|
 |
|
RESEARCH PAPER |
|
|
|
| Year : 2010 | Volume
: 1
| Issue : 1 | Page : 24-31 |
| |
Effect of vitamin E alone and in combination with lycopene on biochemical and histopathological alterations in isoproterenol-induced myocardial infarction in rats
Aman Upaganlawar, Hardik Gandhi, R Balaraman
Pharmacy Department, Faculty of Technology and Engineering, The M. S. University of Baroda, Vadodara-390 002, Gujarat, India
| Date of Web Publication | 21-Jun-2010 |
Correspondence Address:
Aman Upaganlawar
Pharmacy Department, Faculty of Technology and Engineering, The M. S. University of Baroda, Vadodara-390 002, Gujarat
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0976-500X.64532
 Abstract | | |
Background: The present study has been designed to evaluate the combined cardioprotective effect of vitamin E and lycopene on biochemical and histopathological alteration in isoproterenol-induced myocardial infarction in rats. Materials and Methods: Adult male albino rats of Wistar strain were treated with isoproterenol (200 mg/kg, s.c.) for 2 days at an interval of 24 h to develop myocardial infarction. Vitamin E (100 mg/kg/day, p.o.) and lycopene (10 mg/kg/day, p.o.) were administered alone and in combination for 30 days. Change in body weight and organ weight were monitored. Levels of serum marker enzymes (AST, ALT, LDH and CK-MB), lipid peroxidation, endogenous antioxidants (GSH, GPX, GST, SOD and CAT), membrane bound enzymes (Na + /K + ATPases, Mg 2+ ATPases and Ca 2+ ATPases) were evaluated. LDH isoenzyme separation was carried out using gel electrophoresis. Histopathology of heart tissue was performed. Results: Induction of rats with isoproterenol resulted in a significant elevation in organ weight, lipid peroxidation, serum marker enzymes (AST, ALT, CK-MB and LDH), and Ca 2+ ATPases, whereas it caused a significant (P < 0.001) decrease in body weight, activities of endogenous antioxidants (GSH, GP X , GST, SOD and CAT), Na + /K + and Mg 2+ ATPases. ISO treated rats showed high intensity band of LDH1-LDH2 isoenzymes. Treatment with the combination of Vitamin E and lycopene for 30 days significantly attenuated these changes as compared to the individual treatment and ISO treated groups. Histopathological observations were also in correlation with the biochemical parameters. Conclusion: These findings indicate the synergistic cardioprotective effects of vitamin E and lycopene during ISO-induced myocardial infarction in rats.
Keywords: Isoproterenol, myocardial infarction, oxidative stress, vitamin E, lycopene
How to cite this article:
Upaganlawar A, Gandhi H, Balaraman R. Effect of vitamin E alone and in combination with lycopene on biochemical and histopathological alterations in isoproterenol-induced myocardial infarction in rats. J Pharmacol Pharmacother 2010;1:24-31 |
How to cite this URL:
Upaganlawar A, Gandhi H, Balaraman R. Effect of vitamin E alone and in combination with lycopene on biochemical and histopathological alterations in isoproterenol-induced myocardial infarction in rats. J Pharmacol Pharmacother [serial online] 2010 [cited 2021 Dec 1];1:24-31. Available from: http://www.jpharmacol.com/text.asp?2010/1/1/24/64532 |
| Introduction | |  |
Myocardial infarction commonly known as heart attack is a disease that occurs when the blood supply to a part of the heart is interrupted, causing the death of heart tissue. [1] It is a complex phenomenon affecting the mechanical, electrical, structural and biochemical properties of the heart. [2] It is well recognized that there is an increasing generation of reactive oxygen species such as superoxide anion and hydroxyl radicals and other reactive species in ischemic tissue, bringing about oxidative damage of membrane lipids, proteins, carbohydrates, and DNAs. [3] Energy depletion of the cells and necrotic type cell death was also found due to oxidative stress. [4] Hence, therapeutic intervention with antioxidants may be useful in preventing these deleterious changes.
