Scholarly article on topic 'Dietary red palm oil supplementation decreases infarct size in cholesterol fed rats'

Dietary red palm oil supplementation decreases infarct size in cholesterol fed rats Academic research paper on "Basic medicine"

Share paper
Academic journal
Lipids Health Dis
OECD Field of science

Academic research paper on topic "Dietary red palm oil supplementation decreases infarct size in cholesterol fed rats"

RESEARCH Open Access

Dietary red palm oil supplementation decreases infarct size in cholesterol fed rats

1 "I- O-!" 1 1 ^ 1 ^ o

Gergo Szucs ', Dirk J Bester ', Krisztina Kupai , Tamas Csont ,, Csaba Csonka ,, Adriaan J Esterhuyse , Peter Ferdinandy1,3 and Jacques Van Rooyen2*


Background and Aims: The effect of red palm oil (RPO) supplementation on infarct size after ischaemia/ reperfusion in a cholesterol enriched diet-induced hyperlipidemic animal model has not been reported. Previous studies reported results on the effect of RPO in a normal diet, whilst evidence of protection has been linked to improved functional recovery, prosurvival kinase, anti-apoptosis and NO-cGMP. Therefore, we aimed to investigate the effects of dietary RPO supplementation in a cholesterol-enriched diet-induced hyperlipidemic rat model and to investigate the involvement of matrix metalloproteinase 2 (MMP2) inhibition as a possible mechanism of protection.

Materials and Methods: Male Wistar rats were fed either a standard rat chow diet (Norm) or a 2% cholesterol-enriched diet (Chol) for nine weeks. Additionally, two more groups received the same treatment, however, at the week 4, diet was supplemented with RPO for the last five weeks (Norm+RPO and Chol+RPO), respectively. After the feeding period hearts were isolated, perfused according to Langendorff and subjected to 30 minutes of normothermic global ischaemia followed by two hours of reperfusion. Infarct size was measured by 2,3,5-triphenyltetrazolium chloride staining at the end of reperfusion.

Results: Cholesterol-enriched diet increased myocardial infarct size from 23.5 ± 3.0% to 37.2 ± 3.6% (p < 0.05) when compared to normal diet. RPO supplementation significantly reduced infarct size either in Norm+RPO or in Chol+RPO (to 9.2 ± 1.0% and 26.9 ± 3.0%), respectively. Infarct size in Chol+RPO was comparable to the Norm group. MMP2 activity before ischaemia was significantly reduced in the Chol+RPO group when compared to the Chol group. However, the MMP2 activity of the hearts of the RPO fed rats was significantly increased when compared to the normal diet group after ischaemia.

Conclusions: For the first time it was shown that dietary RPO supplementation attenuated the increased susceptibility of the hearts in cholesterol fed rats to ischaemia/reperfusion injury. This was shown by reduced infarct size. For the first time we also show that red palm oil supplementation altered pre-ischaemic levels of MMP-2, which may indicate that myocardial MMP2 may be implicated as a possible role player in RPO mediated protection against ischaemia/reperfusion injury in hearts of cholesterol supplemented rats.


Many cardiovascular ischaemia/reperfusion injury studies use healthy rats for their research protocols. In clinical conditions, unhealthy diets and lifestyle are normally associated with increased risk of myocardial infarction [1].

* Correspondence: vanrooyenj@cput.acza t Contributed equally

2Department of BiomedicalSciences, Faculty of Health and Wellness Sciences, Cape Peninsula University of Technology, Symphony Way, Bellville, 7535, South Africa

Fulllist of author information is available at the end of the article

Bio Med Central

Previous studies using healthy animals contributed to elucidating certain mechanisms of cardiovascular protection. However, it has recently been shown that cholesterol feeding reverses the beneficial effects of preconditioning [2]. One such a model is a mildly dislipidaemic rat model, where the rat is supplemented with low doses of cholesterol for a short time period. In this model, peroxynitrite was increased with a subsequent reduction of myocardial function [3]. This ultimately led to contractile failure of the myocardium, or myocardial stunning injury. Additionally, this model was shown to inhibit the

© 2011 Szucs et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

cardioprotective effects of myocardial preconditioning [2]. Osipov and co-workers (2009) demonstrated in an in vivo hypercholesterolaemic pig model increased infarct size when compared with normal control animals [4]. The authors concluded that increased infarct size in hypercho-lesterolaemic hearts was associated with increased oxida-tive stress and inflammation, together with downregulation of cell survival pathways and induction of apoptosis.

