Mediators of Inflammation

Volume 2014 (2014), Article ID 523684, 8 pages

http://dx.doi.org/10.1155/2014/523684

Research Article

Epigallocatechin Gallate Attenuates Proliferation and Oxidative Stress in Human Vascular Smooth Muscle Cells Induced by Interleukin-1 via Heme Oxygenase-1

Po-Len Liu,¹ Jung-Tung Liu,2,3 Hsuan-Fu Kuo,⁴ Inn-Wen Chong,1,5 and Chong-Chao Hsieh⁵

¹Department of Respiratory Therapy, College of Medicine, and Department of Medical Research, Translational Research Center, Kaohsiung Medical University, Kaohsiung 807, Taiwan

²School of Medicine, College of Medicine, Chung Shan Medical University, Taichung 402, Taiwan

³Department of Neurosurgery, Chung Shan Medical University Hospital, Taichung 402, Taiwan

⁴Department of Internal Medicine, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 801, Taiwan

⁵Department of Internal Medicine, Department of Chest Surgery, Division of Cardiovascular Surgery and Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan

Received 13 June 2014; Accepted 8 August 2014; Published 7 September 2014

Academic Editor: Yung-Hsiang Chen

Copyright © 2014 Po-Len Liu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Proliferation of vascular smooth muscle cells (VSMCs) triggered by inflammatory stimuli and oxidative stress contributes importantly to atherogenesis. The association of green tea consumption with cardiovascular protection has been well documented in epidemiological observations, however, the underlying mechanisms remain unclear. This study aimed to elucidate the effects of the most active green tea catechin derivative, (−)-epigallocatechin-3-gallate (EGCG), in human aortic smooth muscle cells (HASMCs), focusing particularly on the role of a potent anti-inflammatory and antioxidative enzyme heme oxygenase-1 (HO-1). We found that pretreatment of EGCG dose- and time-dependently induced HO-1 protein levels in HASMCs. EGCG inhibited interleukin- (IL-)1-induced HASMC proliferation and oxidative stress in a dose-dependent manner. The HO-1 inducer CoPPIX decreased IL-1-induced cell proliferation, whereas the HO-1 enzyme inhibitor ZnPPIX significantly reversed EGCG-caused growth inhibition in IL-1-treated HASMCs. At the molecular level, EGCG treatment significantly activated nuclear factor erythroid-2-related factor (Nrf2) transcription activities. These results suggest that EGCG might serve as a complementary and alternative medicine in the treatment of these pathologies by inducing HO-1 expression and subsequently decreasing VSMC proliferation.

1. Introduction

Atherosclerosis, the major pathological condition for most stroke syndromes, has been the intense focus of basic, clinical, and epidemiological studies. These studies have direct bearing on the prevention of atherothrombotic brain infarction [1–3]. Atherosclerosis is typically multifactorial, most often dependent on oxidative stress-related risk factors such as hypercholesterolemia, diabetes, smoking, hypertension, and obesity. Complications of atherosclerosis remain the leading cause of morbidity and mortality in industrialized countries [4–6].

The migration of smooth muscle cells into the intima, followed by their proliferation, is a central theme of atherosclerosis and restenosis. Various studies suggest that these events are preceded and accompanied by oxidative stress and inflammation [7–9]. Cytokines of the interleukin-1 (IL-1β) family play a pivotal role in regulating inflammatory responses, and extensive studies have been performed to determine whether IL-1β modifies the inflammatory response [10, 11]. IL-1β induces a substantial increase in the expression of inflammatory factors by vascular smooth muscle cells (VSMCs), and these factors promote leukocyte recruitment and infiltration into the arterial wall and stimulate VSMC proliferation [12, 13]. Recent studies have shown increased levels of IL-1β in human atherosclerotic lesions [14].

The consumption of green tea has attracted attention because of its beneficial effects on health. The association of green tea consumption with cardiovascular protection has been well documented in epidemiological observations [15]. The polyphenolic catechins found in green tea include (−)-epigallocatechin-3-gallate (EGCG) (Figure 1), (−)-epicatechin-3-gallate (ECG), (−)-epigallocatechin (EGC), and epicatechin (EC). These phenolic compounds appear to interfere with the molecular processes underlying the initiation, progression, and rupture of atherosclerotic plaques [16]. EGCG is the most abundant and most active catechin derivative and has been reported to exhibit both anti-inflammatory and antiatherogenic properties in experimental studies associated with its antioxidative activity [17].

Figure 1: Chemical structure of (−)-epigallocatechin-3-gallate (EGCG), the most abundant and most active catechin derivative from green tea.

