Vol 76, No 3 (2017)
Original article
Published online: 2017-02-02

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An investigation on cardioprotective potential of Marrubium vulgare aqueous fraction against ischaemia-reperfusion injury in isolated rat heart

A. Garjani1, D. Tila, S. Hamedeyazdan, H. Vaez, M. Rameshrad, M. Pashaii, F. Fathiazad2
Pubmed: 28198525
Folia Morphol 2017;76(3):361-371.

Abstract

Background: The aim of this study was to evaluate the cardioprotective effects of aqueous fraction of Marrubium vulgare hydroalcoholic extract on cardiac parameters in ischaemic-reperfused isolated rat hearts.

Materials and methods: The aerial parts of the plant were extracted with methanol 70% by maceration. The water-soluble portion of the total hydroalcoholic extract was prepared with liquid-liquid extraction (LLE). Afterwards, the antioxidant activity, total phenolic and flavonoids content of the aqueous fraction were determined. In order to evaluate the effects of the aqueous fraction on cardiac parameters and ischaemia-reperfusion (I/R) injury, the Langendroff method was used on male Wistar rats. Harvested hearts were cannulated immediately to the Langendroff apparatus and subjected into 30 min regional ischaemia and 2 h reperfusion, either by a modified Krebs-Henseleit buffer (KHB) solution or enriched KHB solution with plant extract (10, 20, 40 μg/mL).

Results: The aqueous fraction was found to be a scavenger of DPPH radical with RC50 value of 47 μg/mL. The total phenolic and flavonoids content of the fraction was 6.05 g gallic acid equivalent and 36.13 mg quercetin equivalent per 100 g of dry plant material. In addition, 40 μg/mL of Marrubium vulgare aqueous fraction significantly decreased infarct size in comparison to control group. All doses considerably reduced the total ventricular ectopic beats during 30 min of ischaemia. The extract at dose of 40 μg/mL noticeably decreased the arrhythmias during the first 30 min of reperfusion.

Conclusions: The results of the study indicated aqueous fraction of Marrubium vulgare possesses a protective effect against I/R injuries in isolated rat hearts

