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. 2022 Mar 18;21(2):1261-1270.
doi: 10.1007/s40200-022-01012-4. eCollection 2022 Dec.

Cardioprotective effect of Hrudroga Chintamani Rasa in isoproterenol induced cardiotoxicity in male Sprague Dawley rats

Affiliations

Cardioprotective effect of Hrudroga Chintamani Rasa in isoproterenol induced cardiotoxicity in male Sprague Dawley rats

Ankit P Laddha et al. J Diabetes Metab Disord. .

Erratum in

Abstract

Purpose: Ayurvedic system, a traditional medicinal system has mentioned a preparation Bruhat Vata Chintamani Rasa (Suvarnayukta) for management of heart diseases. Hrudroga Chintamani Rasa (HCR) is a formulation containing Bruhat Vata Chintamani Rasa and a few additional ingredients having beneficial effects in heart diseases. The present study was designed to investigate the cardioprotective activity of the Hrudroga Chintamani Rasa in isoproterenol (ISO)-induced myocardial infarction in rats.

Methods: Male Sprague Dawley rats were treated with HCR at a dose of 56.16 and 112.32 mg/kg for 30 days. Animals received ISO (85 mg/kg. s.c.) on 28th and 29th day at an interval of 24 h.

Result: Disease control animals treated with HCR at a dose of 56.16 mg/kg and 112.32 mg/kg to rats showed a significant reduction in elevated levels of aspartate aminotransferase (AST), lactate dehydrogenase (LDH), and creatine phosphokinase MB (CK-MB), and prevented loss of depleted antioxidant enzymes from the cardiac tissue. ISO-altered electrocardiogram pattern and haemodynamic parameters were also brought about to normal by treatment with HCR. HCR treatment also improved the levels of 5' adenosine monophosphate-activated protein kinase (AMPK) and Silent information regulator 1 (SIRT1) which have potent role in antioxidant defence mechanism. Histopathological findings also showed HCR treatment prevented cardiac tissue from damage.

Conclusion: HCR treatment showed a significant cardioprotective effect in ISO-induced cardiotoxicity in rats probably because of the potent antioxidant activity.

Supplementary information: The online version contains supplementary material available at 10.1007/s40200-022-01012-4.

Keywords: Ayurvedic system; Cardio toxicity; Cardiovascular; Hrudroga Chintamani Rasa; Isoproterenol; Myocardial infarction.

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Conflict of interest statement

Conflict of interestThe author(s) declared the following potential conflict of interest with respect to the research, authorship, and/or publication of this article: One of the co-author is from Shree Dhootapapeshwar Limited, which has funded the study. The first and corresponding author declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Effect of HCR on systolic blood pressure, diastolic pressure and mean arterial blood pressure. All values are expressed as Mean ± S.E.M. (n = 6). **p < 0.01 and *p < 0.05 when compared with disease control. ###p < 0.001 compared with normal control
Fig. 2
Fig. 2
Effect of HCR on left ventricular end-diastolic pressure (LVEDP) and rate of ventricular contractility (+ dp/dt and –dp/dt). All values are expressed as Mean ± S.E.M. (n = 6). ***p < 0.001, **p < 0.01 and *p < 0.05 when compared with disease control. ###p < 0.001 compared with normal control
Fig. 3
Fig. 3
Effect of HCR on biochemical parameters. All values are expressed as Mean ± S.E.M. (n = 6). ***p < 0.001, **p < 0.01 and *p < 0.05 when compared with disease control. ###p < 0.001 compared with normal control
Fig. 4
Fig. 4
Effect of HCR on 5' adenosine monophosphate-activated protein kinase (AMPK) and Silent information regulator 1 (SIRT1) levels. All values are expressed as Mean ± S.E.M. (n = 6). *p < 0.05 when compared with disease control. ###p < 0.001 and ##p < 0.01 compared with normal control
Fig. 5
Fig. 5
Effect of HCR on cardiac troponin (cTn-I) level. All values are expressed as Mean ± S.E.M. (n = 6). *p < 0.05 when compared with disease control. ###p < 0.001 and ##p < 0.01 compared with normal control
Fig. 6
Fig. 6
Effect of HCR on cardiac histopathology (H& E Staining, 100X) N Tissue necrosis, D Degeneration, A Angiogenesis, L Lymphocytic infiltration, C Collagen cardiac muscle
Fig. 7
Fig. 7
Effect of HCR on cardiac histopathology (Masson-Trichrome Staining, 400X)

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References

    1. Prabhakaran D, Jeemon P, Roy A. Cardiovascular Diseases in India: Current Epidemiology and Future Directions. Circulation. Lippincott Williams and Wilkins. 2016;133:1605–20. Available from: 10.1161/CIRCULATIONAHA.114.008729 - PubMed
    1. Fan Y. Cardioprotective Effect of Rhapontigenin in Isoproterenol-Induced Myocardial Infarction in a Rat Model. Pharmacology. S. Karger AG. 2019;103:291–302. Available from: https://www.karger.com/Article/FullText/496800 - PubMed
    1. Burton KP, McCord JM, Ghai G. Myocardial alterations due to free-radical generation. Am J Physiol - Hear Circ Physiol. 1984;15. Available from: https://pubmed.ncbi.nlm.nih.gov/6331179/ - PubMed
    1. Rona G. Catecholamine cardiotoxicity. J Mol Cell Cardiol. 1985;291–306. Available from: https://pubmed.ncbi.nlm.nih.gov/3894676/ - PubMed
    1. Amalraj A, Gopi S. Medicinal properties of Terminalia arjuna (Roxb.) Wight & Arn.: A review. J Tradit Complement Med National Tai wan University. 2017;65–78. Available from: https://pubmed.ncbi.nlm.nih.gov/28053890/ - PMC - PubMed