Naringin Reverses High-Cholesterol Diet-Induced Vascular Dysfunction and Oxidative Stress in Rats via Regulating LOX-1 and NADPH Oxidase Subunit Expression

Pengnet, Sirinat; Prommaouan, Sakdina; Sumarithum, Phinsuda; Malakul, Wachirawadee

doi:https://doi.org/10.1155/2019/3708497

BioMed Research International

On this page

Abstract Introduction Materials and Methods Results Discussion Conclusion Abbreviations Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 3708497 | https://doi.org/10.1155/2019/3708497

Naringin Reverses High-Cholesterol Diet-Induced Vascular Dysfunction and Oxidative Stress in Rats via Regulating LOX-1 and NADPH Oxidase Subunit Expression

Sirinat Pengnet,^1,2Sakdina Prommaouan,¹Phinsuda Sumarithum,¹and Wachirawadee Malakul¹

Academic Editor: Mauro S. Oliveira

Received01 Jul 2019

Accepted10 Sept 2019

Published24 Oct 2019

Abstract

Hypercholesterolaemia is associated with oxidative stress and endothelial dysfunction and leads to the development of atherosclerosis. Naringin exhibits cardiovascular protective and antioxidant properties. Therefore, the aim of this study was to assess the effect of naringin administration on vascular oxidative stress and endothelial dysfunction in hypercholesterolaemic rats and to elucidate its underlying mechanism. Sprague Dawley rats were fed a diet with 1.5% cholesterol (HCD) for 8 weeks to induce hypercholesterolaemia. Naringin (100 mg/kg body weight) was orally administrated to rats during the last 4 weeks of the diet treatment. After 8 weeks, the thoracic aorta was isolated to determine vascular function and nitric oxide (NO) levels. The aortic superoxide anion () level was detected using dihydroethidium (DHE) fluorescence staining. Protein expression of lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), nicotinamide adenine dinucleotide phosphate (NADPH) oxidase subunits, and inducible nitric oxide synthase (iNOS), as well as oxidative damage markers, was also evaluated in aortae. Naringin treatment of hypercholesterolaemic rats enhanced aortic NO levels, restored endothelium-dependent responses to acetylcholine (ACh), and reduced aortic levels. Furthermore, naringin treatment decreased LOX-1, NADPH oxidase subunits (p47^phox, Nox2, and Nox4), and iNOS as well as oxidative damage markers (3-nitrotyrosine (3-NT) and 4-hydroxynonenal (4-HNE)) expression in aortic tissues from hypercholesterolaemic rats. These results demonstrate that naringin treatment improves endothelium dysfunction in hypercholesterolaemic rats, at least partially by decreasing oxidative stress via downregulation of LOX-1 and NADPH oxidase.

1. Introduction

Atherosclerotic cardiovascular disease is a major cause of morbidity and mortality worldwide [1]. Hypercholesterolaemia has been shown to be a major risk factor for atherosclerosis, associated with increasing oxidative stress and impaired endothelial function [2, 3]. The normal endothelium plays an important role in maintaining vascular homeostasis and regulating basal vascular tone through the production of several vasoactive substances, including nitric oxide (NO) and endothelin [4]. Dysregulation of endothelial function is thought to be one of the earliest manifestations of atherosclerosis and is characterized by reduced endothelium-dependent vasodilation, which is mainly mediated by NO [5].

Accumulating evidence has shown that reactive oxygen species (ROS) generated during hypercholesterolaemia are involved in key processes in the development and progression of atherosclerosis, including endothelial dysfunction and oxidative modification of low-density lipoprotein (oxLDL) [6, 7]. ROS triggers LDL cholesterol oxidation to form oxLDL, resulting in the upregulated expression of lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), an endothelial cell receptor for oxLDL [7]. Upregulated LOX-1 expression has been found in many pathological diseases, including hypercholesterolaemia [7]. Increased LOX-1 expression further stimulates the production of ROS, including superoxide () and hydrogen peroxide (H₂O₂), through the activation of β-nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, thereby contributing to the enhancement of NO catabolism and the generation of peroxynitrite (ONOO⁻) [8, 9].

Vascular NADPH oxidase is one of the major sources of ROS generation in hypercholesterolaemia, atherosclerosis, hypertension, and diabetes and is often considered as a target for therapeutic intervention [10]. NADPH oxidase consists of multiple catalytic subunits, such as NOX (NOX1-5), as well as several regulatory subunits, such as p47^phox, p67^phox, and RAC [10]. Among the NOX catalytic subunits, Nox2, Nox1, and Nox4 have been detected in the cardiovascular system in many pathological diseases, such as hypercholesterolaemia, hypertension, and diabetes [11–13]. There is increasing evidence that ROS derived from NADPH oxidase not only decreases intracellular NO, but also increases LOX-1 expression, leading to further overproduction of ROS [8, 9, 14]. Excessive ROS attacks all macromolecules, including proteins, lipids, and nucleic acids, which is deleterious to various tissues and cells [15]. Therefore, natural products and compounds that suppress the expression of vascular NADPH oxidase and LOX-1 may offer therapeutic benefits to ameliorate the development of ROS-induced adverse vascular changes associated with hypercholesterolaemia.

