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Gentianella acuta mitigates cardiovascular damage and inflammation in diet‑induced hypercholesterolaemic rats
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- Published online on: September 6, 2021 https://doi.org/10.3892/etm.2021.10694
- Article Number: 1259
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Copyright : © Si et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY 4.0].
Abstract
Introduction
Cardiovascular disease (CVD) is an important health concern and has been the focus of considerable research. In China, there are an estimated 330 million patients with CVD, and CVD accounts for >40% of all disease-related resident deaths and has been identified as the leading cause of mortality (1). The mortality, incidence and prevalence rates of CVD continue to increase globally (1). Atherosclerosis (AS) is a major cause of CVD and the result of several factors, among which lipid metabolism disorders are the leading contributor. In modern society, lipid metabolism disorders are caused by hypercholesterolaemia and induce an inflammatory response that is involved in all processes of AS (2,3). The nuclear transcription factor controlling their release is phosphorylated (p)-nuclear factor κB (NF-κB), which has been revealed to induce an increase in the production of inflammatory and adhesion factors (4-6). Usually, NF-κB and the inhibitory protein inhibitor of NF-κB-α (IκBα) exist as a complex and are inactive. However, when cells are stimulated or activated, the inhibitor of NF-κB kinase β (IKKβ) phosphorylates and degrades IκBα, thus activating NF-κB. p-NF-κB translocates into the nucleus, binds to related genes and regulates their transcription (7-10). In addition, numerous studies have reported that oxidative stress is an important cause of AS and is closely associated with NF-κB (11-13). Therefore, the occurrence of AS is closely linked to the IKK/IκB/NF-κB pathway.
Gentianella acuta (Michx.) Hulten (G. acuta) belongs to the Gentianella genus of the Gentianaceae family, also known as the bitter gentian (14). The Elunchun people have been using G. acuta to treat arrhythmias and other heart diseases for thousands of years (15,16). Previous studies on G. acuta mainly have focused on traditional efficacy, such as liver protection, and anti-arrhythmic, antioxidant and hypoglycaemic effects; however, further discoveries have been made in other fields (17); for example, the bioactive substances of G. acuta have been revealed to exert a beneficial effect on aberrant intestinal motility (18-20). Li et al (18) reported treatment with water extract of G. acuta could ameliorate cardiac structural disorders, excessive collagenous fiber accumulation in the heart and cardiac malfunction by regulating the NF-κB pathway in a model of myocardial fibrosis. Wang et al (21) indicated that xanthones from G. acuta exerted cardioprotective effects on myocardial ischemia/reperfusion (I/R) injury through its antioxidant and anti-apoptosis properties. Yang et al (22) indicated that the aqueous extract of G. acuta may improve isoproterenol-induced myocardial fibrosis through the inhibition of the tumour growth factor (TGF)-β1/Smads signalling pathway. Numerous studies (16,18,23-25) have reported that G. acuta exerted a protective effect against injury of the heart and the aorta of rats under various conditions, such as I/R. However, the effect and specific mechanism of action of G. acuta in cardiovascular damage and inflammation under hypercholesterolaemic conditions remain unclear. The aim of the present study was to explore the potential role of G. acuta in mitigating cardiovascular damage and inflammation in diet-induced hypercholesterolaemic rats.
Materials and methods
Collection and preparation of plant materials
G. acuta was purchased from The Darhan Muminggan Joint Banner mongolian medicine plantation, Hulunbeier district of Inner Mongolia and was identified and authenticated by Professor Yu-Ping Yan in the field of medicinal plants (College of Pharmacy, Hebei University of Chinese Medicine, Shijiazhuang, China). The plants were air-dried and then chopped. G. acuta (64.51 g) was soaked in 1,400 ml 25˚C distilled water for 30 min. The mixture was boiled in two batches and combined twice with the filtrate. The mixture was used at a quantity of 537 ml to obtain a suspension of G. acuta with a concentration of 0.12 g/ml.
