Ginseng Berry Extract Prevents Atherogenesis via Anti-Inflammatory Action by Upregulating Phase II Gene Expression

Ginseng berry possesses higher ginsenoside content than its root, which has been traditionally used in herbal medicine for many human diseases, including atherosclerosis. We here examined the antiatherogenic effects of the Korean ginseng berry extract (KGBE) and investigated its underlying mechanism of action in vitro and in vivo. Administration of KGBE decreased atherosclerotic lesions, which was inversely correlated with the expression levels of phase II genes to include heme oxygenase-1 (HO-1) and glutamine-cysteine ligase (GCL). Furthermore, KGBE administration suppressed NF-κB-mediated expression of atherogenic inflammatory genes (TNF-α, IL-1β, iNOS, COX-2, ICAM-1, and VCAM-1), without altering serum cholesterol levels, in ApoE−/− mice fed a high fat-diet. Treatment with KGBE increased phase II gene expression and suppressed lipopolysaccharide-induced reactive oxygen species production, NF-κB activation, and inflammatory gene expression in primary macrophages. Importantly, these cellular events were blocked by selective inhibitors of HO-1 and GCL. In addition, these inhibitors reversed the suppressive effect of KGBE on TNF-α-mediated induction of ICAM-1 and VCAM-1, resulting in decreased interaction between endothelial cells and monocytes. These results suggest that KGBE ameliorates atherosclerosis by inhibiting NF-κB-mediated expression of atherogenic genes via upregulation of phase II enzymes and thus has therapeutic or preventive potential for atherosclerosis.


Introduction
Although hyperlipidemia plays an important role in the pathogenesis of atherosclerosis [1], it is currently regarded as an inflammatory response of endothelial cell dysfunction at the initiation of atherosclerotic plaque formation [2]. Numerous evidences demonstrate that the pharmacological effects of statins, well-known antiatherogenic drugs on cardiovascular disease are closely correlated to their lipidlowering and anti-inflammatory activities [3]. Recent studies demonstrated that anti-inflammatory compounds prevent the development of atherosclerosis, without altering blood lipid profiles in hyperlipidemic mice [4,5], indicating that anti-inflammatory compounds may be used as therapeutic drugs for the treatment of atherosclerosis.
Inflammatory genes, such as tumor necrosis factorα (TNF-α), interleukin-1β (IL-1β), inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2), are highly expressed during atherosclerotic development [2,6]. Of these gene products, iNOS and COX-2 synthesize nitric oxide (NO) and prostaglandin E 2 (PGE 2 ), respectively, and are involved in the pathogenesis of atherosclerosis. However, TNF-α and IL-1β promote the expression of intercellular 2 Evidence-Based Complementary and Alternative Medicine adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) in endothelial cells in atherosclerotic lesions [7]. Moreover, the interaction between endothelial cells and monocytes resulted in an increase in the transmigration of circulating monocytes to the intimal area of the vascular walls. Importantly, the expression of these genes is tightly regulated by activation of the transcription factor nuclear factor-κB (NF-κB) [8].
NF-κB is a key player in inflammation gene expression and has a crucial role in atherosclerosis. In resting cells, NF-κB exists in a heterodimeric inactive form in the cytosol bound to the distinct inhibitor κB (IκB). Inflammatory stimulants activate the IκB kinase (IKK), which induces phosphorylation and proteasomal degradation of IκB. Liberated NF-κB translocates from the cytosol to the nucleus, where it promotes transcriptional induction of various inflammatory genes [8]. Recent studies have also demonstrated that herbal medicines and natural compounds can regulate NF-κB-mediated inflammation-associated gene expression by upregulation of phase II antioxidant enzymes, including heme oxygenase-1 (HO-1) and glutamine-cysteine ligase (GCL) [9,10]. Importantly, these enzymes inhibit intracellular accumulation of reactive oxygen species (ROS) involved in redox-dependent NF-κB activation [11].
The root of Panax ginseng contains ginsenosides as active components, which are major contributors to its pharmacological activities, including anti-inflammatory and antiatherosclerotic effects [12]. These components are distributed in many parts of the ginseng plant, including the root, berry, and leaf. Different parts of the plant contain distinct ginsenoside profiles [13], and these parts may possess different pharmacological activities. Recent studies demonstrate that ginseng berry exhibits more potent antihyperglycemic activity and antiobesity effects in a mouse model than those of its root [14,15]. Indeed, the ginseng berry has a different ginsenoside profile and higher ginsenoside content than its root [16]. Thus, the ginseng berry may exert more potent pharmacological effects on various human diseases than those of its root. However, the pharmacological effects of ginseng berry on atherosclerosis have not been studied.
The current study sought to determine if the Korean ginseng berry extract (KGBE) regulates atherosclerosis and to identify its underlying mechanism. We herein, demonstrate that KGBE suppressed atherosclerotic lesion development by inhibiting NF-κB-mediated atherogenic inflammatory gene expression via the induction of the phase II antioxidant enzymes HO-1 and GCL, without lowering serum lipid levels, in a hyperlipidemic mouse model. These results provide new insights into the therapeutic potential of KGBE for the treatment of atherosclerosis.

