Open Access Open Access  Restricted Access Subscription Access

Cardioprotective Effect of Banaba on Myocardial Ischemia/Reperfusion Injury in Rats


Affiliations
1 Bhopal – 462044, Madhya Pradesh, India
2 Department of Pharmacy, Sumandeep Vidyapeeth Deemed to be University, Piparia, Vadodara – 391760, Gujarat, India
3 Parul Institute of Pharmacy & Research, Parul University, Vadodara – 391760, Gujarat, India
 

The ethanol extract of Banaba (Lagerstroemia speciosa L.) leaves, was investigated for their effects on ischemia/reperfusion (I/R) injury induced by occlusion of the left descending coronary artery (LCA) for 1 h, followed by re-opening again for 1 h. Banaba ethanol extract (100 mg/kg) intraperitonially (i.p.) was administered 30 min after induction of ischemia. During I/R period, the hemodynamics and ECG parameters were measured. Oxidative stress markers like reduced glutathione (GSH), Superoxide dismutase (SOD), malondialdehyde (MDA), activities of myeloperoxidase (MPO), creatine kinase (CK) and myocardial infarct area were significantly (P<0.05) reduced in Wistar rats after Banaba treatment. The apoptotic activity and histological observations were influenced by Banaba. The cardioprotective effect of Banaba could be attributed to its ability to improve the antioxidant mechanism, anti-inflammatory and anti-apoptotic activity in ischemic animals.

Keywords

Antioxidant, Anti-inflammatory and Anti-apoptotic, Lagerstroemia speciosa L.
Font Size