Naringin is one of the flavonoids found in citrus fruit and has been reported to have antioxidant, antiapoptotic, anti-inflammatory, antihypercholesterolaemic, and cardioprotective properties [16–22]. Several studies have shown that it reduces the levels of plasma lipids and inflammatory markers and increases antioxidant activity in animal and human models of hyperlipidaemia [23, 24]. Additionally, naringin increased NO production which improved endothelial function in hypertensive rats [25]; normalized systolic blood pressure and improved vascular dysfunction and ventricular diastolic dysfunction in high-carbohydrate, high-fat diet-fed rats [26]; and ameliorated the impairment of endothelial function induced by high-fructose feeding [27]. Therefore, naringin is a useful compound for preventing the development and progression of atherosclerosis. However, its potential mechanisms in high-cholesterol diet-induced hypercholesterolaemic rats have not yet been clarified. We hypothesized that reduced ROS sources and decreased oxidative stress might be involved in improved endothelial function produced by naringin treatment in hypercholesterolaemic rats. Therefore, we sought to examine whether oral administration of naringin can decrease oxidative stress and improve endothelial function in hypercholesterolaemic rats.

2. Materials and Methods

2.1. Animal Experiments

The animal protocols for the study were approved by the Institutional Animal Care Committee of Naresuan University (ethical approval number: 5801001; approval date: January 28, 2015). Forty male Sprague Dawley (SD) rats weighing 180–200 g were purchased from the National Laboratory Animal Center at Salaya, Mahidol University, Thailand. The animals were housed in the animal room of the Center for Animal Research at Naresuan University at a controlled ambient temperature of 22 ± 1.0°C, with a 12-hour light/dark cycle. After an acclimatization period of 1 week, the rats were randomly divided into two groups: control and hypercholesterolaemic. Control rats were given a standard rat chow diet, while hypercholesterolaemic rats were given a high-cholesterol diet (HCD) for 8 weeks. The HCD was prepared according to a previous study [28] with slight modifications consisting of 1.5% cholesterol, 0.37% cholic acid, and 20% palm oil. After 4 weeks, the HCD induced hypercholesterolaemia in the rats, and then the control and hypercholesterolaemic groups were further divided into the following four subgroups: control (C, n = 10), control plus naringin (CN, n = 10), HCD (HC, n = 10), and HCD plus naringin (HCN, n = 10). Naringin (100 mg/kg) or vehicle (1% carboxymethylcellulose) was administered daily by oral gavage for the last 4 weeks of the study (from 5^th week to 8^th week of diet treatment). The dosage of naringin was used according to previous studies [26, 27], which reported that its administration restored impaired endothelial function in rats. At the end of the experiment, the rats were anaesthetized with an intraperitoneal injection of sodium pentobarbital (50 mg/kg/BW), and blood samples were collected via cardiac puncture for the analysis of lipid levels. Serum levels of total cholesterol (TC), triglyceride (TG), and high-density lipoprotein cholesterol (HDL-C) were measured using commercial test kits (Human, Wiesbaden, Germany). Low-density lipoprotein cholesterol (LDL-C) was calculated using the formula of Friedewald et al. [LDL-C=TC-HDL-C-(TG/5)] [29]. The atherogenic index of plasma (AIP) was calculated using the formula of Niroumand et al. [log (TG/HDL-C)] [30]. The atherogenic coefficient (AC) was calculated using the formula [(TC-HDL-C)/HDL-C]. The cardiac risk ratio (CRR) was calculated using the formula [TC/HDL-C].

2.2. Preparation of Isolated Aortic Rings

After the rats were euthanized, the descending thoracic aorta was dissected and cleaned of the surrounding connective tissues and superficial fat. One part of the isolated thoracic aorta was placed in Krebs bicarbonate solution (composition (mM): NaCl, 118.0; KCl, 4.7; MgSO₄·7H₂O, 1.2; KH₂PO₄, 1.1; NaHCO₃, 25.0; D-glucose, 11.0; and CaCl₂·2H₂O, 2.5) for vasorelaxation response experiments, while another part was immediately frozen for nitrate and nitrite assays and western blot analysis.

2.3. Vascular Function Studies

The isolated thoracic aortae were cut into ring segments 2-3 mm in length, which were suspended between two stainless steel hooks linked to an isometric force transducer (AD Instruments Ltd, Australia) and connected to a Bridge Amplifier (PowerLab, AD Instruments Ltd., Australia) for isometric tension testing. Each aortic ring was placed in a 20 ml organ bath chamber containing Krebs bicarbonate buffer, maintained at 37°C with a pH of 7.4, and bubbled with a gas mixture (95% O₂ and 5% CO₂). Resting tensions of the aortic rings were maintained at 1 g, and the rings were allowed to equilibrate for 30 min. Bath contents were then replaced with an isotonic, 123 mM potassium physiological salt solution (KPSS) in which all the NaCl was replaced with KCl (123 mmol/L) to induce maximum contraction (KPSS_max). The tissue was washed with fresh Krebs bicarbonate buffer, and the integrity of the endothelium was tested. For these tests, the aortic rings were then submaximally precontracted between 40% and 60% of the KPSS_max response with phenylephrine (PE, 1 nM–10 μM). After the contractions were stabilized, acetylcholine (ACh, 10 μM) was added to confirm the presence of endothelium.

Cumulative concentration-response curves to the endothelium-dependent relaxant ACh (1 nM–10 μM) and the endothelium-independent relaxant sodium nitroprusside (SNP, 1 nM–10 μM) were determined in vessels precontracted with PE (1 nM–10 μM). The relaxation responses were continuously recorded until maximum relaxation was achieved.