Heme oxygenase-1 (HO-1) is a member of the heat shock protein family. Its expression is triggered by diverse stress inducing stimuli including hypoxia, heavy metals, UV radiation, and reactive oxygen species (ROS) [18–20]. HO-1 can catalyze heme to carbon monoxide and bilirubin with a concurrent release of iron. The physiologic functions of HO-1 entail antioxidation, anti-inflammation, antiproliferation, and antiapoptosis effects [21]. Recent studies suggest that plant-derived chemical substances may act as inducers of the response protein HO-1 and can maximize the intrinsic antioxidant potential of compounds [22].

In this study, we analyzed the potency of EGCG as an inducer of HO-1 expression in human aortic smooth muscle cells (HASMCs) and explored whether this contributed to the protective effects of this polyphenolic compound against smooth muscle cell proliferation and oxidative stress.

2. Materials and Methods

2.1. Cell Culture

HASMCs (Cascade Biologics, OR, USA) were grown and passaged as described previously [23, 24]. Cells were used at passages 3–8. The purity of HASMC cultures was verified by immunostaining with a monoclonal antibody directed against smooth-muscle-specific α-actin (R&D Systems, MN, USA). Before treatment or stimulation with reagents, the cells were serum starved for 24 h.

2.2. Western Blot Analysis

Total cell lysates were prepared in lysis buffer (20 mM Tris-HCl, 150 mM NaCl, 1 mM EDTA, 1 mM EGTA, 1% Triton, 2.5 mM sodium pyrophosphate, 1 mM glycerophosphate, 1 mM Na₃VO₄, 1 μg/mL leupeptin, and 1 mM PMSF, pH 7.5). The protein concentration was determined with a Bio-Rad protein assay reagent (BIO-RAD, CA, USA) and the samples were stored at −70°C [25].

Western blot analysis was used to determine the changes in cell levels of HO-1 in HASMCs. Proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to polyvinylidene fluoride (PVDF) membrane, and then the membranes were blocked with 5% milk. The PVDF membranes were probed with goat anti-HO-1 antibody (R&D Systems, MN, USA) at 1 : 1000 and then incubated with horseradish peroxidase- (HRP-) conjugated secondary antibodies and the proteins were visualized with an enhanced chemiluminescence detection kit (Amersham Biosciences, NJ, USA). Mouse anti-β-actin (Labvision/NeoMarkers, CA, USA) antibodies were used as loading controls. Protein expression levels will be quantified as optical densities, using ImageQuant software [26].

2.3. BrdU Incorporation Assay for Cell Proliferation

HASMCs were seeded on 96-well plates at a density of 1 × 10⁴ cells/well. Cells were incubated with various concentrations of EGCG for 24 h and then stimulated with 50 ng/mL of IL-1β for 8 h. DNA synthesis was measured using a 5-bromo-20-deoxyuridine (BrdU) cell proliferation kit (Calbiochem, Darmstadt, Germany). Briefly, after 4 h of incubation with IL-1β, BrdU labeling solution (BrdU concentration: 10 μM) was added to the cells and incubated for another 4 h. After removing the culture medium, the cells were fixed and nucleases were added to partially digest cellular DNA. Anti-BrdU antibody was then added before adding the mouse IgG-peroxidase conjugate. The signal was developed with tetramethylbenzidine solution in the dark. A spectrophotometric plate reader to measure absorbance was used at dual wavelengths of 450 nm/595 nm [27].

2.4. Cell Cycle Analyses with Flow Cytometry

Analysis of the DNA content and the movement of the cells through the mitotic cycle were performed by flow cytometry 24 h after cell stimulation. HASMCs were harvested and fixed in 70% ethanol; then cells were washed with ice-cold PBS and incubated with RNAase (Sigma, MO, USA) and propidium iodide (Sigma, MO, USA). Cell cycle phase analysis was performed by flow cytometry using a FACScan (Becton Dickinson, NJ, USA), and the percentage of cells in different phases of the cell cycle was analyzed using ModFitLT software (BD, NJ, USA) [28].

2.5. Detection of ROS Production

The effect of EGCG on ROS production in HASMCs was determined by a fluorometric assay using DCFH-DA as the probe. This method is based on the oxidation by H₂O₂ of nonfluorescent DCFH-DA to fluorescent 2′,7′-dichlorofluorescin (DCF). Confluent HASMCs (10⁴ cells/well) in 48-well plates will be pretreated with various concentrations of EGCG. The cells were washed with HBSS, then HBSS containing 10 μM DCFH-DA was added, and incubation continued for 45 min at 37°C. The fluorescence intensity (relative fluorescence units) was measured at 485 nm excitation and 530 nm emission using a Fluorescence Microplate Reader [29].

2.6. Measurement of Glutathione (GSH) and Thiobarbituric Acid Reactive Substances (TBARS) Levels

Intracellular GSH levels were measured using a colorimetric assay (Bioxytech GSH-400; OxisResearch, Portland, OR). Briefly, cells were washed with PBS, and metaphosphoric acid (5%) was added to the cells, which were then scraped off. The mixture was centrifuged at 3,000 g for 5 min at 4°C, and the supernatant was measured at 400 nm after a chemical reaction with reagent R1 (4-chloro-1-methyl-7-trifluromethyl-quinolinium methylsulfate) and reagent R2 (30% NaOH). A known concentration of GSH was used to generate a standard curve [30].

