Cardioprotective role of royal jelly in the prevention of celecoxib-mediated cardiotoxicity in adult male albino rats

• Published in: Journal of cardiothoracic surgery 2024-03, Vol.19 (1), p.135-135, Article 135
• Main Authors: Eleiwa, Naglaa Z H, Khalifa, Hesham A M I, Nazim, Heba A
• Format: Article
• Language: English
• Subjects: Albinism; Animals; Anti-inflammatory agents; Anti-inflammatory drugs; Antioxidants; Antioxidants - therapeutic use; Apoptosis; Arthritis; BAX gene; BAX protein; Bcl-2 protein; bcl-2-Associated X Protein - pharmacology; bcl-2-Associated X Protein - therapeutic use; Biomarkers; Cardiac; Cardiotoxicity; Cardiotoxicity - drug therapy; Cardiotoxicity - etiology; Cardiotoxicity - prevention & control; Celecoxib; Celecoxib - pharmacology; Celecoxib - therapeutic use; Chronic pain; COX-2 inhibitor; Creatine; Creatine kinase; Cyclooxygenase-2; Enzymes; Fatty Acids; FDA approval; Genes; Heart; Heart attacks; Humans; Inflammation; Kinases; L-Lactate dehydrogenase; Lactate; Lactate dehydrogenase; Male; Males; Nonsteroidal anti-inflammatory drugs; Oxidants; Oxidative Stress; Oxidizing agents; Rats; Royal Jelly; Serum; Serum levels; Superoxide; Superoxide dismutase; Toxicity; Variance analysis
• ISSN: 1749-8090; 1749-8090
• DOI: 10.1186/s13019-024-02593-2

Celecoxib, a cyclooxygenase-2 selective inhibitor non-steroidal anti-inflammatory drugs, is used for the management of short- and long-term pain as well as in other inflammatory conditions. Unfortunately, its chronic use is highly associated with serious abnormal cardiovascular events. The current study was designed to explore the effect of long-term administration of celecoxib on the cardiac tissues of male albino rats. The study also examined the alleged cardioprotective effect of royal jelly. Thirty, male albino rats were randomly divided into 3 equal groups; 10 each: (1) rats served as the control group and received no drug; (2) rats received celecoxib (50 mg/kg/day, orally), for 30 consecutive days; (3) rats received celecoxib (50 mg/kg/day, orally) plus royal jelly (300 mg/kg/day, orally) for 30 consecutive days. Sera were collected to assay cardiac enzymes and oxidant/antioxidant status. Rats were euthanatized and cardiac tissues were dissected for quantitative estimation of apoptotic genes (Bax) and anti-apoptotic gene (Bcl-2). Long-term celecoxib administration caused cardiotoxicity in male albino rats as manifested by significant elevation of serum levels of creatine phosphokinase (CPK), creatine kinase-MB (CK-MB), and lactate dehydrogenase (LDH), with ameliorative effects of royal jelly against celecoxib-induced cardiotoxicity as manifested by significantly decrease in serum CPK, CK-MB, and LDH levels. It also showed a significant decrease in the oxidative stress indicator malondialdehyde (MDA) levels and the bax gene. Additionally, it demonstrated significant increases in the bcl-2 gene and superoxide dismutase (SOD) levels, which contribute to its therapeutic effects against celecoxib-induced cardiotoxicity. Long-term celecoxib administration caused cardiotoxicity in male albino rats with protective effect of royal jelly being given together. It could be concluded that royal jelly may prove a useful adjunct in patients being prescribed celecoxib. Not applicable.