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Imbalance in superoxide dismutase/thioredoxin reductase activities in hypercholesterolemic subjects: relationship with low density lipoprotein oxidation
Lipids in Health and Disease volume 11, Article number: 79 (2012)
There is a relationship among hypercholesterolemia, oxidative stress and inflammation in the atherogenesis. Thus, the objective of the present study was to assess paraoxonase (PON1), superoxide dismutase (SOD) and thioredoxin reductase (TrxR-1) activities and their relationship with lipids, oxidative stress and inflammation in subjects with different low density lipoprotein-cholesterol (LDL) levels.
Serum lipids, highly sensitive C-reactive protein (hs-CRP), lipid and protein oxidation, oxidized LDL (LDLox) and LDLox autoantibodies (LDLoxAB) levels and enzymes activities were measured in a total of 116 subjects that were divided into the following groups according to their LDL levels: low-LDL group (LDL < 100 mg/dL, n = 23), intermediate-LDL group (LDL 100–160 mg/dL, n = 50) and high-LDL group (LDL > 160 mg/dL, n = 43).
The LDLox and hs-CRP levels increased in the high-LDL group (2.7- and 3.7- fold, respectively), whereas the intermediate and high-LDL groups had higher LDLoxAB (2.2- and 3.1-fold) when compared to low-LDL group (p < 0.05). Similarly, SOD activity, the atherogenic index (AI) and protein oxidation were also higher in the intermediate (1.3-, 1.3- and 1.2-fold) and high-LDL (1.6-, 2.3- and 1.6-fold) groups when compared to the low-LDL group (p < 0.05). Lipid oxidation and SOD/TrxR-1 ratio increased only in the high-LDL group (1.3- and 1.6-fold) when compared to the low-LDL group (p < 0.05). The SOD/TrxR-1 ratio was positively correlated to TBARS (r = 0.23, p < 0.05), LDLox (r = 0.18, p < 0.05), LDLoxAB (r = 0.21, p < 0.05), LDL (r = 0.19, p < 0.05) and AI (r = 0.22, p < 0.05). PON1 and TrxR-1 activities were similar among groups.
Some oxidative events initiate when LDL levels are clinically acceptable. Moreover, hypercholesterolemic patients have an imbalance in SOD and TrxR-1 activities that is positively associated to LDL oxidation.
Atherosclerosis is the main underlying mechanism of leading causes of death, such as heart and brain disorders. Hypercholesterolemia (HC), especially high levels of low density lipoprotein-cholesterol (LDL), seems to be an important risk factor accounting for severe atherosclerotic diseases, since LDL enters into the vessel walls by a concentration-dependent mechanism. Once into the endothelium, LDL suffers oxidative attack by reactive oxygen species (ROS) on its lipid and protein components, generating oxidized LDL (LDLox). Additionally, LDLox can initiate and enhance the inflammatory process, which plays a pivotal role in the development of atherosclerotic changes. Accordingly, the level of highly sensitive C-reactive protein (hs-CRP), an inflammatory marker, is enhanced in patients with high levels of total cholesterol.
It has been suggested that high density lipoprotein (HDL) protects LDL particles from the oxidative process and subsequent inflammation. This protective action of HDL is due to its associated enzyme paraoxonase 1 (PON1). Although PON1 activity is inversely associated to the incidence of coronary artery disease, there is no data on the behavior of PON1 during different stages of HC.
Since superoxide anion is thought to be one of the most important reactive oxygen species in the pathogenesis of atherosclerotic coronary artery diseases, extracellular superoxide dismutase (EC-SOD) plays a central role in cardiovascular antioxidant mechanisms. This SOD isoenzyme is mainly synthesized and secreted from vascular smooth muscle cells and macrophages and is the predominant arterial SOD isoform. Thioredoxin reductase (TrxR-1) is a redox-active selenoprotein that efficiently regenerates oxidized thioredoxin protein (Trx-1) to its reduced form. Reduced Trx-1 has an antioxidant function because it maintains the reduced state of many proteins. Furthermore, TrxR-1 is overexpressed and released during oxidative stress and has been detected in plasma. Although elevated Trx-1 levels have been found during HC and heart failure in humans[10, 11], few reports are available on the behavior of TrxR-1 during coronary events or in patients with major risk factors, such as HC[12, 13].
