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 Table of Contents  
ORIGINAL ARTICLE
Year : 2018  |  Volume : 16  |  Issue : 1  |  Page : 58-65

Role of inflammation versus hypercholesterolemia in the development of atherosclerosis in male albino rats


Department of Physiology, Faculty of Medicine, Zagazig University, Zagazig, Egypt

Date of Submission18-Jun-2018
Date of Acceptance15-Aug-2018
Date of Web Publication20-Nov-2018

Correspondence Address:
Randa S Gomaa
Department of Physiology, Faculty of Medicine, Zagazig University, Zagazig, 44519
Egypt
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/AZMJ.AZMJ_54_18

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  Abstract 


Background Atherosclerosis (AS) is a chronic condition in which dyslipidemia had been contributed to its development, along with evidence proving an inflammatory cause.
Objective The aim was to determine the relation between dietary hypercholesterolemia and AS with a trial to evaluate the role of inflammation in development of AS in male albino rats.
Materials and methods A total of 30 adult male albino rats were divided into two main groups: control group (n=6) and high-cholesterol diet (HCD)-fed group (n=24), which was subdivided into four subgroups (n=6): HCD-fed, HCD-fed with methotrexate, HCD-fed with cholestyramine, and HCD-fed with statin groups. Serum total cholesterol (TC), triglycerides, high-density lipoprotein (HDL) cholesterol, non-HDL cholesterol, low-density lipoprotein (LDL)-cholesterol, very LDL-cholesterol, atherogenic index, LDL/HDL ratio, and inflammatory markers such as inerlukin-6, tumor necrotic factor-α, and highly sensitive C-reactive protein were estimated. Carotid artery histopathology was done.
Results HCD produced marked disturbance in lipid profile and increased inflammatory markers and atherosclerotic changes in carotid artery. Administration of statin and cholestyramine significantly improved this dyslipidemia. Elevated inflammatory markers were significantly decreased by administration of methotrexate and statin. Atherosclerotic changes in carotid artery decreased significantly in rats pretreated with methotrexate and statin.
Conclusion Atherosclerotic condition is closely associated with excessive intake of cholesterol-rich diet; however, inflammation has a central role in the pathogenesis of the atherosclerotic process, as atherosclerotic changes could be reduced despite disturbed lipid profile by anti-inflammatory medication. Further studies are recommended for more evaluation of the role of anti-inflammatory drugs in reduction of clinical outcomes in atherosclerotic conditions.

Keywords: atherosclerosis, dyslipidemia, high-cholesterol diet, inflammation


How to cite this article:
Ibrahim SM, Gomaa RS, Ismail SI, Ibrahim HS. Role of inflammation versus hypercholesterolemia in the development of atherosclerosis in male albino rats. Al-Azhar Assiut Med J 2018;16:58-65

How to cite this URL:
Ibrahim SM, Gomaa RS, Ismail SI, Ibrahim HS. Role of inflammation versus hypercholesterolemia in the development of atherosclerosis in male albino rats. Al-Azhar Assiut Med J [serial online] 2018 [cited 2018 Dec 18];16:58-65. Available from: http://www.azmj.eg.net/text.asp?2018/16/1/58/244150




  Introduction Top


Cardiovascular diseases (CVDs) are still the leading cause of morbidity and mortality worldwide. Coronary heart disease is a serious health threat in the developed world and responsible for ∼20% of all deaths [1]. Dietary cholesterol causes increase in blood cholesterol level, which leads to arterial wall lesions [2]. The International Atherosclerosis Society recommends decreasing dietary cholesterol as a strategy for lowering low-density lipoprotein cholesterol (LDL-C) [3]. It was reported that dietary cholesterol increases CVD risk [4]. However, Ravnskov et al. [5] reported that there is a lack of an association or an inverse association between LDL-C level and cardiovascular mortality.

Atherosclerosis (AS) is a complex disease of the arterial wall characterized by the formation of atherosclerotic plaques, which lead to progressive occlusion of arteries. These lesions remain silent for decades but over time, they may cause stenosis or rupture. This can lead to distal ischemia and thrombosis, with clinical consequences such as myocardial infarction and stroke [6]. Despite being a multifactorial disease, elevated concentrations of cholesterol, mainly transported by LDL-C particles, promote atherosclerotic lesions [7].

The idea that AS is a predominantly lipid-driven disease has dominated the field of CVD. The concept of atherogenesis has changed owing to new evidence that AS is predominantly a chronic low-grade inflammatory disease of the vessel wall [6]. Chronic inflammation has become recognized as a contributory factor in the development of atherosclerotic CVD and other diverse chronic diseases, with new evidence continually being added that supports AS being an inflammatory condition [8]. In AS, inflammation starts and evolves in response to cholesterol accumulation in the arterial intima of the large and medium arteries. However, innate and adaptive immune responses play a pivotal role throughout the initiation, progression, and clinical consequences of atherosclerotic diseases [6].