Red palm oil (RPO) is an antioxidant rich oil which contains approximately 50% saturated and 50% unsaturated fatty acids [5,6]. Carotenoids and vitamin E (75% of which is tocotrienol) are the most abundant antioxi-dants in this oil. Both of these antioxidants are contained at a level of at least 500 ppm in RPO [5,6]. The cocktail of antioxidants within RPO is believed to have synergistic effects [7,8]. The oil offers cardioprotection, by activation of several different protective pathways which work synergistically together [9].

Dietary RPO supplementation has previously been shown to offer protection against ischaemia/reperfusion injury in the isolated perfused heart [10-12]. Esterhuyse and co-workers (2005) [10] showed that dietary RPO supplementation could improve post ischaemic functional recovery in rats fed a standard rat chow diet (SRC), and rats fed a SRC plus 2% cholesterol for six weeks [10]. They suggested that RPO mediated protection against ischae-mia/reperfusion injury may be induced through different pathways in hearts of SRC fed and cholesterol fed rats.

Matrix metalloproteinases (MMPs) are calcium and zinc dependent endopeptidases. Under normal physiological conditions they facilitate cell migration and tissue remodeling [13]. Recently it was found that MMP2 plays a role in ischaemia/reperfusion damage in the heart [14]. Increased MMP2 activity has also been associated with hypercholesterolaemic diets [2]. This may be due to the increased peroxynitrite production within the myocardium [3]. ROS, and peroxynitrite have been shown to activate MMP2 through redox modification of the regulatory site of this enzyme [15-18]. This redox modification leads to activity being displayed in the 75 and 72 kDa isoforms of the enzyme, while only the 64 kDa isoform is active if MMP2 is activated in the classical manner [16,18]. Activated MMP2 damages cardiomyocytes during reperfusion. This is achieved by cleaving the contractile protein regulatory element, troponin I and possibly other structural and cytoskeletal proteins [19-24]. Activation of MMP2 during an ischaemic insult is therefore normally associated with decreased functional recovery and larger infarct size of the heart [14,25-28]. This has been confirmed through inhibition of MMP2 by antibodies or chemical agents [29-33].

In a recent study [34] it was shown that red palm oil reduced infarct size in a model of ischaemia/reperfusion injury. However, this model investigated only healthy

hearts. The intention of the current study was therefore to use a high cholesterol feeding model to ensure that the model is more clinically relevant and to establish confirmation that red palm oil protection are indeed applicable in unhealthy diets, as was previously argued. In all red palm oil fed studies up to date [9-12], results have indicated post-ischaemic involvement of certain cellular biochemical pathways. However, none of these studies provided any evidence of pre-ischaemic protection by red palm oil.

The aims of this study were: 1) to investigate the effects of dietary RPO supplementation on myocardial infarct size in the hearts of rats on a cholesterol-enriched diet and 2) to determine whether MMP2 activity was altered by RPO supplementation, both pre- and post-ischaemically.

Materials and Methods

All rats received humane animal care in accordance with the Guide for the Care and Use of Laboratory Animals, published by the United States National Institutes of Health (NIH publication 8523, revised 1985).