2.4. Preparation of Aortic Homogenate

One of the aorta parts previously isolated was homogenized with RIPA lysis buffer (1% phosphatase and 1% protease inhibitor), centrifuged at 10,000 rpm for 10 min at 4°C to obtain the supernatants, and then stored at −80°C until analysis. The total protein level of the aortic homogenate was determined by using a bicinchoninic acid (BCA) assay and measuring the absorbance at 500 nm. Bovine serum albumin was used as the standard control.

2.5. Determination of Nitrate and Nitrite Levels in Aortic Tissue

Nitrate and nitrite levels in the aortic tissue were determined using a Nitrate/Nitrite Colorimetric Assay Kit (Cayman Chemical Company, Ann Arbor, MI, USA). Nitrate and nitrite levels were measured by using a microplate reader at a wavelength of 540 nm (Synergy™ HT, Winooski, USA).

2.6. Superoxide Detection

Superoxide generation in the aortic tissue was determined with dihydroethidium (DHE, 5 μM). Aortic tissues were embedded in freezing medium, cut into 30 μm thick sections, and incubated at 37°C protected from light for 30 min with the fluorescent probe DHE. In the presence of superoxide, DHE is oxidized to ethidium, which yields bright red fluorescence. After washing with PBS, the aortic sections were mounted and covered with a coverslip, and images were captured immediately with a fluorescent microscope at excitation and emission wavelengths of 520 and 610 nm, respectively. Superoxide generation was analysed with ImageJ software.

2.7. Western Blot Analysis

Protein expression levels of LOX-1, NADPH oxidase subunits (p47^phox, Nox2, and Nox4), iNOS, and oxidative stress markers (3-NT and 4-HNE) in the aortic tissue were determined. Each sample of aortic homogenate (20 μg proteins) was separated by using a sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) system. After electrophoresis, the proteins were transferred to a polyvinylidene difluoride (PVDF) membrane. The blotted membranes were blocked with 5% skimmed milk for 1 hour at room temperature, followed by overnight incubation at 4°C with anti-LOX-1 (1 : 1000), anti-p47^phox (1 : 1000), anti-Nox4 (1 : 1000), anti-Nox2 (1 : 1000), anti-iNOS (1 : 1000), anti-3-NT (1 : 500), anti-4-HNE (1 :2000), and anti-β-actin (1 : 5000). The membranes were washed three times in Tris-buffered saline containing 0.2% Tween-20 (TBS-T) and then incubated with a goat anti-rabbit IgG-conjugated secondary antibody for 1 hr. After washing, specific proteins were detected using an enhanced chemiluminescence (ECL) system (Millipore, Billerica, MA, USA) and assayed by using Image Lab™ software (Bio-Rad Laboratories, Hercules, CA, USA). Data were expressed as percentages of the control.

2.8. Drugs and Chemicals

Naringin (purity > 90%), cholic acid, ACh, SNP, and PE were purchased from Sigma (St Louis, MO, USA). Primary antibodies against p47^phox, Nox2, iNOS, and 3-NT were purchased from Merck Millipore (Darmstadt, Germany), β-actin was purchased from Cell Signaling Technology (Danvers, MA, USA), LOX-1 and Nox4 were purchased from Boster Biological Technology Co., Ltd. (Pleasanton, CA, USA), and 4-HNE was purchased from Abcam (Cambridge, MA, USA). Goat anti-rabbit IgG-conjugated secondary antibody was purchased from Santa Cruz Biotechnology (Dallas, TX, USA).

2.9. Statistical Analyses

The results were expressed as the mean ± SEM. Concentration-response curves were analysed using nonlinear regression to calculate the sensitivity of the concentration (pEC50). The maximum relaxation (R_max) response to ACh and SNP was analysed as percentages of PE-induced contraction. The results were analysed by one-way analysis of variance (ANOVA) coupled with the Newman–Keuls multiple comparison test or Dunnet’s test, where appropriate, using GraphPad Prism version 5. Statistical significance was indicated by a value of less than 0.05.

3. Results

3.1. Body Weight, Lipid Levels, and Atherogenic Indices

The body weights and lipid profiles (TC, TG, LDL-C, and HDL-C) of the rats are shown in Table 1. There was no difference in initial body weight between the four groups of rats. At the end of the study, the final body weight of HCD-fed rats was significantly greater than that of control rats. Treatment with naringin for 4 weeks did not affect the body weight of normal rats, but significantly reduced the final weight of HCD-fed rats (Table 1). Feeding the rats with a HCD for 8 weeks caused a significant increase in TC, TG, and LDL-C and a decrease in HDL-C compared with control rats. Four weeks of treatment with naringin reversed the changes in the lipid profile induced by HCD in the HCN group (Table 1); however, the treatment did not change lipid levels in normal rats. As shown in Table 1, all atherogenic indices of the HC group were found to be increased compared with the control group. However, there were significant reductions () in all atherogenic indices of the HCN group when compared with the HC group.

3.2. Effect of Naringin on Vascular Relaxation

Both the sensitivity (pEC₅₀) and maximum relaxation (R_max) to ACh were significantly decreased in the aortic rings of hypercholesterolaemic rats compared with those of control rats (Figure 1(a) and Table 2), indicating that hypercholesterolaemia impaired endothelium-dependent relaxation in rat aortae. Treatment with naringin did not affect ACh-induced vasorelaxation in normal rats but increased the sensitivity and maximum relaxation to ACh in hypercholesterolaemic rats (Figure 1(a) and Table 2). In addition, there was no significant difference in the sensitivity and maximum relaxation to the endothelium-independent agonist SNP in the aortae of all groups (Figure 1(b)).