Preparation of Korean Ginseng Berry Extract (KGBE)
and Korean Red Ginseng Extract (KRGE). Korean ginseng berry was harvested, and the seeds were separated and removed. Next, the remnants were dried in hot air and refluxed with 70% ethanol for 10 h. After the extract was filtered and concentrated under reduced pressure at 45 • C, KGBE powder was finally obtained by lyophilization and stored at −20 • C until use. On the other hand, Korean red ginseng was extracted with reflux with 70% ethanol for 10 h. The extract was filtered according to a conventional method and concentrated under reduced pressure. KRGE powder was obtained by lyophilization and stored at −20 • C until use. The lyophilized extracts were dissolved in culture medium before use and mixed with mouse chow diets. For comparison and standardization of ginsenoside composition, seven major ginsenosides were analyzed in KGBE and KRGE through HPLC. Ginsenoside compositions and HPLC chromatograms of both extracts were summarized in Figures 1(a)-1(c).

Western Blot
Analysis. Whole-cell lysates as well as cytosolic and nuclear fractions were prepared as previously described [17]. Samples (30 μg protein) were separated on SDS-PAGE and transferred onto nitrocellulose membranes. The membranes were blocked with 5% nonfat-dried milk and hybridized with primary and secondary antibodies against target proteins. Protein bands were visualized by incubating membranes with chemiluminescent solution for 2 min and exposure to X-ray film.  method [17]. Amplification conditions were as follows: denaturation at 94 • C for 5 min for the first cycle and for 45 s starting from the second cycle, annealing at 56 • C for 30 s for HO-1, GCL-catalytic subunit (GCLC), and βactin. Final extension was performed at 72 • C for 10 min. The primers used were 5 -GGCCCTGGAAGAGGAGATA-3 (sense) and 5 -GCTGGATGTGCTTTTGGTG-3 (antisense) for the HO-1, 5 -CACTGCCAGAACACAGACCC-3 (sense) and 5 -ATGGTCTGGCTGAGAAGCCT-3 for the GCLC and 5 -TCCTTCGTTGCCGGTCCACA-3 (sense) and 5 -CGTCTCCGGAGTCCATCACA-3 (antisense) for the βactin. The amplification conditions and primer sequences for TNF-α, IL-1β, iNOS, COX-2, ICAM-1, and VCAM-1 were the same as previously described [17,18]. The PCR products were separated on a 1% agarose gel and stained with ethidium bromide.

Reverse Transcription-Polymerase
2.6. Analysis of NF-κB Activation Pathway. Cells were pretreated with 100 μg/mL KGBE and inhibitors (20 μM SnPP and 20 μM BSO) for 30 min and then stimulated with 100 ng/mL LPS for 30 min in the presence or absence of the proteasome enzyme inhibitors and 5 μM MG132. Phosphorylation of IKK and IκB and nuclear translocation of the NF-κB p65 subunit were examined by Western blotting and immunohistochemical methods as described previously [17]. Electrophoretic gel mobility shift assay (EMSA) was performed for the measurement of NF-κB-DNA-binding activity using 32 P-labeled double-stranded NF-κB-specific oligonucleotide and nuclear extracts [17]. Supershift and competitive assays were performed following preincubation of the nuclear extracts with 2 μg of NF-κB p65 antibody or an excess (100-fold) of cold probe at room temperature for 30 min. For assay for promoter activity, cells were transfected with piNOS-Luc or pNF-κB-Luc in combination with pcDNA3-β-galactosidase using a lipofectamine method as described previously [17]. The cells were cultured for 20 h in fresh medium containing 5% fetal bovine serum and exposed to KGBE for 4 h, followed by stimulation with LPS for 12 h. Luciferase activity was measured in cell lysates by luminometer. Relative luciferase activity was calculated by normalization with β-galactosidase. Bedding was changed once a week, and the temperature and humidity were controlled. The mice were given water and food ad libitum. Body weights and food intake were measured weekly at regular times. After 16 weeks, mice were sacrificed by cervical dislocation, and the serum levels of total cholesterol (TC), high-density lipoprotein-cholesterol (HDL-C), lowdensity lipoprotein-cholesterol (LDL-C), and triglyceride were measured using a 7020 Automatic Analyzer (Hitachi, Japan).