Animals and experimental design
The Ethics Committee of Hebei University of Chinese Medicine (Shijiazhuang, China) approved and supervised the present study (approval no. DWLL2018016). A total of 32 specific-pathogen free male Sprague-Dawley (SD) rats, aged 6-7 weeks, weighing 160-180 g, were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. (license no. SCXK 2016-0006) and all rats had free access to food and water. They were kept at room temperature with 60% humidity and 12-h light/dark cycle. After 1-week adaptive feeding, the rats were randomized into four groups (8) as follows: i) Control group (Control); ii) control administration group (Control-G), iii) model group (Model); and iv) model administration group (Model-G). While animals in the Model and Model-G groups received a high-fat diet (high-fat feed ratio, 80.4% basic feed + 2% cholesterol + 10% lard + 0.5% sodium cholate + 0.1% propylthiouracil + 5% sugar + 2% yolk powder) to induce preliminary hypercholesterolaemia, Control and Control-G animals received normal feed (100% basic feed: 248.48 g/kg crude protein + 65.18 g/kg crude fat). Normal and high-fat feed were provided and prepared by Hebei Medical University (Shijiazhuang, China). On the basis of the previous study, a 1.2 g/kg G. acuta dosage solution was designed (26). After the third week of modelling, the rats of the Control-G and Model-G groups were administered water extract of G. acuta and the other groups were treated with the same 10 ml/kg of physiological saline for 2 weeks.
At the end of the experiment, all rats were only administered water for the final 12 h. All rats were anesthetized with 50 mg/kg pentobarbital sodium (Merck KGaA) and euthanized using cervical dislocation. Following anaesthesia, blood was collected from the inferior vena cava for analysis of blood indicators. The serum was separated by centrifugation at 12,000 x g for 15 min at 4˚C and stored in a refrigerator at -80˚C for further analysis. The heart was weighed and fixed with the thoracic aorta in 10% (v/v) formalin 24 h at room temperature for histopathological studies, and the rest of heart and thoracic aorta were stored at -80˚C.
Blood biochemical index test
The serum levels of total cholesterol (TC; cat. no. OSR6216; Beckman Coulter, Inc.), triglycerides (TG; cat. no. OSR61118; Beckman Coulter, Inc.), low-density lipoprotein (LDL; cat. no. A113-1-1; Nanjing Jiancheng Bioengineering Institute), high-density lipoprotein (HDL; cat. no. A112-1-1; Nanjing Jiancheng Bioengineering Institute), lactate dehydrogenase (LDH; cat. no. A020-1-2; Nanjing Jiancheng Bioengineering Institute), creatine kinase (CK; cat. no. A032-1-1; Nanjing Jiancheng Bioengineering Institute), tumour necrosis factor-α (TNF-α; cat. no. SXR063; Shanghai Senxiong Biotech Industry, Co., Ltd.) and interleukin-10 (IL-10; cat. no. SXR035; Shanghai Senxiong Biotech Industry, Co., Ltd.) were assessed strictly according to the manufacturer's instructions.
Histopathological examination of the heart and thoracic aorta
The heart and thoracic aortas isolated from each group were fixed in 10% (v/v) formalin in 50 mm potassium phosphate buffer (pH 7.0) for 24 h at 4˚C. The tissues were subsequently embedded in paraffin, cut into 4-µm sections, and stained 5 min at room temperature with hematoxylin and then 1 min with eosin at room temperature. The sections were observed and images were captured using a light microscope with a Leica DFC 320 digital camera (magnification, x400; Leica Microsystems, Inc.).