Experimental design

Male Wistar rats were divided into four groups. Rats in these groups were placed on the following diets, respectively:

Group 1: Standard rat chow diet for 9 weeks (Norm)

Group 2: 2% cholesterol-enriched diet for 9 weeks (Chol)

Group 3: Standard rat chow supplemented with 200 |jl RPO (Norm+RPO) per day for the last 5 weeks of the 9 week period

Group 4: 2% cholesterol-enriched diet for nine weeks supplemented with 200 ^l RPO per day for the last 5 weeks of the 9 week period (Chol+RPO)

Rats were individually housed to ensure that each animal received equal amounts of supplements. RPO and supplements were prepared on a daily basis in order to prevent spoiling. Rats were allowed ad libitum access to food and water.

Isolated heart perfusion

After the feeding period, rats were anaesthetized using diethyl ether. Hearts were isolated, mounted on a Lan-gendorff perfusion apparatus, and were perfused at 37°C using a Krebs-Henseleit buffer solution which was constantly gassed with 5% carbon dioxide, 95% oxygen and a constant perfusion pressure of 100 cmH20 was maintained. After mounting, hearts were subjected to 10 minutes of stabilization, followed by 30 minutes of normothermic global ischaemia and 120 minutes of reperfusion. At the end of the perfusion protocol ventricular tissue was frozen at -20°C overnight.

Infarct size determination

Frozen hearts were cut into 2 mm thick cross-sectional slices. These slices were stained in 2,3,5-triphenyltetra-zolium chloride (TTC) for 10 minutes at 37°C. After TTC staining, the slices were transferred to a formalin solution for ten minutes and then placed in phosphate buffer (pH 7.4) [35,36]. Heart slices were then placed between two sheets of glass and scanned into a computer and analyzed using infarct size planimetry software (Infarctsize™ 1.0 Pharmahungary, Szeged, Hungary) in a blinded manner. Infarct size was represented as percentage of the area at risk.

MMP2 zymography

Coronary effluent collected for 10 minutes before ischaemia and the first 10 minutes of reperfusion was concentrated by ultra filtration using Amicon ultra filtration tubes. The concentrated coronary flow was then subjected to gelatin zymography.

Gelatinolytic activities of MMPs were examined as previously described [18]. Briefly, polyacrylamide gels were copolymerized with gelatin, and a constant amount of protein was separated by electrophoresis in each lane. Following electrophoresis, gels were washed with 2.5% Triton X-100 and incubated for 20 hours at 37°C in incubation buffer. Gels were then stained with 0.05% Coomassie Brilliant Blue in a mixture of methanol/acetic acid/water and destained in aqueous 4% methanol/8% acetic acid. Zymograms were digitally scanned, and band intensities were quantified using Quantity One software (Bio-Rad, Hercules, CA) and expressed as a ratio to the internal standard.

Serum cholesterol and triglyceride measurement

Serum cholesterol and triglyceride were measured using a test kit supplied by Diagnosticum Zrt. (Budapest, Hungary) as described previously [37].


All values are presented as mean ± SEM. Differences among means were analyzed by two-way ANOVA followed by an appropriate post hoc test to make all pair-wise comparisons and comparisons of each group to the respective control. P was considered significant if it was less than 0.05.


Animal mass

The body and heart weight of the RPO supplemented rats were significantly decreased when compared to the Norm group and also to the Chol+RPO group after the feeding period (Table 1).

Perfusion data

There were no significant differences in the coronary effluent of any of the groups after the supplementation period. Coronary effluent of all groups except the RPO group was significantly decreased after ischaemia, when compared to their baseline values. There were no significant differences in the heart rates before or after ischae-mia (Table 2).

Infarct size

Cholesterol-enriched diet alone increased myocardial infarct size from 23.5 ± 3.0% to 37.2 ± 3.6% (p < 0.05) when compared to normal diet. RPO supplementation significantly reduced infarct size in Norm+RPO and also in Chol+RPO (9.2 ± 1.0% and 26.9 ± 3.0%), respectively (Figure 1). Infarct size in Chol+RPO group was comparable to the group fed with normal diet.