Analysis of Atherosclerosis in Atherosclerotic Mice.
After mice were euthanized with carbon dioxide inhalation, the right atria were removed, and hearts and aortas were perfused with phosphate-buffered saline through the left ventricle. Analyses of en face and aortic sinus plaque lesions were performed as described previously [19].

Measurements of Nitric Oxide Metabolites, ROS, Cytokines, and PGE 2 .
Nitrite and nitrite plus nitrate (NO x ), stable oxidized products of NO, were measured in the culture media and serum using Griess reagents and a reductase-based colorimetric assay kit (Alexis San Diego, CA), respectively [17]. TNF-α, IL-1β and PGE 2 levels were determined in sera and culture media using ELISA kits. Macrophages were pretreated with 100 μg/mL KGBE in the presence or absence of 20 μM SnPP and 20 μM BSO for 30 min, followed by stimulation with LPS for 1 h. Intracellular ROS accumulation was determined using the H 2 O 2 -sensitive fluorescent dye, DCFH 2 -DA [17].
2.11. Statistical Analysis. All data are presented as the mean ± standard deviation (SD) of at least three independent experiments. Student's t-test was also performed to identify which group difference accounted for the significant overall analysis of variance. P < 0.05 was considered statistically significant.

KGBE Prevents Atherogenesis without Improving Serum
Lipid Profiles in ApoE −/− Mice. We analyzed major seven saponin components in KGBE and KRGE extracts. Of them, the six ginsenosides, Rb2, Rc, Rd, Re, Rg1, and Rg2, showed high levels in KGBE as compared with those of KRGE, which is a well-known ginseng product (Figure 1(a)). The extraction yields of KGBE and KRGE were 22.8% and 47.9%, respectively. We first investigated whether KGBE exerts an antiatherosclerotic effect in HFD-fed ApoE −/−  b)). In addition, HFD-fed mice developed significant plaque lesions in the intima of their aortic sinuses, compared with NCD-fed control mice, and this plaque lesions were statistically reduced by supplementation with KGBE (P < 0.01), but not with KRGE (P = 0.07) (Figures 2(c) and 2(d)). Taken together, these results indicate that KGBE elicits a higher antiatherogenic effect than KRGE. We also assessed whether KGBE regulates serum lipid levels in ApoE −/− mice fed a HFD (Table 1). No significant changes were observed in triglyceride, TC, LDL-C, and HDL-C levels between mice fed HFD alone and HFD supplemented with KGBE or KRGE. These results suggest that KGBE prevents atherosclerotic development without lowering serum lipid levels. Although not shown, the body weight between mice fed a HFD alone and in combination with KGBE was not statistically different. In addition, no notable differences in liver damage were observed between the two groups as determined by serum levels of glutamate-oxaloacetate transaminase and glutamate-pyruvate transaminase (data not shown).

KGBE Inhibits the Production of Inflammatory Mediators in HFD-Fed ApoE
Monocytes/macrophages infiltrate atherosclerotic lesion areas and increase the expression of inflammatory genes, such as TNF-α, IL-1β and iNOS, which play an important role in development and progression of atherosclerosis [2,6]. Thus, we next examined the effects of KGBE on the expression of these genes in aortic tissues and their gene product levels in sera. The levels of TNF-α and IL-1β mRNAs and their secreted proteins were significantly increased in aortic tissues and sera from mice fed a HFD, respectively, and these increases were reduced by supplementation with KGBE (Figures 3(a) and 3(b)). In addition, iNOS expression and NO production were also increased in aortic tissues and sera from mice fed a HFD, respectively, and these increases were significantly attenuated by KGBE (Figure 3(c)). Furthermore, all observed antiinflammatory effects of KGBE were substantially higher than those of KRGE (Figures 3(a)-3(c)).

