Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 33093
Alcoholic Extract of Terminalia Arjuna Protects Rabbit Heart against Ischemic-Reperfusion Injury: Role of Antioxidant Enzymes and Heat Shock Protein
Authors: K. Gauthaman, T.S. Mohamed Saleem, V. Ravi, Sita Sharan Patel, S. Niranjali Devaraj
Abstract:
The present study was designed to investigate the cardio protective role of chronic oral administration of alcoholic extract of Terminalia arjuna in in-vivo ischemic reperfusion injury and the induction of HSP72. Rabbits, divided into three groups, and were administered with the alcoholic extract of the bark powder of Terminalia arjuna (TAAE) by oral gavage [6.75mg/kg: (T1) and 9.75mg/kg: (T2), 6 days /week for 12 weeks]. In open-chest Ketamine pentobarbitone anaesthetized rabbits, the left anterior descending coronary artery was occluded for 15 min of ischemia followed by 60 min of reperfusion. In the vehicle-treated group, ischemic-reperfusion injury (IRI) was evidenced by depression of global hemodynamic function (MAP, HR, LVEDP, peak LV (+) & (- ) (dP/dt) along with depletion of HEP compounds. Oxidative stress in IRI was evidenced by, raised levels of myocardial TBARS and depletion of endogenous myocardial antioxidants GSH, SOD and catalase. Western blot analysis showed a single band corresponding to 72 kDa in homogenates of hearts from rabbits treated with both the doses. In the alcoholic extract of the bark powder of Terminalia arjuna treatment groups, both the doses had better recovery of myocardial hemodynamic function, with significant reduction in TBARS, and rise in SOD, GSH, catalase were observed. The results of the present study suggest that the alcoholic extract of the bark powder of Terminalia arjuna in rabbit induces myocardial HSP 72 and augments myocardial endogenous antioxidants, without causing any cellular injury and offered better cardioprotection against oxidative stress associated with myocardial IR injury.Keywords: Antioxidants, HSP72, Ischemic reperfusion injury, Terminalia arjuna.
Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1333116
Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 2300References:
[1] E. Braunwald and R. A. Kloner, "The stunned myocardium prolonged post ischemic ventricular dysfunction," Circulation., 1982, vol. 66, pp. 1146-1149.
[2] J. L. Park and B. R. Lucchest, "Mechanism of Myocardial ischemic reperfusion injury," Ann Thorac Surg., 1999, vol. 68, pp. 1905-1912.
[3] G. Ambrosio, J. T. Flaherty, C. Dullio, I. Tritto, G. Sanoro, P. P. Ellia, M. Condorelli, and M. Chiariello, "Oxygen radicals generated at reflow induce peroxidation of membrane lipids in reperfused hearts," J Clin Invest., 1991, Vol. 87, pp. 2056-2066.
[4] R. Ferrari, C. Ceconi, S. Curello, A. Cargnoni, E. Pasini and O. Visioli, "The occurrence of oxidative stress during reperfusion in experimental animals and men". Cardiovascular Drugs and Therapeutics., 1991, Vol. 5, pp. 277-288.
[5] J. G. Gross, R. K. Judy, and C. W. David, "Mechanism of post ischemic contractile dysfunction," Ann Thoracic Surge., 1999, vol. 68, pp. 1898- 1904.
[6] R. Bolli, "The Late Phase of Preconditioning," Circ. Res., 2000, vol. 87, pp. 972-983.
[7] K. Gauthaman, M. Maulik, R. Kumari, S. C. Manchanda, A. K. Dinda and S.K. Maulik, "Effect of chronic treatment with bark of Terminalia arjuna: A study on the isolated ischemic reperfused rat heart," Journal of Ethnopharmacology., 2001, vol. 75 (2-3), pp. 197-201.
[8] K. Karthikeyan, B. R. Bai, K. Gauthaman, K. S. Sathish and S. N. Devaraj, "Cardioprotective effect of the alcoholic extract of Terminalia arjuna bark in an in vivo model of myocardial ischemic reperfusion injury," Life Sci., 2003, vol. 73(21), pp. 2727-2739.
[9] K. Gauthaman, S. K. Banerjee, A. K. Dinda, C. C. Ghosh and S. K. Maulik, "Terminalia arjuna (Roxb.) protects rabbit heart against ischemic-reperfusion injury: role of antioxidant enzymes and heat shock protein," Journal of Ethnopharmacology., 2005, vol. 96, pp. 403-409.
[10] D. M. Yellon, and D. J. Hausenloy, "Myocardial reperfusion injury," N Engl J Med., 2007, vol. 357, pp. 1121-1135.
[11] K. Gauthaman, T. S. Mohamed Saleem, V. Ravi and S. Niranjali Devaraj, "Cardioprotective properties of Methanolic extract of Terminalia arjuna Linn Bark in an in vitro model of Myocardial ischemic reperfusion injury in rats," Int. J.Pharmacol.Biol.Sci., vol. 2 (1), 2008, pp. 13-28.
[12] A. A. Knowlton, "The role of heat shock protein in heart," Journal of Molecular & Cellular cardiology., 1995, vol. 27, pp. 121-31.
[13] E. K. Hiodromitis, G. K. Karavolias, E. Bofilis, D. M. Yellon and D.T. Kremastinos, "Enhanced protection of heat shock in myocardial infarction: inhibition of detrimental effect of systemic hyperthermia," Cardiovascular Drugs Therapy., 1999, vol. 13 (3), pp. 223-231.