Before ischaemia activity of the 75kDa isoform of MMP2 was significantly lower in the Chol+RPO group when compared to the Chol group (228 ± 28 arbitrary units versus 450 ± 34 arbitrary units; Figure 2). After ischaemia MMP2 (72kDa isoform) activity of the RPO supplemented group was significantly increased when compared to rats with normal diet (2472 ± 132 arbitrary units versus 2007 ± 68 arbitrary units; Figure 3).

Serum lipid profile

There were no significant differences in the serum total cholesterol and triglyceride level among groups (Table 3).


Our results show that dietary RPO supplementation reversed the negative effects of cholesterol supplementation in the ischaemia/reperfusion rat heart model. Furthermore, dietary RPO supplementation reduced myocardial infarct size in cholesterol supplemented rats. Previous studies have shown that dietary RPO supplementation improved functional recovery of cholesterol fed rats after ischaemia [10,12]. In the present study cholesterol supplementation was carried out for a longer period (nine weeks versus six weeks in previous studies). This indicates that RPO could effectively protect hearts against ischaemia/ reperfusion injury, despite a longer duration of cholesterol feeding. Osipov and co-workers (2009) found that hypercholesterolaemic pigs had increased left ventricular function throughout the ischaemia/reperfusion period when compared to normal pigs [4]. This was, however, associated with an increased infarct size and increased apoptotic markers. Our results together with previous

Table 1 Animal mass and heart mass after a nine week diet

Norm Chol Norm+RPO Chol+RPO

Animal mass (g) 494.0 ±18.1 472.6 ± 13.5 381.3 ± 7.6* 511.5 ± 14.4

Heart mass (g) 1.6 ± 0.1 1.7 ± 0.1 1.4 ± 0.1* 1.7 ± 0.1

Values are mean ± SEM, n = 8; *p < 0.05 versus Norm and Chol+RPO

studies [10,12] showed that dietary RPO can attenuate the harmful effects of cholesterol supplementation in the ischaemia/reperfusion model. Our total serum cholesterol results were not increased in the cholesterol fed rats. This was expected, as a previous study employed a similar model of cholesterol feeding in rats, without achieving significant changes in serum cholesterol [38]. The effects of the cholesterol feeding on the cardiovascular system are however clearly discussed in the study of Giricz and co-workers (2003) through the depletion of nitric oxide, and our current study by increased myocardial infarct size [38].

Coronary flow in the Norm group was reduced by 70%, in the Chol group by 64%, in the Chol+RPO group by 57% and in the Norm+RPO group by 33% after ischaemia. This indicates that RPO attenuated the fall in coronary flow after ischaemia. This may suggest that RPO supplementation improves vascular function during reperfusion.

MMP2 activity was measured before ischaemia in the cholesterol supplemented groups and compared to a Norm control group and a RPO supplemented group, as it may be expected that the cholesterol supplemented groups may have increased oxidative stress after supplementation. As increased oxidative stress leads to activation of MMP2 through redox modification of it's regulatory subunit, this would be associated with changes in MMP2 activity before ischaemia which would be expected to be absent in normal rats [2,15-18]. Our results demonstrate for the first time that dietary RPO supplementation may alter myocar-dial oxidative stress before ischaemia in cholesterol fed rats, as MMP2 activity was reduced before ischaemia. The reduction in MMP2 activity before ischaemia in rats supplemented with both cholesterol and RPO suggests that RPO was able to reduce oxidative stress in these rats. This would most probably be achieved through quenching of ROS, which is generated in greater proportions in cholesterol supplemented rats [3,38]. Increased generation of ROS and oxidative stress would normally be associated

with activation of MMP2 [15,17,18]. As increased activity of MMP2 may lead to either cardiac remodeling, or tissue damage [21-24], this reduction in MMP2 activity may play a role in RPO mediated protection against ischaemia/ reperfusion injury. However, MMP2 activity of the Norm +RPO was increased during reperfusion, when compared to normal rats without RPO supplementation. This would normally be associated with increased myocardial susceptibility to ischaemia/reperfusion injury [14,25-28]. RPO was able to reduce myocardial infarct size in cholesterol fed rats, despite increased activity of MMP2 in reperfusion found in normal rats. This suggests MMP2 activity may only play a protective role in cholesterol fed rats, and that other protective pathways are responsible for RPO mediated protection in normal rats.