(a)

(b)

3.3. Effects of Naringin on Aortic Nitrate and Nitrite Levels

The levels of aortic nitrate and nitrite were decreased in hypercholesterolaemic rats when compared with the levels in the control rats (hypercholesterolaemic 1.76 ± 0.43 vs. control 4.59 ± 0.28 μM/mg protein, ) (Figure 2). Naringin treatment did not affect the levels of nitrate and nitrite in the aortae of control rats but significantly increased nitrate and nitrite levels in hypercholesterolaemic aortae to the levels observed in control rats. These results indicate that treatment with naringin enhances nitrate and nitrite levels in the aortic tissues of hypercholesterolaemic rats.

3.4. Effect of Naringin on Superoxide Production

To evaluate superoxide anion levels in aortic tissue, DHE fluorescent staining was performed on aortic sections from each group; it revealed that superoxide levels in aortic tissues were significantly higher in HCD-fed rats than in control rats (Figure 3). However, DHE-derived signals were markedly attenuated in aortae from hypercholesterolaemic rats treated with naringin compared with untreated hypercholesterolaemic rats.

(a)

(b)

(c)

(d)

(e)

3.5. Effect of Naringin on LOX-1, NADPH Oxidase Subunits, iNOS, and Oxidative Stress Marker Expression

Western blotting demonstrated that HCD-fed rats showed significantly increased expression of LOX-1, NADPH oxidase subunits (p47^phox, Nox2, and Nox4), iNOS, and oxidative stress markers (3-NT and 4-HNE) in the aortic tissues as compared with control rats (Figures 4 and 5). Treatment of hypercholesterolaemic rats with naringin significantly decreased LOX-1, NADPH oxidase subunits (p47^phox, Nox2, and Nox4), iNOS, and oxidative stress markers (3-NT and 4-HNE) expression in aortic tissues (Figures 4 and 5); however, this treatment did not alter these values in normal rats.

(a)

(b)

(c)

(d)

(e)

(a)

(b)

(c)

(d)

4. Discussion

Our results show that the treatment of hypercholesterolaemic rats with naringin for 4 weeks restores endothelium-dependent relaxation and NO levels in aortae. Furthermore, naringin treatment also decreased oxidative stress markers, including O₂⁻, 4-HNE, and 3-NT, in aortic tissues of hypercholesterolaemic rats. In addition, we showed that the mechanisms associated with improvements in endothelial damage and oxidative stress involve the downregulation of LOX-1, NADPH oxidase subunits, and iNOS.

It is widely accepted that hypercholesterolaemia is one of the major risk factors for CVD and is characterized by abnormally high levels of serum total and LDL cholesterol [31]. It is well established that LDL cholesterol and especially its oxidized form (oxLDL) play important roles in impaired endothelial function and the pathogenesis of atherosclerosis [6, 32]. Numerous studies have shown that the consumption of a HCD causes serum lipid abnormalities and oxidative stress, thereby initiating endothelial dysfunction [33, 34]. Using standard diets supplemented with cholesterol and cholic acid to induce hypercholesterolaemia in rats in our study caused increased serum levels of TC, TG, and LDL-C and a decreased HDL-C level, indicating that a hypercholesterolaemic model was successfully induced by a HCD in the present study. Naringin was reported to exhibit hypocholesterolaemic activity by lowering cholesterol synthesis through the decreased activities of hepatic 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase [19] and acyl-coenzyme A-cholesterol O-acyltransferase (ACAT) [35, 36]. Our data showed that after 4 weeks of administration of naringin, serum lipid levels from animals fed with high-cholesterol diets were found to be effectively decreased in HCD-fed rats. Additionally, atherogenic coefficient/indices, powerful indicators of the risk of cardiovascular diseases, were decreased in hypercholesterolaemic rats treated with naringin, indicating that naringin treatment reduced atherogenic risk in hypercholesterolaemia.

Endothelial dysfunction is considered an important early marker of atherosclerosis and characterized by impaired endothelium-dependent relaxation and reduced NO bioavailability [37]. The endothelium plays a crucial role in the regulation of tone by mainly synthesizing and releasing NO [4]. Several studies demonstrated that NO is the major mediator of endothelium-dependent relaxation of rat aortae and that mechanism of vasorelaxation is impaired in many pathological diseases, including hypercholesterolaemia and diabetes [5, 38, 39]. Endothelium-derived NO is synthesized by nitric oxide synthase (NOS) [37]. In vascular tissues, there are two principal types of NOS isoforms, endothelial NOS (eNOS) and inducible NOS (iNOS) [37]. eNOS has a protective vascular effect, whereas iNOS can produce a large amount of NO accompanied by increased generation of ROS, including OONO⁻, which are detrimental to vascular tissues [37]. Consistent with previous studies [40, 41], our results also demonstrate endothelial dysfunction in aortae of untreated hypercholesterolaemic rats, as shown by decreased ACh-induced endothelium-dependent vasorelaxation and reduced aortic content of the NO metabolites nitrite and nitrate. These findings indicated impaired endothelial function induced by hypercholesterolaemia related to reduced endothelium-derived NO levels. Previously, naringin was shown to restore the reduced ACh-induced vasorelaxation in the aortic rings of stroke-prone spontaneously hypertensive rats (SHRSP) [25] and of high-carbohydrate, high-fat diet-fed rats [26]. We found that naringin treatment for 4 weeks ameliorated the impairment of endothelium-dependent relaxation in hypercholesterolaemic rats, evidenced by an increase in the sensitivity and maximum relaxation of thoracic aortae in response to ACh. However, naringin treatment did not affect endothelium-independent relaxation of aortas in response to SNP. Furthermore, our results also demonstrated that naringin treatment increased the content of the NO metabolites nitrite and nitrate in aortic tissues of hypercholesterolaemic rats. These findings suggest that chronic treatment with naringin increases NO bioavailability and improves hypercholesterolaemia-induced endothelial dysfunction.