On basis of these data, determining the relation between dietary hypercholesterolemia and AS with a trial to evaluate role of inflammation in atherosclerotic process in male albino rats is the objective of the current study.


  Materials and methods Top


A total of 30 adult male albino rats 12 weeks old weighing 180–200 g were obtained from the Animal House Faculty of Veterinary Medicine, Zagazig University. They were kept in steel wire cages (six/cage) in the animal house in Faculty of Medicine of Zagazig University under hygienic conditions. Animals had free access to water, were kept at room temperature, and were maintained on a 12-h light/dark cycle [9]. The rats were accommodated to animal house conditions for 1 : for 2 weeks before the experiments were carried out [10]. The experimental protocols were approved by Physiology Department and by Institutional Review Board (IRB) Committee, Faculty of Medicine, Zagazig University, Egypt.

The animals were divided into two main groups:
  1. Group I (n=6) (control): the rats were fed on normal diet, which consisted of 25.8% protein, 62.8% carbohydrate, and 11.4% fat [11].
  2. Group II (n=24): the rats were fed on high-cholesterol diet (HCD) composed of cow fat (4%), cholic acid (0.2%), cholesterol (1%), egg yolk (7%), methyl thiouracil (0.2%), corn starch (35%) sodium chloride (1%), wheat bran (6.6%), and wheat flour (45%) [12].


These animals were subdivided into four subgroups, with 6 rats each:
  1. Group IIa: rats were fed HCD.
  2. Group IIb: rats were fed HCD with methotrexate (tablets 2.5 mg SANDOZ, Egypt) as anti-inflammatory drug by dose 0.3 mg/kg/twice per week with 3-day interval by oral route in the morning before eating [13].
  3. Group IIc: rats were fed HCD with cholestyramine (sachets 4 g SANDOZ) as lipid-lowering drug by dose 0.5 gm/kg/day by oral route in the morning before eating [14].
  4. Group IId: rats were fed HCD with simvastatin (tablets 40 mg Gulf Pharmaceutical Industries, Julphar, Egypt) as lipid-lowering and anti-inflammatory drug by dose 10 mg/kg/day by oral route in the morning before eating [15].


Experimental protocol

The experiment lasted for 6 weeks after acclimatization of the rats to the experimental conditions, and then the rats were killed by decapitation after 12 h of fasting under anesthesia (chloral hydrate) inhalation. Blood samples were obtained by exsanguination at the time of killing, collected and allowed to clot for 2 h at room temperature before centrifugation. Sera were stored at −20°C until analysis. Repeated freezing and thawing was avoided. Then, the carotid artery was rapidly removed, dissected from the connective tissues, and fixed in 10% neutral-buffered formalin. Sections of 5 μm were stained with hematoxylin and eosin and then were examined and photographed by light microscopy for histopathology. The thickness of tunica media was measured from photographs of 400× magnification using Digimizer 4.3.2. Image analysis software (Med Calc Software, Belgium). The values of the thickness from each sample were finally statistically compared.

The sera were examined for levels of TC by colorimetric method [16] and triglyceride levels (TG) and high-density lipoprotein-cholesterol (HDL-C) by an enzymatic assay [17]. Calculation of non-high density lipoprotein cholesterol level (non-HDL-C) was done by the following formula: non-HDL-C=TC–HDL-C [18]. Low-density lipoprotein-cholesterol (LDL-C) was calculated using Friedewald’s formula [19]: LDL-C=[TC–(HDL–TG)/5]. Very low-density lipoprotein-cholesterol (VLDL-C) was calculated as follows: VLDL-C=TG/5 [19]. LDL/HDL ratio was calculated [20]. The atherogenic index (AI) was calculated from the formula: AI=(TC–HDL)/HDL [21].

Estimation of serum highly sensitive C-reactive protein (HS-CRP) level was done by immune-enzymatic assay technique described by Buduneli et al. [22]. Estimation of serum inerlukin-6 (IL-6) level was done by using rat ELISA kits (Bio Basic Inc., Ohio, USA) [23]. Serum tumor necrotic factor-α (TNF-α) level was determined by using rat ELISA kits (Bio Basic Inc.) according to Fernando et al. [24].

Statistical analysis

Results were presented as mean±SD. Statistical analysis was performed using the statistical package for the social sciences, version 19.0 (SPSS; SPSS Inc., Chicago, Illinois, USA). Repeated measures of analysis of variance was applied followed by least significance differences for multiple comparisons. Levels of significance (P) were considered to be statistically significant when P value was less than 0.05 [25].