Considering the link among HC, oxidative stress and inflammation in the atherogenesis, this study reported the behavior of PON1 activity, as well as, the antioxidants SOD and TrxR-1 activities in the different stages of HC development. We also investigated the associations among the activity of these enzymes, oxidative stress and inflammatory markers and circulating lipids in the blood of subjects with different LDL levels.
Population characteristics are shown in Table 1. No significant difference was found among groups concerning age (p > 0.05). Total cholesterol (TC) levels increased significantly along with the increase in LDL levels among groups (p < 0.05). Triglycerides (TG) levels were also higher in the intermediate- and high-LDL groups when compared to the low-LDL group (p < 0.05), but no difference was observed between the high- and intermediate-LDL groups. In contrast, intermediate-LDL group had higher HDL levels than the other groups (p < 0.05). In addition, the atherogenic index (AI) increased in groups along with the increase in LDL levels (p < 0.05, Table 1).
One-way ANOVA revealed that patients from the high-LDL group showed significantly increased thiobarbituric acid reactive substances (TBARS) levels when compared to the low- and intermediate-LDL groups (p < 0.05, Table 2). On the other hand, protein carbonyl content increased in the intermediate- and high-LDL groups when compared to the low-LDL group (p < 0.05, Table 2), but no significant differences were found between the intermediate- and high-LDL groups. LDL levels affected LDLox and the levels of the inflammatory marker hs-CRP in the same way of TBARS levels, as it can be revealed by the nonparametric Kruskal-Wallis test (p < 0.05, Table 2). The LDLox autoantibodies (LDLoxAB) levels of patients from the intermediate- and high-LDL groups were significantly higher than those from the low-LDL group (p < 0.05, Table 2).
SOD activity was significantly higher in patients from the intermediate- and high-LDL groups compared to the low-LDL group (p < 0.05) and significant differences were found between the intermediate and high-LDL groups (Figure 1A). No significant differences were observed in TrxR-1 or PON1 activities among groups (p > 0.05, Figure 1B and1C). Because TrxR-1 could be important to reduce the hydrogen peroxide (H2O2) that is generated during the dismutation of superoxide anion radical by SOD, we have also assessed the SOD/TrxR-1 ratio to verify a possible imbalance between these activities. The SOD/TrxR-1 ratio increased in the high-LDL group when compared to the low-LDL group, but no difference was observed between the low- and intermediate-LDL groups or between the intermediate- and high-LDL groups (p < 0.05, Figure 1D).
LDL levels were positively correlated to TC, TG, TBARS levels, protein carbonyl content, LDLox, LDLoxAB and hs-CRP levels as well as to AI, SOD activity and SOD/TrxR-1 ratio (p < 0.05, Table 3). In contrast, LDL levels had no significant correlation with HDL levels, TrxR-1 or PON1 activities (p > 0.05, Table 3). A positive correlation was observed between TrxR-1and SOD activities (p < 0.05, Table 3). Despite the lack of additional associations of TrxR-1 with oxidative or inflammatory markers, SOD/TrxR-1 ratio was positively correlated with TBARS, LDLox and LDLoxAB levels, as well as, with the AI (p < 0.05, Table 3). Hs-CRP levels were positively correlated with LDLox as well as with LDLoxAB levels (p < 0.05, Figure 2A and2B). In addition, we also found a positive correlation between TBARS and LDLox levels (p < 0.05, Figure 2C). PON1 activity had no correlation with oxidative or inflammatory markers in the present study (p > 0.05, Table 3).