KGBE Elicits the Anti-Inflammatory Effect in RAW264.7
Macrophage Cells. Immune-activated macrophages express a variety of inflammatory genes, such as iNOS, COX-2, TNF-α, and IL-1β, which are major contributing factors in the pathogenesis of atherosclerosis [2,6]. Experiments were performed to determine whether KGBE influences the expression of these genes in LPS-stimulated RAW264.7 cells. As expected, LPS-stimulated RAW264.7 cells increased expression of the inflammation-associated enzymes, iNOS and COX-2, as determined by Western blot and RT-PCR analyses, and these increases were inhibited in a dose-dependent manner by cotreatment with KGBE (Figure 4(a)). Similarly, treatment with KGBE inhibited LPS-induced production of nitrite (a stable oxidized product of NO) and PGE 2 in a dose-dependent manner with an IC 50 value of ∼40 μg/mL (Figures 4(b) and 4(c)). In addition, KGBE inhibited LPS-induced expression of the inflammatory cytokine genes, TNF-α, and IL-1β, in a dose-dependent manner (Figure 4(d)), and these inhibitory effects were highly correlated with increased levels of TNF-α and IL-1β in the culture media of LPS-stimulated RAW264.7 cells (Figures 4(e) and 4(f)). Under the same experimental conditions, KGBE did not reduce cell viability as measured by the crystal violet staining method (data not shown).
These results suggest that KGBE regulates inflammatory gene expression in immune-activated macrophages. such, we next examined the in vitro and in vivo effect of KGBE on the expression of phase II genes and their role in KGBE-mediated anti-inflammatory activity. The expression of HO-1 and GCLC was slightly increased in aortic tissues from ApoE −/− mice fed a HFD alone and further increased by supplementation with KGBE ( Figure 5(a)). In addition, treatment with KGBE increased expression levels of HO-1 and GCLC in peritoneal macrophages isolated from ApoE −/− mice ( Figure 5(b)). Thus, we analyzed the functional role of these enzymes in KGBE-mediated anti-inflammatory activity using their respective inhibitors. The suppressive effects of KGBE on iNOS expression and NO production were reduced by co-treatment with either the HO-1 inhibitor SnPP or the GCL inhibitor BSO and synergistically reversed by combined treatment with both inhibitors (Figure 5(c)). These inhibitors also reduced the KGBE-mediated suppressive effects on COX-2 expression and PGE 2 production in LPS-stimulated primary macrophages ( Figure 5(d)). Moreover, treatment with SnPP and BSO together attenuated the inhibitory effects of KGBE on TNF-α and IL-1β mRNA expression and protein levels in the culture media of LPS-stimulated macrophages (Figures 5(e) and 5(f)). These results suggest that KGBE decreases inflammatory gene expression probably by upregulating HO-1 and GCLC.

KGBE Inhibits LPS-Induced ROS Generation and NF-κB Activation by Increasing HO-1 and GCLC Expression.
Although high levels of ROS induce cytotoxicity, appropriate levels of ROS contribute to the activation of intracellular signal cascades, including NF-κB pathway [21]. Therefore, we investigated whether KGBE regulates intracellular ROS levels in LPS-stimulated macrophages. KGBE effectively suppressed LPS-induced increases in intracellular ROS levels, and this effect was attenuated by combined treatment with SnPP and BSO (Figure 6(a)). We next examined the functional role of HO-1 and GCLC in KGBE-mediated regulation of NF-κB activation. KGBE inhibited LPS-induced translocation of the cytosolic NF-κB p65 subunit into the nucleus, thereby retaining its cytosolic level, and this inhibitory effect was reversed by combined treatment with SnPP and BSO, as determined by confocal microscopy and Western blot analysis (Figures 6(b) and 6(c)). We further confirmed the inhibitory effect of KGBE on the functional activation of NF-κB by performing an EMSA. Treatment with KGBE suppressed LPS-induced increase in DNA-binding activity of NF-κB in the nuclear extracts from macrophages stimulated with LPS, and this inhibitory effect was significantly reduced by combined treatment with SnPP and BSO ( Figure 6(d)). The specific binding of NF-κB to DNA was confirmed by a competitive assay with a cold probe and a supershift assay with an antibody against the NF-κB subunit p65. We further examined the effect of KGBE on iNOS promoter activity and NF-κB-Luc reporter activity. KGBE significantly inhibited LPSinduced increases in the transcriptional activities of iNOS promoter and NF-κB-Luc construct, which were reduced by combined treatment with SnPP and BSO ( Figure 6(e)). We next examined the effect of KGBE on the signaling cascade responsible for IκB degradation. Treatment with KGBE suppressed LPS-induced phosphorylation of IKKα at threonine 23 and IKKαβ at serines 180/181, resulting in phosphorylation and degradation of IκB, and these effects were attenuated by combined treatment with SnPP and BSO ( Figure 6(f)). These results indicate that KGBE can inhibit LPS-induced NF-κB activation by suppressing IKKdependent IκB degradation via upregulation of phase II enzymes and subsequent reduction of intracellular ROS levels.