  Results Top


Effect of HCD and HCD with medication on lipid profile

There was increase in serum levels of TC, TG, non-HDL-C, LDL-C, VLDL-C, HDL/LDL, and AI with decrease in HDL-C level in all HCD-fed groups in comparison with the control group. Administration of simvastatin and cholestyramine significantly increased serum HDL-C level and decreased serum levels of TC, TG, non-HDL-C, LDL-C, VLDL-C, HDL/LDL and AI, whereas methotrexate did not change serum lipid profile levels in comparison with HCD-fed rats ([Table 1]).
Table 1 Comparison of lipid profile parameters in all studied groups

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Effect of HCD and HCD with medication on inflammatory markers

There was an increase in serum levels of IL6, TNF-α, and HS-CRP in all HCD-fed groups in comparison with the control group. Administration of cholestyramine did not change serum inflammatory marker levels in comparison with HCD-fed rats whereas methotrexate and simvastatin administration significantly decreased the serum levels of IL6, TNF-α, and HS-CRP in comparison with HCD-fed and HCD-fed cholestyramine-treated rats ([Table 2]).
Table 2 Comparison of inflammatory markers in all studied groups

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Histopathological findings

Group I

The wall of the carotid artery showed normal architecture with normal 3 layers: tunica intima with smooth and regular surface that is composed of a continuous layer of flat endothelial cells (I), tunica media that is formed of several layers of regularly arranged smooth muscle fibers (M), and tunica adventia that is formed of loose connective tissue (A) ([Figure 1]–slide I).
Figure 1 Photograph of transverse sections (TC) of carotid artery. (Slide I): TC of carotid artery of control group (group I) showing normal histological structures of intima, media, and adventitia. (Slide IIa): TC of carotid artery of group IIa shows atherogenic changes in form of marked intimal thickening and subintimal atheromatous plaque (a) with atheromatous cap formation formed of foamy histocytes (b), fibrous bands, and scattered inflammatory cells (c) with ulceration of intimal lining (d). (Slide IIb): TC of carotid artery of group IIb shows that methotrexate administration prevented to a large extent the development of atherosclerotic changes as indicated by very thin atheromatous plaque with less inflammatory cellular infiltration and some foam cells formation with nearly normal thickness of media. (Slide IIc): TC of carotid artery of group IIc shows that cholestyramine produced slight improvement in the atherogenic changes in the form of slight reduction in the thickness of subintimal atheromatous plaque (↑) with needle-like cholesterol clefts formation, foamy histocytes, fibrous bands, and inflammatory cells infiltration with intimal ulceration (a), thickening, and protrusion in the lumen (b). (Slide IId): TC of carotid artery of group IId shows that simvastatin administration prevented to a large extent the development of atherosclerotic changes as indicated by minimal intimal thickening, less inflammatory cellular infiltration, less foam cells, and less cholesterol clefts with nearly normal thickness of media.

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Groups IIa

The wall of carotid artery showed atherogenic changes in form of marked intimal thickening and subintimal atheromatous plaque (a) with atheromatous cap formation formed of foamy histocytes (b), fibrous bands, and scattered inflammatory cells (c) with ulceration of intimal lining (d) ([Figure 1]–slide IIa).

In group IIb

Methotrexate administration prevented to a large extent the development of atherosclerotic changes as indicated by very thin atheromatous plaque with less inflammatory cellular infiltration and some foam cells formation with nearly normal thickness of media ([Figure 1]–slide IIb).

In group IIc

Cholestyramine produced slight improvement in the atherogenic changes in the form of slight reduction in the thickness of subintimal atheromatous plaque (↑) with needle-like cholesterol clefts formation, foamy histocytes, fibrous bands, and inflammatory cells infiltration with intimal ulceration (a), thickening, and protrusion in the lumen (b) ([Figure 1]–slide IIc).

In group IId

Simvastatin administration prevented to a large extent the development of atherosclerotic changes as indicated by minimal intimal thickening, less inflammatory cellular infiltration, less foam cells, and less cholesterol clefts with nearly normal thickness of media ([Figure 1]–slide IId).

Effect of HCD and HCD with medication on carotid intima media thickness (CIMT)

CIMT was 30.7±3.8 μm, 49.9±3 μm, 39.9±0.7 μm, 48.4±2.8 μm, and 38.9± 0.69 μm in groups I, IIa, IIb, IIc, and IId, respectively. There was a significant increase in CIMT in all HCD-fed groups in comparison with control group. Administration of cholestyramine did not change CIMT in comparison with HCD-fed rats whereas methotrexate and simvastatin administration significantly decreased CIMT in comparison with HCD-fed and HCD-fed cholestyramine-treated rats ([Figure 2]).
Figure 2 Comparison of carotid intima media thickness in all studied groups. n=6 in each group − Data are represented as mean±standard deviation. CIMT, carotid intima media thickness. P<0.05. *Significant when compared with control group, (a) significant when compared with group IIa, (b) significant when compared with group IIb, (c) significant when compared with group IIc.