Isoproterenol, a β-adrenergic agonist, has been found to cause severe stress in the myocardium resulting in infarct like necrosis of the heart muscle.[5] Some of the mechanisms proposed to explain ISO-induced damage to cardiac myocytes include hypoxia due to myocardial hyperactivity, coronary hypotension, calcium overload, hypertrophy, depletion of energy reserve and excessive production of free radicals resulting from oxidative metabolism of catecholamine. [6]
Vitamin E in humans is the major antioxidant in lipid phases. [7] Vitamin E has been shown to slow or inhibit the oxidative modification of LDL that is responsible for the development and progression of atherosclerosis in human and animals. [8] It has been shown to reduce smooth muscle cell proliferation, [9] platelet adherence and aggregation, [10] protein kinase C activation [11] and isoproterenol-induced myocardial infarction in rats. [12] Epidemiological data indicated an inverse association between cardiovascular risk and vitamin E intake from dietary sources and/or supplements. [13] Despite these promising experimental and epidemiological data, most randomized controlled trials have failed to confirm the role of vitamin E supplementation in cardiovascular prevention. [14]
Lycopene is a natural pigment synthesized by plants and microorganisms. It is highly lipophilic and is most commonly located within cell membranes and other lipid components. It is therefore expected that in the lipophilic environment, lycopene will have maximum ROS scavenging effects. In epidemiological studies and supplementation human trials, lycopene was found to reduce cardiovascular risks due to its antioxidant properties. [15] Lycopene, because of its high number of conjugated double bonds, exhibits higher singlet oxygen quenching ability compared to β-carotene or α-tocopherol.[16] Chronic administration of lycopene can protect myocardium against ischemia reperfusion injury. [17]
Several studies have shown that antioxidants are uniquely different from one another and work synergistically and more effectively when they are used in combinations. [12],[18],[19] In vitro study showed that lycopene and vitamin E acts synergistically in microsomal membranes [20] and LDL oxidation. [21] The interaction of vitamin E with lycopene during myocardial oxidative stress induced injury has not been previously evaluated. Hence, the present study was designed to evaluate the effect of vitamin E alone and in combination with lycopene on tissue defense system, lipid peroxidation status and histopathological alterations during ISO-induced myocardial infarction in rats.
| Materials and Methods | | |
Materials
Lycopene powder (10%) was gifted by Genesis Lab Ltd, Mumbai. Vitamin E (DL-α-Tocopherol acetate) and (±)-Isoproterenol hydrochloride were purchased from Sigma Aldrich Co. St. Louis. MO. USA. All other chemicals were of analytical grade.
Experimental animals
Male adult albino rats (Wistar strain) weighing between 200 and 230 g were used in the present study. All experiments were approved by the Institutional Animal Ethics Committee (IAEC) of the Institute. The animals were housed in an air conditioned room and were kept in standard laboratory conditions under natural light and dark cycle (12 h light/ dark) maintained at an ambient temperature 25 ± 2°C. The animals were fed standard pellet diet (Amrut feeds, Pranav Agro Industries Ltd. Pune, India) and water ad libitum.
Pilot study for dose fixation
Lycopene at the doses of 5, 10 and 15 mg/kg/day and vitamin E at the doses of 25, 50 and 100 mg/kg/day were screened in isoproterenol-induced myocardial infarction in rats. The optimum dose exhibiting maximum cardioprotective effect during 30 days was evaluated by estimating serum lactate dehydrogenase, creatine phospokinase-MB and the level of tissue lipid peroxidation. Lycopene (10 mg/kg/day, p.o.) and vitamin E (100 mg/kg/day, p.o.) were found to be most effective in functional recovery of biochemical alterations. Hence, these doses were selected for further evaluation (alone as well as in combination) in the present study.
Experimental design and protocol
Animals were randomly allocated into six main groups comprising 10 rats in each group. Six animals were used for biochemical estimations and four animals for histopathological study. Group I: Control: animals received vehicle for 30 days and normal saline on 29 th and 30 th day. Group II: animals received vehicle for 30 days and intoxicated with ISO (200mg/kg, s.c.) on 29 th and 30 th day at an interval of 24 h. Group III: Vitamin E (100 mg/kg/day, p.o.) and lycopene (10 mg/kg/day, p.o.) in combination for 30 days. Group IV: Vitamin E (100 mg/kg, p. o.) for 30 days and challenged with ISO on 29 th and 30 th day. Groups V: lycopene (10 mg/kg, p. o.) for 30 days in olive oil [17] and challenged with ISO on 29 th and 30 th day. Group VI: Vitamin E (100 mg/kg, p.o.) and lycopene (10 mg/kg, p.o.) in combination for 30 days and challenged with ISO on 29 th and 30 th day. Olive oil was used as vehicle for vitamin E and lycopene. Control and ISO treated groups also received same volume of olive oil thought the treatment period.
