Limits...
Antioxidant, lipid lowering, and membrane stabilization effect of sesamol against doxorubicin-induced cardiomyopathy in experimental rats.

Chennuru A, Saleem MT - Biomed Res Int (2013)

Bottom Line: Sesamol has cardioprotective activity through normalization of doxorubicin-induced-altered biochemical parameters.Biochemical study was further supported by histopathological study, which shows that sesamol offered myocardial protection from necrotic damage.From these findings, it has been concluded that the sesamol has significant cardioprotection against doxorubicin induced cardiomyopathy via amelioration of oxidative stress, lipid lowering, and membrane stabilization effect.

View Article: PubMed Central - PubMed

Affiliation: Department of Pharmacology, Annamacharya College of Pharmacy, Rajampet, Andhrapradesh 516126, India.

ABSTRACT
The present study was designed to evaluate the cardioprotective effect of sesamol against doxorubicin-induced cardiomyopathy in rats. In this study, the cardioprotective effect of sesamol against doxorubicin induced cardiomyopathy in experimental rats was evaluated at the dosage of 50 mg/kg bw. Doxorubicin was administered to rats at a total cumulative dose of 15 mg/kg through intraperitoneal route for 2 weeks in six-divided dose on 8th, 10th, 14th, 16th, 18th, and 21st day. After the last dose administration, the endogenous antioxidants and lipid peroxidation were estimated in heart tissue homogenate. Cardiac biomarkers such as troponin T, LDH, CK, and AST and lipid profiles such as cholesterol, triglycerides, HDL, LDL, and VLDL were estimated in serum. Sesamol has cardioprotective activity through normalization of doxorubicin-induced-altered biochemical parameters. Biochemical study was further supported by histopathological study, which shows that sesamol offered myocardial protection from necrotic damage. From these findings, it has been concluded that the sesamol has significant cardioprotection against doxorubicin induced cardiomyopathy via amelioration of oxidative stress, lipid lowering, and membrane stabilization effect.

Show MeSH

Related in: MedlinePlus

Light microscopical analysis of heart tissue: (G1) heart of rat received saline, (G2) heart of rat received sesamol, (G3) heart of rat received DOX, and (G4) heart of rat received sesamol+DOX.
© Copyright Policy
Related In: Results  -  Collection

License
getmorefigures.php?uid=PMC3818820&req=5

fig2: Light microscopical analysis of heart tissue: (G1) heart of rat received saline, (G2) heart of rat received sesamol, (G3) heart of rat received DOX, and (G4) heart of rat received sesamol+DOX.

Mentions: Light microscopical section of heart tissue (Figure 2) of saline treated rat (G1) and sesamol treated rat (G2) show normal architecture of myocardium. Rats treated with DOX (G3) shows severe myocardial necrosis with subendocardial loss of muscles. Rats treated with sesamol+DOX show well-preserved myocardium when compared to DOX (G3) treated group.


Antioxidant, lipid lowering, and membrane stabilization effect of sesamol against doxorubicin-induced cardiomyopathy in experimental rats.

Chennuru A, Saleem MT - Biomed Res Int (2013)

Light microscopical analysis of heart tissue: (G1) heart of rat received saline, (G2) heart of rat received sesamol, (G3) heart of rat received DOX, and (G4) heart of rat received sesamol+DOX.
© Copyright Policy
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3818820&req=5

fig2: Light microscopical analysis of heart tissue: (G1) heart of rat received saline, (G2) heart of rat received sesamol, (G3) heart of rat received DOX, and (G4) heart of rat received sesamol+DOX.
Mentions: Light microscopical section of heart tissue (Figure 2) of saline treated rat (G1) and sesamol treated rat (G2) show normal architecture of myocardium. Rats treated with DOX (G3) shows severe myocardial necrosis with subendocardial loss of muscles. Rats treated with sesamol+DOX show well-preserved myocardium when compared to DOX (G3) treated group.

Bottom Line: Sesamol has cardioprotective activity through normalization of doxorubicin-induced-altered biochemical parameters.Biochemical study was further supported by histopathological study, which shows that sesamol offered myocardial protection from necrotic damage.From these findings, it has been concluded that the sesamol has significant cardioprotection against doxorubicin induced cardiomyopathy via amelioration of oxidative stress, lipid lowering, and membrane stabilization effect.

View Article: PubMed Central - PubMed

Affiliation: Department of Pharmacology, Annamacharya College of Pharmacy, Rajampet, Andhrapradesh 516126, India.

ABSTRACT
The present study was designed to evaluate the cardioprotective effect of sesamol against doxorubicin-induced cardiomyopathy in rats. In this study, the cardioprotective effect of sesamol against doxorubicin induced cardiomyopathy in experimental rats was evaluated at the dosage of 50 mg/kg bw. Doxorubicin was administered to rats at a total cumulative dose of 15 mg/kg through intraperitoneal route for 2 weeks in six-divided dose on 8th, 10th, 14th, 16th, 18th, and 21st day. After the last dose administration, the endogenous antioxidants and lipid peroxidation were estimated in heart tissue homogenate. Cardiac biomarkers such as troponin T, LDH, CK, and AST and lipid profiles such as cholesterol, triglycerides, HDL, LDL, and VLDL were estimated in serum. Sesamol has cardioprotective activity through normalization of doxorubicin-induced-altered biochemical parameters. Biochemical study was further supported by histopathological study, which shows that sesamol offered myocardial protection from necrotic damage. From these findings, it has been concluded that the sesamol has significant cardioprotection against doxorubicin induced cardiomyopathy via amelioration of oxidative stress, lipid lowering, and membrane stabilization effect.

Show MeSH
Related in: MedlinePlus