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  Discussion Top


Data of the present study revealed marked disturbance in lipid profile of rats fed with cholesterol-rich diet manifested by increased serum levels of TC, TG, LDL-C, VLDL-C as well as non-HDL-C, LDL/HDL, and AI parallel to a decrease in HDL-C level.

These results are in agreement with many other researchers who reported that feeding animals with cholesterol-rich diet is commonly used as a model for induction of hypercholesterolemia to study the etiology of hypercholesterolemia-related metabolic disorders and the efficiency of anti-hypercholesterolemia agents [26],[27],[28].

Moreover, it was found that the serum TC, non-HDL-C, LDL-C, and LDL/HDL of animals fed high-cholesterol high-fat diet increased significantly [29], and it was reported that cholesterol is an undisputed risk factor in CVD, and the total lifelong cholesterol burden defines the risk [30].

Non-HDL-C contains more atherogenic cholesterol than LDL-C [18] and has been suggested to be a surrogate marker of small, dense LDL-C [31]. Zhang et al. [32] showed that the use of non-HDL-C is ahead of LDL-C in predicting the severity of coronary AS [33].

LDL/HDL is an important parameter in detection of atherosclerotic diseases, and it was considered to be an indicator with greater predictive value than isolated parameters used independently [34].

In contrast, it was reported that epidemiologic studies have found no [35] or little [36] association between cholesterol intake and CVD risk.

The recently ACCELERATE trial that examined whether the addition of evacetrapib to standard medical therapy reduces the risk of cardiovascular (CV) morbidity and mortality in patients with high-risk vascular disease dumbfounded many experts by failing to demonstrate any cardiovascular benefit of evacetrapib, a novel cholesteryl ester transfer protein inhibitor, despite dramatically lowering LDL-C and raising HDL-C in high-risk patients with coronary disease. It is now clear that lowering cholesterol through diet or with different classes of drugs does not significantly prolong life or consistently prevent CVD, and cholesterol paradox is supported [37].

In addition, Dehghan et al. [38] found in their prospective urban rural epidemiology (PURE) study that high carbohydrate intake but not total fat and individual types of fat was associated with higher risk of total mortality. Total fat and types of fat were not associated with CVD mortality, whereas saturated fat had an inverse association with stroke. They recommended that global dietary guidelines should be reconsidered in light of these findings.

The results of the present study showed that administration of simvastatin and cholestyramine but not methotrexate significantly improved dyslipidemia produced by HCD.

Simvastatin is commonly used to reduce blood lipids and to treat CVDs including myocardial infarction, stroke, and hypertension [39] and is useful for high-risk patients with hypercholesterolemia in primary prevention settings [40]. It possesses additional pleiotropic effects, including antioxidant, anti-inflammatory, and immunemodulatory properties [41].

Although methotrexate directly targets the inflammatory process of atherogenesis, methotrexate not only attenuated systemic inflammation but additionally decreased cardiovascular events, suggesting that a direct treatment of inflammation may reduce the risk of CVD [42]. Moreover, it was reported that methotrexate also may have direct anti-atherosclerotic effects; in the cholesterol-fed rabbit model, methotrexate reduced new atheroma formation by 75% and reduced multiple biomarkers of macrophage function within the vessel wall [43].

Cardiovascular inflammation reduction trial (CIRT) proposed that the reduction in CVD events in patients with prior MI and either type II diabetes or metabolic syndrome, conditions associated with persistent inflammation, by using methotrexate was derived from its effect on vascular inflammation [44].

However, cholestyramine is one of bile acid substrates that selectively bind and remove bile acid molecules from the gastrointestinal tract, decreasing plasma cholesterol levels [45].

The present results revealed that TNF-α, IL6, and HS-CRP are elevated in HCD-fed rats and HCD-fed rats pretreated with cholestyramine when compared with controls but significantly decreased in HCD-fed rats pretreated with methotrexate and simvastatin when compared with HCD group and HCD pretreated with cholestyramine group. Atherosclerotic changes in carotid artery decreased significantly in rats pretreated with methotrexate and simvastatin with minimal improvement in cholestyramine pretreated groups.

TNF-α has been implicated in the pathogenesis of chronic systemic inflammatory conditions and in the development of atherogenesis and vascular inflammation [46], whereas IL-6 was shown to be produced by macrophages in atherosclerotic mice [47]. It has been reported that high IL-6 concentrations have been associated with increased risk of MI in healthy men and has an early peak at the acute phase of MI related to plaque instability [48].

