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Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model

The present study was conducted to investigate whether caffeic acid phenethyl ester (CAPE), an active component of propolis extract, has a protective effect on amphotericin B induced nephrotoxicity in rat models. Male Wistar-Albino rats were randomly divided into four groups: (I) control group (n =...

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Autores principales: Altuntaş, Atila, Yılmaz, H. Ramazan, Altuntaş, Ayşegül, Uz, Efkan, Demir, Murat, Gökçimen, Alparslan, Aksu, Oğuzhan, Bayram, Dilek Şenol, Sezer, Mehmet Tuğrul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084592/
https://www.ncbi.nlm.nih.gov/pubmed/25032223
http://dx.doi.org/10.1155/2014/702981
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author Altuntaş, Atila
Yılmaz, H. Ramazan
Altuntaş, Ayşegül
Uz, Efkan
Demir, Murat
Gökçimen, Alparslan
Aksu, Oğuzhan
Bayram, Dilek Şenol
Sezer, Mehmet Tuğrul
author_facet Altuntaş, Atila
Yılmaz, H. Ramazan
Altuntaş, Ayşegül
Uz, Efkan
Demir, Murat
Gökçimen, Alparslan
Aksu, Oğuzhan
Bayram, Dilek Şenol
Sezer, Mehmet Tuğrul
author_sort Altuntaş, Atila
collection PubMed
description The present study was conducted to investigate whether caffeic acid phenethyl ester (CAPE), an active component of propolis extract, has a protective effect on amphotericin B induced nephrotoxicity in rat models. Male Wistar-Albino rats were randomly divided into four groups: (I) control group (n = 10), (II) CAPE group (n = 9) which received 10 μmol/kg CAPE intraperitoneally (i.p.), (III) amphotericin B group (n = 7) which received one dose of 50 mg/kg amphotericin B, and (IV) amphotericin B plus CAPE group (n = 7) which received 10 μmol/kg CAPE i.p. and one dose of 50 mg/kg amphotericin B. The left kidney was evaluated histopathologically for nephrotoxicity. Levels of malondialdehyde (MDA), nitric oxide (NO), enzyme activities including catalase (CAT), and superoxide dismutase (SOD) were measured in the right kidney. Histopathological damage was prominent in the amphotericin B group compared to controls, and the severity of damage was lowered by CAPE administration. The activity of SOD, MDA, and NO levels increased and catalase activity decreased in the amphotericin B group compared to the control group (P = 0.0001, P = 0.003, P = 0.0001, and P = 0.0001, resp.). Amphotericin B plus CAPE treatment caused a significant decrease in MDA, NO levels, and SOD activity (P = 0.04, P = 0.02, and P = 0.0001, resp.) and caused an increase in CAT activity compared with amphotericin B treatment alone (P = 0.005). CAPE treatment seems to be an effective adjuvant agent for the prevention of amphotericin B nephrotoxicity in rat models.
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spelling pubmed-40845922014-07-16 Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model Altuntaş, Atila Yılmaz, H. Ramazan Altuntaş, Ayşegül Uz, Efkan Demir, Murat Gökçimen, Alparslan Aksu, Oğuzhan Bayram, Dilek Şenol Sezer, Mehmet Tuğrul Biomed Res Int Research Article The present study was conducted to investigate whether caffeic acid phenethyl ester (CAPE), an active component of propolis extract, has a protective effect on amphotericin B induced nephrotoxicity in rat models. Male Wistar-Albino rats were randomly divided into four groups: (I) control group (n = 10), (II) CAPE group (n = 9) which received 10 μmol/kg CAPE intraperitoneally (i.p.), (III) amphotericin B group (n = 7) which received one dose of 50 mg/kg amphotericin B, and (IV) amphotericin B plus CAPE group (n = 7) which received 10 μmol/kg CAPE i.p. and one dose of 50 mg/kg amphotericin B. The left kidney was evaluated histopathologically for nephrotoxicity. Levels of malondialdehyde (MDA), nitric oxide (NO), enzyme activities including catalase (CAT), and superoxide dismutase (SOD) were measured in the right kidney. Histopathological damage was prominent in the amphotericin B group compared to controls, and the severity of damage was lowered by CAPE administration. The activity of SOD, MDA, and NO levels increased and catalase activity decreased in the amphotericin B group compared to the control group (P = 0.0001, P = 0.003, P = 0.0001, and P = 0.0001, resp.). Amphotericin B plus CAPE treatment caused a significant decrease in MDA, NO levels, and SOD activity (P = 0.04, P = 0.02, and P = 0.0001, resp.) and caused an increase in CAT activity compared with amphotericin B treatment alone (P = 0.005). CAPE treatment seems to be an effective adjuvant agent for the prevention of amphotericin B nephrotoxicity in rat models. Hindawi Publishing Corporation 2014 2014-06-16 /pmc/articles/PMC4084592/ /pubmed/25032223 http://dx.doi.org/10.1155/2014/702981 Text en Copyright © 2014 Atila Altuntaş et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Altuntaş, Atila
Yılmaz, H. Ramazan
Altuntaş, Ayşegül
Uz, Efkan
Demir, Murat
Gökçimen, Alparslan
Aksu, Oğuzhan
Bayram, Dilek Şenol
Sezer, Mehmet Tuğrul
Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model
title Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model
title_full Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model
title_fullStr Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model
title_full_unstemmed Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model
title_short Caffeic Acid Phenethyl Ester Protects against Amphotericin B Induced Nephrotoxicity in Rat Model
title_sort caffeic acid phenethyl ester protects against amphotericin b induced nephrotoxicity in rat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084592/
https://www.ncbi.nlm.nih.gov/pubmed/25032223
http://dx.doi.org/10.1155/2014/702981
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