Lipid peroxidation was quantified by measuring TBARS by spectrophotometric assay (Beckman Coulter, DU 640 spectrophotometer, Germany) according to a previous study. The level of lipid peroxides, expressed as nanomoles of malondialdehyde (MDA) per milligram of protein, was calculated from the absorbance at 532 nm using tetraethoxypropane (TEP) as an external standard [30].

2.7. Nuclear Extract Preparation and Electrophoretic Mobility Shift Assay (EMSA)

Nuclear protein extracts were prepared as previously described [19]. In brief, cells were scraped off the plates in an ice-cold HEPES buffer. After centrifugation at 300 g for 10 minutes at 4°C, the cells were solubilized with the above buffer with 0.1% Triton X-100 and centrifuged at 12,000 g for 10 minutes at 4°C. The nuclear pellets were resuspended in a buffer (10 mM HEPES, pH 7.9, 1.5 mM MgCl₂, 0.42 M NaCl, 1 mM DTT, 0.2 mM EDTA, 1.0 mM PMSF, 25% glycerol, 0.5 mM PMSF, 2 μg/mL aprotinin, 2 μg/mL pepstatin, and 2 μg/mL leupeptin), incubated for 30 minutes at 4°C, and centrifuged at 15,000 g for 30 minutes at 4°C.

The probe for nuclear factor E2-related factor-2 (Nrf2) gel shift assays was a synthetic double-stranded oligonucleotide (5′-AGA TTT TGC TGA GTC ACC AGT CCC-3′) containing the consensus Nrf2 binding site with antioxidant response element (ARE) [31]. For EMSA, doubled-stranded DNA was end-labeled with dig-dUTP using terminal transferase (Roche, Germany). The DNA-binding reaction was performed with 5 μg nuclear proteins and 0.8 ng digoxin-labeled oligonucleotide at room temperature for 15 minutes. Nuclear extract-oligonucleotide mixtures were separated from the unbound DNA probe by electrophoresis through a native 6% polyacrylamide gel in 0.5× TBE (Tris-Borate-EDTA buffer, pH 8.0). The digoxin-labeled oligonucleotide was detected with anti-digoxin antibody conjugated with alkaline phosphatase [32].

2.8. Statistical Analyses

Values will be expressed as means ± standard deviation (SD). Statistical evaluation was performed using Student’s t-test or one-way ANOVA followed by Dunnett’s test. A value of <0.05 was considered significant.

3. Results

3.1. EGCG Increases HO-1 Expression in HASMCs

To test the effects of EGCG on HO-1 expression in HASMCs, EGCG (12.5, 25, 37.5, and 50 μM) was added in culture medium with HASMCs for 24 h, and Western blot was performed for HO-1 protein expression. As shown in Figure 2(a), EGCG dose-dependently increased HO-1 protein expression in HASMCs. Moreover, EGCG time-dependently (6, 12, 18, and 24 h) increased HO-1 protein expression in HASMCs.

(a)

(b)

Figure 2: EGCG (a) dose- and (b) time-dependently induces HO-1 protein expression in HASMCs. Data are expressed as mean SD of three independent experiments. compared with medium alone condition.

3.2. Inhibitory Effect of EGCG on Proliferation and Oxidative Stress in HASMCs Induced by IL-1β

To investigate whether EGCG inhibits the proliferation of HASMCs induced by inflammatory cytokine IL-1β, HASMCs cells were incubated with IL-1β (50 ng/mL) with EGCG (10–50 μM) for 24 h, and BrdU incorporation assay was performed. EGCG had a dose-dependent effect to reduce proliferation of IL-1β-treated HASMCs. The significance was found in 30, 40, and 50 μM concentration (Figure 3(a)).

(a)

(b)

Figure 3: EGCG dose-dependently inhibits (a) cell proliferation and (b) ROS production in IL-1β-treated HASMCs. Data are expressed as mean SD of three independent experiments. versus control group; versus IL-1β-treated group.

Flow cytometric analysis was then used to determine whether the EGCG-induced cell growth inhibition was due to arrest at a specific point of the cell cycle. As shown in Table 1, flow cytometric analysis of the DNA content in HASMCs showed that EGCG treatment caused a significant increase in the percentage of cells in G₀/G₁ phase and a significant decrease in the S populations relative to IL-1β-treated cells.

Table 1: Effect of EGCG on the cell cycle distribution in IL-1-treated HASMCs.