Elevated plasma cholesterol levels play a dominant role in cardiovascular diseases as can be evidenced by the occurrence of atheroma in the aorta of hypercholesterolemic rabbits. Accordingly, the AI, which reflects the relationship between the non-HDL cholesterol fraction and the HDL cholesterol fraction and is considered a possible indicator of a predisposition to heart disease, was directly correlated to the increase in LDL levels. The injury theory of atherosclerosis holds that circulating LDL accumulates at susceptible sites where the oxidation of its protein and lipid components takes place, generating LDLox. LDLox, in turn, participates in the inflammatory processes, contributing to lesion progression. Our results corroborate this theory, since elevated LDLox levels were found in patients from the high-LDL group. Accordingly, lipid oxidation (TBARS) was also increased in patients from the high-LDL group and we observed a positive correlation between TBARS and LDLox, reinforcing that TBARS levels are at least partially associated to LDLox levels. In contrast to lipid oxidation, protein oxidation seems to start even when LDL levels are considered clinically acceptable, because the protein carbonyl content was increased in the intermediate-LDL group. The delay in the increase of LDL oxidation in the intermediate-LDL group may be related to a protective effect of LDLoxAB that was increased in this group compared to the low-LDL group. This idea is supported by previous studies which demonstrated that even minor modifications of native LDL render it immunogenic and that humoral antibodies are specific for the modifications to apo B[16, 17]. These findings indicate that circulating antibodies respond to oxidative modifications in the protein moiety of LDL. In addition, humoral antibodies to modified LDL may redirect its site of degradation, primarily from plasma to the reticuloendothelial cells of the liver from rabbits. Thus, LDLoxAB could enhance the removal of LDLox from serum and prevent its entrance into the arterial wall. In agreement, an inverse relationship between LDLoxAB and LDLox levels in healthy subjects is in line with the idea that LDLoxAB has a role in the clearance of LDLox from the circulation. Moreover, at low rates of LDL oxidation, it is possible that an immune response might lead to an accelerated macrophage uptake of LDLox and thereby it may play a protective role. When the rate of oxidation is enhanced, however, the immune response might play a pathogenetic role, leading to accelerated macrophage uptake that overwhelms the capacity of the macrophage to handle the ingested LDLox. Thus, we can speculate that the rate of oxidation in the intermediate-LDL group is low and LDLoxAB are still able to counteract LDLox, whereas in the high-LDL group this protection did not occur.
SOD activity increased along with the increase in LDL levels among groups and this increase occurred most likely to counteract the superoxide anion overproduction caused by HC. The increase in SOD activity, along with the increase in protein carbonyl and LDLoxAB levels, even when LDL levels are considered clinically acceptable; indicate that oxidative stress is an early event in the evolution of hyperlipidemia.
The enzyme TrxR-1 along with protein Trx-1 has been recognized as an essential component for cellular redox control and antioxidant defense. In this study, we demonstrated for the first time the behavior of serum TrxR-1 activity during different stages of HC in humans, although an elevation in serum reduced Trx-1 has already been described in patients with HC. Additionally, we have recently demonstrated an increase in serum TrxR-1 activity in hypercholesterolemic rabbits. However, in the present study, we observed no statistically significant differences in TrxR-1 activity among groups. The thioredoxin system (TrxR-1 and Trx-1) acts as a H2O2 scavenging system, reducing H2O2 to H2O. Besides scavenging H2O2, TrxR-1 can indirectly maintain the reduced state of many proteins by regenerating oxidized Trx-1 to its reduced form. Thus, we can speculate that the lack of changes in TrxR-1 activity in the intermediate-LDL group resulted in the increase of protein oxidation in this group. However, no association was found between TrxR-1 activity and protein carbonyl levels. Despite the unchanged activity of TrxR-1 among groups, we found a weak, but significant correlation between TrxR-1 and SOD activities, which could indicate a role for TrxR-1 in the removal of H2O2 produced by SOD. Interestingly, in the high-LDL group, SOD activity had a prominent increase over TrxR-1 activity, as measured by the increased SOD/TrxR-1 ratio. This imbalance in SOD/TrxR-1 activities suggests that TrxR1 activity could be lacking to efficiently remove the H2O2 produced by SOD. Because the SOD/TrxR-1 ratio was positively correlated with TBARS, LDLox and LDLoxAB levels, we can speculate that the imbalance in SOD/TrxR1 ratio could have deleterious effects in hypercholesterolemic subjects due to a peroxide overload. However, this proposal deserves further investigation because glutathione peroxidase and catalase, which are other important enzymes to remove H2O2 in plasma, were not evaluated in the present study. In fact, an imbalance between SOD and catalase activities has been well documented in various oxidative conditions[23, 24], but to the best of our knowledge, this is the first report about an imbalance between SOD and TrxR-1 activity. Because the SOD/TrxR-1 ratio was associated with the AI, we can suggest a possible role of the SOD/TrxR-1 ratio as a marker of cardiovascular events during HC.