Estimation of cardiac marker enzymes
On day 31, blood was collected from retro-orbital plexus under mild ether anesthesia (approx. 2 ml). Blood was centrifuged at 2000 rpm for 20 min to separate serum (Remi centrifuge). Serum lactate dehydrogenase (LDH) and creatine phospokinase-MB (CK-MB) were determined by using standard kits from Reckon Diagnostic Ltd., India. Serum aspartate transaminase (AST) and serum alanine transaminase (ALT) were estimated by using the standard kit from Span Diagnostic Pvt Ltd., India. All estimations were carried out using UV spectrophotometer (Shimadzu, India).
Separation of LDH-isoenzymes
LDH-isoenzymes were separated by agarose gel electrophoresis. [22] Agarose gel (1%w/v) was prepared and poured immediately on the glass slide. After the gel sets properly, 10 μl of serum samples was loaded into the wells. After the run, the gel was removed and stained by the following method. The staining solution contained 1.0 ml of 1 M lithium lactate, 1.0 ml of 1 M sodium chloride, 1.0 ml of 5 mM magnesium chloride, 2.5 ml of 0.1% w/v nitroblue tetrazolium, 0.25 ml of 0.1%w/v phenazinemethosulphate, 2.5 ml of 0.5 M phosphate buffer (pH 7.5) and 10 mg of NAD in a total volume of 10 ml. The photographs were taken using AlphaEase Fc Imaging system, USA.
Estimation of myocardial lipid peroxidation and antioxidant enzymes
The animals were scarified using overdose of pentobarbital sodium. Hearts were excised, weighed and homogenized in chilled tris HCl buffer (10 mM, pH 7.4) at a concentration of 10% (w/v). The homogenates were centrifuged at 10,000 rpm at 0 o C for 20 min using Remi C-24 high speed cooling centrifuge. The clear supernatant was used for the assay of lipid peroxidation, [23] superoxide dismutase, [24] catalase, [25] reduced glutathione, [26] glutathione peroxidase [27] and glutathione S transferase. [28]
Estimation of membrane bound ATPases
The sediment after centrifugation of tissue homogenate was resuspended in ice-cold tris buffer (10 mM, pH 7.4) to get a final concentration of 10%w/v and were used for the estimation of Na + /K + ATPase, [29] Ca 2+ ATPase [30] and Mg 2+ ATPase. [31] Protein was estimated according to the method of Lowery et al. [32]
Histopathological study
After decapitation, the heart was rapidly dissected out and washed immediately with saline and fixed in 10% buffered formalin. Hearts which were stored in 10% formalin were embedded in paraffin sections cut at 5 μm and were stained with hematoxyline and eosin. The stained sections were examined under Olympus (Magnus MLX series) India Pvt Ltd. Photomicroscope and photographed (10X). Four hearts from each group were assessed for light microscopic studies. A minimum of 10 fields per slide were examined and graded for severity of changes using scores on a scale of severe (+ + +), moderate (+ +), mild (+) and absence (A).
Statistical analysis
Results are presented as mean ± S.E.M. One-way analysis of variance (ANOVA) followed by Bonferroni multiple comparisons using a computer based fitting program (GraphPad Prism 5). Differences were considered to be statistically significant when P < 0.05. P > 0.05 was considered as non significant.
| Results | | |
0Effect of vitamin E alone and in combination with lycopene on body weight, heart weight and heart / body weight ratio in ISO treated rats
As shown in [Table 1], body weight at the end of experiment period in ISO treated group was found to be significantly (P < 0.01) decreased, whereas the heart weight and its ratio with body weight was found to be significantly (P < 0.01) increased as compared to control group. Treatment with vitamin E and lycopene in combination for 30 days significantly (P < 0.01) increased the body weight and significantly (P < 0.05, P < 0.01) decreased the heart weight and heart / body weight ratio as compared to ISO treated group.
Effect of vitamin E alone and in combination with lycopene on serum cardiac marker enzymes in ISO treated rats
[Figure 1] and [Figure 2] show the effect of vitamin E and lycopene combination on serum cardiac marker enzymes. Rats treated with ISO led to a significant (P < 0.001) increase in the activities of serum marker enzymes such as AST, ALT, LDH and CK-MB as compared to the control groups. Treatment with vitamin E and lycopene in combination for 30 days and challenged with ISO showed a significant (P < 0.001) reduction in the activities of all serum cardiac marker enzymes as compared to the ISO, vitamin E + ISO and lycopene + ISO treated groups. Combined effect of antioxidants was found to be more effective in maintaining serum marker enzymes as compared to individual antioxidants.