Considerable evidence indicates that overproduction of ROS under hypercholesterolaemic conditions causes the inactivation of NO and the development of endothelial dysfunction, as well as the oxidative modification of LDL [7, 42]. In vascular tissues, ROS are generated via several sources such as NADPH oxidase, xanthine oxidase, cyclooxygenase, uncoupled NOS, and mitochondria [10]. Several lines of evidence indicate that vascular NADPH oxidase plays a critical role in promoting ROS-induced vascular damage and atherogenesis [10]. NADPH oxidase consists of membrane-bound core catalytic subunits, such as Nox1–5 and Duox1-2, and cytosolic/regulatory subunits, such as p47^phox, p67^phox, and RAC [10]. Assembly of the membrane NADPH oxidase complex is activated by translocation of cytoplasmic subunits, such as the p47^phox and p67^phox subunits to the plasma membrane, which results in the generation of ROS, including and H₂O₂ [10]. There is evidence that Nox2 and Nox4 are the major isoforms of endothelial NADPH oxidase and are upregulated in various pathological diseases, including hyperlipidaemia [43, 44]. Our study showed that aortic expression of Nox2, Nox4, and p47^phox was increased in hypercholesterolaemic rats. Furthermore, in aortic tissues from the hypercholesterolaemic group incubated with DHE, there was an enhancement of red fluorescence, suggesting an increase in vascular levels. These findings were reversed by naringin treatment. In agreement with these results, similar changes in NOX subunits expression were associated with naringin treatment in other tissues of streptozotocin- (STZ-) induced diabetic models [45].

LOX-1, a receptor for oxLDL, has been reported to play a vital role in the activation of NADPH oxidase-derived ROS and is expressed on endothelial cells and smooth muscle cells [46]. Under hypercholesterolaemic conditions, elevated LDL-C is oxidized by ROS and turned into oxLDL [7]. The uptake of oxLDL into the endothelium via the receptor LOX-1 leads to the activation of NADPH oxidase followed by the quick enhancement of intracellular ROS, which causes macromolecular damage, including protein oxidation, lipid peroxidation, and endothelial dysfunction [8, 15]. ROS, particularly , react with NO, thereby decreasing the availability of NO for vasorelaxation and generating OONO⁻, a highly reactive and cytotoxic molecule [15]. Furthermore, excessive NO produced by iNOS also promotes the formation of OONO⁻, which induces the nitration of protein-bound tyrosine residues, causing further oxidative damage to the vasculature [37, 47].

In an animal model of hyperlipidaemia, LOX-1 expression was found to be increased in the aorta of hyperlipidaemic mice [7]. In addition, hyperlipidaemia has been shown to trigger upregulation of 3-NT, a marker of peroxynitrite-induced protein nitration, and 4-HNE, an oxidized product from polyunsaturated fatty acid, in vascular tissues [44]. These observations were confirmed by the findings of our present study, which demonstrated that the aortic expressions of LOX-1, 3-NT, and 4-HNE, as well as iNOS expression, were enhanced in hypercholesterolaemic rats. These findings indicated the presence of oxidative damage in vascular tissues of hypercholesterolaemic rats.

Naringin has been demonstrated to exhibit strong antioxidant activities in scavenging free radicals [24, 48]. Previous studies showed that naringin decreased oxidative stress markers, such as malondialdehyde (MDA), and increased the activity of endogenous antioxidants, such as superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), in various tissues of high-fat diet-fed animals and in diabetic animals [24, 48]. Therefore, our study further examined the inhibitory effects of naringin on protein expression associated with oxidative stress. The present study, for the first time, showed the beneficial suppression of aortic expression of LOX-1 in hypercholesterolaemic rats by naringin, indicating that its antiatherosclerotic effect might be associated with a decrease in LOX-1 expression. Furthermore, naringin treatment reduced the expression of aortic oxidative stress markers 3-NT and 4-HNE, as well as the expression of iNOS in hypercholesterolaemic rats. All of the above results suggest that the beneficial effect of naringin on endothelial function in hypercholesterolaemia might be associated with the downregulation of LOX-1 and NADPH oxidase subunits. In addition, the decrease in both NADPH oxidase-derived and iNOS-derived NO by naringin treatment contributes to the prevention of OONO⁻ generation and NO inactivation, resulting in subsequent improvement of endothelial function.

5. Conclusion

The present study shows that naringin treatment for 4 weeks improves endothelial function in the aortae of hypercholesterolaemic rats. The mechanism related to the beneficial effects of naringin administration on hypercholesterolaemia is the reduction of oxidative stress in aortic tissues, possibly due to the downregulation of LOX-1 and the oxidative enzymes NADPH oxidase and iNOS. The reduction of ROS production leads to increased NO bioavailability and improved endothelium-dependent vasorelaxation in aortae of hypercholesterolaemic rats.