Justification for the Use of Statins in Prevention; an Intervention Trial Evaluating Rosuvastatin (JUPITER) is a trial that was conducted to determine if patients with elevated CRP level without hyperlipidemia might benefit from statin therapy and confirmed the strong relationship between CRP and CVDs [49]. It was concluded that estimation of HS-CRP can be considered as a better predictor for CVD than the serum LDL-cholesterol [50].It was reported that that during the AS, proinflammatory mediators (IL-6 and TNF-α) were activated. Consequently, for the treatment of atherogenesis, anti-inflammatory therapy was also needed [51]. It was reported that atherosclerotic plaque initiation and progression associated with the roles of inflammatory cells and cytokines [52].

Moreover, the results of Canakinumab Anti-inflammatory Thrombosis Outcomes Study (CANTOS) trial showed that anti-inflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid level lowering [53].

In contrast, other studies considered AS a predominantly lipid-driven disease. They reported that the possible mechanisms implicated in the pathogenesis of AS have made considerable ‘response to lipoprotein retention’ hypothesis as the initiating process in AS [54],[55],[56].

It was claimed that the augmented level of the serum cholesterol is the imperative feature of the atherogenesis, which was confirmed by an epidemiological study that showed correlation in the LDL, TC, and the severity of the AS [57]. AS is considered as a clinical condition of the cholesterol. Wang et al. [58] considered the hardening and narrowing the arteries as a consequence of manufacturing of the fatty material.

Current treatment guidelines and recommendations target LDL-C and non-HDL-C reduction to decrease CVD risk [59]. It was reported that control of LDL-C remains a cornerstone of CHD risk management and that the risk modification by cholesterol-lowering treatment is proved [60].


  Conclusion Top


Atherosclerotic condition is closely associated with excessive intake of cholesterol-rich diet; however, inflammation has a central role in the pathogenesis of the atherosclerotic process as atherosclerotic changes could be reduced despite disturbed lipid profile by anti-inflammatory medication. Further studies are recommended for more evaluation of the role of anti-inflammatory drugs in reduction of the clinical outcomes in atherosclerotic conditions.

Aknowledgements

The histopathological assessment in the current study was done by Professor Dr Kamal Ahmed Al Kashishy, Professor of Pathology, Faculty of Medicine, Zagazig University.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Cassar A, Holmes DR, Rihal CS, Gersh BJ. Chronic coronary artery disease: diagnosis and management. Mayo Clin Proc 2009; 84:1130–1146.  Back to cited text no. 1
    
2.
Gordon T. The diet-heart idea. Outline of a history. Am J Epidemiol 1988; 127:220–225.  Back to cited text no. 2
    
3.
Ariyo AA, Thach C, Tracy R. Lp(a) Lipoprotein, vascular disease, and mortality in the elderly. N Engl J Med 2003; 349:2108–2115.  Back to cited text no. 3
    
4.
D’Agostino RB, Vasan RS, Pencina MJ, Wolf PA, Cobain M, Massaro JM, Kannel WB.General cardiovascular risk profile for use in primary care: the Framingham heart study. Circulation 2008; 117:743–753.  Back to cited text no. 4
    
5.
Ravnskov U, Diamond DM, Hama R, Hamazaki T, Hammarskjöld B, Hynes N et al. Lack of an association or an inverse association between low density-lipoprotein cholesterol and mortality in the elderly: a systematic review. Br Med J Open 2016; 6:e 010401.  Back to cited text no. 5
    
6.
Lorenzatti AJ, Retzlaff BM. Unmet needs in the management of atherosclerotic cardiovascular disease: Is there a role for emerging anti-inflammatory interventions? Int J Cardiol 2016; 221:581–586.  Back to cited text no. 6
    
7.
Stone GW, Maehara A, Lansky AJ, de Bruyne B, Cristea E, Mintz GS et al. A prospective natural-history study of coronary atherosclerosis. N Engl J Med 2011; 364:226–235.  Back to cited text no. 7
    
8.
Gimbrone MA, García-Cardeña G. Endothelial cell dysfunction and the pathobiology of atherosclerosis. Circ Res 2016; 118:620–636.  Back to cited text no. 8
    
9.
Dray C, Knauf C, Daviaud D, Waget A, Boucher J, Buléon M, Carpéné C. Apelin stimulates glucose utilization in normal and obese insulin-resistant mice. Cell Metab 2008; 8:437–445.  Back to cited text no. 9
    