Similar to TrxR-1, the behavior of PON1 activity at different stages of HC has not been demonstrated yet. PON1 is believed to be responsible for the antioxidant effects of HDL and its activity is inversely associated with the progression of atherosclerosis and the incidence of coronary artery disease. In agreement, previous results from our group revealed diminished serum PON1 activity along with atherosclerotic plaque in the aorta of hypercholesterolemic rabbits. Moreover, a large prospective study pointed low serum PON1 activity as an independent risk factor for coronary events in men at high risk of coronary heart disease. However, we did not found differences in PON1 activity among the three studied groups or significant correlations between LDL levels and PON1 activity. This could be explained by an established balance between PON1 inactivation by oxidant species and PON1 elevation in order to provide a protective mechanism against oxidant species and atherosclerotic plaque progression. These differences in PON1 activity between previous studies and ours can be due the fact that studies concerning PON1 and cardiovascular diseases usually evaluated the relationship between serum enzyme activity and plaque formation or cardiovascular events such as myocardial infarction. Here, we evaluated the relationship between PON1 activity and another known predicting factor for cardiovascular diseases, the LDL levels. Moreover, PON1 seems not play a role in early atherosclerosis, although it may play a role in a later stage of cardiovascular diseases. Since the atheroma formation was not evaluated in this study, we can speculate that unchanged PON1 activity and the lack of associations between PON1, LDL and LDLox levels are most likely because LDL levels evaluated in this study corresponded to early stages of atherosclerosis.
The involvement of oxidative stress in the initiation and progression of the inflammatory process is well documented. Accordingly, we observed a significant correlation between LDLox and hs-CRP, which is an inflammatory marker. Moreover, serum hs-CRP levels were increased in the high-LDL group. Despite the changes in SOD and SOD/TrxR-1 ratio that accompanied the increase in LDL levels, no relationship was found between hs-CRP levels and antioxidant enzymes. This lack of correlation has already been described in the serum of patients with rheumatoid arthritis, although both parameters had been changed by the disease. Although the extracellular reduced Trx-1 has proinflammatory effects by potentiating cytokine release from fibroblasts and monocytes, our results reveal that TrxR-1 seems to have no relationship with the inflammatory response during HC.
In conclusion, the present study demonstrated that some oxidative events initiate even when LDL levels are clinically acceptable. Moreover, hypercholesterolemic patients show an imbalance in SOD/TrxR-1 activities, which may play a role in the oxidative stress, because it is positively associated to LDL oxidation.
The population studied consisted of patients from LABIMED (Santa Maria, RS, Brazil). All subjects gave written informed consent to participate in the study. The work was carried out in accordance with The Code of Ethics of the World Medical Association and the protocol was approved by the Research Ethics Committee of the Federal University of Santa Maria (Protocol number: 23081.019182/2007-10). Subjects were divided into three groups according to the serum LDL levels, as follows: low-LDL group comprised subjects with LDL levels < 100 mg/dL (2.6 mmol/L); intermediate-LDL group comprised subjects with LDL levels ranging from 100 to 160 mg/dL (2.6-4.15 mmol/L); and high-LDL group comprised subjects with LDL levels > 160 mg/dL (4.15 mmol/L). These LDL ranges were selected according to the National Cholesterol Education Program, where LDL levels < 100 mg/dL are considered safe; between 100 and 160 mg/dL are clinically acceptable, but close to the limit; and LDL levels > 160 mg/dL are considered to be well above the safe limit for risk of cardiovascular diseases. Male and female subjects ageing 28 to 87 years-old were included in the study. Smokers, obese and hypertensive patients as well as patients with infectious diseases, metabolic syndrome and with blood glucose levels > 95 mg/dL were excluded from the study. Patients undergoing drug or vitamin treatment were also excluded from the study.