Abbreviations

TC:	Total cholesterol
TG:	Triglyceride
LDL-C:	Low-density lipoprotein cholesterol
HDL-C:	High-density lipoprotein cholesterol
AC:	Atherogenic coefficient
CRR:	Cardiac risk ratio
AIP:	Atherogenic index of plasma
NO:	Nitric oxide
eNOS:	Endothelial NO synthase
ACh:	Acetylcholine
SNP:	Sodium nitroprusside
PE:	Phenylephrine
LOX-1:	Lectin-like oxidized low-density lipoprotein receptor-1
NADPH oxidase:	Nicotinamide adenine dinucleotide phosphate oxidase
iNOS:	Inducible nitric oxide synthase
3-NT:	3-Nitrotyrosine
4-HNE:	4-Hydroxynonenal
:	Superoxide anion.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Acknowledgments

This work was supported by grants from the National Research Council of Thailand (NRCT).

References

S. Mendis, “Global progress in prevention of cardiovascular disease,” Cardiovascular Diagnosis and Therapy, vol. 67, no. 1, pp. S32–S38, 2017.
View at: Publisher Site | Google Scholar
S. Yang, L. Liu, L. Meng, and X. Hu, “Capsaicin is beneficial to hyperlipidemia, oxidative stress, endothelial dysfunction, and atherosclerosis in Guinea pigs fed on a high-fat diet,” Chemico-Biological Interactions, vol. 297, pp. 1–7, 2019.
View at: Publisher Site | Google Scholar
G. Zhang, M. Li, Y. Xu et al., “Antioxidation effect of simvastatin in aorta and Hippocampus: a rabbit model fed high-cholesterol diet,” Oxidative Medicine and Cellular Longevity, vol. 2016, Article ID 6929306, 8 pages, 2016.
View at: Publisher Site | Google Scholar
G. Favero, C. Paganelli, B. Buffoli, L. F. Rodella, and R. Rezzani, “Endothelium and its alterations in cardiovascular diseases: life style intervention,” BioMed Research International, vol. 2014, Article ID 801896, 28 pages, 2014.
View at: Publisher Site | Google Scholar
J. B. Su, “Vascular endothelial dysfunction and pharmacological treatment,” World Journal of Cardiology, vol. 7, no. 11, pp. 719–741, 2015.
View at: Publisher Site | Google Scholar
P. Jin and S. Cong, “LOX-1 and atherosclerotic-related diseases,” Clinica Chimica Acta, vol. 491, pp. 24–29, 2019.
View at: Publisher Site | Google Scholar
L. Gu, W. Bai, S. Li et al., “Celastrol prevents atherosclerosis via inhibiting LOX-1 and oxidative stress,” PLoS One, vol. 8, no. 6, Article ID e65477, p. 11, 2013.
View at: Publisher Site | Google Scholar
H.-C. Ou, W.-C. Chou, C.-H. Hung et al., “Galectin-3 aggravates ox-LDL-induced endothelial dysfunction through LOX-1 mediated signaling pathway,” Environmental Toxicology, vol. 34, no. 7, pp. 825–835, 2019.
View at: Publisher Site | Google Scholar
S. Xu, S. Ogura, J. Chen, P. J. Little, J. Moss, and P. Liu, “LOX-1 in atherosclerosis: biological functions and pharmacological modifiers,” Cellular and Molecular Life Sciences, vol. 70, no. 16, pp. 2859–2872, 2013.
View at: Publisher Site | Google Scholar
D. Burtenshaw, R. Hakimjavadi, E. M. Redmond, and P. A. Cahill, “Nox, reactive oxygen species and regulation of vascular cell fate,” Antioxidants (Basel), vol. 6, no. 4, p. 90, 2017.
View at: Publisher Site | Google Scholar
I. M. Fenyo, I. C. Florea, M. Raicu, and A. Manea, “Tyrphostin AG490 reduces NAPDH oxidase activity and expression in the aorta of hypercholesterolemic apolipoprotein E-deficient mice,” Vascular Pharmacology, vol. 54, no. 3–6, pp. 100–106, 2011.
View at: Publisher Site | Google Scholar
A. M. Briones, F. Tabet, G. E. Callera et al., “Differential regulation of Nox1, Nox2 and Nox4 in vascular smooth muscle cells from WKY and SHR,” Journal of the American Society of Hypertension, vol. 5, no. 3, pp. 137–153, 2011.
View at: Publisher Site | Google Scholar
S.-A. Manea, M.-L. Antonescu, I. M. Fenyo, M. Raicu, M. Simionescu, and A. Manea, “Epigenetic regulation of vascular NADPH oxidase expression and reactive oxygen species production by histone deacetylase-dependent mechanisms in experimental diabetes,” Redox Biology, vol. 16, pp. 332–343, 2018.
View at: Publisher Site | Google Scholar
Q. Jiang, D. Wang, Y. Han, Z. Han, W. Zhong, and C. Wang, “Modulation of oxidized-LDL receptor-1 (LOX1) contributes to the antiatherosclerosis effect of oleanolic acid,” The International Journal of Biochemistry & Cell Biology, vol. 69, pp. 142–152, 2015.
View at: Publisher Site | Google Scholar
A. Phaniendra, D. B. Jestadi, and L. Periyasamy, “Free radicals: properties, sources, targets, and their implication in various diseases,” Indian Journal of Clinical Biochemistry, vol. 30, no. 1, pp. 11–26, 2015.
View at: Publisher Site | Google Scholar
