while concomitantly increasing mRNA and protein levels of Sirt1, suggesting that quercetin may decrease MMP expression via deacetylation at the MMP promoter. Consistent with this, we observed that, in alveolar macrophages. quercetin decreases LPS-induced histone H4 acetylation at the MMP9 and MMP12 promoter NF-κB binding sites, thereby decreasing the transcription of MMP9 and MMP12. Furthermore, sirtinol, which inhibits Sirt1 activity, abrogated the effect of quercetin on MMP levels and lung elasticity in elastase/LPS-exposed mice. Together, these data suggest that quercetin prevents further degradation of alveolar walls by decreasing MMP expression, thereby slowing the progression of emphysema in these mice

Quercetin doses ranging between 10 to 100 mg/kg body weight have been used in previous animal studies of allergic airways disease [19, 20, 59]. Beneficial effects of quercetin were observed at doses as low as 10 mg/kg body weight. For example, we showed that 0.2 mg (approximately 10 mg/kg) inhibited eosinophilic inflammation and airways responsiveness in cockroach allergen-sensitized and challenged mice [19]. At this dose, quercetin levels of 0.25 μM were achieved. In the present study, plasma quercetin levels of 0.131 μM were reached. This dose was well-tolerated and was sufficient to prevent progression of emphysema. Our previous study showed that quercetin concentrations as low as 0.1 μM suppress airway epithelial cell cytokine expression in vitro [19]. It is also possible that enteral administration of quercetin produces sufficient gut levels to modulate lung inflammation, perhaps by altering the microbiome. Normally, human quercetin plasma concentrations are in the low nanomolar range, but upon supplementation it may increase to the high nanomolar or low micromolar range [60], suggesting that the concentration of quercetin required to prevent progression of emphysema can be achieved in humans. It is possible that absorption and availability can be further increased by using glycosylated form of quercetin [61]. These levels of quercetin were reported to be safe in humans with no adverse effects (reviewed in [62]). On the other hand, a handful of in vitro studies suggested that quercetin metabolites may be harmful and in fact may increase oxidative stress in lung epithelial cells [63, 64]. Further studies are needed to determine the appropriate dosage and form of quercetin (glycosylated versus aglycosylated) for administration to human patients.

Conclusions

In summary, we have demonstrated that quercetin, a plant polyphenol, reduces oxidative stress, inflammation and MMP levels in elastase/LPS treated mice which show typical features of COPD. Quercetin also prevented progression of emphysema in these mice. Even after cessation of smoking, COPD patients show progressive emphysematous changes due to persistent oxidative stress and protease burden in the airways [24]. The possibility that quercetin, which reduces inflammation and MMP levels while preventing progression of emphysema, may be beneficial in patients with COPD merits clinical testing.

Declarations

Acknowledgements

We thank Marisa Linn for processing lung tissue for histology. This work was supported by the National Institutes of Health (AT004793 to U.S.).

Authors’ Affiliations

(1)
Department of Pediatrics and Communicable Diseases, University of Michigan
(2)
Department of Internal Medicine, University of Michigan
(3)
Department of Family Medicine, University of Michigan
(4)
Department of Molecular and Integrative Physiology, University of Michigan
(5)
Department of Foods and Nutrition, Purdue University