The aim of this study was to investigate whether MMP2 activity was involved in RPO mediated protection of cholesterol fed rat hearts against ischaemia/reperfu-sion. Our results suggest that MMP2 activity may play a role in RPO mediated protection of the hearts of the cholesterol fed rats, but not the hearts of SRC fed rats. This suggests that more pathways of protection may play a role in this protection. Kruger and co-workers (2007) [12] found that RPO supplementation of cholesterol fed rats led to decreased phosphorylation of pro-apoptotic molecules, p38 and JNK. This coincided with increased phosphorylation of the pro-survival kinase ERK early in reperfusion, which leads to reduced apoptosis. Apoptosis has been shown to play a role in the detrimental effects of hypercholesterolaemia in the heart. Inhibition of apop-tosis may therefore explain the protective effects of RPO in this model [12].


For the first time we showed that dietary RPO supplementation attenuated increased susceptibility of cholesterol fed rat hearts to ischaemia/reperfusion injury as evidenced by reduced infarct size. Myocardial MMP2

Table 2 Coronary effluent (CE) collected for 10 min to measure MMP activity and heart rate (HR) before and after ischaemia

CE before ischaemia (mL/10 min) CE after ischaemia (mL/10 min) HR before ischaemia (BPM) HR after ischaemia (BPM)

Norm 205.0 ± 5.7 59.2 ± 4.0* 387.4 ± 56.5 338.0 ± 128.6

Chol 185.9 ± 21.7 67.1 ± 6.5* 390.8 ± 37.3 346.0 ± 115.3

Norm+RPO 152.5 ± 12.9 100.0 ± 6.9 344.1 ± 12.0 328.0 ± 40.7

Chol+RPO 141.9 ± 12.5 61.9 ± 3.8* 327.3 ± 17.6 339.0 ± 29.2

Values are mean ± SEM, n = 8; *p < 0.05 versus the corresponding "before ischaemia" values.

Chol +RPO

Norm +RPO

Figure 1 Myocardial infarct size in rats fed different diets for nine weeks. Infarct size is expressed as a percentage of the area at risk, values are mean ± SEM, n = 8; *p < 0.05 versus corresponding non-RPO treated groups; #p < 0.05 versus corresponding normaldiet.

Norm Chol


Chol Norm Chol


Figure 2 MMP2 activity in coronary effluent collected for 10 minutes before ischaemia. Values are mean ± SEM, n = 8; *p < 0.05 versus corresponding non-RPO treated groups; #p < 0.05 versus corresponding normaldiet.

1500 -

■ V! 1000 -

3000 n

2000 -

1000 -

Norm Chol


Chol Norm Chol


Figure 3 MMP2 activity in coronary effluent collected for the first 10 minutes of reperfusion. Values are mean ± SEM, n = 8; *p < 0.05 versus corresponding non-RPO treated groups; #p < 0.05 versus corresponding normal diet.

Table 3 Serum total cholesterol and serum triglyceride levels of rats after nine weeks of diet

Norm Chol Norm+RPO Chol+RPO

Total cholesterol 1.96 ± 0.05 1.91 ± 0.05 2.15 ± 0.23 1.79 ± 0.04


Triglycerides 0.72 ± 0.06 0.80 ± 0.08 0.71 ± 0.06 0.80 ± 0.07


Values are mean ± SEM, n = 8.

activity was reduced in cholesterol and RPO supplemented rat hearts before ischaemia (Figure 2), but not after ischaemia (Figure 3) associated with decreased infarct size. This may suggest a different or additional mechanism of protection.