Blood sample collection
Blood samples were collected after a 12-h overnight fasting by venous puncture into Vacutainer® (BD Diagnostics, Plymouth, UK) tubes with no anticoagulant. Blood samples were routinely centrifuged within 1 h of collection at 2500 × g for 15 min, and aliquots of serum samples were immediately used to assess TC, TG, HDL, LDLox, LDLoxAB, hs-CRP, TBARS levels and TrxR-1 activity. Then, serum samples were stored at −20°C for a maximum of 4 weeks before remaining measurements.
TC and TG concentrations were measured by standard enzymatic methods using Ortho-Clinical Diagnostics® reagents on a fully automated analyzer (Vitros 950® dry chemistry system; Johnson & Johnson, Rochester, NY, USA). HDL cholesterol was measured after precipitation of apolipoprotein B-containing lipoproteins with dextran sulfate and magnesium chloride, as previously described. LDL was estimated with the Friedewald equation. The AI was calculated as (TC - HDL cholesterol)/HDL cholesterol as previously reported.
Oxidative stress markers
LDLox was determined by a capture ELISA according to the manufacturer instructions (Mercodia AB, Uppsala, Sweden) and as described before. Serum samples were added to microplate wells coated with high affinity antibodies for LDLox. A peroxidase-conjugated antibody and tetramethylbenzidine (TMB) as substrate for peroxidase were used. The intensity of the yellow color, which is directly proportional to the LDLox concentration, was read at 450 nm. A standard curve was generated from standard LDLox. LDLoxAB was determined using ELISA as described by Wu and Lefvert. Serum samples were added to microplate wells coated with high affinity antigen (LDLox). The methodology was similar to that used to quantify LDLox and the intensity of the yellow color that was directly proportional to the LDLoxAB concentration was read at 450 nm. A standard curve was generated from standard LDLoxAB. Lipid peroxidation, measured as TBARS levels, was assessed after the addition of 7.2 mM of butylated hydroxytoluene to prevent further oxidation. The reaction with thiobarbituric acid and extraction with n-butanol was performed as previously described and the reaction product was determined at 535 nm using a standard curve of 1,1,3,3-tetraethoxypropane. Protein oxidation was assessed as protein carbonyl content based on the reaction of the carbonyl groups with 2,4-dinitrophenylhydrazine to form 2,4-dinitrophenylhydrazone. Samples were read at 370 nm and carbonyl content was calculated using the molar absorption coefficient for aliphatic hydrazones (22,000 M-1 cm-1). SOD activity was determined at 480 nm using 50 mM glycine buffer, pH 10.2, and 1 mM epinephrine at 30°C. SOD activity was expressed as the amount of enzyme that inhibits the auto-oxidation of epinephrine to adrenochrome by 50%, which is equal to 1 unit. TrxR-1 activity was determined using 5,5′-dithiobis (2-nitrobenzoic acid) (DTNB) and reduced adenine dinucleotide phosphate. The method is based on the reduction of DTNB, which is indicated by an increase in absorbance at 412 nm.
PON1 activity was assessed by measuring the rate of paraoxon hydrolysis to yield p-nitrophenol, at 412 nm and 25°C. The amount of p-nitrophenol generated was calculated using the molar extinction coefficient 17,000 M-1 cm-1 and 1 U of PON1 activity is defined as 1 nmol of p-nitrophenol generated per minute.
Hs-CRP was measured by nephelometry according to the manufacturer instructions (Dade Behring, Newark, DE, USA).
Data were analyzed by one-way analysis of variance (ANOVA) followed by unequal N HSD test when appropriate. Data that did not exhibit normal distribution were transformed (log or square root transformation) in order to meet ANOVA assumptions before analysis. When a variable was found not following normal distribution even after log or square root transformation, it was analyzed by the nonparametric Kruskal-Wallis ANOVA followed by the post hoc Dunn’s test when appropriate. The associations between variables were evaluated by Pearson’s correlation for variables that had normal distribution and by Spearman’s rank order correlation for variables that did not exhibit normal distribution. Results were considered significant when p < 0.05.