References

  1. Rahman I, Adcock IM: Oxidative stress and redox regulation of lung inflammation in COPD. Eur Respir J 2006, 28:219–242.View ArticlePubMedGoogle Scholar
  2. MacNee W, Rahman I: Is oxidative stress central to the pathogenesis of chronic obstructive pulmonary disease? Trends Mol Med 2001, 7:55–62.View ArticlePubMedGoogle Scholar
  3. Sydbom A, Blomberg A, Parnia S, Stenfors N, Sandstrom T, Dahlen SE: Health effects of diesel exhaust emissions. Eur Respir J 2001, 17:733–746.View ArticlePubMedGoogle Scholar
  4. Nowak D, Kasielski M, Antczak A, Pietras T, Bialasiewicz P: Increased content of thiobarbituric acid-reactive substances and hydrogen peroxide in the expired breath condensate of patients with stable chronic obstructive pulmonary disease: no significant effect of cigarette smoking. Respir Med 1999, 93:389–396.View ArticlePubMedGoogle Scholar
  5. Chung KF, Adcock IM: Multifaceted mechanisms in COPD: inflammation, immunity, and tissue repair and destruction. Eur Respir J 2008, 31:1334–1356.View ArticlePubMedGoogle Scholar
  6. Ito K, Ito M, Elliott WM, Cosio B, Caramori G, Kon OM, Barczyk A, Hayashi S, Adcock IM, Hogg JC, et al.: Decreased histone deacetylase activity in chronic obstructive pulmonary disease. N Engl J Med 2005, 352:1967–1976.View ArticlePubMedGoogle Scholar
  7. Nakamaru Y, Vuppusetty C, Wada H, Milne JC, Ito M, Rossios C, Elliot M, Hogg J, Kharitonov S, Goto H, et al.: A protein deacetylase SIRT1 is a negative regulator of metalloproteinase-9. FASEB J 2009, 23:2810–2819.View ArticlePubMedGoogle Scholar
  8. Hasday JD, Bascom R, Costa JJ, Fitzgerald T, Dubin W: Bacterial endotoxin is an active component of cigarette smoke. Chest 1999, 115:829–835.View ArticlePubMedGoogle Scholar
  9. Larsson L, Szponar B, Pehrson C: Tobacco smoking increases dramatically air concentrations of endotoxin. Indoor Air 2004, 14:421–424.View ArticlePubMedGoogle Scholar
  10. Sebastian A, Pehrson C, Larsson L: Elevated concentrations of endotoxin in indoor air due to cigarette smoking. J Environ Monit 2006, 8:519–522.View ArticlePubMedGoogle Scholar
  11. Jagielo PJ, Thorne PS, Watt JL, Frees KL, Quinn TJ, Schwartz DA: Grain dust and endotoxin inhalation challenges produce similar inflammatory responses in normal subjects. Chest 1996, 110:263–270.View ArticlePubMedGoogle Scholar
  12. Michel O, Duchateau J, Plat G, Cantinieaux B, Hotimsky A, Gerain J, Sergysels R: Blood inflammatory response to inhaled endotoxin in normal subjects. Clin Exp Allergy 1995, 25:73–79.View ArticlePubMedGoogle Scholar
  13. Kaneko Y, Takashima K, Suzuki N, Yamana K: Effects of theophylline on chronic inflammatory lung injury induced by LPS exposure in Guinea pigs. Allergol Int 2007, 56:445–456.View ArticlePubMedGoogle Scholar
  14. Vernooy JH, Dentener MA, van Suylen RJ, Buurman WA, Wouters EF: Long-term intratracheal lipopolysaccharide exposure in mice results in chronic lung inflammation and persistent pathology. Am J Respir Cell Mol Biol 2002, 26:152–159.View ArticlePubMedGoogle Scholar
  15. Sajjan U, Ganesan S, Comstock AT, Shim J, Wang Q, Nagarkar DR, Zhao Y, Goldsmith AM, Sonstein J, Linn MJ, et al.: Elastase- and LPS-exposed mice display altered responses to rhinovirus infection. Am J Physiol Lung Cell Mol Physiol 2009, 297:L931–944.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Kandaswami C, Middleton E Jr: Free radical scavenging and antioxidant activity of plant flavonoids. Adv Exp Med Biol 1994, 366:351–376.View ArticlePubMedGoogle Scholar
  17. Robak J, Gryglewski RJ: Flavonoids are scavengers of superoxide anions. Biochem Pharmacol 1988, 37:837–841.View ArticlePubMedGoogle Scholar
  18. Walker EH, Pacold ME, Perisic O, Stephens L, Hawkins PT, Wymann MP, Williams RL: Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine. Mol Cell 2000, 6:909–919.View ArticlePubMedGoogle Scholar
  19. Nanua S, Zick SM, Andrade JE, Sajjan US, Burgess JR, Lukacs NW, Hershenson MB: Quercetin blocks airway epithelial cell chemokine expression. Am J Respir Cell Mol Biol 2006, 35:602–610.View ArticlePubMedPubMed CentralGoogle Scholar