KGBE Inhibits the Expression of Adhesion Molecules in
Endothelial Cells. NF-κB is also critical modulator of ICAM-1 and VCAM-1 expression, which are involved in vascular inflammation responsible for atherosclerotic development [22]. We hypothesized that KGBE could inhibit the expression of ICAM-1 and VCAM-1 via upregulation of HO-1 and GCLC. Thus, we examined the effect of KGBE on the expression of adhesion molecules in TNF-α-stimulated endothelial cells. As expected, KGBE treatment suppressed TNF-αinduced ICAM-1 and VCAM-1 expression in HUVECs, and its suppressive effect was significantly attenuated by treatment with both SnPP and BSO (Figure 7(a)). We next examined the effect of KGBE on leukocyte-endothelial cell interaction. KGBE effectively inhibited adhesion of leukocytes to HUVECs stimulated with TNF-α, and this inhibition was reversed by treatment with both SnPP and BSO (Figures  7(b) and 7(c)). We further investigated the in vivo effect of KGBE on ICAM-1 and VCAM-1 expression in aortic tissues of hyperlipidemic mice. ICAM-1 and VCAM-1 mRNA levels were significantly upregulated in aortic tissues from HFD-fed mice, and these increases were inhibited by administration of KGBE (Figure 7(d)).