Phase
IL-1
EGCG + IL-1
value

Sub-G₁
2.2% ± 1.1%
3.7% ± 1.2%
0.186

G₀/G₁
54.2% ± 7.9%
75.4% ± 8.3%
0.033*

S
31.6% ± 5.3%
11.3% ± 4.3%
0.007*

G₂/M
12.0% ± 2.3%
9.6% ± 2.5%
0.288

< 0.05.

To directly evaluate the effect of EGCG on ROS production, we evaluated ROS level in IL-1β-treated HASMCs. As shown in Figure 3(b), treatment with IL-1β (50 ng/mL) for 30 min caused a higher increase of fluorescence compared with control cells. However, pretreatment of HASMCs for 30 min with EGCG (10–50 μM) dose-dependently and significantly inhibited IL-1β-induced ROS generation.

In addition, Table 2 shows that EGCG treatment caused a significant increase of GSH content and a significant decrease of TBARS content relative to IL-1β-treated cells.

Table 2: The GSH and TBARS levels in EGCG and IL-1-treated HASMCs.

IL-1
EGCG + IL-1
value

GSH

(nmol/mg protein)
27.3 ± 2.4
42.5 ± 3.5
0.003*

TBARS

(nmol/mg protein)
7.2 ± 1.4
3.4 ± 1.8
0.045*

< 0.05.

3.3. EGCG Attenuates IL-1β-Induced Proliferation via HO-1

We assayed the effect of HO-1 expression on IL-1β-induced cell proliferation. As shown in Figure 4, we found that the HO-1 inducer CoPPIX decreased IL-1β-induced cell proliferation, whereas the HO-1 enzyme inhibitor, ZnPPIX, significantly reversed EGCG-caused growth inhibition in IL-1β-treated HASMCs.

Figure 4: CoPPIX and ZnPPIX modulate proliferation inhibitory effect of EGCG in IL-1β-treated HASMCs. Data are expressed as mean SD of three independent experiments. versus control group; versus IL-1β-treated group; versus EGCG and IL-1β-treated group.

3.4. EGCG Activates Nrf2 in HASMCs

Activation of Nrf2 increases Nrf2 accumulation in the nucleus. It has been suggested that the regulation of Nrf2 transcriptional activation of HO-1 relies on subcellular distribution rather than induction of this transcription factor through de novo synthesis [31, 33]. Thus, we determined nuclear activation of Nrf2 in both control and EGCG-treated cells. As shown by EMSA in Figure 5, EGCG treatment significantly activated Nrf2 transcription activities through binding specifically to the ARE found in the promoters of target genes.

Figure 5: Effect of EGCG on Nrf-2 activation. Data are expressed as mean SD of three independent experiments. versus control group.

4. Discussion

The present study showed that, for the first time, green tea EGCG attenuated IL-1β-induced proliferation of HASMCs via HO-1-related mechanisms. EGCG treatment induced the arrest of cell cycle progression and increased ROS production as results in GSH deficiency and lipid peroxidation in VSMCs. Our data also suggest that Nrf-2 mediated HO-1 expression may play a pivotal role for the antiproliferative effect of EGCG on VSMCs.

Atherosclerosis causes clinical diseases through luminal narrowing of the brain (ischemic stroke), heart, and peripheral vessels. Oxidative stress contributes to the progression of cerebrovascular disease. It can induce important processes leading to cerebral aneurysm formation including direct endothelial damage as well as smooth muscle cell phenotypic switching to a proliferative and inflammatory phenotype [34]. Epidemiological studies indicated that regular consumption of green tea is associated with a reduced risk of coronary heart disease [35, 36]. In vitro investigations have indicated that green tea polyphenolic compounds are able to inhibit several key events of the atherogenic process such as proliferation and migration of VSMCs by redox-sensitive mechanisms. EGCG-mediated HO-1 induction has been shown to occur in endothelial cells [31, 37–39], epithelial cells [40], neurons [41], kidney [42, 43], and pulmonary cells [44–46]. In the present study, the antioxidant properties of EGCG were further reported to protect against cardiovascular diseases by inhibiting inflammatory cytokine-induced VSMC proliferation via HO-1 induction. Thus, our results elucidated the relationship with inflammation, ROS, and regulation of atheroprotective genes HO-1 and how the regulation of these activities by EGCG can lead to a prevention of vascular diseases.

During atherogenesis, chronic inflammation and oxidative stress play a crucial role in VSMC activation. To eliminate the oxidative stress, endogenous antioxidant enzymes including HO-1 induction are evoked. The beneficial effects of HO-1 upregulation have been reported in a series of animal models [47]. Induction HO-1 induction is mediated by various mechanisms, including the blockade of immune response and increased production of carbon oxide [48]. HO-1 protects VSMCs from oxidative damage and against VSMC proliferation [49, 50]. In the present study, EGCG dose- and time-dependently induced HO-1 expression in HASMCs. Consistent with our results, EGCG also increases HO-1 expression and shows anti-inflammatory capacity in various cells such as endothelial cells [31, 37, 39] and monocytic cells [51]. All these findings suggest that EGCG is a strong inducer of HO-1 and such induction may be independent of various cell types.