  20. Rogerio AP, Kanashiro A, Fontanari C, da Silva EV, Lucisano-Valim YM, Soares EG, Faccioli LH: Anti-inflammatory activity of quercetin and isoquercitrin in experimental murine allergic asthma. Inflamm Res 2007, 56:402–408.View ArticlePubMedGoogle Scholar
  21. Hwang MK, Song NR, Kang NJ, Lee KW, Lee HJ: Activation of phosphatidylinositol 3-kinase is required for tumor necrosis factor-alpha-induced upregulation of matrix metalloproteinase-9: its direct inhibition by quercetin. Int J Biochem Cell Biol 2009, 41:1592–1600.View ArticlePubMedGoogle Scholar
  22. Newcomb DC, Sajjan US, Nagarkar DR, Wang Q, Nanua S, Zhou Y, McHenry CL, Hennrick KT, Tsai WC, Bentley JK, et al.: Human rhinovirus 1B exposure induces phosphatidylinositol 3-kinase-dependent airway inflammation in mice. Am J Respir Crit Care Med 2008, 177:1111–1121.View ArticlePubMedPubMed CentralGoogle Scholar
  23. Mercer PF, Shute JK, Bhowmik A, Donaldson GC, Wedzicha JA, Warner JA: MMP-9, TIMP-1 and inflammatory cells in sputum from COPD patients during exacerbation. Respir Res 2005, 6:151.View ArticlePubMedPubMed CentralGoogle Scholar
  24. Louhelainen N, Rytila P, Haahtela T, Kinnula VL, Djukanovic R: Persistence of oxidant and protease burden in the airways after smoking cessation. BMC Pulm Med 2009, 9:25.View ArticlePubMedPubMed CentralGoogle Scholar
  25. Finlay GA, O'Driscoll LR, Russell KJ, D'Arcy EM, Masterson JB, FitzGerald MX, O'Connor CM: Matrix metalloproteinase expression and production by alveolar macrophages in emphysema. Am J Respir Crit Care Med 1997, 156:240–247.View ArticlePubMedGoogle Scholar
  26. Segura-Valdez L, Pardo A, Gaxiola M, Uhal BD, Becerril C, Selman M: Upregulation of gelatinases A and B, collagenases 1 and 2, and increased parenchymal cell death in COPD. Chest 2000, 117:684–694.View ArticlePubMedGoogle Scholar
  27. Zheng T, Zhu Z, Wang Z, Homer RJ, Ma B, Riese RJ Jr, Chapman HA Jr, Shapiro SD, Elias JA: Inducible targeting of IL-13 to the adult lung causes matrix metalloproteinase- and cathepsin-dependent emphysema. J Clin Invest 2000, 106:1081–1093.View ArticlePubMedPubMed CentralGoogle Scholar
  28. Hwang JW, Chung S, Sundar IK, Yao H, Arunachalam G, McBurney MW, Rahman I: Cigarette smoke-induced autophagy is regulated by SIRT1-PARP-1-dependent mechanism: Implication in pathogenesis of COPD. Aarch Biochem Biophy 2010, 500:203–209.View ArticleGoogle Scholar
  29. Tabak C, Arts IC, Smit HA, Heederik D, Kromhout D: Chronic obstructive pulmonary disease and intake of catechins, flavonols, and flavones: the MORGEN Study. Am J Respir Crit Care Med 2001, 164:61–64.View ArticlePubMedGoogle Scholar
  30. Santus P, Sola A, Carlucci P, Fumagalli F, Di Gennaro A, Mondoni M, Carnini C, Centanni S, Sala A: Lipid peroxidation and 5-lipoxygenase activity in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2005, 171:838–843.View ArticlePubMedGoogle Scholar
  31. Walda IC, Tabak C, Smit HA, Rasanen L, Fidanza F, Menotti A, Nissinen A, Feskens EJ, Kromhout D: Diet and 20-year chronic obstructive pulmonary disease mortality in middle-aged men from three European countries. Eur J Clin Nutr 2002, 56:638–643.View ArticlePubMedGoogle Scholar
  32. Culpitt SV, Rogers DF, Fenwick PS, Shah P, De Matos C, Russell RE, Barnes PJ, Donnelly LE: Inhibition by red wine extract, resveratrol, of cytokine release by alveolar macrophages in COPD. Thorax 2003, 58:942–946.View ArticlePubMedPubMed CentralGoogle Scholar
  33. Kode A, Rajendrasozhan S, Caito S, Yang SR, Megson IL, Rahman I: Resveratrol induces glutathione synthesis by activation of Nrf2 and protects against cigarette smoke-mediated oxidative stress in human lung epithelial cells. Am J Physiol Lung Cell Mol Physiol 2008, 294:L478–488.View ArticlePubMedGoogle Scholar
  34. Biswas SK, McClure D, Jimenez LA, Megson IL, Rahman I: Curcumin induces glutathione biosynthesis and inhibits NF-kappaB activation and interleukin-8 release in alveolar epithelial cells: mechanism of free radical scavenging activity. Antioxidants & redox signaling 2005, 7:32–41.View ArticleGoogle Scholar