M. Rajadurai and P. S. M. Prince, “Preventive effect of naringin on cardiac mitochondrial enzymes during isoproterenol-induced myocardial infarction in rats: a transmission electron microscopic study,” Journal of Biochemical and Molecular Toxicology, vol. 21, no. 6, pp. 354–361, 2007.
View at: Publisher Site | Google Scholar
Q.-J. Cui, L.-Y. Wang, Z.-X. Wei, and W.-S. Qu, “Continual naringin treatment benefits the recovery of traumatic brain injury in rats through reducing oxidative and inflammatory alterations,” Neurochemical Research, vol. 39, no. 7, pp. 1254–1262, 2014.
View at: Publisher Site | Google Scholar
A. D. Kandhare, P. Ghosh, and S. L. Bodhankar, “Naringin, a flavanone glycoside, promotes angiogenesis and inhibits endothelial apoptosis through modulation of inflammatory and growth factor expression in diabetic foot ulcer in rats,” Chemico-Biological Interactions, vol. 219, pp. 101–112, 2014.
View at: Publisher Site | Google Scholar
M. Rajadurai and P. S. M. Prince, “Preventive effect of naringin on lipids, lipoproteins and lipid metabolic enzymes in isoproterenol-induced myocardial infarction in Wistar rats,” Journal of Biochemical and Molecular Toxicology, vol. 20, no. 4, pp. 191–197, 2006.
View at: Publisher Site | Google Scholar
M. Rajadurai and P. S. M. Prince, “Preventive effect of naringin on lipid peroxides and antioxidants in isoproterenol-induced cardiotoxicity in Wistar rats: biochemical and histopathological evidences,” Toxicology, vol. 228, no. 2-3, pp. 259–268, 2006.
View at: Publisher Site | Google Scholar
M. Rajadurai and P. S. M. Prince, “Preventive effect of naringin on cardiac markers, electrocardiographic patterns and lysosomal hydrolases in normal and isoproterenol-induced myocardial infarction in Wistar rats,” Toxicology, vol. 230, no. 2-3, pp. 178–188, 2007.
View at: Publisher Site | Google Scholar
M. Rajadurai and P. S. M. Prince, “Preventive effect of naringin on isoproterenol-induced cardiotoxicity in Wistar rats: an in vivo and in vitro study,” Toxicology, vol. 232, no. 3, pp. 216–225, 2007.
View at: Publisher Site | Google Scholar
A. Chanet, D. Milenkovic, C. Deval et al., “Naringin, the major grapefruit flavonoid, specifically affects atherosclerosis development in diet-induced hypercholesterolemia in mice,” The Journal of Nutritional Biochemistry, vol. 23, no. 5, pp. 469–477, 2012.
View at: Publisher Site | Google Scholar
P. Pu, D.-M. Gao, S. Mohamed et al., “Naringin ameliorates metabolic syndrome by activating AMP-activated protein kinase in mice fed a high-fat diet,” Archives of Biochemistry and Biophysics, vol. 518, no. 1, pp. 61–70, 2012.
View at: Publisher Site | Google Scholar
M. Ikemura, Y. Sasaki, J. C. Giddings, and J. Yamamoto, “Preventive effects of hesperidin, glucosyl hesperidin and naringin on hypertension and cerebral thrombosis in stroke-prone spontaneously hypertensive rats,” Phytotherapy Research, vol. 26, no. 9, pp. 1272–1277, 2012.
View at: Publisher Site | Google Scholar
M. A. Alam, K. Kauter, and L. Brown, “Naringin improves diet-induced cardiovascular dysfunction and obesity in high carbohydrate, high fat diet-fed rats,” Nutrients, vol. 5, no. 3, pp. 637–650, 2013.
View at: Publisher Site | Google Scholar
W. Malakul, S. Pengnet, C. Kumchoom, and S. Tunsophon, “Naringin ameliorates endothelial dysfunction in fructose-fed rats,” Experimental and Therapeutic Medicine, vol. 15, no. 3, pp. 3140–3146, 2018.
View at: Publisher Site | Google Scholar
W. Malakul, S. Thirawarapan, W. Suvitayavat, and O. L. Woodman, “Type 1 diabetes and hypercholesterolaemia reveal the contribution of endothelium-derived hyperpolarizing factor to endothelium-dependent relaxation of the rat aorta,” Clinical and Experimental Pharmacology and Physiology, vol. 35, no. 2, pp. 192–200, 2008.
View at: Google Scholar
W. T. Friedewald, R. I. Levy, and D. S. Fredrickson, “Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge,” Clinical Chemistry, vol. 18, no. 6, pp. 499–502, 1972.
View at: Google Scholar
S. Niroumand, M. Khajedaluee, M. Khadem-Rezaiyan et al., “Atherogenic Index of Plasma (AIP): a marker of cardiovascular disease,” Medical Journal of the Islamic Republic of Iran, vol. 29, p. 240, 2015.
View at: Google Scholar
K. Tjaden, E. Pardali, and J. Waltenberger, “Hypercholesterolemia induces vascular cell dysfunction: molecular basis for atherosclerosis,” Austin Journal of Vascular Medicine, vol. 2, no. 1, p. 1011, 2015.
View at: Google Scholar
A. Pirillo, G. D. Norata, and A. L. Catapano, “LOX-1, OxLDL, and atherosclerosis,” Mediators of Inflammation, vol. 2013, Article ID 152786, 12 pages, 2013.