Effect of vitamin E alone and in combination with lycopene on lipid peroxidation and antioxidant enzymes in ISO treated rats
[Figure 3] indicates the level of lipid peroxides (LPO) in the hearts of control and experimental group of rats. Maximum induction of LPO was observed in ISO intoxicated rats. The change in LPO was significantly decreased in rats treated with vitamin E and lycopene compared to vitamin E+ISO, lycopene+ISO and ISO intoxicated rats.
[Table 2] shows the activities of antioxidant enzymes such as GPX, GST, SOD, CAT and level of GSH in the heart of control and experimental group of rats. Rats injected with ISO showed a significant (P < 0.001) decrease in the activities of GPX, GST, SOD, CAT and the level of GSH as compared to control groups [Table 2]. Vitamin E in combination with lycopene significantly (P < 0.001) normalized all the parameters and was found to be more effective than vitamin E+ISO, lycopene+ISO and ISO treatment groups.
Effect of vitamin E alone and in combination with lycopene on membrane bound ATPases in ISO treated rats
[Figure 4] shows a significant (P < 0.001) decrease in the activities of Na + /K + ATPase and Mg 2+ ATPase whereas a significant (P < 0.001) increase in the activity of Ca 2+ ATPase in ISO administered rats as compared to the control group. Vitamin E did not produce any significant effect on Mg 2+ ATPase activity. Combination of vitamin E and lycopene showed a significant (P < 0.001) increase in activities of Na + /K + ATPase, Mg 2+ ATPase, and a significant reduction in the activity of Ca 2+ ATPase as compared to vitamin E+ISO, lycopene+ISO and ISO treatment groups.
Effect of vitamin E alone and in combination with lycopene on LDH-isoenzymes separation in ISO treated rats
Agarose gel electrophoretic separation of serum LDH-isoenzyme patterns of normal and ISO-induced rats are depicted in [Figure 5]. ISO induction caused an increase in the intensity of LDH-1 and LDH-2 isoenzyme bands compared to normal control rats. Treatment with vitamin E and lycopene in combination significantly decreased the intensity of LDH-1 and LDH-2 isoenzyme bands compared to ISO-intoxicated rats, vit.E+ISO and lycopene+ISO groups [Figure 5].
Effect of vitamin E alone and in combination with lycopene on histopathological alterations in ISO treated rats
[Figure 6]a shows the light micrograph of control heart showing normal architecture without any fraying or infarction. Light micrograph of isoproterenol-intoxicated group shows focal confluent necrosis of muscle fibers with inflammatory cell infiltration, and edema with fragmentation of muscle fibers [Figure 6]b. Treatment with vitamin E +ISO group showed myonecrosis with less edema and inflammatory cells [Figure 6]c.
Lycopene+ISO treated rat heart shows mild edema with significant reduction in infarction, showing normal myocardial architecture [Figure 6]d. Combination of vitamin E and lycopene showed less necrosis and edema, whereas absence of inflammatory cells [Figure 6]e. [Table 3] shows the change in the degree of histopathological scoring after treatment with the combination of vitamin E and lycopene.
| Discussion | | |
ISO in large doses induces morphological and functional alterations in the heart leading to myocardial necrosis. It also produces excessive free radicals resulting from oxidative metabolism of catecholamine. There are increasing evidences that cardiotoxicity of ISO occurs because of generation of free radicals and oxidative stress. [1],[12],[18] In the present study, there was a significant decrease in the body weight, significant increase in heart weight and heart/body weight ratio in isoproterenol treated rats. Increase in the ratio is suggestive of cardiac hypertrophy which may be due to ventricular stiffness, increased water content, edematous intermuscular space and extensive necrosis of cardiac muscle followed by invasion of the damaged tissue by inflammatory cells. [33],[34] Treatment with vitamin E and lycopene significantly decreased the heart/body weight ratio, suggesting that the combination could effectively suppress the stimulus for hypertrophy.
The present study reveals that ISO treatment results in marked elevation in the levels of cardiac serum marker enzymes like AST, ALT, LDH and CK-MB. Results of present study are in line with those reported by Kurian et al, 2005. [35] These cardio specific marker enzymes are released from the heart into the blood during myocardial damage due to deficiency of oxygen supply or glucose, the cell membrane become permeable or may rupture and results in the leakage of enzymes in the serum. [36] Combination of vitamin E and lycopene synergistically normalized the levels of serum biomarker enzymes compared to vitamin E+ISO and lycopene+ISO treatment groups. This protection might be due to the effect of vitamin E in combination with lycopene on the myocardium, which had reduced the extent of myocardial damage induced by ISO and thereby restricting the leakage of these enzymes from the myocardium, suggesting the membrane stabilizing potential of the combination.