This work was supported by a Collaborative Research Grant between Hungary (ZA-35/2006) and South Africa (NRF: 62212) and by grants from the NationalOffice for Research and Technology (Jedlik-NKFP-A1-2006-029, Med-Food, Baross DA-TECH-07-2008-0041, TAM0P-4.2.2-08/1/2008-0013, TAMOP-4.2.1/B-09/1/K0NV-2010-0005). T. Csont holds a "Janos Bolyai Felowship"

from the Hungarian Academy of Sciences. The red palm oilused in this study was supplied by Carotino SDN BHD (company number: 69046-T), Johar-Bahru, Malaysia.

Author details

Cardiovascular Research Group, University of Szeged, Dom ter 9, Szeged, H-6720, Hungary. 2Department of BiomedicalSciences, Faculty of Health and Wellness Sciences, Cape Peninsula University of Technology, Symphony Way, Bellville, 7535, South Africa. " 6722, Hungary.

'Pharmahungary Group, Hajnoczy u 6, Szeged,

Authors' contributions

GS was involved in allexperimental procedures, and played an important role in writing and editing the manuscript. DB was equally involved in experimentalwork and drafted the manuscript. KK contributed to all experimentalwork and data processing. She was also involved in the editing of the manuscript. TC was involved in the planning the study, interpretation of results and editing of the manuscript. CC, AE, PF and JvR were involved in planning the study, interpretation of the results and editing the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Received: 23 March 2011 Accepted: 20 June 2011 Published: 20 June 2011


1. Ferdinandy P, Szilvassy Z, Baxter GF: Adaptation to myocardial stress in disease states: is preconditioning a healthy heart phenomenon? Trends Pharmacol Sci 1998, 19(6):223-229.

2. Ferdinandy P, Schulz R, Baxter GF: Interaction of cardiovascular risk factors with myocardial ischemia/reperfusion injury, preconditioning, and postconditioning. Pharmacol Rev 2007, 59(4):418-458.

3. Onody A, Csonka C, Giricz Z, Ferdinandy P: Hyperlipidemia induced by a cholesterol-rich diet leads to enhanced peroxynitrite formation in rat hearts. Cardiovasc Res 2003, 58(3):663-670.

4. Osipov RM, Bianchi C, Feng J, Clements RT, Liu Y, Robich MP, Glazer HP, Sodha NR, Sellke FW: Effect of hypercholesterolemia on myocardial necrosis and apoptosis in the setting of ischemia-reperfusion. Circulation 2009, 120(1 1 Suppl):S22-30.

5. Nagendran B, Unnithan UR, Choo YM, Sundram K: Characteristics of red palm oil, a carotene- and vitamin E-rich refined oil for food uses. Food Nutr Bull 2000, 21(2):189-194.

6. Sundram K, Sambanthamurthi R, Tan YA: Palm fruit chemistry and nutrition. Asia Pac J Clin Nutr 2003, 12(3):355-362.

7. Wilson TA, Nicolosi RJ, Kotyla T, Sundram K, Kritchevsky D: Different palm oil preparations reduce plasma cholesterol concentrations and aortic cholesterol accumulation compared to coconut oil in hypercholesterolemic hamsters. J Nutr Biochem 2005, 16(10):633-640.

8. Schroeder MT, Becker EM, Skibsted LH: Molecular mechanism of antioxidant synergism of tocotrienols and carotenoids in palm oil. J Agric Food Chem 2006, 54(9):3445-3453.

9. van Rooyen J, Esterhuyse AJ, Engelbrecht AM, du Toit EF: Health benefits of a natural carotenoid rich oil: a proposed mechanism of protection against ischaemia/reperfusion injury. Asia Pac J Clin Nutr 2008,17(Suppl 1)316-319.

10. Esterhuyse AJ, du Toit EF, Benade AJ, van Rooyen J: Dietary red palm oil improves reperfusion cardiac function in the isolated perfused rat heart of animals fed a high cholesterol diet. Prostaglandins Leukot Essent Fatty Acids 2005, 72(3):153-161.