Cell cycle is a major convergent point in VSMC proliferation. This process is controlled by multiple protein kinases and regulatory cyclins [52]. Negative regulators of the protein kinases and cyclins, therefore arresting the cell cycle at G₀/G₁ phase [48]. In the present study, EGCG inhibited DNA synthesis and arrested the cell cycle at G₀/G₁ phase. Thus, the protein levels of negative regulators of the protein kinases and cyclins need to be further investigated. Nevertheless, based on these findings, it is reasonable to speculate that the inhibitory effects of EGCG on VSMC proliferation are mediated by the induction of a cell cycle arrest.

Oxidative stress is defined as the imbalanced redox status in which prooxidants overwhelm antioxidant capacity, resulting in increased production of ROS. ROS have been implicated in the pathogenesis of virtually every stage of atherosclerosis [7, 8, 53]. ROS, especially superoxide anion and hydrogen peroxide, are important signaling molecules in cardiovascular cells. ROS participate in growth, apoptosis, and migration of VSMCs; these events play important roles in vascular diseases, suggesting that the sources of ROS and the signaling pathways that they modify may represent important therapeutic targets [54]. Numerous studies have shown that ROS influence cellular processes in vascular remodeling by turning on several intracellular signaling cascades. ROS potently activate mitogen-activated protein kinase members important in cell growth and differentiation, which induce expression of proinflammatory genes that play a role in the vascular inflammation associated with hypertension and atherosclerosis [54]. The present study provides the direct evidences that EGCG could maintain the concentrations of intracellular antioxidants found in biological systems. EGCG maintained GSH amounts in inflammatory cytokine-stressed HASMCs resulting in decreased TBARS.

Advances in signal transduction network indicate that a battery of redox-sensitive transcription factors, such Nrf2, and their upstream kinases play an important regulatory role in HO-1 gene induction [55]. The transcription factor Nrf2 plays an essential role in the ARE-mediated expression of phase II detoxifying and antioxidant enzymes and in the activation of other stress inducible genes. These genes may play a vital role in the prevention of cell dysfunction as a result of free radical production [56]. In the present study, Nrf2 was found to be markedly induced in HASMCs exposed to EGCG. The translocation of Nrf2 into the nucleus with treatment of EGCG was also found to be associated with increases in its ARE transcriptional activity. Our data therefore suggest that EGCG may induce many ARE-associated genes via its potent induction of Nrf2.

5. Conclusions

In summary, our results demonstrated that (1) EGCG dose- and time-dependently induces HO-1 expression in HASMCs; (2) EGCG dose-dependently inhibits IL-1β-induced HASMC proliferation and cell cycle arrest; (3) EGCG dose-dependently reduces IL-1β-induced oxidative stress in HASMC; and (4) Nrf-2 mediated HO-1 expression may play a pivotal role for the antiproliferative effect of EGCG on VSMCs. Thus, EGCG may likely fulfill the definition of a pharmacological preconditioning agent for preventing cerebrovascular and cardiovascular diseases.

Conflict of Interests

The authors declare that they have no conflict of interests.

Acknowledgments

This work was supported in part by the Kaohsiung Medical University (KMUH102-2M18) and the Ministry of Science and Technology, Taiwan (MOST 103-2314-B-037-051 and NSC 102-2314-B-037-067).

References

F. M. Yatsu and M. Fisher, “Atherosclerosis: current concepts on pathogenesis and interventional therapies,” Annals of Neurology, vol. 26, no. 1, pp. 3–12, 1989.

M. Fisher, “Atherosclerosis: cellular aspects and potential interventions,” Cerebrovascular and Brain Metabolism Reviews, vol. 3, no. 2, pp. 114–133, 1991.

L. Liu, X. Xu, J. Li, X. Li, and W. Sheng, “Lentiviral-mediated shRNA silencing of PDE4D gene inhibits platelet-derived growth factor-induced proliferation and migration of rat aortic smooth muscle cells,” Stroke Research and Treatment, vol. 2011, Article ID 534257, 7 pages, 2011.

J. Patel, K. M. Channon, and E. McNeill, “The downstream regulation of chemokine receptor signalling: implications for atherosclerosis,” Mediators of Inflammation, vol. 2013, Article ID 459520, 12 pages, 2013.

O. Zimmermann, K. Li, and M. Zaczkiewicz, “C-reactive protein in human atherogenesis: facts and fiction,” Mediators of Inflammation, vol. 2014, Article ID 561428, 6 pages, 2014.

F. Strang and H. Schunkert, “C-reactive protein and coronary heart disease: all said—is not it?” Mediators of Inflammation, vol. 2014, Article ID 757123, 7 pages, 2014.