LDH is a cytosolic enzyme, which exists in five different isoforms (LDH 1 to LDH 5). In the cardiac tissue, LDH 1 and LDH 2 predominate. Hence, detection of elevated concentration of these enzymes becomes a definitive diagnostic criterion for cardiac toxicity. In the present study, we observed an increase in the intensity of LDH1 and LDH2 isoenzyme in serum of isoproterenol treated rats which may be due to ISO-induced necrosis in rats. [37] Vitamin E and lycopene in combination reduces the intensity of LDH1 and LDH2 isoenzyme. This could be due to reduction in the degree of damage and thereby reduction in leakage of enzymes from myocardium.
Significant increase in the level of lipid peroxidation and a significant decrease in the activities of GSH, GPX, GST, SOD and CAT were observed in ISO intoxicated rats, which suggests the involvement of oxidative stress in ISO toxicity. This result is in line with the earlier reported studies. [38] Elevation of lipid peroxides in ISO treated rats could be attributed to the accumulation of lipids in the heart and the irreversible damage to myocardial membranes. Reduction in the activity of SOD and CAT in the present study may be due to the increased generation of highly cytotoxic free radicals due to auto oxidation of catecholamine. GSH exerts its function by reaction with superoxide radical, peroxy radicals and singlet oxygen followed by the formation of oxidized glutathione and other disulfides. [30] The unavailability of GSH may decrease the activity of GPx and GST in ISO treated rats. Combined treatment of vitamin E and lycopene restored the level of LPO and endogenous antioxidants to that of control group indicating the potential antioxidant effects of this combination. Lycopene was found to be more effective in restoring the LPO and antioxidant enzymes than vitamin E.
Membrane bound ATPases plays an important role in the contraction and relaxation of the cardiac muscle by maintaining the normal ion levels inside the myocyte. Na + /K + ATPase and Mg 2+ ATPase are the '-SH' group containing enzymes and is lipid dependant. Reduction in the activity of these enzymes might be due to enhanced lipid peroxidation by free radicals. Reduced activity of Mg 2+ ATPase and Na + /K + ATPase may be responsible for ionic imbalance caused by ISO which damages the membranous proteins. Result of the present study also shows enhanced activity of Ca 2+ ATPase; it may be due to activation of adenylate cyclase activity. Calcium overload in the myocardial cells during ischemia activates the Ca 2+ dependant ATPase of the membrane depleting high energy phosphate stores, thereby indirectly inhibiting Na + and K + transport and inactivating Na + /K + ATPase. [2] Treatment with vitamin E and lycopene in combination increased the activities of Na + /K + ATPase and Mg 2+ ATPase and decreased the activity of Ca 2+ ATPase in ISO group. This could be due to the ability of vitamin E and lycopene to protect the '-SH' group from oxidative damage through the inhibition of peroxidation of membrane lipids.
Histopathological findings of vitamin E and lycopene alone and their combination shows a near normal morphology of cardiac muscle. Combination of vitamin E and lycopene shows better morphological protection than alone antioxidant treated groups by absence of necrosis and inflammatory cells which is in accordance with biochemical changes. These data further confirmed the cardioprotective action of the combination of vitamin E and lycopene.
Both vitamin E and lycopene are lipid soluble antioxidants. Vitamin E is a chain breaking antioxidant in human plasma and is a low density lipoprotein. [11] It could effectively trap the lipid peroxyl radical to inhibit the free radical initiated lipid peroxidation. Lycopene is a well-known singlet oxygen scavenger and other excited species. During singlet oxygen quenching, energy is transferred from singlet oxygen to lycopene molecule, converting it to the energy rich triplet state. [39] Further it was reported that the synergistic effects of lycopene and vitamin E combination may be due to the regeneration of vitamin E from its α-tocopheroxyl radical by lycopene.[40] This may possibly be the reason for the better effect of vitamin E and lycopene in attenuating cardiac dysfunction through lowering of cardiac marker enzymes and LPO. In conclusion, the results of the present study indicate that the combined treatment with vitamin E and lycopene synergistically prevents the ISO-induced myocardial infarction than an individual antioxidant treatment in rats.
| Acknowledgment | | |
Authors are thankful to All India Council for Technical Education (AICTE) for providing financial assistance in the form of National Doctoral Fellowship (AICTE File No. 1-10/RID/NDF-PG/(30)/2007-08) for this work. Authors are also thankful to Dr. Vikas Toke, Jyot pathology, Baroda for carrying out the histopathological study.