[14] S. K. Powers, M. Locke and H. A. Demirel, "Exercise, heat shock proteins, and myocardial protection from I-R injury," Med Sci Sports Exerc., Mar 2001, vol 33 (3), pp. 386-392.
[15] K. Gauthaman and S. Niranjali Devaraj, "Terminalia arjuna barks protects rat hearts with induction of the 72 kDa Heat shock protein (HSP 72)," Biomedicine., 2003, (3&4), pp. 26-30.
[16] C. G. Caroline, A. Mohamed and H. Y. Magdi, "Heat stress proteins and myocardial protection: Experimental model or potential clinical tool?" The International Journal of Biochemistry and Cell Biology, 1999, vol 31, pp. 559-573.
[17] A. K. Nadkarni, Indian Materia Medica vol.1, Bombay: Popular Prakashan (Pvt.) Ltd., India. 1976.
[18] A. B. Vaidya, "Terminalia arjuna in cardiovascular therapy," J Assoc Physicians India ., April 1994 , vol. 42 (4), pp. 281-282.
[19] Y. B. Tripathi, "Terminalia arjuna extract modulates the contraction of rat aorta induced by KCl and norepinephrine," Phytotherapy Research., 1993, vol. 7, pp. 320-322.
[20] S. Dwivedi, "Antianginal and cardioprotective effects of Terminalia arjuna, an indigenous drug, in coronary heart disease," Journal Association Physician India., 1994, vol. 42 (4), pp. 287-289.
[21] M. Gautham, M. Sunit, and K. D. Dipak, "Evaluation of Antioxidant Effectiveness of a few selected Vegetables," Enviromental & Nutrional Interactions., 1997, vol. 1, pp. 287-297.
[22] S. K. Maulik, R. Kumari, M. Maulik., S. C. Manchanda and S. K. Gupta, "Captopril and its time of administration in myocardial ischemicreperfusion injury," Pharmacol Res., 2001, vol. 44 (2), pp. 123-127.
[23] W. Lamprecht, F. Stan, H. Weisser, and F. Heinz, "Determination of creatine phosphate and adenosine triphosphate with creatine kinase," In: Methods of Enzymatic Analysis., Bergmayer, H.U. (Ed.). Academic Press: New York 1974, pp. 1776-1778.
[24] P. Kakkar, B. Das and P. N. Viswanathan, "A modified spectrophotometric assay of superoxide dismutase" Indian Journal Biochemistry Biophysics., 1984, vol. 21, pp. 130-132.
[25] H. Aebi, Catalase, In: Bergmeyer HU, editor. Methods of Enzymatic Analysis. Verlag: Chemic Academic Press Inc., 1974, pp. 673-85.
[26] G. L. Ellman, "Tissue sulphydryl groups," Archive Biochemistry Biophysics., 1959, vol. 82, pp. 70-77.
[27] H. Okhawa, N. Oohishi and K. Yagi, "Assay for Lipid peroxides in animal tissues by thiobarbituric acid reaction," Annals of Biochemistry., 1979, vol. 95, pp. 351-358.
[28] M. M. Hutter, R. E. Sievers, V. Barbose and C.L. Wolfe, "Heat shock protein induction in rat hearts. A direct correlation between the amount of heat shock protein induced and the degree of myocardial protection" Circulation., 1994, vol. 89, pp. 355-360.
[29] M. M. Bradford, "A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding," Analytical Biochemistry., 1976, vol. 7 (72), pp. 248-254.
[30] V Pathania, N. Syal, M. H. Hundal, and K. L. Khanduja, "Geriforte stimulates antioxidant defense system," Indian Journal of Experimental Biology., 1998, vol. 36, pp. 414- 417.
[31] S. K. Banerjee, A. K. Dinda, S. C. Manchanda and S. K. Maulik, "Chronic garlic administration protects rat heart against oxidative stress induced by ischemic reperfusion injury," BMC Pharmacology., 2002, vol. 2 (1), 16.
[32] A. L. Miller, "Botanical influences on cardiovascular disease," Alternative Medical Review., 1998, vol. 3 (6), pp. 422-431.
[33] H. Yamasaki, H. Uefuji, and Y. Sakihama, Arch Biochem. Biophys., 1996; 332(1), 183-186.
[34] J. C. Tilak, T. P. A. Devasagayam, T. Kon, Y. Naito and T. Yoshikawa, "Protection by an medicinal plant, Terminalia arjuna, and its active component, Baicalein against superoxide and singlet oxygen," In International conference on natural products, free radicals and padioprotectors in health (NFR - 200) and III annual meeting of SFRR - India., Jan17- 19, 2004, pp. 21-22.
[35] P. K. Singal, A. K. Dhalla, M. Hill, and T. P. Thomas, "Endogenous antioxidant changes in the myocardium in response to acute and chronic stress conditions," Molecular cell biochemistry, 1993, vol. 129, pp. 179- 186.
[36] S. D. Seth, M. Maulik, C. K. Katiyar, and S. K. Mauilk, "Role of lipistat in protection against isoproterenol induced myocardial necrosis in rats: A biochemical and histopathological study," Indian Journal of Physiology and Pharmacology., 1998, vol. 42 (1), pp. 101-106.
[37] D. K. Das, and N. Maulik, In "Cell Biology of Trauma", eds. By Lemasters J.L., Oliver C., Boca Raton CRC press 1995, pp 193-211.
[38] S. E. Steare and D. M. Yellon, "The potential for endogenous myocardial antioxidant to protect the myocardium against ischemicreperfusion injury; refreshing the parts exogenous antioxidants can not reach," J. Mol. Cell. Cardiol., 1995, vol. 27, pp. 65-74.