Immunohistochemical analysis of IKKβ, p-IKKβ, IκBα and p-IκBα in the heart and thoracic aorta
Each section was dewaxed with a dimethylbenzene gradient and dehydrated using an alcohol gradient. The sections were then incubated with 3% H2O2 for 15 min in the dark, blocked with 100% goat serum for 20 min at room temperature (cat. no. ZLI-9056; ZSGB-BIO; OriGene Technologies, Inc.), and then rinsed three times with PBS. The primary antibodies [IKKβ (1:100; cat. no. A2087; ABclonal Biotech Co., Ltd.), p-IKKβ (1:400; cat. no. bs-5398R), IκBα (1:800; cat. no. bsm-33441M) and p-IκBα (1:200; cat. no. bs-5515R; all from BIOSS)] were incubated with the sections at 4˚C overnight. Next, rabbit two-step HRP-secondary antibody polymers (cat. no. PV-6001; ZSGB-BIO; OriGene Technologies, Inc.) were added for 60 min at room temperature and then the avidin-biotin-peroxidase complex (cat. no. PK-6200; Vector Laboratories, Inc.; Maravai LifeSciences) was added for 120 min at room temperature. The sections were stained with diaminobenzidine (DAB) reagent 10 min at room temperature, dehydrated with alcohol gradient and DAB and finally mounted using neutral balsam. The sections were viewed under a light microscope (magnification, x400) and analyzed using ImageJ software (v. d1.47; National Institutes of Health).
Western blot analysis for p-IKKβ, p-IκBα and p-NF-κB in the heart and p-NF-κB in the thoracic aorta
The protein extract from the frozen tissues of the heart and thoracic aorta were determined using a BCA Protein Assay Kit (cat. no. P0010; Beyotime Institute of Biotechnology) to ensure 20 µg protein per lane and were separated by 10% SDS-PAGE and then transferred onto polyvinylidene difluoride membranes. Membranes were blocked 4˚C for 5 h with 5% non-fat dry milk in Tris-buffered saline with 0.05% Tween-20 and left overnight. The blots were incubated with primary antibodies for GAPDH (1:1,000; cat. no. bs-0755R; BIOSS), IKKβ (1:100; cat. no. AF6013; Affinity Biosciences), p-IKKβ (1:400; cat. no. bs-5398R), IκBα (1:800; cat. no. bsm-33441M), p-IκBα (1:200; cat. no. bs-5515R; all from BIOSS), NF-κB (1:1,000; product no. 8242; Cell Signaling Technology, Inc.), p-NF-κB (1:250; cat. no. ab247871; Abcam) overnight at 4˚C and then incubated with a secondary antibody (1:10,000; cat. no. ZB2301; ZSGB-BIO; OriGene Technologies, Inc.) conjugated to horseradish peroxidase (1:6,500; Biosharp Life Sciences) for 2 h at room temperature. After the treatment of Super ECL Detection Reagent (cat. no. 36208ES60; Shanghai Yeasen Biotechnology Co., Ltd.), the protein bands were quantified by transmittance densitometry using ImageJ software (v. d1.47; National Institutes of Health). The relative protein band intensity was expressed as the ratio of each protein to the reference GAPDH.
Statistical analysis
All statistical analyses were completed using SPSS 22.0 software (IBM Corp). The data are presented as the mean ± SD. Differences among the four groups were assessed using one-way analysis of variance followed by Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference.
Results
Effects of G. acuta on serum lipids
Compared with the Control group, the TG, TC and LDL levels of the Model and Model-G groups were significantly increased, while the HDL level was significantly decreased (P<0.05). In addition, the levels of TG, TC and LDL were significantly decreased, and those of HDL were significantly increased in the Model-G group compared with those in the Model group (Fig. 1; P<0.05).
Effects of G. acuta on IL-10 and TNF-α in the serum
Compared with the Control group, the TNF-α levels in the Model group were increased >2-fold (P<0.05). Compared with the Model group, TNF-α was significantly decreased in the Model-G group (P<0.05). The IL-10 levels in the Model group were significantly decreased compared with those in the Control and Model-G groups (Fig. 2; P>0.05).