11. Bester DJ, van Rooyen J, du Toit EF, Esterhuyse AJ: Red palm oil protects against the consequences of oxidative stress when supplemented with dislipidaemic diets. Medical Technology SA 2006, 20(1):3-10.

12. Kruger MJ, Engelbrecht AM, Esterhuyse J, du Toit EF, van Rooyen J: Dietary red palm oil reduces ischaemia-reperfusion injury in rats fed a hypercholesterolaemic diet. Br J Nutr 2007, 97(4):653-660.

13. Nagase H, Woessner JF Jr: Matrix metalloproteinases. J Biol Chem 1999, 274(31):21491-21494.

14. Cheung PY, Sawicki G, Wozniak M, Wang W, Radomski MW, Schulz R: Matrix metalloproteinase-2 contributes to ischemia-reperfusion injury in the heart. Circulation 2000, 101(15):1833-1839.

Rajagopalan S, Meng XP, Ramasamy S, Harrison DG, Galis ZS: Reactive oxygen species produced by macrophage-derived foam cells regulate the activity of vascular matrix metalloproteinases in vitro. Implications for atherosclerotic plaque stability. J Clin Invest 1996, 98(11):2572-2579. Okamoto T, Akaike T, Sawa T, Miyamoto Y, van der Vliet A, Maeda H: Activation of matrix metalloproteinases by peroxynitrite-induced protein S-glutathiolation via disulfide S-oxide formation. J Biol Chem 2001, 276(31):29596-29602.

Siwik DA, Pagano PJ, Colucci WS: Oxidative stress regulates collagen synthesis and matrix metalloproteinase activity in cardiac fibroblasts. Am

J Physiol Cell Physiol 2001, 280(1):C53-60.

Kupai K, Szucs G, Cseh S, Hajdu I, Csonka C, Csont T, Ferdinandy P: Matrix

metalloproteinase activity assays: Importance of zymography. J

Pharmacol Toxicol Methods 2010, 61(2):205-209.

Hein S, Scheffold T, Schaper J: Ischemia induces early changes to

cytoskeletal and contractile proteins in diseased human myocardium. J

Thorac Cardiovasc Surg 1995, 110(1):89-98.

Matsumura Y, Saeki E, Inoue M, Hori M, Kamada T, Kusuoka H:

Inhomogeneous disappearance of myofilament-related cytoskeletal

proteins in stunned myocardium of guinea pig. Circ Res 1996,


Gao WD, Atar D, Liu Y, Perez NG, Murphy AM, Marban E: Role of troponin I proteolysis in the pathogenesis of stunned myocardium. Circ Res 1997, 80(3):393-399.

Bolli R, Marban E: Molecular and cellular mechanisms of myocardial stunning. Physiol Rev 1999, 79(2):609-634.

McDonough JL, Arrell DK, Van Eyk JE: Troponin I degradation and

covalent complex formation accompanies myocardial ischemia/

reperfusion injury. Circ Res 1999, 84(1):9-20.

Wang W, Schulze CJ, Suarez-Pinzon WL, Dyck JR, Sawicki G, Schulz R:

Intracellular action of matrix metalloproteinase-2 accounts for acute

myocardial ischemia and reperfusion injury. Circulation 2002,


Hayashidani S, Tsutsui H, Ikeuchi M, Shiomi T, Matsusaka H, Kubota T, Imanaka-Yoshida K, Itoh T, Takeshita A: Targeted deletion of MMP-2 attenuates early LV rupture and late remodeling after experimental myocardial infarction. Am J Physiol Heart Circ Physiol 2003, 285(3): H1229-35.