| References | | |
| 1. | Rajadurai M, Stanely Mainzen Prince P. Preventive effect of naringin on cardiac markers, electrocardiographic patterns and lysosomal hydrolases in normal and isoproterenol-induced myocardial infarction in wistar rats. Toxicology 2007;230:178-88.  |
| 2. | Petrich ER, Schanne OF, Zumino AP. Electrophysiological responses to ischemia and reperfusion. In: Karmazyn M, editor. Myocardial ischemia: Mechanism, reperfusion, protection. Basel: Birkhauser Verlag; 1996. p. 115-33. |
| 3. | Dikshit M, Van Oosten MH, de Graff S, Srimal RC. Free radical scavenger mechanisms in experimentally induced ischemia in the rabbit heart and protective effect of verapamil. Arch Int Pharmacodyn Ther 1992;318:55-65. |
| 4. | Radons J, Heller B, Bόrkle A, Hartmann B, Rodriguez ML, Krφncke KD, et al. Nitric oxide toxicity in islet cells involves poly (ADP-ribose) polymerase activation and concomitant NAD+ depletion. Biochem Biophys Res Commun 1994;199:270-7. |
| 5. | Wexler BC. Myocardial infarction in young vs. old male rats: pathophysiological changes. Am Heart J 1978;96:70-80. |
| 6. | Mohanty I, Arya DS, Dinda A, Talwar KK, Joshi S, Gupta SK. Mechanisms of cardioprotective effects of Withania somnifera in experimentally induced myocardial infarction. Basic Clin Pharmacol Toxicol 2004;94:184-90. |
| 7. | Traber MG, Sies H. Vitamin E in humans: Demand and delivery. Annu Rev Nutr 1996;16:321-47. |
| 8. | Verlangieri AJ, Bush MJ. Effects of dl-(±)-α-tocopherol supplementation on experimentally induced primate atherosclerosis. J Am Coll Nutr 1992;11:131-8. |
| 9. | Meydani M. Vitamin E. Lancet 1995;345:170-5. |
| 10. | Steiner M. Influence of vitamin E on platelet functions in humans. J Am Coll Nutr 1991;10:466-73. |
| 11. | Bursell SE, King GL. Can protein kinase C inhibition and vitamin E prevent the development of diabetic vascular complications? Diabetes Res Clin Pract 1999;45:169-82. |
| 12. | Upaganlawar A, Gandhi C, Balaraman R. Effect of green tea and vitamin E combination on isoproterenol induced myocardial infarction in rats. Plant Foods Hum Nutr 2009;64:75-80. |
| 13. | Jha P, Flather M, Lonn E, Farkouh M, Yusuf S. The antioxidant vitamins and cardiovascular disease: A critical review of epidemiologic and clinical trial data. Ann Intern Med 1995;123:860-72. |
| 14. | Vivekananthan DP, Penn MS, Sapp SK, Hsu A, Topol EJ. Use of antioxidant vitamins for the prevention of cardiovascular disease: Meta-analysis of randomised trials. Lancet 2003;361:2017-23. |
| 15. | Gerster H. The potential role of lycopene for human health. J Am Coll Nutr 1997;16:109-26. |
| 16. | Di Mascio P, Kaiser S, Sies H. Lycopene as the most efficient biological carotenoid singlet oxygen quencher. Arch Biochem Biophys 1989;274:532-8. |
| 17. | Bansal P, Gupta SK, Ojha SK, Nandave M, Mittal R, Kumari S, et al. Cardioprotective effect of lycopene in the experimental model of myocardial ischemia-reperfusion injury. Mol Cell Biochem 2006;289:1-9. |
| 18. | Punithavathi VR, Prince PS. Combined effects of quercetin and α-tocopherol on lipids and glycoprotein components in isoproterenol induced myocardial infarcted Wistar rats. Chem Biol Interact 2009;181:322-7. |
| 19. | Yogeeta SK, Gnanapragasam A, Kumar SS, Subhashini R, Sathivel A, Devaki T. Synergistic interactions of Ferulic acid with Ascorbic acid: Its cardioprotective role during isoproterenol induced myocardial infarction in rats. Mol Cell Biochem 2006;283:139-46. |
| 20. | Palozza P, Krinsky NI. Antioxidant effects of carotenoids on biological membranes. Acta Med Rom 1993;31:131-40. |
| 21. | McKenzie D, Henderson AR. Electrophoresis of lactate dehydrogenase isoenzymes. Clin Chem 1983;29:189-95. |