One-way analysis of variance
Highly sensitive C-reactive protein
Oxidized low-density lipoprotein
Oxidized low-density lipoprotein antibodies
Superoxide dismutase/ Thioredoxin reductase 1 ratio
Thiobarbituric acid reactive substances
Thioredoxin reductase 1.
Steinberg D, Gotto AM: Preventing coronary artery disease by lowering cholesterol levels: fifty years from bench to bedside. J Am Med Ass. 1999, 282: 2043-2050. 10.1001/jama.282.21.2043.
Batlouni M: Hipótese oxidativa da aterosclerose. Arq Bras Cardiol. 1997, 68: 55-63.
Packard RRS, Libby P: Inflammation in atherosclerosis: from vascular biology to biomarker discovery and risk prediction. Clin Chem. 2008, 54: 24-38.
Aviram M, Rosenblat M, Bisgaier CL, Newton RS, Primo-Parmo SL, La Du BN: Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions. A possible peroxidative role for paraoxonase. J Clin Invest. 1998, 101: 1581-1590. 10.1172/JCI1649
Aviram M: Does paraoxonase play a role in susceptibility to cardiovascular disease? Mol. Med Today. 1999, 5: 381-386. 10.1016/S1357-4310(99)01546-4.
Cai H, Harrison DG: Endothelial dysfunction in cardiovascular diseases: the role of oxidant stress. Circ Res. 2000, 87: 840-844. 10.1161/01.RES.87.10.840
Stralin P, Karlsson K, Johansson BO, Marklund SL: The interstitium of the human arterial wall contains very large amounts of extracellular superoxide dismutase. Arterioscler Thromb Vasc Biol. 1995, 15: 2032-2036. 10.1161/01.ATV.15.11.2032
Arnér ESJ, Holmgren A: Physiological functions of thioredoxin and thioredoxin reductase. Eur J Biochem. 2000, 267: 6102-6109. 10.1046/j.1432-1327.2000.01701.x
Söderberg A, Sahaf B, Rosén A: Thioredoxine reductase, a redoxactive selenoprotein, is secreted by normal and neoplastic cells: presence in human plasma. Cancer Res. 2000, 60: 2281-2289.
Kunihisa M, Chiharu K, Nakamura H, Makita T, Ishii K, Okuda N, Yodoi J, Sasayama S: Serum thioredoxin and α-tocopherol concentrations in patients with major risk factors. Circ J. 2005, 69: 291-294. 10.1253/circj.69.291
Kishimoto C, Shioji K, Nakamura H, Nakayama Y, Yodoi J, Sasayama S: Serum thioredoxin (TRX) levels in patients with heart failure. Jpn Circ J. 2001, 65: 491-494. 10.1253/jcj.65.491
Wu Y, Yang L, Zhong L: Decreased serum levels of thioredoxin in patients with coronary artery disease plus hyperhomocysteinemia is strongly associated with the disease severity. Atherosclerosis. 2010, 212: 351-355. 10.1016/j.atherosclerosis.2010.06.002
Jekell A, Hossain A, Alehagen U, Dahlström U, Rose’ A: Elevated circulating levels of thioredoxin and stress in chronic heart failure. Eur J Heart Fail. 2004, 6: 883-890.
Augusti PR, Conterato GMM, Somacal S, Sobieski R, Quatrin A, Maurer L, Rocha MP, Denardin IT, Emanuelli T: Astaxanthin reduces oxidative stress, but not aortic damage in atherosclerotic rabbits. J Cardiovasc Pharmacol Ther. 2009, 14: 314-322. 10.1177/1074248409350136
Fassini PG, Noda RW, Ferreira ES, Silva MA, Neves VA, Demonte A: Soybean glycinin improves HDL-C and suppresses the effects of rosuvastatin on hypercholesterolemic rats. Lipid Health Dis. 2011, 10: 165-10.1186/1476-511X-10-165. 10.1186/1476-511X-10-165
Witztum JL, Steinbrecher UP, Fisher M, Kesaniemi A: Nonenzymatic glucosylation of homologous LDL and albumin render them inununogenic in the guinea pig. Proc Natl Acad Set U S A. 1983, 80: 2757-2761. 10.1073/pnas.80.9.2757.