View at: Publisher Site | Google Scholar
A. R. El-Sheakh, H. A. Ghoneim, G. M. Suddek, and E. S. M. Ammar, “Attenuation of oxidative stress, inflammation, and endothelial dysfunction in hypercholesterolemic rabbits by allicin,” Canadian Journal of Physiology and Pharmacology, vol. 94, no. 2, pp. 216–224, 2016.
View at: Publisher Site | Google Scholar
H. M. Al-Muzafar and K. A. Amin, “Efficacy of functional foods mixture in improving hypercholesterolemia, inflammatory and endothelial dysfunction biomarkers-induced by high cholesterol diet,” Lipids in Health and Disease, vol. 16, no. 1, p. 194, 2017.
View at: Publisher Site | Google Scholar
C.-H. Lee, T.-S. Jeong, Y.-K. Choi et al., “Anti-atherogenic effect of citrus flavonoids, naringin and naringenin, associated with hepatic ACAT and aortic VCAM-1 and MCP-1 in high cholesterol-fed rabbits,” Biochemical and Biophysical Research Communications, vol. 284, no. 3, pp. 681–688, 2001.
View at: Publisher Site | Google Scholar
S. Jeon, Y. B. Park, and M.-S. Choi, “Antihypercholesterolemic property of naringin alters plasma and tissue lipids, cholesterol-regulating enzymes, fecal sterol and tissue morphology in rabbits1,” Clinical Nutrition, vol. 23, no. 5, pp. 1025–1034, 2004.
View at: Publisher Site | Google Scholar
Y. Zhao, P. M. Vanhoutte, and S. W. S. Leung, “Vascular nitric oxide: beyond eNOS,” Journal of Pharmacological Sciences, vol. 129, no. 2, pp. 83–94, 2015.
View at: Publisher Site | Google Scholar
D. H. Choi, Y. J. Lee, J. S. Kim, D. G. Kang, and H. S. Lee, “Cynanchum wilfordiiameliorates hypertension and endothelial dysfunction in rats fed with high fat/cholesterol diets,” Immunopharmacology and Immunotoxicology, vol. 34, no. 1, pp. 4–11, 2012.
View at: Publisher Site | Google Scholar
C.-W. Lu, Y. Lin, Y.-P. Lei, L. Wang, Z.-M. He, and Y. Xiong, “Pyrrolidine dithiocarbamate ameliorates endothelial dysfunction in thoracic aorta of diabetic rats by preserving vascular DDAH activity,” PLoS One, vol. 12, no. 7, Article ID e0179908, 2017.
View at: Publisher Site | Google Scholar
D. H. Choi, Y. J. Lee, H. C. Oh et al., “Improved endothelial dysfunction by cynanchum wilfordii in apolipoprotein E−/− mice fed a high fat/cholesterol diet,” Journal of Medicinal Food, vol. 15, no. 2, pp. 169–179, 2012.
View at: Publisher Site | Google Scholar
J.-H. Wu, Q.-H. Wang, F. Li et al., “Suppression of diet-induced hypercholesterolemia by turtle jelly, a traditional Chinese functional food, in rats,” Evidence-Based Complementary and Alternative Medicine, vol. 2012, Article ID 320304, 15 pages, 2012.
View at: Publisher Site | Google Scholar
C. M. Balarini, M. A. Leal, I. B. Gomes et al., “Sildenafil restores endothelial function in the apolipoprotein E knockout mouse,” Journal of Translational Medicine, vol. 11, no. 1, p. 3, 2013.
View at: Publisher Site | Google Scholar
K. Tang, F. Wang, Y. Zeng, X. Chen, and X. Xu, “Salusin-α attenuates hepatic steatosis and atherosclerosis in high fat diet-fed low density lipoprotein receptor deficient mice,” European Journal of Pharmacology, vol. 830, pp. 76–86, 2018.
View at: Publisher Site | Google Scholar
K.-P. Shen, H.-L. Lin, W.-T. Chang et al., “Eugenosedin-A ameliorates hyperlipidemia-induced vascular endothelial dysfunction via inhibition of α1-adrenoceptor/5-HT activity and NADPH oxidase expression,” The Kaohsiung Journal of Medical Sciences, vol. 30, no. 3, pp. 116–124, 2014.
View at: Publisher Site | Google Scholar
J. Zhang, S. Yang, H. Li, F. Chen, and J. Shi, “Naringin ameliorates diabetic nephropathy by inhibiting NADPH oxidase 4,” European Journal of Pharmacology, vol. 804, pp. 1–6, 2017.
View at: Publisher Site | Google Scholar
S. Balzan and V. Lubrano, “LOX-1 receptor: a potential link in atherosclerosis and cancer,” Life Sciences, vol. 198, pp. 79–86, 2018.
View at: Publisher Site | Google Scholar
S. Bartesaghi and R. Radi, “Fundamentals on the biochemistry of peroxynitrite and protein tyrosine nitration,” Redox Biology, vol. 14, pp. 618–625, 2018.
View at: Publisher Site | Google Scholar
R. Butchi Akondi, P. Kumar, A. Annapurna, and M. Pujari, “Protective effect of rutin and naringin on sperm quality in streptozotocin (STZ) induced type 1 diabetic rats,” Iranian Journal of Pharmaceutical Research, vol. 10, no. 3, pp. 585–596, 2011.
View at: Google Scholar

Copyright

Copyright © 2019 Sirinat Pengnet 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.

PDF Download Citation

Download other formats

Order printed copies

Views

1771

Downloads

1365

Citations