| 22. | Fuhrman B, Volkova N, Rosenblat M, Aviram M. Lycopene synergistically inhibits LDL oxidation in combination with vitamin E, glabridin, rosmarinic acid, carnosic acid, or garlic. Antioxid Redox Signal 2000;3:491-506. |
| 23. | Slater TF, Sawyer BC. The stimulatory effect of carbon tetrachloride and other halogenalkane or peroxidative reactions in the rat liver function in vitro. Biochem J 1971;123:805-15. |
| 24. | Misra HP, Fridovich I. The role of superoxide anion in the autooxidation of epinephrine and a simple assay of superoxide dismutase. J Biol Chem 1972;247:3170-5. |
| 25. | Aebi H. Catalase in vitro. Methods Enzymol 1984;105:121-6. |
| 26. | Moron MS, Depierre JW, Mannervik B. Levels of glutathione, glutathione reductase and glutathione S transferase activities in rat lung and liver. Biochim Biophys Acta 1979;582:67-8. |
| 27. | Rotruck JT, Pope AL, Ganther HE, Swanson AB, Hafeman DG, Hoekstra WG. Selenium: biochemical role as a component of glutathione peroxidase. Science 1979;179:588-90. |
| 28. | Habig WH, Jakoby WB. Assay of differentiation of glutathione S-transferases. Methods Enzymol 1981;77:398-405. |
| 29. | Bonting SL. Membrane ion transport. In: Pembroski TM, Schmidt TH, Blumchen G, editors. Bio-Behavioral Base of Coronary Heart Disease. Vol. 1. London: Wiley Inter Science; 1970. p. 254-363. |
| 30. | Hjertιn S, Pan H. Purification and characterization of two form of low affinity calcium ion ATPase from erythrocyte membrane. Biochim Biophys Acta 1983;728:281-8. |
| 31. | Ohnishi T, Suzuki T, Suzuki Y, Ozawa K. A Comparative study of plasma membrane Mg 2+ ATPase activities in normal, regenerating and malignant cells. Biochim Biophys Acta 1982;684:67-4. |
| 32. | Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193:265-75. |
| 33. | Nirmala C, Puvanakrishnan R. Protective role of curcumin against isoproterenol induced myocardial infarction in rats. Mol Cell Biochem 1996;159:85-3. |
| 34. | Weber KT, Brilla CG. Pathological hypertrophy and cardiac interstitium: fibrosis and renin-angiotensin-aldosterone system. Circulation 1991;83:1849-65. |
| 35. | Kurian GA, Philip S, Varghese T. Effect of aqueous extract of the Desmodium gangeticum DC root in the severity of myocardial infarction. J Ethnopharmacol 2005;97:457-61. |
| 36. | Arya DS, Bansal P, Ojha SK, Nandave M, Mohanty I, Gupta SK. Pyruvate provide cardioprotection in the experimental model of myocardial ischemia reperfusion injury. Life Sci 2006;79:38-4. |
| 37. | Priscilla DH, Prince PS. Cardioprotective effect of gallic acid on cardiac troponin-t, cardiac marker enzymes, lipid peroxidation products and antioxidants in experimentally induced myocardial infarction in Wistar rats. Chem Biol Interact 2009;179:118-24. |
| 38. | Rajadurai M, Stanely Mainzen Prince P. Preventive effect of naringin on lipid peroxide and antioxidant in isoproterenol- induced cardiotoxicity in Wistar rats: biochemical and histopathological evidences. Toxicology 2006;228:259-68. |
| 39. | Wertz K, Siler U, Goralczyk R. Lycopene: modes of action to promote prostate health. Arch Biochem Biophys 2004;430:127-34. |
| 40. | Palozza P, Krinsky NI. β-carotene and α-tocopherol are synergistic antioxidants. Arch Biochem Biophys 1992;297:184-97. |
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
[Table 1], [Table 2], [Table 3]
| This article has been cited by | | 1 |
The beneficial effects of antioxidants combination on cardiac injury induced by tetrachloromethane |
|
| Aliah R. Alshanwani, Laila M. Faddah, Hanan Hagar, Ahlam M. Alhusaini, Sameerah Shaheen, Raeesa A. Mohammad, Fatima M. B. Alharbi, Alaa AlHarthii, Amira M. Badr | | Drug and Chemical Toxicology. 2020; : 1 | | [Pubmed] | [DOI] | | | 2 |