Effects of G. acuta on CK and LDH in the serum
The CK and LDH levels of the Model group were significantly higher compared with those of the Control and Model-G groups (P<0.05). Compared with the Model group, the level of CK and LDH were significantly decreased in the Model-G group (P<0.05; Fig. 3).
Effects of G. acuta on morphological and histological changes in the heart
The cardiomyocytes in the Control group were arranged in an orderly manner with uniform nuclei, uniform H&E staining of the cytoplasm and obvious striations. The arrangement of cardiomyocytes in the Model group was disordered, with burrs, slightly blurry striations, and certain sections were revealed to have lipid droplets. The arrangement of cardiomyocytes in the Model-G group was improved and appeared orderly (Fig. 4).
Effect of G. acuta on IKK/IκB/NF-κB in the heart
The IKKβ, p-IKKβ and p-IκBα protein expression levels of the Model group were markedly higher compared with those in the other three groups. While changes in the expression of IκBα were not significant among the four groups, the levels of p-IKKβ/IKKβ and p-IκBα/IκBα in the Model group were significantly higher than the other groups (Fig. 5A-C). Compared with the Control and Model-G groups, the protein levels of p-IKKβ/IKKβ, p-IκBα/IκBα and p-NF-κB/NF-κB in the Model group were significantly increased (Fig. 5D-G).
Effects of G. acuta on morphological and histological changes in the thoracic aorta
The arterial intima in the Control group was relatively smooth, with clear boundaries between the intima, media and adventitia, and endothelial cell layer continuity. The intima of the arteries of the Model group was uneven, and some endothelial cells had lost their continuity. Intimal concavity was improved in the Model-G group. The intima of the Control-G group was damaged (Fig. 6).
Effect of G. acuta on IKK/IκB/NF-κB in the thoracic aorta
The IKKβ, p-IKKβ and p-IκBα protein expression levels of the Model group were significantly higher compared with those in the other three groups. While the changes in the expression of IκBα were not significant among the four groups, the levels of p-IKKβ/IKKβ and p-IκBα/IκBα in the Model group were higher than the other three groups (Fig. 7A-C). Compared with the Model group, the levels of p-NF-κB/NF-κB in the Control and Model-G groups were significantly decreased (Fig. 7D and E).
Discussion
Several studies have reported that hypercholesterolaemia is not only a risk factor for AS development, but also an important cause of the exacerbation of AS (27,28). It has been revealed that G. acuta exerts a protective effect against myocardial ischemia (19). On this basis, its anti-AS effects and mechanism were studied herein. In the present study, a rat model of hypercholesterolaemia was established using a high-fat diet (29) to explore the effect and mechanisms of G. acuta in mitigating cardiovascular damage and inflammation.
Hypercholesterolaemia model rats exhibited increases in serum lipids and inflammatory factors, aortic muscular layer thickening and widespread myocardial structural disruption. These histopathological changes in the body were important formative indices of hypercholesterolaemia, with some beneficial changes appearing in the Model-G group, such as improved aortic wall structure and neatly arranged myocardial cells. Lipid deposition has been identified as an important cause of AS, which can lead to the increase of free radicals, thereby damaging endothelial cell function (30-32). Thus, the release of protective factors is reduced, leading to a reduction in the tightness of endothelial cells and increased permeability, which in turn results in increased lipid deposition, forming a vicious circle (33). As a consequence of a continuous high-fat diet, LDL is elevated and deposited in the endothelial cells of the arteries in which it is oxidized to ox-LDL, which can cause necrosis and disintegration of macrophages, release of lipids from atheromatous necrosis and plaque formation (34). When comparing the Model-G and the Model groups, it was revealed that G. acuta could effectively reduce the serum lipid level with further increasing the level of HDL.