User

Notifications
JOURNAL COVERS
  

  • Ferrari R, Alfieri O, Curello S. Occurrence of oxidative stress using reperfusion of the human heart. Circulation. 1990; 81:201–11. https://doi.org/10.1161/01.CIR.81.1.201. PMid:2297827
  • Verma S, Fedak PWM, Weisel RD, Butany J, Rao V, Maitland A, et al. Fundamentals of reperfusion injury for the clinical cardiologist. Circulation. 2002; 105:2332–6. https://doi.org/10.1161/01.CIR.0000016602.96363.36
  • Mohanty I, Arya DS, Dinda A, Joshi S, Talwar KK, Gupta SK. Protective effects of Curcuma longa on ischemiareperfusion induced myocardial injuries and their mechanisms. Life Sciences. 2004; 75:1701–11. https://doi.org/10.1016/j.lfs.2004.02.032. PMid:15268970
  • Stangl V, Rodiger O, Frank TM, Bohm M, Stangl K, Baumann G, Felix SB. Influence of polymorphonuclear leukocytes and plasma on coronary vasomotion after ischemia. Annals of Thoracic Surgery. 1999; 68:442–6. https://doi.org/10.1016/ S0003-4975(99)00550-0
  • Baldus S, Heitzer T, Eiserich JP, Lau YD, Mollnau H, Ortak M, et al. Myeloperoxidase enhances nitric oxide catabolism during myocardial ischemia and reperfusion. Free Radical Biology and Medicine. 2004; 37:902–11. https://doi.org/10.1016/j.freeradbiomed.2004.06.003. PMid:15304260
  • Saks VA, Khuchua ZA, Vasilyeva EV, Belikova OY, Kuznetsov AV. Metabolic compartmentation and substrate channeling in muscle cells: role of coupled creatine kinases in in vivo regulation of cellular respiration: a synthesis Molecular and Cellular Biochemistry. 1994; 133:155–92. https://doi.org/10.1007/BF01267954. PMid:7808453
  • Tienfenbacher CP, Kaptiza J, Dietz V, Lee CH, Niroomand F. Reduction of myocardial infarct size by fluvastatin. The American Journal of Physiology-Heart and Circulatory Physiology. 2003; 285:H59–64. https://doi.org/10.1152/ ajpheart.00782.2002. PMid:12623790
  • Hattori K, Sukenobu N, Sasaki T, Takasuga S, Hayashi T, Kasai R, et al. Activation of Insulin Receptors by Lagerstroemin. Journal of Pharmacological Sciences. 2003; 93:69–73. https://doi.org/10.1254/jphs.93.69. PMid:14501154
  • Yamaguchi Y, Yamada K, Yoshikawa N, Nakamura K, Haginaka J, Kunitomo M. Corosolic acid prevents oxidative stress, inflammation and hypertension in SHR/NDmer-cp rats, a model of metabolic syndrome. Life Sciences. 2006; 79:2474–9. https://doi.org/10.1016/j.lfs.2006.08.007. PMid:16959274
  • Shinghala JR, Balaraman R. Antihypertensive effect of 5-HT1A agonist buspirone and 5HT2B antagonist in experimentally induced hypertension in rats. Pharmacology. 2005; 73(3):129–39. https://doi.org/10.1159/000082114. PMid:15539790
  • Bradley PP, Priebat DA, Christensen RD, Rothstein G. Measurement of cutaneous inflammation: Estimation of neutrophil content with an enzyme marker. The Journal of Investigative Dermatology. 1982; 78:206–9. https://doi.org/10.1111/1523-1747.ep12506462. PMid:6276474
  • Misra HP, Fridovich L. The role of superoxide anions in the auto-oxidation of epinephrine and simple assay for superoxide dismutase. Journal of Biological Chemistry. 1972; 247:3170–5.
  • Aebi H. Catalase in vitro. Methods in Enzymology. 1984; 105:121–6. https://doi.org/10.1016/S0076-6879(84)05016-3
  • Moron MS, Depierre JW, Mannervik B. Levels of glutathione, glutathione reductase and glutathione S-transeferase activities in rat lung and liver. Biochimica et Biophysica Acta. 1979; 582:67–78. https://doi.org/10.1016/0304-4165(79)90289-7
  • Slater TF, Sawyer BC. The stimulatory effect of carbon tetrachloride and other halogenoalkanes or peroxidative reactions in rat liver fractions in vitro. Biochemical Journal. 1971; 123:805–14. https://doi.org/10.1042/bj1230805. PMid:4399399. PMCid:PMC1177080
  • Lowery OH, Rosenbrough NJ, Farr Al, Randall RJ. Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry. 1951; 193:265–75.
  • Simonian NA, Getz RL, Leveque JC, Konardi C, Coyle JT. Kainic acid induced apoptosis in neurons. Neuroscience. 1996; 75:1047–55. https://doi.org/10.1016/0306-4522(96)00326-0
  • Kleber AG. ST-segment elevation in the electrocardiogram: A sign of myocardial ischemia. Cardiovascular Research. 2000; 45:111–18. https://doi.org/10.1016/S0008-6363(99)00301-6
  • Kleber AG, Janse MJ, Van Capelle FJC, Durrer D. Mechanism and time course of S-T and T-Q segment changes during acute regional myocardial ischemia in the pig heart determined by extracellular and intracellular recordings. Circulation Research. 1978; 42:603–13. https://doi.org/10.1161/01.RES.42.5.603. PMid:639183
  • Das DK, Cordis GA, Rao PS, Liu XK, Maity S. Highperformance liquid chromatographic detection of hydroxylated benzoic acids as an indirect measure of hydroxyl radical in heart: its possible link with the myocardial reperfusion injury. Journal of Chromatography. 1991; 536:273–82. https://doi.org/10.1016/S00219673(01)89260-8
  • Shankar RA, Hideg K, Zweier JL, Kuppusamy P. Targeted antioxidant properties of N-[(tetramethyl-3-pyrroline3-carboxamido)propyl] phthalimide and its nitroxide metabolite in preventing postischemic myocardial injury. Journal of Pharmacology and Experimental Therapeutics. 2000; 292:838–45.
  • Wang QD, Pernow J, Sjoquist P, Ryden L. Pharmacological possibilities for protection against myocardial reperfusion injury. Cardiovascular Research. 2002; 55:25–37. https:// doi.org/10.1016/S0008-6363(02)00261-4. PMid:12062706
  • Becker LB. New concepts in reactive oxygen species and cardiovascular reperfusion physiology. Cardiovascular Research. 2004; 61:461–70. https://doi.org/10.1016/j.cardiores.2003.10.025. PMid:14962477
  • Kutala VK, Khan M, Mandal R, Ganesan L, Tridandapani S, Kalai T, et al. Attenuation of myocardial ischemia-reperfusion injury by trimetazidine derivatives functionalized with antioxidant properties. Journal of Pharmacology and Experimental Therapeutics. 2006; 317(3):921–8. https://doi.org/10.1124/jpet.105.100834. PMid:16467453
  • Hamilton KL, Staib JL, Phillips T, Hess A, Lennon SL, Powers SK. Exercise, antioxidants, and hsp72: Protection against myocardial ischemia/reperfusion. Free Radical Biology and Medicine. 2003; 34:800–9. https://doi.org/10.1016/S08915849(02)01431-4
  • Wang M, Baker L, Tsai BM, Meldrum KK, Meldrum DR. Sex differences in the myocardial inflammatory response to ischemia-reperfusion injury. The American Journal of Physiology-Endocrinology and Metabolism. 2005; 288:E321–6. https://doi.org/10.1152/ajpendo.00278.2004. PMid:15367393
  • Roof RL, Duvdevani R, Stein DG. Gender influences outcome of brain injury; progesterone plays a protective role. Brain Research. 1993; 607:333–6. https://doi.org/10.1016/0006-8993(93)91526-X
  • Scartezzini P, Speroni E. Review on some plants of Indian traditional medicine with antioxidant activity. Journal of Ethanopharmacology. 2000; 71:23–43. https://doi.org/10.1016/S0378-8741(00)00213-0
  • Sobel BE, Bresnahan GF, Shell WE, Yoder RD. Estimation of infarct size in man and its relation to prognosis. Circulation. 1972; 46:640–8. https://doi.org/10.1161/01.CIR.46.4.640. PMid:5072765
  • Itoh G, Tamura J, Suzuki M, Suzuki Y, Ikeda H, Koike M, et al. DNA fragmentation of human infarcted myocardial cells demonstrated by the nick end labeling method and DNA agarose gel electrophoresis. The American Journal of Pathology. 1995; 146:1325–31.
  • Majno G, Joris I. Apoptosis, oncosis, and necrosis: An overview of cell death. The American Journal of Pathology. 1995; 146:3–15.
  • Gottlieb RA, Burleson KO, Kloner RA, Babior BM, Engler RL. Reperfusion injury induces apoptosis in rabbit cardiomyocytes. The Journal of Clinical Investigations 1994; 94:1621–8. https://doi.org/10.1172/JCI117504. PMid: 7929838. PMCid:PMC295322
  • Gottlieb RA, Giesing HA, Engler RL, Babior BM. The acid deoxyribonuclease of neutrophils: A possible participant in apoptosis-associated genome destruction. Blood. 1995; 86:2414–18. https://doi.org/10.1182/blood.V86.6.2414.bloodjournal8662414. PMid:7662989
  • Galang N, Sasaki H, Maulik N. Apoptotic cell death during ischemia/reperfusion and its attenuation by antioxidant therapy. Toxicology. 2000; 148:111–18. https://doi.org/10.1016/S0300-483X(00)00201-8
  • Vakeva AP, Agah A, Rollins SA. Myocardial infarction and apoptosis after myocardial ischemia and reperfusion: role of the acute myocardial terminal complement components and inhibition by anti-C5 therapy. Circulation. 1998; 97:2259–67. https://doi.org/10.1161/01.CIR.97.22.2259. PMid:9631876
  • Fliss H, Gattinger D. Apoptosis in ischemic and reperfused rat myocardium. Circulation Research. 1996; 79:949–56. https://doi.org/10.1161/01.RES.79.5.949. PMid:8888687
  • Liu F, Kim JK, Li Y, Liu XQ, Li J, Chen X. An extract of Lagerstroemia speciosa L. has insulin-like glucose uptakestimulatory and adipocyte differentiation-inhibitory Activities in 3T3-L1 cells. Journal of Nutrition. 2001; 131:2242–7. https:// doi.org/10.1093/jn/131.9.2242. PMid:11533261

