Caffeic acid phenethyl ester modulates methotrexate-induced oxidative stress in testes of rat

The aim of this study was to investigate the possible protective role of caffeic acid phenethyl ester on testicular toxicity of methotrexate in rats. Nineteen male rats were divided into three groups as follows: group I, control; group II, methotrexate-treated; group III, methotrexate + caffeic acid...

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Veröffentlicht in:Human & experimental toxicology 2008-07, Vol.27 (7), p.547-552
Hauptverfasser: Armagan, A, Uzar, E, Uz, E, Yilmaz, HR, Kutluhan, S, Koyuncuoglu, HR, Soyupek, S, Cam, H, Serel, TA
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container_end_page 552
container_issue 7
container_start_page 547
container_title Human & experimental toxicology
container_volume 27
creator Armagan, A
Uzar, E
Uz, E
Yilmaz, HR
Kutluhan, S
Koyuncuoglu, HR
Soyupek, S
Cam, H
Serel, TA
description The aim of this study was to investigate the possible protective role of caffeic acid phenethyl ester on testicular toxicity of methotrexate in rats. Nineteen male rats were divided into three groups as follows: group I, control; group II, methotrexate-treated; group III, methotrexate + caffeic acid phenethyl ester-treated. In the second day of experiment, a single dose of methotrexate was intraperitoneally administered to groups II and III, although a daily single dose of caffeic acid phenethyl ester was intraperitoneally administered to group III for 7 days. At the end of the experiment, the testes of the animals were removed and weighed. In the tissue, the level of lipid peroxidation as malondialdehyde and activities of superoxide dismutase were higher in the methotrexate group than in the control group. Lipid peroxidation levels and superoxide dismutase activities were decreased in caffeic acid phenethyl ester + methotrexate group compared with methotrexate group. The activities of catalase in the methotrexate group decreased insignificantly although its activities were significantly increased by caffeic acid phenethyl ester administration. The activity of glutathione peroxidase did not change in the groups. There was significant difference in body weight between control and methotrexate-induced groups. In conclusion, the administration of methotrexate causes elevation of oxidative stress although treatment with caffeic acid phenethyl ester has protective effects on the oxidative stress in testes.
doi_str_mv 10.1177/0960327108092293
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Nineteen male rats were divided into three groups as follows: group I, control; group II, methotrexate-treated; group III, methotrexate + caffeic acid phenethyl ester-treated. In the second day of experiment, a single dose of methotrexate was intraperitoneally administered to groups II and III, although a daily single dose of caffeic acid phenethyl ester was intraperitoneally administered to group III for 7 days. At the end of the experiment, the testes of the animals were removed and weighed. In the tissue, the level of lipid peroxidation as malondialdehyde and activities of superoxide dismutase were higher in the methotrexate group than in the control group. Lipid peroxidation levels and superoxide dismutase activities were decreased in caffeic acid phenethyl ester + methotrexate group compared with methotrexate group. The activities of catalase in the methotrexate group decreased insignificantly although its activities were significantly increased by caffeic acid phenethyl ester administration. The activity of glutathione peroxidase did not change in the groups. There was significant difference in body weight between control and methotrexate-induced groups. In conclusion, the administration of methotrexate causes elevation of oxidative stress although treatment with caffeic acid phenethyl ester has protective effects on the oxidative stress in testes.</description><identifier>ISSN: 0960-3271</identifier><identifier>EISSN: 1477-0903</identifier><identifier>DOI: 10.1177/0960327108092293</identifier><identifier>PMID: 18829730</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Antimetabolites, Antineoplastic - toxicity ; Antioxidants ; Biological and medical sciences ; Body Weight - drug effects ; Caffeic Acids - pharmacology ; Chemotherapy ; Cytotoxins - pharmacology ; Drug Antagonism ; Drug toxicity and drugs side effects treatment ; Enzymes ; Injections, Intraperitoneal ; Lipid Peroxidation - drug effects ; Male ; Males ; Malondialdehyde ; Medical sciences ; Methotrexate - toxicity ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Organ Size - drug effects ; Oxidation ; Oxidative Stress - drug effects ; Pharmacology. 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Nineteen male rats were divided into three groups as follows: group I, control; group II, methotrexate-treated; group III, methotrexate + caffeic acid phenethyl ester-treated. In the second day of experiment, a single dose of methotrexate was intraperitoneally administered to groups II and III, although a daily single dose of caffeic acid phenethyl ester was intraperitoneally administered to group III for 7 days. At the end of the experiment, the testes of the animals were removed and weighed. In the tissue, the level of lipid peroxidation as malondialdehyde and activities of superoxide dismutase were higher in the methotrexate group than in the control group. Lipid peroxidation levels and superoxide dismutase activities were decreased in caffeic acid phenethyl ester + methotrexate group compared with methotrexate group. The activities of catalase in the methotrexate group decreased insignificantly although its activities were significantly increased by caffeic acid phenethyl ester administration. The activity of glutathione peroxidase did not change in the groups. There was significant difference in body weight between control and methotrexate-induced groups. 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Nineteen male rats were divided into three groups as follows: group I, control; group II, methotrexate-treated; group III, methotrexate + caffeic acid phenethyl ester-treated. In the second day of experiment, a single dose of methotrexate was intraperitoneally administered to groups II and III, although a daily single dose of caffeic acid phenethyl ester was intraperitoneally administered to group III for 7 days. At the end of the experiment, the testes of the animals were removed and weighed. In the tissue, the level of lipid peroxidation as malondialdehyde and activities of superoxide dismutase were higher in the methotrexate group than in the control group. Lipid peroxidation levels and superoxide dismutase activities were decreased in caffeic acid phenethyl ester + methotrexate group compared with methotrexate group. The activities of catalase in the methotrexate group decreased insignificantly although its activities were significantly increased by caffeic acid phenethyl ester administration. The activity of glutathione peroxidase did not change in the groups. There was significant difference in body weight between control and methotrexate-induced groups. In conclusion, the administration of methotrexate causes elevation of oxidative stress although treatment with caffeic acid phenethyl ester has protective effects on the oxidative stress in testes.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>18829730</pmid><doi>10.1177/0960327108092293</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Antimetabolites, Antineoplastic - toxicity
Antioxidants
Biological and medical sciences
Body Weight - drug effects
Caffeic Acids - pharmacology
Chemotherapy
Cytotoxins - pharmacology
Drug Antagonism
Drug toxicity and drugs side effects treatment
Enzymes
Injections, Intraperitoneal
Lipid Peroxidation - drug effects
Male
Males
Malondialdehyde
Medical sciences
Methotrexate - toxicity
Miscellaneous (drug allergy, mutagens, teratogens...)
Organ Size - drug effects
Oxidation
Oxidative Stress - drug effects
Pharmacology. Drug treatments
Phenylethyl Alcohol - analogs & derivatives
Phenylethyl Alcohol - pharmacology
Rats
Rats, Wistar
Rodents
Side effects
Superoxide Dismutase - metabolism
Testis - drug effects
Testis - metabolism
Testis - pathology
Toxicology
Urogenital system
title Caffeic acid phenethyl ester modulates methotrexate-induced oxidative stress in testes of rat
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