A change in TNF-α and IL-10 levels in the serum of hypercholesterolaemic rats was also observed. TNF-α and IL-10 are important inflammatory factors leading to AS. TNF-α has been reported to promote the production of various inflammatory cytokines through T cells and has been identified as an important indicator of inflammation (35). Conversely, IL-10 has been reported to inhibit mononuclear macrophages from performing specific immune functions, such as the release of inflammatory mediators (36). Compared with the Control group, the levels of TNF-α were significantly increased, and those of IL-10 were decreased in the Model group. Following treatment with G. acuta, TNF-α and IL-10 levels were significantly altered in the Model group. These results demonstrated that the inflammatory response induced by the high-fat diet was inhibited by G. acuta.
CK and LDH have been revealed to be important indices reflecting functional heart status (37). Compared with the control group, the levels of CK and LDH in the blood vessels of the Model group were significantly decreased, indicating the protective effect of G. acuta in the heart. It was also revealed by H&E staining that the arrangement of cardiomyocytes in the Model-G group was improved and appeared orderly. These results further demonstrated that G. acuta effectively alleviated cardiovascular damage and inflammation in diet-induced hypercholesterolaemic rats.
NF-κB has been identified as an important nuclear factor that controls inflammatory cytokines and is normally bound to IκB in the cytoplasm. After NF-κB has been activated and translocated to the nucleus, several downstream inflammation-related factors, such as TNF-α and IL-6, promote its synthesis and release. Such factors are important causes of the occurrence and deterioration of AS (38-40). As a pattern recognition receptor, activated IKK is a major upstream target for NF-κB regulation. Multiple members of the IKK family, such as IKKα and IKKβ, have important regulatory effects on the activity of NF-κB. Both of these have been revealed to phosphorylate the IκB protein at different serine residues, while the main function has been assumed by IKKβ (41). Thus, IKKβ is an important indicator of NF-κB activation. When G. acuta was administered, the expression of p-IKKβ/IKKβ and p-IκBα/IκBα both in the heart and thoracic aorta in the Model-G group were significantly decreased. Compared with the Model group, the phosphorylation ratio of IKKβ, IκBα, NF-κB in the heart and NF-κB in thoracic aorta was decreased in the Model-G group. In addition, G. acuta significantly decreased the expression levels of IKKβ, p-IKKβ and p-IκBα in endothelial cells of the thoracic aorta, indicating its protective role. These results demonstrated that the anti-inflammatory effect of G. acuta may be mediated by inhibiting the IKKβ/IκBα/NF-κB pathway in the heart as well as the thoracic aorta.
In conclusion, G. acuta mitigated cardiovascular damage and inflammation in diet-induced hypercholesterolaemic rats, possibly through the inhibition of the IKK-β/IκB/NF-κB pathway. Thus, G. acuta may prove useful in the treatment of hypercholesterolaemia.
A limitation of the present study was that it lacked direct assessment of physiological parameters and immunohistochemical analysis could reveal the expression levels but was weaker in protein comparison than western blotting in thoracic aorta. In addition, G. acuta water extract was selected, but water extract is comprised of numerous components and these were not fractionated and explored individually.
Acknowledgements
The authors would like to thank Professor Gang Cao and Professor Huazhou Xu (School of Basic Medicine, Hebei University of Chinese Medicine, Shijiazhuang, China) for technical assistance.
Funding
Funding: The present was supported by the National Natural Science Foundation of China (grant no. 81573698), the innovative research program for postgraduate of Hebei University of Chinese Medicine (grant no. XCXZZSS2021003) and the 333 Talent Project of Hebei (grant no. 2020-7).
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Authors' contributions
DM and ZM conceived the project and designed the experiments. AL and SG carried out the experiments. MS, MW and YH established the rat model of hypercholesterolaemia and carried out the experiments. YH conducted the statistical analysis. MS and MW wrote the manuscript and confirmed the authenticity of the raw data. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The Ethics Committee of Hebei University of Chinese Medicine (Shijiazhuang, China) approved and supervised the present study (approval no. DWLL2018016). The animal treatments in this study were in compliance with the Laboratory Animal Management of National Animal Science and Technology Commission's Regulations (Beijing, China).
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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