10.
Amessou M, Bortoli S, Liemans V, Collinet M, Desbuquois B, Brichard S, Girard J. Treatment of streptozotocin-induced diabetic rats with vanadate and phlorizin prevents the over-expression of the liver insulin receptor gene. Eur J Endocrinol 1999; 140:79–86.  Back to cited text no. 10
    
11.
Messier C, Whately K, Liang J, Du L, Puissant D. The effects of a high-fat, high-fructose, and combination diet on learning, weight, and glucose regulation in C57BL/6 mice. Behavioral Brain Res 2007; 178:139–145.  Back to cited text no. 11
    
12.
Pengzhan Y, Ning L, Xiguang L, Gefei Z, Quanbin Z, Pengcheng L. Anti hyperlipidemic activity of high sulfate content derivative of polysaccharide extracted from Ulva pertusa (Chlorophyta). Pharmacol Res 2003; 48:543–549.  Back to cited text no. 12
    
13.
Bauerova K, Paulovicova E, Mihalova D, Drafi F, Strosova M, Mascia C et al. Combined methotrexate and coenzyme Q10 therapy in adjuvant-induced arthritis evaluated using parameters of inflammation and oxidative stress. Acta Biochim Pol 2010; 57:347–354.  Back to cited text no. 13
    
14.
Choi MK, Song IS, Kim DD, Chung SJ, Shim CK. Decreased biliaryexecretion of tributylmethyl ammonium in cholestyramine pretreated rats due to decrease formation of ion pair complexes with hepatic bile salts. Biopharm Drug Dispos 2007; 28:485–490.  Back to cited text no. 14
    
15.
Lin C, Huang P, Lai CF, Chen J. Simvastatin attenuates oxidative stress, NF-κB activation and artery calcification in LDLR-/- mice fed with high fat diet via down-regulation of tumor necrosis factor-α and TNF receptor 1. PLoS One 2015; 10:e0143686.  Back to cited text no. 15
    
16.
Tietz NW. Clinical guide to laboratory tests. USA: WB Saunders Co.; 1995.  Back to cited text no. 16
    
17.
Nauck M, März W, Jarausch J, Cobbaert C, Sägers A, Bernard D et al. Multicenter evaluation of a homogeneous assay for HDL-C without sample pretreatment. Clin Chem 1997; 43:1622–1629.  Back to cited text no. 17
    
18.
Garg R, Vasamreddy CR, Blumenthal RS. Non-high-density lipoprotein cholesterol: why lower is better. Prev Cardiol 2005; 8:173–177.  Back to cited text no. 18
    
19.
Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem 1972; 18:499–502.  Back to cited text no. 19
    
20.
Kastelein JJ, van der Steeg WA, Holme I, Gaffney M, Cater NB, Barter P et al. Lipids, apolipoproteins, and their ratios in relation to cardiovascular events with statin treatment. Circulation 2008; 117:3002–3009.  Back to cited text no. 20
    
21.
Yang LR, Shi HY, Hao G, Li W, Le WG. Increasing oxidative stress with progressive hyperlipidemia in human: relation between malondialdehyde and atherogenic index. J Clin Biochem Nutr 2008; 43:154–158.  Back to cited text no. 21
    
22.
Buduneli E, Buduneli N, Vardar-Şengül S, Kardeşler L, Atilla G, Lappin DF, Kinane FD. Systemic low-dose doxycycline and alendronate administration and serum interleukin-1 beta, osteocalcin and C-reactive protein levels in rats. J Periodontol 2005; 76:1927–1933.  Back to cited text no. 22
    
23.
Song DK, Suh HW, Huh SO, Jung JS, Ihn BM, Choi IG, Kim YH. Central GABAA and GABAB receptor modulation of basal and stress-induced plasma interleukin-6 levels in mice. J Pharmacol Exp Ther 1998; 287:144–149.  Back to cited text no. 23
    
24.
Fernando B, Marley R, Holt S, Anand R, Harry D, Sanderson P et al. N-acetylcysteine prevents development of the hyper dynamic circulation in the portal hypertensive rat. Hepatology 1998; 28:689–694.  Back to cited text no. 24
    
25.
Knapp GR, Miller MC. Tests of statistical significance: regression and correlation. In: Clinical epidemiology and biostatistics. 1st ed. Baltimore, Maryland: Williams & Wilkins, Indiana University; 1992. 255–274.  Back to cited text no. 25
    
26.
Kabiri N, Asgary S, Setorki M. Lipid lowering by hydroalcoholic extracts of Amaranthus Caudatus L induces regression of rabbit’s atherosclerotic lesions. Lipids Health Dis 2011; 10:1–8.  Back to cited text no. 26
    
