Key result
Caffeic acid phenethyl ester significantly attenuated cisplatin-induced nephrotoxicity by reducing malondialdehyde levels from 1.84 to 1.30 nmol/mg (p=0.001) and decreasing inflammation.
Why the study?
Cisplatin is an antineoplastic chemotherapeutic that may induce nephrotoxicity, and this study aimed to determine the potential therapeutic effects of caffeic acid phenethyl ester in cisplatin-induced nephrotoxicity in rats.
Does caffeic acid phenethyl ester reduce cisplatin-induced nephrotoxicity in rats?
Does caffeic acid phenethyl ester reduce cisplatin-induced nephrotoxicity in rats?
Caffeic acid phenethyl ester (CAPE) ameliorates cisplatin-induced nephrotoxicity in rats by reducing oxidative stress and inflammation.
Answers are grounded in this paper and cite their sources.
May attenuate CP nephrotoxicity in rats; leaves open translation to human chemotherapy.
The aim of this study is to determine the potential therapeutic effects of CAPE in CP-induced nephrotoxicity in rats. Cisplatin (CP) is an antineoplastic chemotherapeutic used for treatment of many cancer types but its applications may induce nephrotoxicity. Caffeic acid phenethyl ester (CAPE) is an active component of propolis and it has several important physiological activities. Rats were divided into four groups: Control, CAPE (10 mol/kg/i.p), CP (7 mg/kg/i.p), and CP+CAPE (7 mg/kg/i.p, CP and 10 mol/kg/i.p, CAPE). After administrations, animals were sacrificed, and kidney tissues were extracted. Histopathological changes were evaluated and TNF- and IL-6 immunostaining were performed. Moreover, tissue SOD, CAT and MDA levels were measured by ELISA assay to assessment of oxidative stress and lipid peroxidation. CP group showed histopathological deterioration compared to the Control group and CAPE treatment attenuated this damage. When compared with Control and CAPE group, an increase in TNF- and IL-6 immunoreactivities and tissue MDA levels were observed in the CP group while a decrease in tissue SOD and CAT levels were detected. Furthermore, an improvement was observed in the CP+CAPE compared to the CP group. We suggest that CAPE can be used as a therapeutic agent to attenuate the toxic effects of cisplatin, thanks to its antioxidant and anti-inflammatory properties.
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Ceylan et al. (2021) studied Cisplatin-induced nephrotoxicity (n=38). Caffeic acid phenethyl ester (CAPE) vs. Cisplatin alone was evaluated on Kidney tissue malondialdehyde (MDA) levels (nmol/mg) (p=0.001). Caffeic acid phenethyl ester significantly attenuated cisplatin-induced nephrotoxicity by reducing malondialdehyde levels from 1.84 to 1.30 nmol/mg (p=0.001) and decreasing inflammation.
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