Cardioprotective Potential of Albizzia lebbeck: Insights Isoproterenol-Induced Myocardial Infarction in Rats

Jump To References Section

Authors

  • Department of Pharmacology, SIMS College of Pharmacy, Guntur - 522509, Andhra Pradesh ,IN
  • Department of Pharmacology, SIMS College of Pharmacy, Guntur - 522509, Andhra Pradesh ,IN
  • Department of Pharmacology, SIMS College of Pharmacy, Guntur - 522509, Andhra Pradesh ,IN
  • Department of Pharmacology, SIMS College of Pharmacy, Guntur - 522509, Andhra Pradesh ,IN
  • Department of Pharmaceutical Analysis, SIMS College of Pharmacy, Guntur - 522509, Andhra Pradesh ,IN
  • Department of Pharmaceutical Analysis, SIMS College of Pharmacy, Guntur - 522509, Andhra Pradesh ,IN

DOI:

https://doi.org/10.18311/ti/2024/v31i1/35749

Keywords:

Antioxidant Enzymes, Cardiac Biomarkers, CVD Risk Factors, Histopathology, Medicinal Plants, Oxidative Stress

Abstract

This study investigates the cardioprotective potential of Albizzia lebbeck (Shirish) ethanol leaf extract against Isoproterenol (ISO)-induced myocardial infarction in Wistar albino rats. Cardiovascular Diseases (CVDs) are a major global health concern, contributing significantly to morbidity and mortality. A. lebbeck, a medicinal plant with documented pharmacological activities, has not been scientifically studied for its cardioprotective properties. The research utilised a rat model of ISO-induced myocardial infarction, a well-established experimental approach to study preventive effects on myocardial damage. The study included the isolation and preparation of A. lebbeck ethanol leaf extract (MEAL) and its administration at different doses (200 mg/kg and 400 mg/kg) to ISO-treated rats. Various parameters, including relative organ weight, cardiac biomarkers (cTnI, LDH, CK-MB), total proteins, oxidative stress markers (SOD, MDA), and histopathological changes, were assessed. The results revealed that ISO administration induced cardiac hypertrophy, increased serum biomarkers, and oxidative stress, indicating myocardial damage. Treatment with MEAL, especially at the higher dose (400 mg/kg), significantly mitigated these effects. MEAL administration reduced the heart-to-body weight ratio, normalised serum biomarkers, restored endogenous antioxidant enzyme levels, and showed a protective effect against structural damage in histopathological examination. In conclusion, A. lebbeck ethanol leaf extract demonstrated significant cardioprotective effects against ISO-induced myocardial infarction in rats. These findings suggest the potential of A. lebbeck as a natural therapeutic agent for preventing or ameliorating cardiac damage associated with stress-induced conditions. Further research is warranted to elucidate the specific mechanisms underlying its cardioprotective properties and explore its potential clinical applications.

Downloads

Download data is not yet available.

Published

2024-02-28

How to Cite

Anusha, V. L., Yerragopu, A. K., Kiran, N. S., Rajesh, A., Sirisha, Y., & Harini, A. L. (2024). Cardioprotective Potential of <i>Albizzia lebbeck</i>: Insights Isoproterenol-Induced Myocardial Infarction in Rats. Toxicology International, 31(1), 121–129. https://doi.org/10.18311/ti/2024/v31i1/35749
Received 2023-11-30
Accepted 2024-02-01
Published 2024-02-28

 

References

Kadali VN, Kindangi KR, Pola SR, Ramesh T, Sandeep BV. Cardio-protective plants present in west Godavari district of Andhra Pradesh, India: A short review. Int J Pharmacogn. 2016; 3:19-25.

Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: A systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012; 380(9859):2095-128. https://doi. org/10.1016/S0140-6736(12)61728-0 PMid:23245604

Barnes AS. Emerging modifiable risk factors for cardiovascular disease in women: Obesity, physical activity, and sedentary behavior. Texas Hear Inst J. 2013; 40(3):293-5.

Malakar AK, Choudhury D, Halder B, Paul P, Uddin A, Chakraborty S. A review on coronary artery disease, its risk factors, and therapeutics. J Cell Physiol. 2019; 234(10):16812-23. https://doi.org/10.1002/jcp.28350. PMid:30790284 DOI: https://doi.org/10.1002/jcp.28350

Pencina MJ, Navar AM, Wojdyla D, Sanchez RJ, Khan I, Elassal J, et al. Quantifying importance of major risk factors for coronary heart disease. Circulation. 2019; 139(13):1603-11. https://doi.org/10.1161/CIRCULATIONAHA.117.031855 PMid:30586759 PMCid:PMC6433489 DOI: https://doi.org/10.1161/CIRCULATIONAHA.117.031855

Pěsíc M, Stanković S. Development of natural product drugs in a sustainable manner. Brief for United Nations Global Sustainable Development Report; 2015.

SS Agarwal. Paridhavi M. Herbal Drug Technology. Vol 9. University Press (India) Private Limited; 2007.