Steinbrecher UP, Fisher M, Witztum JL, Curtiss LK: Immunogenicity of homologous low density lipoprotein after methylation, ethylation, acetylation or carbamylation: generation of antibodies specific for derivatized lysine. Lipid Res. 1984, 25: 1109-1116.
Wiklund O, Witztum JL, Carew TE, Pittman RC, Elam RL, Steinberget D: Turnover and tissue sites of degradation of glucosylated low density lipoprotein in normal and immunized rabbits. J Lipid Res. 1987, 28: 1098-1109.
Shoji T, Nishizawa Y, Fukumoto M, Shimamura K, Kimura J, Kanda H, Emoto M, Kawagishi T, Morii H: Inverse relationship between circulating oxidized low density lipoprotein (oxLDL) and anti-oxLDL antibody levels in healthy subjects. Atherosclerosis. 2000, 148: 171-177. 10.1016/S0021-9150(99)00218-X
Yla-Herttuala S, Palinski W, Butler SW, Picard S, Steinberg D, Witztum JL: Rabbit and human atherosclerotic lesions contain IgG that recognizes epitopes of oxidized LDL. Arterioscler Thromb Vasc Biol. 1994, 14: 32-40. 10.1161/01.ATV.14.1.32.
Ohara Y, Peterson TE, Harrison DG: Hypercholesterolemia increases endothelial superoxide anion production. J Clin Invest. 1993, 91: 2546-2551. 10.1172/JCI116491
Augusti PR, Quatrin A, Somacal S, Conterato GMM, Sobieski R, Ruviaro AR, Maurer LH, Duarte MMF, Roehrs M, Emanuelli T: Astaxanthin prevents changes in the activities of thioredoxin reductase and paraoxonase in hypercholesterolemic rabbits. J Clin Biochem Nutr. 10.3164/jcbn.11-74. in press,
Bambini-Junior V, Rodrigues L, Behr GA, Moreira JCF, Riesgo R, Gottfried C: Animal model of autism induced by prenatal exposure to valproate: behavioral changes and liver parameters. Brain Res. 2011, 1408: 8-16.
Pinho RA, Andrades ME, Oliveira MR, Pirola AC, Zago MS, Silveira PCL, Dal-Pizzol F, Moreira JCF: Imbalance in SOD/CAT activities in rat skeletal muscles submitted to treadmill training exercise. Cell Biol Int. 2006, 30: 848-853. 10.1016/j.cellbi.2006.03.011
Mackness B, Durrington P, McElduff P, Yarnell J, Azam N, Watt M, Mackness M: Low paraoxonase activity predicts coronary events in the Caerphilly prospective study. Circulation. 2003, 107: 2775-2779. 10.1161/01.CIR.0000070954.00271.13
Aviram M, Rosenblat M, Billecke S, Erogul J, Sorenson R, Bisgaier CL, Newton RS, La Du B: Human serum paraoxonase (PON 1) is inactivated by oxidized low density lipoprotein and preserved by antioxidants. Free Rad Biol Med. 1999, 26: 892-904. 10.1016/S0891-5849(98)00272-X
Mackness B, Hunt R, Durrington PN, Mackness MI: Increased immunolocalization of paraoxonase, clusterin, and apolipoprotein A-I in the human artery wall with the progression of atherosclerosis. Arterioscler Thromb Vasc Biol. 1997, 17: 1233-1238. 10.1161/01.ATV.17.7.1233
Jayakumari N, Thejaseebai G: High prevalence of low serum paraoxonase-1 in subjects with coronary artery disease. J Clin Biochem Nutr. 2009, 45: 278-284. 10.3164/jcbn.08-255
Van Himbergen TM, Roest M, de Graaf J, Jansen EH, Hattori H, Kastelein JJ, Voorbij HA, Stalenhoef AF, Van Tits LJ: Indications that paraoxonase-1 contributes to plasma high density lipoprotein levels in familial hypercholesterolemia. J Lipid Res. 2005, 46: 445-451.
