Affiliation:
1. Captain Srinivasa Murthy Central Ayurveda Research Institute, Central Council for Research in Ayurvedic Sciences (CCRAS), Arumbakkam, Chennai, Tamil Nadu, India
2. Regional Ayurveda Research Institute, CCRAS, Pune, Maharashtra, India
3. National Ayurveda Research Institute for Panchakarma, Cheruthuruthy, Kerala, India
Abstract
Abstract
BACKGROUND:
Ayurvedic medicine provides fundamental knowledge of the concepts and components involved in traditional medicine. Hridayarnava Rasa (H. Rasa) is an Ayurvedic formulation, composed of herbal constituents and metallo-mineral ingredients. Individual components of H. Rasa were reported to treat various ailments; however, very few evidence-based studies on the formulation were available in other aspects of H. Rasa. The present study was focused on the evidence-based assessment of the test of H. Rasa in experimentally induced atherosclerotic cardiovascular disease (ASCVD).
METHODS:
A total of 24 male New Zealand rabbits were randomly distributed into six groups of four rabbits each. Group I rabbits were fed with a standard pellet diet; group II was induced with ASCVD; groups III, IV, and V were induced with ASCVD plus different doses of H. Rasa, and group VI was induced with ASCVD plus atorvastatin supplementation.
RESULTS:
Plasma lactate dehydrogenase, creatine kinase, aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase, γ-glutamyltransferase, total cholesterol, triglycerides, low-density lipoprotein cholesterol (LDLc), very LDLc, AST:ALT ratio, hydroxy-3-methyl glutaryl coenzyme reductase activity, collagen, and elastin were significantly increased, whereas high-density lipoprotein cholesterol levels were significantly decreased in ASCVD induced group. This was supported by CD68 levels of the aorta by immunohistochemistry. Changes were reversed in H. Rasa-treated groups of different doses of the drug.
CONCLUSION:
These results suggest that a high-fat diet accelerates the development of ASCVD in a time-dependent manner, and H. Rasa protects the aorta by maintaining the lipids, lipoproteins, and marker enzymes in a dose-dependent manner similar to atorvastatin.