27.
Akioka K, Kawaguchi H, Kitajima S, Miura N, Noguchi M, Horiuchi M et al. Investigation of necessity of sodium cholate and minimal required amount of cholesterol for dietary induction of atherosclerosis in microminipigs. In Vivo 2014; 28:81–90.  Back to cited text no. 27
    
28.
Rzepecka-Stojko A, Stojko J, Jasik K, Buszman E. Anti-atherogenic activity of polyphenol-rich extract from bee pollen. Nutrients 2017; 9:1369.  Back to cited text no. 28
    
29.
Zhao Y, Xianga L, Liua Y, Niua M, Yuana J, Chena H. Atherosclerosis induced by a high-cholesterol and high-fat diet in the inbred strain of the Wuzhishan Miniature Pig. Anim Biotechnol 2017; 29:110–118.  Back to cited text no. 29
    
30.
Holvena KB, Ulvenb SM, Bogsruda MP. Hyperlipidemia and cardiovascular disease with focus on familial hypercholesterolemia. Curr Opin Lipidol 2017; 28:445–447.  Back to cited text no. 30
    
31.
Moriyama K, Takahashi E. Non-HDL cholesterol is a more superior predictor of small-dense LDL cholesterol than LDL cholesterol in Japanese subjects with TG levels <400 mg/dL. J Atheroscler Thromb 2016; 23:1126–1137.  Back to cited text no. 31
    
32.
Zhang Y, Wu NQ, Li S, Zhu CG, Guo YL, Qing P et al. Non-HDL-C is a better predictor for the severity of coronary atherosclerosis compared with LDL-C. Heart Lung Circ 2016; 25:975–981.  Back to cited text no. 32
    
33.
Millán J, Pintó X, Muñoz A, Zúñiga M, Rubiés-Prat J, Pallardo LF et al. Lipoprotein ratios: physiological significance and clinical usefulness in cardiovascular prevention. Vasc Health Risk Mana 2009; 5:757–765.  Back to cited text no. 33
    
34.
Kunutsor KS, Francesco ZF, Jouni KJ, Sudhir KS, Laukkanen AJ. Is high serum LDL/HDL cholesterol ratio an emerging risk factor for sudden cardiac death? Findings from the KIHD study. J Atheroscler Thromb 2017; 24:600–608.  Back to cited text no. 34
    
35.
Paik HY, Kim CI, Moon HK, Yoon JS, Joung H, Shim JE, Jung HJ. Dietary goals and dietary guidelines for korean adults. Korean J Nutr 2008; 41:887–899.  Back to cited text no. 35
    
36.
Konner M, Eaton SB. Paleolithic nutrition: twenty-five years later. Nutr Clin Pract 2010; 25:594–602.  Back to cited text no. 36
    
37.
Du Broff R. Cholesterol paradox: a correlate does not a surrogate make. Evid Based Med 2017; 22:15–19.  Back to cited text no. 37
    
38.
Dehghan M, Mente A, Zhang X, Swaminathan S, Li W, Mohan V et al. Associations of fats and carbohydrate intake with cardiovascular disease and mortality in 18 countries from five continents (PURE): a prospective cohort study. Lancet 2017; 390:2050–2062.  Back to cited text no. 38
    
39.
Wang J, Zhu H, Yang Z, Liu Z. Antioxidative effects of hesperetin against lead acetate-induced oxidative stress in rats. Ind J Pharmacol 2013; 45:395–398.  Back to cited text no. 39
    
40.
Stone NJ, Robinson JG, Lichtenstein AH, Merz NB, Blum CB, Eckel RH et al. 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association task force on practice guidelines. Circulation 2014; 129:1–45.  Back to cited text no. 40
    
41.
Jarcho JA, Keaney JF. Proof that lower is better-LDL cholesterol and improve-it. N Engl J 2015; 372:2448–2450.  Back to cited text no. 41
    
42.
Micha R, Imamura F, Wyler von Ballmoos M, Solomon DH, Hernán MA, Ridker PM, Mozaffarian D. Systematic review and meta-analysis of methotrexate use and risk of cardiovascular disease. Am J Cardiol 2011; 108:1362–1370.  Back to cited text no. 42
    
43.
Bulgarelli A, Martins Dias AA, Caramelli B, Maranhao RC. Treatment with methotrexate inhibits atherogenesis in cholesterol-fed rabbits. J Cardiovasc Pharmacol 2012; 59:308–314.  Back to cited text no. 43
    
44.
Everett MB, Pradhan DA, Solomon HD, Paynter N, Macfadyen J, Zaharris E et al. Rationale and Design of the Cardiovascular Inflammation Reduction Trial (CIRT): a test of the inflammatory hypothesis of atherothrombosis. Am Heart J 2013; 166:199–207.  Back to cited text no. 44
    