  35. Meja KK, Rajendrasozhan S, Adenuga D, Biswas SK, Sundar IK, Spooner G, Marwick JA, Chakravarty P, Fletcher D, Whittaker P, et al.: Curcumin restores corticosteroid function in monocytes exposed to oxidants by maintaining HDAC2. Am J Respir Cell Mol Biol 2008, 39:312–323.View ArticlePubMedPubMed CentralGoogle Scholar
  36. Shishodia S, Potdar P, Gairola CG, Aggarwal BB: Curcumin (diferuloylmethane) down-regulates cigarette smoke-induced NF-kappaB activation through inhibition of IkappaBalpha kinase in human lung epithelial cells: correlation with suppression of COX-2, MMP-9 and cyclin D1. Carcinogenesis 2003, 24:1269–1279.View ArticlePubMedGoogle Scholar
  37. Suzuki M, Betsuyaku T, Ito Y, Nagai K, Odajima N, Moriyama C, Nasuhara Y, Nishimura M: Curcumin attenuates elastase- and cigarette smoke-induced pulmonary emphysema in mice. Am J Physiol Lung Cell Mol Physiol 2009, 296:L614–623.View ArticlePubMedGoogle Scholar
  38. Kasielski M, Nowak D: Long-term administration of N-acetylcysteine decreases hydrogen peroxide exhalation in subjects with chronic obstructive pulmonary disease. Respir Med 2001, 95:448–456.View ArticlePubMedGoogle Scholar
  39. Maestrelli P, Paska C, Saetta M, Turato G, Nowicki Y, Monti S, Formichi B, Miniati M, Fabbri LM: Decreased haem oxygenase-1 and increased inducible nitric oxide synthase in the lung of severe COPD patients. Eur Respir J 2003, 21:971–976.View ArticlePubMedGoogle Scholar
  40. Ichinose M, Sugiura H, Yamagata S, Koarai A, Shirato K: Increase in reactive nitrogen species production in chronic obstructive pulmonary disease airways. Am J Respir Crit Care Med 2000, 162:701–706.View ArticlePubMedGoogle Scholar
  41. Shinohara T, Kaneko T, Nagashima Y, Ueda A, Tagawa A, Ishigatsubo Y: Adenovirus-mediated transfer and overexpression of heme oxygenase 1 cDNA in lungs attenuates elastase-induced pulmonary emphysema in mice. Hum Gene Ther 2005, 16:318–327.View ArticlePubMedGoogle Scholar
  42. Chen JC, Ho FM, Pei-Dawn Lee C, Chen CP, Jeng KC, Hsu HB, Lee ST, Wen Tung W, Lin WW: Inhibition of iNOS gene expression by quercetin is mediated by the inhibition of IkappaB kinase, nuclear factor-kappa B and STAT1, and depends on heme oxygenase-1 induction in mouse BV-2 microglia. Eur J Pharmacol 2005, 521:9–20.View ArticlePubMedGoogle Scholar
  43. Comalada M, Ballester I, Bailon E, Sierra S, Xaus J, Galvez J, de Medina FS, Zarzuelo A: Inhibition of pro-inflammatory markers in primary bone marrow-derived mouse macrophages by naturally occurring flavonoids: analysis of the structure-activity relationship. Biochem Pharmacol 2006, 72:1010–1021.View ArticlePubMedGoogle Scholar
  44. Mu MM, Chakravortty D, Sugiyama T, Koide N, Takahashi K, Mori I, Yoshida T, Yokochi T: The inhibitory action of quercetin on lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophage cells. J Endotoxin Res 2001, 7:431–438.View ArticlePubMedGoogle Scholar
  45. Minamoto K, Harada H, Lama VN, Fedarau MA, Pinsky DJ: Reciprocal regulation of airway rejection by the inducible gas-forming enzymes heme oxygenase and nitric oxide synthase. J Exp Med 2005, 202:283–294.View ArticlePubMedPubMed CentralGoogle Scholar
  46. Davies SP, Reddy H, Caivano M, Cohen P: Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J 2000, 351:95–105.View ArticlePubMedPubMed CentralGoogle Scholar
  47. Agullo G, Gamet-Payrastre L, Manenti S, Viala C, Remesy C, Chap H, Payrastre B: Relationship between flavonoid structure and inhibition of phosphatidylinositol 3-kinase: A comparison with tyrosine kinase and protein kinase C inhibition. Biochem Pharmocol 1997, 53:1649–1657.View ArticleGoogle Scholar
  48. Huang Y-T, Hwang J-J, Lee P-P, Ke F-C, Huang J-H, Huang C-J, Kandaswami C, Middleton E Jr, Lee M-T: Effects of luteolin and quercetin, inhibitors of tyrosine kinase, on cell growth and metastasis-associated properties in A431 cells overexpressing epidermal growth factor receptor. Br J Pharmacol 1999, 128:999–1010.View ArticlePubMedPubMed CentralGoogle Scholar