Hassan LG, Umar KJ, Atiku I. Nutritional evaluation of A. lebbeck (L.) pods as source of feeds for livestock. Am J Food Technol. 2007; 2(5):435-9. https://doi.org/10.3923/ ajft.2007.435.439 DOI: https://doi.org/10.3923/ajft.2007.435.439

Khalil MI, Ahmmed I, Ahmed R, Tanvir EM, Afroz R, Paul S, et al. Amelioration of isoproterenol-induced oxidative damage in rat myocardium by Withania somnifera leaf extract. Biomed Res Int. 2015; 2015:1-10. https://doi.org/10.1155/2015/624159 PMid:26539517 PMCid:PMC4619872 DOI: https://doi.org/10.1155/2015/624159

Huang H, Geng Q, Yao H, Shen Z, Wu Z, Miao X, et al. Protective effect of scutellarin on myocardial infarction induced by isoprenaline in rats. Iran J Basic Med Sci. 2018; 21(3):267-76.

Sivakumar B, Velmurugan C, Bhargava A, Kumar PL. Diuretic activity of methanolic extract of Albizia lebbeck. Res Rev J Pharmacol Toxicol Stud. 2013;1(1):3-5.

Murugesan M, Revathi R, Manju V. Cardioprotective effect of fenugreek on isoproterenol-induced myocardial infarction in rats. Indian J Pharmacol. 2011; 43(5):516-19. https://doi.org/10.4103/0253-7613.84957 PMid:22021992 PMCid:PMC3195119 DOI: https://doi.org/10.4103/0253-7613.84957

Flack CP, Woollen JW. Prevention of interference by dextran with biuret-type assay of serum proteins. Clin Chem. 1984; 30(4):559-61. https://doi.org/10.1093/clinchem/30.4.559 PMid:6200256 DOI: https://doi.org/10.1093/clinchem/30.4.559

MacDonald RP. Serum lactic dehydrogenase-a diagnostic aid in myocardial infarction. J Am Med Assoc. 1957; 165(1):35. https://doi.org/10.1001/jama.1957.02980190037009 PMid:13462739 DOI: https://doi.org/10.1001/jama.1957.02980190037009

Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem. 1974; 47(3):469-74. https://doi.org/10.1111/j.1432-1033.1974. tb03714.x PMid:4215654 DOI: https://doi.org/10.1111/j.1432-1033.1974.tb03714.x

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95(2):351-8. https://doi.org/10.1016/0003- 2697(79)90738-3 PMid:36810 DOI: https://doi.org/10.1016/0003-2697(79)90738-3

Mert H, Yilmaz H, Irak K, Yildirim S, Mert N. Investigation of the protective effect of kefir against isoproterenol induced myocardial infarction in rats. Korean J Food Sci Anim Resour. 2018; 38(2):259-72.

Rajadurai M, Prince PSM. 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(2-3):178-88. https://doi.org/10.1016/j.tox.2006.11.053 PMid:17188415 DOI: https://doi.org/10.1016/j.tox.2006.11.053

Nirmala C, Puvanakrishnan R. Protective role of curcumin against isoproterenol induced myocardial infarction in rats. Mol Cell Biochem. 1996; 159(2):85-93. https://doi. org/10.1007/BF00420910 PMid:8858558 DOI: https://doi.org/10.1007/BF00420910

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(3):457-61. https://doi.org/10.1016/j.jep.2004.11.028 PMid:15740881 DOI: https://doi.org/10.1016/j.jep.2004.11.028

Arya DS, Bansal P, Ojha SK, Nandave M, Mohanty I, Gupta SK. Pyruvate provides cardioprotection in the experimental model of myocardial ischemic reperfusion injury. Life Sci. 2006; 79(1):38-44. https://doi.org/10.1016/j.lfs.2005.12.039 PMid:16457854 DOI: https://doi.org/10.1016/j.lfs.2005.12.039

Maghamiour N, Safaie N. High Creatine Kinase (CK)-MB and Lactate dehydrogenase in the absence of myocardial injury or infarction: A case report. J Cardiovasc Thorac Res. 2014; 6(1):69-70.

Alpert JS, Thygesen K, Antman E, Bassand JP. Myocardial infarction redefined- a consensus document of The Joint European Society of Cardiology/American College of Cardiology Committee for the redefinition of myocardial infarction. J Am Coll Cardiol. 2000; 36(3):959-69. https:// doi.org/10.1016/S0735-1097(00)00804-4 PMid:10987628 DOI: https://doi.org/10.1016/S0735-1097(00)00804-4

Priscilla DH, Prince PSM. 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(2-3):118-24. https://doi.org/10.1016/j. cbi.2008.12.012 PMid:19146839 DOI: https://doi.org/10.1016/j.cbi.2008.12.012

Wei H, Li H, Wan SP, Zeng Q-T, Cheng L-X, Jiang L-L, et al. Cardioprotective effects of malvidin against isoproterenolinduced myocardial infarction in rats: A mechanistic study. Med Sci Monit. 2017; 23:2007-16. https://doi.org/10.12659/ MSM.902196 PMid:28445445 PMCid:PMC5414594 DOI: https://doi.org/10.12659/MSM.902196

Rajadurai M, Prince PSM. Preventive effect of naringin on lipid peroxides and antioxidants in isoproterenolinduced cardiotoxicity in Wistar rats: Biochemical and histopathological evidences. Toxicology. 2006; 228(2-3):259- 68. https://doi.org/10.1016/j.tox.2006.09.005 PMid:17084010 DOI: https://doi.org/10.1016/j.tox.2006.09.005