45.
Heřmánková E, Žák A, Poláková L, Hobzová R, Hromádka R, Širc J. Polymeric bile acid sequestrates: review of design, in vitro binding activities, and hypo cholesterolemic effects. Eur J Med Chem 2017; 6:300–317.  Back to cited text no. 45
    
46.
Ito TK, Yokoyama M, Yoshida Y, Nojima A, Kassai H, Oishi K et al. A crucial role for CDC42 in senescence-associated inflammation and atherosclerosis. PLoS One 2014; 9:e102186.  Back to cited text no. 46
    
47.
Recinos III A, Le Jeune WS, Sun H, Lee CY, Tieu BC, Lu M et al. Angiotensin II induces IL-6 expression and the Jak-STAT3 pathway in aortic adventitia of LDL receptor-deficient mice. Atherosclerosis 2007; 194:125–133.  Back to cited text no. 47
    
48.
Anderson DR, Poterucha JT, Mikuls TR, Duryee MJ, Garvin RP, Klassen LW et al. IL-6 and its receptors in coronary artery disease and acute myocardial infarction. Cytokine 2013; 62:395–400.  Back to cited text no. 48
    
49.
Ridker PM, Darielson E, Fonacca FA, Genest J, Gotto AM, Kastelein JJ et al. On behalves of JUPITER trial study group. Reduction in CRP and LDL-C and cardiovascular event rates after initiation of rosuvastatin: a prospective study of the JUPITER trial. Lancet 2013; 373:1175–1182.  Back to cited text no. 49
    
50.
Datta S, Iqbal Z, Prasad KR. Comparison between serum hs-CRP and LDL cholesterol for search of a better predictor for ischemic heart disease. Indian J Clin Biochem 2011; 26:210–213.  Back to cited text no. 50
    
51.
Voloshyna I, Littlefield MJ, Reiss AB. Atherosclerosis and interferon-gamma: new insights and therapeutic targets. Trends Cardiovasc Med 2014 24:45–51.  Back to cited text no. 51
    
52.
Wu MY, Li CJ, Hou MF, Chu PY. New insights into the role of inflammation in the pathogenesis of atherosclerosis. Int J Mol Sci 2017; 18:2034.  Back to cited text no. 52
    
53.
Ridker PM, Everett BM, Thuren T, MacFadyen JG, Chang WH, Ballantyne C et al. (2017). Anti-inflammatory therapy with canakinumab for atherosclerosis. N Engl J Med 2013; 377:1119–1131.  Back to cited text no. 53
    
54.
Nakashima Y, Fujii H, Sumiyoshi S, Wight TN, Sueishi K. Early human atherosclerosis: accumulation of lipid and proteoglycans in intimal thickenings followed by macrophage infiltration. Arterioscler Thromb Vasc Biol 2007; 27:1159–1165.  Back to cited text no. 54
    
55.
Tabas I, Williams KJ, Boren J. Subendothelial lipoprotein retention as the initiating process in atherosclerosis: update and therapeutic implications. Circulation 2007; 116:1832–1844.  Back to cited text no. 55
    
56.
Ballinger ML, Osman N, Hashimura K, de Haan JB, Jandeleit-Dahm K, Allen T et al. Imatinib inhibits vascular smooth muscle proteoglycan synthesis and reduces LDL binding in vitro and aortic lipid deposition in vivo. J Cell Mol Med 2010; 14:1408–1418.  Back to cited text no. 56
    
57.
Li H, Wang QJ, Zhu DN, Yang Y. Reinioside C, a triterpene saponin of Polygala aureocauda Dunn, exerts hypolipidemic effect on hyperlipidemic mice. Phytother Res 2008; 22:159–164.  Back to cited text no. 57
    
58.
Wang Q, Imamura F, Lemaitre RN, Rimm EB, Wang M, King IB et al. Plasma phospholipid trans-fatty acids levels, cardiovascular diseases, and total mortality: the Cardiovascular Health Study. J Am Heart Assoc 2014; 3:e000914.  Back to cited text no. 58
    
59.
Jacobson TA, Ito MK, Maki KC, Orringer CE, Bays HE, Jones PH et al. National Lipid Association recommendations for patient-centered management of dyslipidemia. Part 1-Full report. J Clin Lipidol 2015; 8:473–488.  Back to cited text no. 59
    
60.
Ference BA, Ginsberg HN, Graham I, Ray KK, Packard CJ, Bruckert E et al. Low-density lipoproteins cause atherosclerotic cardiovascular disease. Evidence from genetic, epidemiologic and clinical studies. A consensus statement from the European, Atherosclerosis Society Consensus Panel. Eur Heart J 2017; 38:2459–2472.  Back to cited text no. 60
    


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