Discussion
This study was undertaken to elucidate the pharmacological effect of KGBE on atherosclerotic development and investigate its underlying mechanism of action. Although administration of KGBE did not alter serum lipid contents, it resulted in a significant decrease in HFD-induced atherosclerotic lesion formation, which was highly correlated with its ability to upregulate the phase II antioxidant enzymes, HO-1, and GCLC. Furthermore, KGBE inhibited the expression of atherogenic inflammatory genes, such as TNF-α, IL-1β, iNOS, ICAM-1, and VCAM-1, in aortic tissues from mice fed a HFD. KGBE also elicited similar regulatory effects on the expression of phase II enzymes and atherogenic inflammatory genes in LPS-stimulated macrophages and TNF-α-activated endothelial cells. We also revealed that inhibition of both HO-1 and GCL activities effectively blocked KGBE-induced inhibitory effects on NF-κB activation and atherogenic gene expression. These results suggest that KGBE prevents the pathogenesis of atherosclerosis by suppressing NF-κB-mediated atherogenic inflammatory gene expression via upregulation of phase II antioxidant enzymes, without improving serum lipid profiles.
The root of Panax ginseng is a well-known herbal medicine used to regulate vascular homeostasis and treat vascular diseases, including atherosclerosis and hypertension [23,24]. Ginseng contains ginsenosides as active components, which contribute to its pharmacological activities [12]. The berry portion of ginseng also contains higher levels of ginsenosides than its root [16]. We also revealed that KGBE used in this  study contains high levels of several ginsenosides, including Rb2, Rc, Rd, Re, Rg1, and Rg2. These evidences suggest that ginseng berry may exert more potent antiatherogenic effects on atherosclerosis than its root. We herein demonstrate that supplementation with KGBE (0.05%, W/W, P < 0.01), but not with KRGE (0.075%, W/W, P > 0.05), elicited the potent inhibitory effect on atherosclerotic plaque formation. It is well accepted that atherosclerosis develops as a consequence Evidence-Based Complementary and Alternative Medicine 11 of high blood levels of cholesterol and triglyceride and chronic inflammatory responses. Although ginseng root extract is shown to lower total cholesterol and triglyceride levels in a hyperlipidemic rat model [25], our results show that KGBE has a greater suppressive effect on atherosclerotic lesion formation than Korean red ginseng extract (KRGE) in mice fed a HFD, without serum lipid-lowering activity. This different antiatherosclerotic effect between extracts of ginseng root and berry may be due to their distinct ginsenoside profiles [13]. These results suggest that the antiatherosclerotic effect of KGBE is not directly associated with its ability to lower blood cholesterol and lipid levels.
Atherosclerosis is a lipid-driven, chronic inflammatory disease of the vessel wall [2]. Immune cells and their mediators directly cause chronic arterial inflammation, which is a well-known factor in the pathogenesis of atherosclerosis. Indeed, anti-inflammatory compounds effectively inhibit atherosclerotic plaque formation in a hyperlipidemic animal model [4,26]. Although our data did not indicate that KGBE reduces blood cholesterol levels, this extract effectively suppressed the serum levels of atherogenic inflammatory mediators, such as TNF-α, IL-1β, and NO, in mice fed a HFD. KGBE also attenuated the mRNA levels of these cytokines and protein levels of iNOS in aortic tissues from hyperlipidemic mice. These results suggest that KGBE suppresses atherosclerotic lesion formation by suppressing inflammatory gene expression, without lowering serum lipid levels.
NF-κB is a key regulator of inflammatory response, and its functional involvement in atherosclerosis is demonstrated by the presence of its activated form in human atherosclerotic plaques [5]. Furthermore, selective inhibition of NF-κB reduces the area of atherosclerotic lesions [4]. Recent studies also demonstrated that anti-inflammatory compounds, which inhibit NF-κB activation, prevent the development of atherosclerosis, without lowering serum lipid levels, in hyperlipidemic mice [4,27]. In addition, the antiatherosclerotic effects of statins are associated with both the reduction of blood LDL-C levels and the suppression of NF-κBmediated inflammatory gene expression [3,28]. These observations suggest that herbal and natural medicines that inhibit NF-κB activation are beneficial in preventing atherosclerosis via suppression of atherogenic inflammatory gene expression. Atherosclerotic lesions are filled with various immune cells, such as monocytes and macrophages, which can orchestrate and elicit inflammatory responses, leading to the production of NF-κB-mediated inflammatory genes [4]. We herein found that treatment with KGBE inhibited NF-κB activation and suppressed the expression of the inflammatory cytokines and enzymes, TNF-α, IL-1β, iNOS, and COX-2 in LPS-stimulated macrophages. Of these gene products, TNF-α is an important contributor in the pathogenesis of atherosclerosis via leukocyte-endothelial cell interactions by upregulating the adhesion molecules ICAM-1 and VCAM-1 in endothelial cells [29], leading to the transmigration of circulating monocytes to the intima and formation of atheroma plaque [30]. We found that KGBE inhibited NF-κB-mediated expression of ICAM-1 and VCAM-1 in TNF-α-stimulated HUVECs, resulting in the inhibition of monocyte-endothelial cell interactions. Moreover, administration of KGBE suppressed HFD-induced increases in adhesion molecule expression