  49. Peet GW, Li J: IkappaB kinases alpha and beta show a random sequential kinetic mechanism and are inhibited by staurosporine and quercetin. J Biol Chem 1999, 274:32655–32661.View ArticlePubMedGoogle Scholar
  50. Vlahos CJ, Matter WF, Hui KY, Brown RF: A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002). J Biol Chem 1994, 269:5241–5248.PubMedGoogle Scholar
  51. Babusyte A, Stravinskaite K, Jeroch J, Lotvall J, Sakalauskas R, Sitkauskiene B: Patterns of airway inflammation and MMP-12 expression in smokers and ex-smokers with COPD. Respir Res 2007, 8:81.View ArticlePubMedPubMed CentralGoogle Scholar
  52. Demedts IK, Morel-Montero A, Lebecque S, Pacheco Y, Cataldo D, Joos GF, Pauwels RA, Brusselle GG: Elevated MMP-12 protein levels in induced sputum from patients with COPD. Thorax 2006, 61:196–201.View ArticlePubMedGoogle Scholar
  53. Ohnishi K, Takagi M, Kurokawa Y, Satomi S, Konttinen YT: Matrix metalloproteinase-mediated extracellular matrix protein degradation in human pulmonary emphysema. Lab Invest 1998, 78:1077–1087.PubMedGoogle Scholar
  54. Deshmukh HS, McLachlan A, Atkinson JJ, Hardie WD, Korfhagen TR, Dietsch M, Liu Y, Di PY, Wesselkamper SC, Borchers MT, et al.: Matrix metalloproteinase-14 mediates a phenotypic shift in the airways to increase mucin production. Am J Respir Crit Care Med 2009, 180:834–845.View ArticlePubMedPubMed CentralGoogle Scholar
  55. Deshmukh HS, Shaver C, Case LM, Dietsch M, Wesselkamper SC, Hardie WD, Korfhagen TR, Corradi M, Nadel JA, Borchers MT, et al.: Acrolein-activated matrix metalloproteinase 9 contributes to persistent mucin production. Am J Respir Cell Mol Biol 2008, 38:446–454.View ArticlePubMedGoogle Scholar
  56. Park HJ, Lee CM, Jung ID, Lee JS, Jeong YI, Chang JH, Chun SH, Kim MJ, Choi IW, Ahn SC, et al.: Quercetin regulates Th1/Th2 balance in a murine model of asthma. Internat Immunopharmacol 2009, 9:261–267.View ArticleGoogle Scholar
  57. Conquer JA, Maiani G, Azzini E, Raguzzini A, Holub BJ: Supplementation with quercetin markedly increases plasma quercetin concentration without effect on selected risk factors for heart disease in healthy subjects. J Nutr 1998, 128:593–597.PubMedGoogle Scholar
  58. Hollman PC, van Trijp JM, Mengelers MJ, de Vries JH, Katan MB: Bioavailability of the dietary antioxidant flavonol quercetin in man. Cancer Lett 1997, 114:139–140.View ArticlePubMedGoogle Scholar
  59. Harwood M, Danielewska-Nikiel B, Borzelleca JF, Flamm GW, Williams GM, Lines TC: A critical review of the data related to the safety of quercetin and lack of evidence of in vivo toxicity, including lack of genotoxic/carcinogenic properties. Food Chem Toxicol 2007, 45:2179–2205.View ArticlePubMedGoogle Scholar
  60. Boots AW, Li H, Schins RP, Duffin R, Heemskerk JW, Bast A, Haenen GR: The quercetin paradox. Toxicol Appl Pharmacol 2007, 222:89–96.View ArticlePubMedGoogle Scholar
  61. Biasutto L, Sassi N, Mattarei A, Marotta E, Cattelan P, Toninello A, Garbisa S, Zoratti M, Paradisi C: Impact of mitochondriotropic quercetin derivatives on mitochondria. Biochim Biophys Acta 2010, 1797:189–196.View ArticlePubMedGoogle Scholar
  62. Papi A, Bellettato CM, Braccioni F, Romagnoli M, Casolari P, Caramori G, Fabbri LM, Johnston SL: Infections and airway inflammation in chronic obstructive pulmonary disease severe exacerbations. Am J Respir Crit Care Med 2006, 173:1114–1121.View ArticlePubMedGoogle Scholar
  63. Rajendrasozhan S, Yang SR, Kinnula VL, Rahman I: SIRT1, an antiinflammatory and antiaging protein, is decreased in lungs of patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2008, 177:861–870.View ArticlePubMedPubMed CentralGoogle Scholar
  64. Mahadeva R, Shapiro SD: Chronic obstructive pulmonary disease 3: Experimental animal models of pulmonary emphysema. Thorax 2002, 57:908–914.View ArticlePubMedPubMed CentralGoogle Scholar

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