Egyptian Journal of Basic and Clinical Pharmacology
Vol. 7 (2017), Issue 1, pp. 47-56
doi:10.11131/2017/101364
Pentoxifylline and Cilostazol Against Rat Heart Injuries Induced by Doxorubicin
Abstract
We investigated the possible protective effects of pentoxifylline (PTX) and cilostazol on doxorubicin (Dox)-induced cardiotoxicity in rats. Rats are randomly assigned into: saline, Dox (I.P. 2.5 mg/kg every other day six injections over two weeks), Dox (I.P. 2.5 mg/kg every other day six injections over two weeks then PTX (50 mg/kg/day/oral), Dox (I.P. 2.5 mg/kg) every other day six injections over two weeks then cilostazol (50 mg/kg/day/oral). After 21 days these animals were sacrificed and serum CK-MB and troponin I levels were determined. Malondialdehyde (MDA), superoxide dismutase (SOD), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and caspase-3 levels also were determined. Heart sections were examinedhistopathologically. Treatment with PTX and cilostazol decreased troponin I and CK-MB while increased SOD activity with decrements in MDA, IL-6, TNF-α, and caspase-3 levels with attenuation of the changes in cardiac histopathology. PTX and cilostazol exert protective effects against Dox-induced cardiotoxicity.
Egyptian Journal of Basic and Clinical Pharmacology
Vol. 7 (2017), Issue 1, pp. 47-56
doi:10.11131/2017/101364
Pentoxifylline and Cilostazol Against Rat Heart Injuries Induced by Doxorubicin
Abstract
We investigated the possible protective effects of pentoxifylline (PTX) and cilostazol on doxorubicin (Dox)-induced cardiotoxicity in rats. Rats are randomly assigned into: saline, Dox (I.P. 2.5 mg/kg every other day six injections over two weeks), Dox (I.P. 2.5 mg/kg every other day six injections over two weeks then PTX (50 mg/kg/day/oral), Dox (I.P. 2.5 mg/kg) every other day six injections over two weeks then cilostazol (50 mg/kg/day/oral). After 21 days these animals were sacrificed and serum CK-MB and troponin I levels were determined. Malondialdehyde (MDA), superoxide dismutase (SOD), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and caspase-3 levels also were determined. Heart sections were examinedhistopathologically. Treatment with PTX and cilostazol decreased troponin I and CK-MB while increased SOD activity with decrements in MDA, IL-6, TNF-α, and caspase-3 levels with attenuation of the changes in cardiac histopathology. PTX and cilostazol exert protective effects against Dox-induced cardiotoxicity.
Egyptian Journal of Basic and Clinical Pharmacology
Vol. 7 (2017), Issue 1, pp. 47-56
doi:10.11131/2017/101364
Pentoxifylline and Cilostazol Against Rat Heart Injuries Induced by Doxorubicin
How to Cite this Article
Noha A. T. Abbas and Soad L. Kabil, “Pentoxifylline and Cilostazol Against Rat Heart Injuries Induced by Doxorubicin,” Egyptian Journal of Basic and Clinical Pharmacology, Vol. 7, Issue 1, pp. 47-56, 2017. doi:10.11131/2017/101364