in a mouse model. These results suggest that KGBE inhibits the expression of atherogenic inflammatory genes via the suppression of NF-κB activation. It is well known that NF-κB is activated by ROS and oxidized LDL, which play crucial roles in the initiation and progression of atherosclerosis [31]. ROS can indirectly elicit IKK-dependent NF-κB activation by promoting redoxsensitive activation of the PI3K/PTEN/Akt and NIK/IKK pathways [17]. Our previous studies demonstrated that natural antioxidants effectively inhibit NF-κB-mediated inflammatory gene expression by blocking intracellular ROS accumulation in LPS-stimulated macrophages [17,32], implicating ROS as an important cellular signal mediator for NF-κB activation. We here found that KGBE significantly reduced intracellular ROS levels, NF-κB activation, iNOS promoter activity, and inflammatory gene expression in cultured macrophages stimulated with LPS. KGBE also inhibited phosphorylation of IKKα and IKKαβ and subsequent phosphorylation-dependent degradation of IκB, which is an endogenous inhibitor of NF-κB. These data indicate that KGBE inhibits atherogenic gene expression via suppression of the redox-sensitive NF-κB activation pathway, particularly regulation of phosphorylation-dependent activation of IKK by decreasing intracellular ROS level (Figure 8).
An increasingly large body of evidence points to a crucial role of Nrf2-dependent phase II enzymes in antiinflammation and anti-atherosclerosis [11,20]. The antiinflammatory effect of phase II antioxidant enzymes is associated with inhibition of NF-κB activation by modulating ROS generation and removal. Of these enzymes, HO-1 and GCL are the most potent antioxidant enzymes. HO-1 catalyzes heme to biologically active products: carbon monoxide and biliverdin/bilirubin, which regulate inflammatory response by acting as potential antioxidants [33]. On the other hand, GCL, a rate-limiting enzyme in glutathione biosynthesis, elevates intracellular GSH levels and redox potential, which are likely to inhibit inflammationassociated gene expression by blocking the redox-sensitive NF-κB activation pathway [34]. Furthermore, the natural compound carnosic acid elevates intracellular GSH levels via upregulation of Nrf2-dependent phase II enzyme GCL expression, leading to suppression of NF-κB activation and inflammatory reaction [35,36]. We here found that KGBE elevated the expression of HO-1 and GCL in vitro and in vivo. Inhibitors of HO-1 (SnPP) and GCL (BSO) significantly reversed the suppressive effects of KGBE on LPSinduced ROS generation, NF-κB activation, and atherogenic inflammatory gene expression in cultured macrophages. In addition, these inhibitors effectively ameliorated the inhibitory effect of KGBE on adhesion molecule expression in TNF-α-stimulated endothelial cells. Of the ginsenosides detected in KGBE, Rb1, Rd, and Re are known to induce Nrf2-mediated phase II genes and/or inhibition of the NF-κB pathway [37][38][39][40], suggesting these ginsenosides as possible candidates in the strong anti-atherogenic activity of KGBE. These results indicate that KGBE inhibits the expression of atherogenic inflammatory genes and adhesion molecules via upregulation of Nrf2-dependent antioxidant genes, HO-1 and GCL, which are responsible for the reduction of intracellular ROS levels ( Figure 8).
Although ginseng berry has not been shown to elicit antiinflammatory and anti-atherogenic effects, we first revealed that KGBE elicited anti-atherogenic and anti-inflammatory effects, with upregulation of phase II antioxidant genes. Increasing evidences have been shown that Nrf2-dependent phase II gene expression plays an important role in preventing chronic inflammation and atherosclerotic pathogenesis [20,41]. Therefore, activators of Nrf2 pathway that increases expression of phase II and antioxidant enzymes can be used as novel therapeutic strategies for restoring cellular redox homeostasis and diminishing NF-κB-mediated inflammation in cardiovascular diseases, including atherosclerosis [42,43]. Indeed, dietary and herbal Nrf2 activators result in the upregulation of multiple endogenous antioxidant mechanisms and decrease the possibility of developing atherosclerotic lesions [11,41]. Our previous report also showed that siRNA-based Nrf2 activation suppresses vascular inflammation in a mouse model [44]. In addition, administration of an Nrf2 activator resulted in significant phase II gene upregulation and decreased atherogenesis in LDLR −/− mice [45], ApoE −/− mice [46], and rabbits fed a high-fat diet [47]. These evidences suggest that KGBE-induced increases in Nrf2-mediated phase II gene expression is linked to its medicinal properties with regard to anti-inflammation and anti-atherogenesis. Our results demonstrate that KGBE might prevent vascular inflammation and atherosclerotic development by inducing Nrf2-mediated phase II gene expression.
Our findings presented herein indicate that KGBE reduces HFD-induced atheromatous lesion formation in a mouse model via an anti-inflammatory mechanism by promoting the expression of HO-1 and GCL, which are responsible for inhibiting NF-κB activation by reducing intracellular ROS levels. These findings suggest that KGBE inhibits the pathogenesis of hyperlipidemic atherosclerosis by suppressing NF-κB-mediated expression of atherogenic inflammatory genes via induction of phase II antioxidant enzymes, such as HO-1 and GCL, without lowering serum lipid levels. Thus, KGBE could be considered as a potential therapeutic and preventive herbal medicine for the treatment of atherosclerosis and its related complications.