Menon B, Singh M, Singh K: Matrix metalloproteinases mediate beta-adrenergic receptor-stimulated apoptosis in adult rat ventricular myocytes. Am J Physiol Cell Physiol 2005, 289(1):C168-76. Bergman MR, Teerlink JR, Mahimkar R, Li L, Zhu BQ, Nguyen A, Dahi S, Karliner JS, Lovett DH: Cardiac matrix metalloproteinase-2 expression independently induces marked ventricular remodeling and systolic dysfunction. Am J Physiol Heart Circ Physiol 2007, 292(4):H1847-60. Fert-Bober J, Leon H, Sawicka J, Basran RS, Devon RM, Schulz R, Sawicki G: Inhibiting matrix metalloproteinase-2 reduces protein release into coronary effluent from isolated rat hearts during ischemia-reperfusion. Basic Res Cardiol 2008, 103(5)431-443.

Clark WM, Lessov N, Lauten JD, Hazel K: Doxycycline treatment reduces ischemic brain damage in transient middle cerebral artery occlusion in the rat. J Mol Neurosci 1997, 9(2):103-108.

Cursio R, Mari B, Louis K, Rostagno P, Saint-Paul MC, Giudicelli J, Bottero V, Anglard P, Yiotakis A, Dive V, Gugenheim J, Auberger P: Rat liver injury after normothermic ischemia is prevented by a phosphinic matrix metalloproteinase inhibitor. FASEB J 2002, 160):93-95. Roach DM, Fitridge RA, Laws PE, Millard SH, Varelias A, Cowled PA: Up-regulation of MMP-2 and MMP-9 leads to degradation of type IV collagen during skeletal muscle reperfusion injury; protection by the MMP inhibitor, doxycycline. Eur J Vasc Endovasc Surg 2002, 23(3):260-269.

Bendeck MP, Conte M, Zhang M, Nili N, Strauss BH, Farwell SM: Doxycycline modulates smooth muscle cell growth, migration, and matrix remodeling after arterial injury. Am J Pathol 2002, 160(3):1089-1095.

Krishnamurthy P, Peterson JT, Subramanian V, Singh M, Singh K: Inhibition of matrix metalloproteinases improves left ventricular function in mice lacking osteopontin after myocardial infarction. Mol Cell Biochem 2009, 322(1-2):53-62.

Bester DJ, Kupai K, Csont T, Szucs G, Csonka C, Esterhuyse AJ, Ferdinandy P, Van Rooyen J: Dietary red palm oil supplementation reduces myocardial

infarct size in an isolated perfused rat heart model. Lipids Health Dis 2010, 9:64.

35. Kocsis GF, Pipis J, Fekete V, Kovacs-Simon A, Odendaal L, Molnar E, Giricz Z, Janaky T, van Rooyen J, Csont T, Ferdinandy P: Lovastatin interferes with the infarct size-limiting effect of ischemic preconditioning and postconditioning in rat hearts. Am J Physiol Heart Circ Physiol 2008, 294(5): H2406-9.

36. Csonka C, Kupai K, Kocsis GF, Novak G, Fekete V, Bencsik P, Csont T, Ferdinandy P: Measurement of myocardial infarct size in preclinical studies. J Pharmacol Toxicol Methods 2010, 61(2) :163-170.

37. Csont T, Bereczki E, Bencsik P, Fodor G, Gorbe A, Zvara A, Csonka C, Puskas LG, Santha M, Ferdinandy P: Hypercholesterolemia increases myocardial oxidative and nitrosative stress thereby leading to cardiac dysfunction in apoB-100 transgenic mice. Cardiovasc Res 2007, 76(1):100-109.

38. Giricz Z, Csonka C, Onody A, Csont T, Ferdinandy P: Role of cholesterol-enriched diet and the mevalonate pathway in cardiac nitric oxide synthesis. Basic Res Cardiol 2003, 98(5):304-310.


Cite this article as: Szucs et al.: Dietary red palm oil supplementation decreases infarct size in cholesterol fed rats. Lipids in Health and Disease

2011 10:103.

Submit your next manuscript to BioMed Central and take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at „- ..■■ . f-f.ntn|