C.-P. Lin, Y.-H. Chen, H.-B. Leu et al., “Anti-inflammatory strategies for homocysteine-related cardiovascular disease,” Frontiers in Bioscience, vol. 14, no. 10, pp. 3836–3845, 2009.

C.-P. Lin, F.-Y. Lin, P.-H. Huang et al., “Endothelial progenitor cell dysfunction in cardiovascular diseases: role of reactive oxygen species and inflammation,” BioMed Research International, vol. 2013, Article ID 845037, 10 pages, 2013.

G. Maiolino, G. Rossitto, P. Caielli, and et al, “The role of oxidized low-density lipoproteins in atherosclerosis: the myths and the facts,” Mediators of Inflammation, vol. 2013, Article ID 714653, 13 pages, 2013.

C. J. Liang, C. W. Lee, and H. C. Sung, “Ganoderma lucidum polysaccharides reduce lipopolysaccharide-induced interleukin-1 beta expression in cultured smooth muscle cells and in thoracic aortas in mice,” Evidence-Based Complementary and Alternative Medicine, vol. 2014, Article ID 305149, 13 pages, 2014.

A. Bebes, F. Kovacs-Solyom, J. Prihoda, et al., “Interleukin-1 receptors are differentially expressed in normal and psoriatic T cells,” Mediators of Inflammation, vol. 2014, Article ID 472625, 9 pages, 2014.

S.-J. Lin, H.-T. Yen, Y.-H. Chen, H.-H. Ku, F.-Y. Lin, and Y.-L. Chen, “Expression of interleukin-1β and interleukin-1 receptor antagonist in oxLDL-treated human aortic smooth muscle cells and in the neointima of cholesterol-fed endothelia-denuded rabbits,” Journal of Cellular Biochemistry, vol. 88, no. 4, pp. 836–847, 2003.

O. Bădulescu, C. Bădescu, M. Ciocoiu, and M. Bădescu, “Interleukin-1-beta and dyslipidemic syndrome as major risk factors for thrombotic complications in type 2 diabetes mellitus,” Mediators of Inflammation, vol. 2013, Article ID 169420, 8 pages, 2013.

A. Qamar and D. J. Rader, “Effect of interleukin 1β inhibition in cardiovascular disease,” Current Opinion in Lipidology, vol. 23, no. 6, pp. 548–553, 2012.

P. Bhardwaj and D. Khanna, “Green tea catechins: defensive role in cardiovascular disorders,” Chinese Journal of Natural Medicines, vol. 11, no. 4, pp. 345–353, 2013.

P. E. Szmitko and S. Verma, “Antiatherogenic potential of red wine: clinician update,” The American Journal of Physiology—Heart and Circulatory Physiology, vol. 288, no. 5, pp. H2023–H2030, 2005.

P. V. A. Babu, H. Si, and D. Liu, “Epigallocatechin gallate reduces vascular inflammation in db/db mice possibly through an NF-κB-mediated mechanism,” Molecular Nutrition & Food Research, vol. 56, no. 9, pp. 1424–1432, 2012.

P.-L. Liu, J.-R. Tsai, A. L. Charles et al., “Resveratrol inhibits human lung adenocarcinoma cell metastasis by suppressing heme oxygenase 1-mediated nuclear factor-κB pathway and subsequently downregulating expression of matrix metalloproteinases,” Molecular Nutrition and Food Research, vol. 54, no. 2, pp. S196–S204, 2010.

J.-R. Tsai, H.-M. Wang, P.-L. Liu et al., “High expression of heme oxygenase-1 is associated with tumor invasiveness and poor clinical outcome in non-small cell lung cancer patients,” Cellular Oncology, vol. 35, no. 6, pp. 461–471, 2012.

X.-H. Li, X. Gong, L. Zhang et al., “Protective effects of polydatin on septic lung injury in mice via upregulation of HO-1,” Mediators of Inflammation, vol. 2013, Article ID 354087, 10 pages, 2013.

A. Grochot-Przeczek, J. Dulak, and A. Jozkowicz, “Haem oxygenase-1: non-canonical roles in physiology and pathology,” Clinical Science, vol. 122, no. 3, pp. 93–103, 2012.

B.-M. Choi, D.-W. Lim, J.-A. Lee, S. S. Gao, D. Y. Kwon, and B.-R. Kim, “Luteolin suppresses cisplatin-induced apoptosis in auditory cells: possible mediation through induction of heme oxygenase-1 expression,” Journal of Medicinal Food, vol. 11, no. 2, pp. 230–236, 2008.

F.-Y. Lin, Y.-H. Chen, Y.-W. Lin et al., “The role of human antigen R, an RNA-binding protein, in mediating the stabilization of toll-like receptor 4 mRNA induced by endotoxin: a novel mechanism involved in vascular inflammation,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 26, no. 12, pp. 2622–2629, 2006.