Possible protective mechanisms exerted by metformin or metformin and vitamin E in isoproterenol-induced cardiac injury |
|
| Nawal M. Al-Rasheed,Nouf M. Al-Rasheed,Danah A. AL-Rabeeah,Heba S. AL-Barrak,Salma A. AL-Salman,Shahd A. Ibrahim,Sulafa A. AL-Hassab,Maha A. Al-Amin,Iman H. Hasan,Hanaa N. Al-Ajmi,Tahani K. AL-Shammari | | Journal of Cellular Biochemistry. 2018; | | [Pubmed] | [DOI] | | | 3 |
Isoproterenol-induced cardiac ischemia and fibrosis: Plant-based approaches for intervention |
|
| Prince Allawadhi,Amit Khurana,Nilofer Sayed,Preeti Kumari,Chandraiah Godugu | | Phytotherapy Research. 2018; | | [Pubmed] | [DOI] | | | 4 |
Molecular assessment of protective effect of Vitex negundo in ISO induced myocardial infarction in rats |
|
| Maruthi Prasad E.,Ramgopal Mopuri,Madhusudana Pulaganti,Mohammed Abdul Kareem,Md. Shahidul Islam,Dase Gowda K.R,Mackraj Irene,Yingli Lu,Lakshmi Devi Kodidhela | | Biomedicine & Pharmacotherapy. 2017; 92: 249 | | [Pubmed] | [DOI] | | | 5 |
Effect of vitamin D on isoprenaline-induced myocardial infarction in rats: possible role of peroxisome proliferator-activated receptor-? |
|
| Ola Ahmed El-Gohary,Mona Maher Allam | | Canadian Journal of Physiology and Pharmacology. 2017; : 1 | | [Pubmed] | [DOI] | | | 6 |
Effects of Caffeine and Lycopene in Experimentally Induced Diabetes Mellitus |
|
| Ozlem Ozmen,Senay Topsakal,Mehmet Haligur,Ahmet Aydogan,Dilnur Dincoglu | | Pancreas. 2016; 45(4): 579 | | [Pubmed] | [DOI] | | | 7 |
Lycopene attenuates inflammation and apoptosis in post-myocardial infarction remodeling by inhibiting the nuclear factor-?B signaling pathway |
|
| QIN HE,WEI ZHOU,CAIJIN XIONG,GANG TAN,MANHUA CHEN | | Molecular Medicine Reports. 2015; 11(1): 374 | | [Pubmed] | [DOI] | | | 8 |
The Biochemical and histopathological effects of estrogen replacement therapy on the heart of ovariectomized female rats subjected to myocardial infarction |
|
| Khaled Abdulqawi,Abeer M. El-Mahalaway,Ola A. EL-Gohary,Ahmed Y. Rezk,Odette Wahba | | Evidence Based Women's Health Journal. 2013; 3(4): 165 | | [Pubmed] | [DOI] | | | 9 |
Tomato lycopene attenuates myocardial infarction induced by isoproterenol: Electrocardiographic, biochemical and anti-apoptotic study |
|
| Upaganlawar, A. and Patel, V. and Balaraman, R. | | Asian Pacific Journal of Tropical Biomedicine. 2012; 2(5): 345-351 | | [Pubmed] | | | 10 |
Tomato lycopene attenuates myocardial infarction induced by isoproterenol: Electrocardiographic, biochemical and anti–apoptotic study |
|
| Aman Upaganlawar,Vaibhav Patel,R Balaraman | | Asian Pacific Journal of Tropical Biomedicine. 2012; 2(5): 345 | | [Pubmed] | [DOI] | | | 11 |
Isoproterenol Induced Myocardial Infarction: Protective Role of Natural Products |
|
| Aman Upaganlawar, Hardik Gandhi, R. Balaraman | | Journal of Pharmacology and Toxicology. 2011; 6(1): 1-17 | | [Pubmed] | [DOI] | | | 12 |
Cardioprotective Effects of Lagenaria siceraria Fruit Juice on Isoproterenol-induced Myocardial Infarction in Wistar Rats: A Biochemical and Histoarchitecture Study |
|
| A Upaganlawar and R Balaraman | | J Young Pharm. 2011; 3(4): 297-303 | | [Pubmed] | [DOI] | | | 13 |
Lycopene prevents 3-nitropropionic acid-induced mitochondrial oxidative stress and dysfunctions in nervous system |
|
| Sandhir, R. and Mehrotra, A. and Kamboj, S.S. | | Neurochemistry International. 2010; 57(5): 579-587 | | [Pubmed] | | | 14 |
Lycopene prevents 3-nitropropionic acid-induced mitochondrial oxidative stress and dysfunctions in nervous system |
|
| Rajat Sandhir,Arpit Mehrotra,Sukhdev S. Kamboj | | Neurochemistry International. 2010; 57(5): 579 | | [Pubmed] | [DOI] | |
|
|
|
|
|
|
|
|