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References

  1. Akhlaghi M, Bandy B. Mechanisms of flavonoid protection against myocardial ischemia-reperfusion injury. J Mol Cell Cardiol. 2009; 46(3): 309–317.
  2. Akther N, Shawl AS, Sultana S, et al. Hepatoprotective activity of Marrubium vulgare against paracetamol induced toxicity. J Pharm Res. 2013; 7(7): 565–570.
  3. Bell RM, Mocanu MM, Yellon DM. Retrograde heart perfusion: the Langendorff technique of isolated heart perfusion. J Mol Cell Cardiol. 2011; 50(6): 940–950.
  4. Berrougui H, Isabelle M, Cherki M, et al. Marrubium vulgare extract inhibits human-LDL oxidation and enhances HDL-mediated cholesterol efflux in THP-1 macrophage. Life Sci. 2006; 80(2): 105–112.
  5. Boudjelal A, Henchiri C, Siracusa L, et al. Compositional analysis and in vivo anti-diabetic activity of wild Algerian Marrubium vulgare L. infusion. Fitoterapia. 2012; 83(2): 286–292.
  6. Dong L, Fan Y, Shao Xu, et al. Vitexin protects against myocardial ischemia/reperfusion injury in Langendorff-perfused rat hearts by attenuating inflammatory response and apoptosis. Food Chem Toxicol. 2011; 49(12): 3211–3216.
  7. Du Yu, Lou H. Catechin and proanthocyanidin B4 from grape seeds prevent doxorubicin-induced toxicity in cardiomyocytes. Eur J Pharmacol. 2008; 591(1-3): 96–101.
  8. Fofie N, Kiendrebeogo M, Coulibaly K, et al. Mineral salt composition and secondary metabolites of ocimum gratissimum L., an anti-hyperglycemic plant. Nat Prod Chem Res. 2016; 4(5).
  9. Gu L, Kelm MA, Hammerstone JF, et al. Concentrations of proanthocyanidins in common foods and estimations of normal consumption. J Nutr. 2004; 134(3): 613–617.
  10. Hamedeyazdan S, Fathiazad F, Sharifi S, et al. Antiproliferative activity of Marrubium persicum extract in the MCF-7 human breast cancer cell line. Asian Pac J Cancer Prev. 2012; 13(11): 5843–5848.
  11. Hort MA, Straliotto MR, Duz MS, et al. Cardioprotective effects of a proanthocyanidin-rich fraction from Croton celtidifolius Baill: focus on atherosclerosis. Food Chem Toxicol. 2012; 50(10): 3769–3775.
  12. Hotta Y, Huang L, Muto T, et al. Positive inotropic effect of purified green tea catechin derivative in guinea pig hearts: the measurements of cellular Ca2+ and nitric oxide release. Eur J Pharmacol. 2006; 552(1-3): 123–130.
  13. Jing W, Chunhua Ma, Shumin W. Effects of acteoside on lipopolysaccharide-induced inflammation in acute lung injury via regulation of NF-κB pathway in vivo and in vitro. Toxicol Appl Pharmacol. 2015; 285(2): 128–135.
  14. Khanna D, Bhardwaj P. Green tea catechins: defensive role in cardiovascular disorders. Chin J Nat Med. 2013; 11(4): 345–353.
  15. Kim AS, Miller EJ, Wright TM, et al. A small molecule AMPK activator protects the heart against ischemia-reperfusion injury. J Mol Cell Cardiol. 2011; 51(1): 24–32.
  16. Korish AA, Arafah MM. Catechin combined with vitamins C and E ameliorates insulin resistance (IR) and atherosclerotic changes in aged rats with chronic renal failure (CRF). Arch Gerontol Geriatr. 2008; 46(1): 25–39.
  17. Kruger M, Davies N, Myburgh K, et al. Proanthocyanidins, anthocyanins and cardiovascular diseases. Food Res Int. 2014; 59: 41–52.
  18. Nazari A, Sadr SS, Faghihi M, et al. The cardioprotective effect of different doses of vasopressin (AVP) against ischemia-reperfusion injuries in the anesthetized rat heart. Peptides. 2011; 32(12): 2459–2466.
  19. Pukalskas A, Venskutonis P, Salido S, et al. Isolation, identification and activity of natural antioxidants from horehound (Marrubium vulgare L.) cultivated in Lithuania. Food Chem. 2012; 130(3): 695–701.
  20. Russell RR, Li Ji, Coven DL, et al. AMP-activated protein kinase mediates ischemic glucose uptake and prevents postischemic cardiac dysfunction, apoptosis, and injury. J Clin Invest. 2004; 114(4): 495–503.
  21. Sahpaz S, Garbacki N, Tits M, et al. Isolation and pharmacological activity of phenylpropanoid esters from Marrubium vulgare. J Ethnopharmacol. 2002; 79(3): 389–392.
  22. Schofield P, Mbugua DM, Pell AN. Analysis of condensed tannins: a review. Animal Feed Science and Technology. 2001; 91(1-2): 21–40.
  23. Sibelius U, Grandel U, Buerke M, et al. Staphylococcal -toxin provokes coronary vasoconstriction and loss in myocardial contractility in perfused rat hearts : role of thromboxane generation. Circulation. 2000; 101(1): 78–85.
  24. Srinivasan R, Chandrasekar MJN, Nanjan MJ, et al. Antioxidant activity of Caesalpinia digyna root. J Ethnopharmacol. 2007; 113(2): 284–291.
  25. Stulzer HK, Tagliari MP, Zampirolo JA, et al. Antioedematogenic effect of marrubiin obtained from Marrubium vulgare. J Ethnopharmacol. 2006; 108(3): 379–384.
  26. Wei Bo, Li WW, Ji J, et al. The cardioprotective effect of sodium tanshinone IIA sulfonate and the optimizing of therapeutic time window in myocardial ischemia/reperfusion injury in rats. Atherosclerosis. 2014; 235(2): 318–327.
  27. Yousefi K, Soraya H, Fathiazad F, et al. Cardioprotective effect of methanolic extract of Marrubium vulgare L. on isoproterenol-induced acute myocardial infarction in rats. Indian J Exp Biol. 2013; 51(8): 653–660.
  28. Zhao Y, Zhao B. Protective effect of natural antioxidants on heart against ischemia-reperfusion damage. Curr Pharm Biotechnol. 2010; 11(8): 868–874.
  29. Zheng J, Lee HC, Bin Sattar MM, et al. Cardioprotective effects of epigallocatechin-3-gallate against doxorubicin-induced cardiomyocyte injury. Eur J Pharmacol. 2011; 652(1-3): 82–88.