F.-Y. Lin, Y.-H. Chen, J.-S. Tasi et al., “Endotoxin induces toll-like receptor 4 expression in vascular smooth muscle cells via NADPH oxidase activation and mitogen-activated protein kinase signaling pathways,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 26, no. 12, pp. 2630–2637, 2006.

J.-W. Chen, Y.-H. Chen, and S.-J. Lin, “Long-term exposure to oxidized low-density lipoprotein enhances tumor necrosis factor-α-stimulated endothelial adhesiveness of monocytes by activating superoxide generation and redox-sensitive pathways,” Free Radical Biology & Medicine, vol. 40, no. 5, pp. 817–826, 2006.

Y.-H. Chen, S.-J. Lin, H.-H. Ku et al., “Salvianolic acid B attenuates VCAM-1 and ICAM-1 expression in TNF-α-treated human aortic endothelial cells,” Journal of Cellular Biochemistry, vol. 82, no. 3, pp. 512–521, 2001.

S.-J. Lin, T.-H. Yang, Y.-H. Chen et al., “Effects of Ginkgo biloba extract on the proliferation of vascular smooth muscle cells in vitro and on intimal thickening and interleukin-1 β expression after balloon injury in cholesterol-fed rabbits in vivo,” Journal of Cellular Biochemistry, vol. 85, no. 3, pp. 572–582, 2002.

P.-L. Liu, Y.-L. Chen, Y.-H. Chen, S.-J. Lin, and Y. R. Kou, “Wood smoke extract induces oxidative stress-mediated caspase-independent apoptosis in human lung endothelial cells: role of AIF and EndoG,” The American Journal of Physiology: Lung Cellular and Molecular Physiology, vol. 289, no. 5, pp. L739–L749, 2005.

J.-W. Chen, Y.-H. Chen, F.-Y. Lin, Y.-L. Chen, and S.-J. Lin, “Ginkgo biloba extract inhibits tumor necrosis factor-α-induced reactive oxygen species generation, transcription factor activation, and cell adhesion molecule expression in human aortic endothelial cells,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 23, no. 9, pp. 1559–1566, 2003.

Y.-H. Chen, F.-Y. Lin, P.-L. Liu et al., “Antioxidative and hepatoprotective effects of magnolol on acetaminophen-induced liver damage in rats,” Archives of Pharmacal Research, vol. 32, no. 2, pp. 221–228, 2009.

Y. Zheng, A. Morris, M. Sunkara, J. Layne, M. Toborek, and B. Hennig, “Epigallocatechin-gallate stimulates NF-E2-related factor and heme oxygenase-1 via caveolin-1 displacement,” Journal of Nutritional Biochemistry, vol. 23, no. 2, pp. 163–168, 2012.

T. Li, Y.-H. Chen, T.-J. Liu et al., “Using DNA microarray to identify Sp1 as a transcriptional regulatory element of insulin-like growth factor 1 in cardiac muscle cells,” Circulation Research, vol. 93, no. 12, pp. 1202–1209, 2003.

A. T. Dinkova-Kostova, W. D. Holtzclaw, R. N. Cole et al., “Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, no. 18, pp. 11908–11913, 2002.

R. M. Starke, N. Chalouhi, M. S. Ali et al., “The role of oxidative stress in cerebral aneurysm formation and rupture,” Current Neurovascular Research, vol. 10, no. 3, pp. 247–255, 2013.

R. Johnson, S. Bryant, and A. L. Huntley, “Green tea and green tea catechin extracts: an overview of the clinical evidence,” Maturitas, vol. 73, no. 4, pp. 280–287, 2012.

N. Khan and H. Mukhtar, “Tea and health: studies in humans,” Current Pharmaceutical Design, vol. 19, no. 34, pp. 6141–6147, 2013.

C. C. Wu, M. C. Hsu, C. W. Hsieh, J. B. Lin, P. H. Lai, and B. S. Wung, “Upregulation of heme oxygenase-1 by Epigallocatechin-3-gallate via the phosphatidylinositol 3-kinase/Akt and ERK pathways,” Life Sciences, vol. 78, no. 25, pp. 2889–2897, 2006.

Y. Zheng, M. Toborek, and B. Hennig, “Epigallocatechin gallate-mediated protection against tumor necrosis factor-α-induced monocyte chemoattractant protein-1 expression is heme oxygenase-1 dependent,” Metabolism: Clinical and Experimental, vol. 59, no. 10, pp. 1528–1535, 2010.

P. Pullikotil, H. Chen, R. Muniyappa et al., “Epigallocatechin gallate induces expression of heme oxygenase-1 in endothelial cells via p38 MAPK and Nrf-2 that suppresses proinflammatory actions of TNF-α,” Journal of Nutritional Biochemistry, vol. 23, no. 9, pp. 1134–1145, 2012.