Lemarechal H, Allanore Y, Chenevier-Gobeaux C, Ekindjian OG, Kahan A, Borderie D: High redox thioredoxin but low thioredoxin reductase activities in the serum of patients with rheumatoid arthritis. Clin Chim Acta. 2006, 367: 156-161. 10.1016/j.cca.2005.12.006
Expert Panel on Detection, Evaluation and Treatment of High Blood Cholesterol in Adults: Executive summary of the third report the National Cholesterol Education Program (Adults Treatment III). JAMA. 2001, 285: 2486-2497. 10.1001/jama.285.19.2486
Bachorik PS, Albers JJ: Precipitation methods for quantification of lipoproteins. Methods Enzymol. 1996, 129: 78-100.
Friedewald WT, Levy RI, Fredrickson DS: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without the use of preparative ultracentrifuge. Clin Chem. 1972, 18: 499-502.
Yang R, Shi Y, Hao G, Li W, Le G: Increasing oxidative stress with progressive hyperlipidemia in human: relation between malondialdehyde and atherogenic index. J Clin Biochem Nutr. 2008, 43: 154-158. 10.3164/jcbn.2008044
Holvoet P, Stassen JM, Van Cleemput J, Collen D, Vanhaecke J: Oxidized low density lipoproteins in patients with transplant-associated coronary artery disease. Arterioscler Thromb Vasc Biol. 1998, 18: 100-107. 10.1161/01.ATV.18.1.100
Wu R, Lefvert AK: Autoantibodies against oxidized low density lipoprotein (OxLDL): characterization of antibody isotype, subclass, affinity and effect on the macrophage uptake of oxLDL. Clin Exp Immunol. 1995, 102: 174-180.
Ohkawa H, Ohishi N, Yagi K: Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979, 95: 351-358. 10.1016/0003-2697(79)90738-3
Levine RL, Garland D, Oliver CN, Amici A, Climent I, Lenz AG, Ahn BW, Shaltiel S, Stadtman ER: Determination of carbonyl content in oxidatively modified proteins. Method Enzymol. 1990, 186: 464-478.
Misra HP, Fridovich I: The role of superoxide anion in the auto-oxidation of epinephrine and a simple assay for superoxide-dismutase. J Biol Chem. 1972, 247: 3170-3175.
Holmgren A, Björnstedt M: Thioredoxin and thioredoxin reductase. Meth Enzymol. 1995, 252: 199-208.
Bolayirli IM, Aslan M, Balci H, Altug T, Hacibekiroglu M, Seven A: Effects of atorvastatin therapy on hypercholesterolemic rabbits with respect to oxidative stress, nitric oxide pathway and homocysteine. Life Sci. 2007, 81: 121-127. 10.1016/j.lfs.2007.04.027
This work was supported by CNPq and FAPERGS. CNPq provided a research fellowship to T. Emanuelli, PhD degree fellowships to P.R. Augusti and G.M.M. Conterato, scientific initiation fellowships to A. Quatrin and A.R. Ruviaro, as well as a technical support fellowship.
The authors declare that they have no competing interests.
SS, AQ, ARR, GMMC, JV and PRA contributed to the experimental work. MMFD contributed to the experimental work, in particular in the quantification of inflammatory marker, oxidized low-density lipoprotein levels and oxidized low-density lipoproteins antibodies analyses. PRA and TE contributed in the design and planning of the study, as well as drafting and critical revision of the manuscript. All the authors contributed to the interpretation and discussion of results related to their part of the work and approved the final version of the paper.
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Augusti, P.R., Ruviaro, A.R., Quatrin, A. et al. Imbalance in superoxide dismutase/thioredoxin reductase activities in hypercholesterolemic subjects: relationship with low density lipoprotein oxidation. Lipids Health Dis 11, 79 (2012) doi:10.1186/1476-511X-11-79
- Atherogenic index
- Oxidized low density lipoprotein
- Superoxide dismutase
- Thioredoxin reductase