Abstract Views: 314

PDF Views: 136




  • Cardioprotective Effect of Banaba on Myocardial Ischemia/Reperfusion Injury in Rats

Abstract Views: 314  |  PDF Views: 136

Authors

Vipin Dhote
Bhopal – 462044, Madhya Pradesh, India
Ramachandran Balaraman
Department of Pharmacy, Sumandeep Vidyapeeth Deemed to be University, Piparia, Vadodara – 391760, Gujarat, India
Muthu K. Mohan Maruga Raja
Parul Institute of Pharmacy & Research, Parul University, Vadodara – 391760, Gujarat, India

Abstract


The ethanol extract of Banaba (Lagerstroemia speciosa L.) leaves, was investigated for their effects on ischemia/reperfusion (I/R) injury induced by occlusion of the left descending coronary artery (LCA) for 1 h, followed by re-opening again for 1 h. Banaba ethanol extract (100 mg/kg) intraperitonially (i.p.) was administered 30 min after induction of ischemia. During I/R period, the hemodynamics and ECG parameters were measured. Oxidative stress markers like reduced glutathione (GSH), Superoxide dismutase (SOD), malondialdehyde (MDA), activities of myeloperoxidase (MPO), creatine kinase (CK) and myocardial infarct area were significantly (P<0.05) reduced in Wistar rats after Banaba treatment. The apoptotic activity and histological observations were influenced by Banaba. The cardioprotective effect of Banaba could be attributed to its ability to improve the antioxidant mechanism, anti-inflammatory and anti-apoptotic activity in ischemic animals.

Keywords


Antioxidant, Anti-inflammatory and Anti-apoptotic, Lagerstroemia speciosa L.

References





DOI: https://doi.org/10.18311/jnr%2F2020%2F25156