H.-K. Na, E.-H. Kim, J.-H. Jung, H.-H. Lee, J.-W. Hyun, and Y.-J. Surh, “(-)-Epigallocatechin gallate induces Nrf2-mediated antioxidant enzyme expression via activation of PI3K and ERK in human mammary epithelial cells,” Archives of Biochemistry and Biophysics, vol. 476, no. 2, pp. 171–177, 2008.

L. Romeo, M. Intrieri, V. D'Agata et al., “The major green tea polyphenol, (-)-epigallocatechin-3-gallate, induces heme oxygenase in rat neurons and acts as an effective neuroprotective agent against oxidative stress,” Journal of the American College of Nutrition, vol. 28, pp. 492S–499S, 2009.

K. Sahin, M. Tuzcu, H. Gencoglu et al., “Epigallocatechin-3-gallate activates Nrf2/HO-1 signaling pathway in cisplatin-induced nephrotoxicity in rats,” Life Sciences, vol. 87, no. 7-8, pp. 240–245, 2010.

Y. Kakuta, M. Okumi, Y. Isaka et al., “Epigallocatechin-3-gallate protects kidneys from ischemia reperfusion injury by HO-1 upregulation and inhibition of macrophage infiltration,” Transplant International, vol. 24, no. 5, pp. 514–522, 2011.

M.-H. Kweon, V. M. Adhami, J.-S. Lee, and H. Mukhtar, “Constitutive overexpression of Nrf2-dependent heme oxygenase-1 in A549 cells contributes to resistance to apoptosis induced by epigallocatechin 3-gallate,” The Journal of Biological Chemistry, vol. 281, no. 44, pp. 33761–33772, 2006.

I.-T. Lee, C.-C. Lin, C.-Y. Lee, P.-W. Hsieh, and C.-M. Yang, “Protective effects of (-)-epigallocatechin-3-gallate against TNF-α-induced lung inflammation via ROS-dependent ICAM-1 inhibition,” Journal of Nutritional Biochemistry, vol. 24, no. 1, pp. 124–136, 2013.

H. You, L. Wei, W. L. Sun, et al., “The green tea extract epigallocatechin-3-gallate inhibits irradiation-induced pulmonary fibrosis in adult rats,” International Journal of Molecular Medicine, vol. 34, no. 1, pp. 92–102, 2014.

M. Zhang, B. H. Zhang, L. Chen, and W. An, “Overexpression of heme oxygenase-1 protects smooth muscle cells against oxidative injury and inhibits cell proliferation,” Cell Research, vol. 12, no. 2, pp. 123–132, 2002.

F. Jiang, R. Jiang, X. Zhu, X. Zhang, and Z. Zhan, “Genipin Inhibits TNF-α-Induced Vascular Smooth Muscle Cell Proliferation and Migration via Induction of HO-1,” PLoS ONE, vol. 8, no. 8, Article ID e74826, 2013.

R. R. Campos, “Oxidative stress in the brain and arterial hypertension,” Hypertension Research, vol. 32, no. 12, pp. 1047–1048, 2009.

J. E. Kim, Y. J. Kang, K. Y. Lee, and H. C. Choi, “Isoproterenol inhibits angiotensin II-stimulated proliferation and reactive oxygen species production in vascular smooth muscle cells through heme oxygenase-1,” Biological and Pharmaceutical Bulletin, vol. 32, no. 6, pp. 1047–1052, 2009.

R. M. Ogborne, S. A. Rushworth, and M. A. O'Connell, “Epigallocatechin activates haem oxygenase-1 expression via protein kinase C and Nrf2,” Biochemical and Biophysical Research Communications, vol. 373, no. 4, pp. 584–588, 2008.

C. J. Sherr, “Cancer cell cycles,” Science, vol. 274, no. 5293, pp. 1672–1677, 1996.

Y.-H. Chen, S.-J. Lin, Y.-L. Chen, P.-L. Liu, and J.-W. Chen, “Anti-inflammatory effects of different drugs/agents with antioxidant property on endothelial expression of adhesion molecules,” Cardiovascular and Hematological Disorders—Drug Targets, vol. 6, no. 4, pp. 279–304, 2006.

A. Fortuño, G. San José, M. U. Moreno, J. Díez, and G. Zalba, “Oxidative stress and vascular remodelling,” Experimental Physiology, vol. 90, no. 4, pp. 457–462, 2005.

E. O. Farombi and Y.-J. Surh, “Heme oxygenase-1 as a potential therapeutic target for hepatoprotection,” Journal of Biochemistry and Molecular Biology, vol. 39, no. 5, pp. 479–491, 2006.

H. S. Marinho, C. Real, L. Cyrne, H. Soares, and F. Antunes, “Hydrogen peroxide sensing, signaling and regulation of transcription factors,” Redox Biology, vol. 2, pp. 535–562, 2014.