Toxic Effect of Cyclophosphamide on Sperm Morphology, Testicular Histology and Blood Oxidant‐Antioxidant Balance, and Protective Roles of Lycopene and Ellagic Acid

:  In this study, the toxic effect of cyclophosphamide (CP) on sperm morphology, testicular histology and blood oxidant–antioxidant balance, and protective roles of lycopene (LC) and ellagic acid (EA) were investigated. For this purpose, 48 healthy, adult, male Sprague‐Dawley rats were divided into...

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Veröffentlicht in:Basic & clinical pharmacology & toxicology 2010-09, Vol.107 (3), p.730-736
Hauptverfasser: Çeribaşi, Ali Osman, Türk, Gaffari, Sönmez, Mustafa, Sakin, Fatih, Ateşşahin, Ahmet
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Türk, Gaffari
Sönmez, Mustafa
Sakin, Fatih
Ateşşahin, Ahmet
description :  In this study, the toxic effect of cyclophosphamide (CP) on sperm morphology, testicular histology and blood oxidant–antioxidant balance, and protective roles of lycopene (LC) and ellagic acid (EA) were investigated. For this purpose, 48 healthy, adult, male Sprague‐Dawley rats were divided into six groups; eight animals in each group. The control group was treated with placebo. LC, EA and CP groups were given alone LC (10 mg/kg/every other day), EA (2 mg/kg/every other day) and CP (15 mg/kg/week) respectively. One of the last two groups received CP + LC, and the other treated with CP + EA. All treatments were maintained for 8 weeks. At the end of the treatment period, morphological abnormalities of sperm, plasma malondialdehyde (MDA) levels and glutathione (GSH) levels, and GSH‐peroxidase (GSH‐Px), catalase (CAT) and superoxide dismutase (SOD) activities in erythrocytes, and testicular histopathological changes were examined. CP administration caused statistically significant increases in tail and total abnormality of sperm, plasma MDA level and erythrocyte SOD activity, and decreases in erythtocyte CAT activity, diameters of seminiferous tubules, germinal cell layer thickness and Johnsen’s Testicular Score along with degeneration, necrosis, immature germ cells, congestion and atrophy in testicular tissue. However, LC or EA treatments to CP‐treated rats markedly improved the CP‐induced lipid peroxidation, and normalized sperm morphology and testicular histopathology. In conclusion, CP‐induced lipid peroxidation leads to the structural damages in spermatozoa and testicular tissue of rats, and also LC or EA have a protective effect on these types of damage.
doi_str_mv 10.1111/j.1742-7843.2010.00571.x
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For this purpose, 48 healthy, adult, male Sprague‐Dawley rats were divided into six groups; eight animals in each group. The control group was treated with placebo. LC, EA and CP groups were given alone LC (10 mg/kg/every other day), EA (2 mg/kg/every other day) and CP (15 mg/kg/week) respectively. One of the last two groups received CP + LC, and the other treated with CP + EA. All treatments were maintained for 8 weeks. At the end of the treatment period, morphological abnormalities of sperm, plasma malondialdehyde (MDA) levels and glutathione (GSH) levels, and GSH‐peroxidase (GSH‐Px), catalase (CAT) and superoxide dismutase (SOD) activities in erythrocytes, and testicular histopathological changes were examined. CP administration caused statistically significant increases in tail and total abnormality of sperm, plasma MDA level and erythrocyte SOD activity, and decreases in erythtocyte CAT activity, diameters of seminiferous tubules, germinal cell layer thickness and Johnsen’s Testicular Score along with degeneration, necrosis, immature germ cells, congestion and atrophy in testicular tissue. However, LC or EA treatments to CP‐treated rats markedly improved the CP‐induced lipid peroxidation, and normalized sperm morphology and testicular histopathology. In conclusion, CP‐induced lipid peroxidation leads to the structural damages in spermatozoa and testicular tissue of rats, and also LC or EA have a protective effect on these types of damage.</description><identifier>ISSN: 1742-7835</identifier><identifier>EISSN: 1742-7843</identifier><identifier>DOI: 10.1111/j.1742-7843.2010.00571.x</identifier><identifier>PMID: 20353483</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Antineoplastic Agents, Alkylating - toxicity ; Antioxidants - metabolism ; Atrophy ; Biological and medical sciences ; Blood ; Carotenoids - therapeutic use ; Catalase ; Catalase - metabolism ; Cyclophosphamide ; Cyclophosphamide - toxicity ; Degeneration ; ellagic acid ; Ellagic Acid - therapeutic use ; Erythrocytes ; Erythrocytes - metabolism ; Germ cells ; Glutathione ; Glutathione - blood ; Glutathione Peroxidase - metabolism ; Lipid peroxidation ; lycopene ; Male ; Malondialdehyde ; Malondialdehyde - blood ; Medical sciences ; Necrosis ; Oxidants - metabolism ; Pharmacology. Drug treatments ; Protective Agents - therapeutic use ; Rats ; Rats, Sprague-Dawley ; Seminiferous tubule ; Sperm ; Spermatozoa - drug effects ; Spermatozoa - pathology ; Statistical analysis ; Superoxide dismutase ; Superoxide Dismutase - metabolism ; Tails ; Testes ; Testis - drug effects ; Testis - pathology</subject><ispartof>Basic &amp; clinical pharmacology &amp; toxicology, 2010-09, Vol.107 (3), p.730-736</ispartof><rights>2010 The Authors. 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For this purpose, 48 healthy, adult, male Sprague‐Dawley rats were divided into six groups; eight animals in each group. The control group was treated with placebo. LC, EA and CP groups were given alone LC (10 mg/kg/every other day), EA (2 mg/kg/every other day) and CP (15 mg/kg/week) respectively. One of the last two groups received CP + LC, and the other treated with CP + EA. All treatments were maintained for 8 weeks. At the end of the treatment period, morphological abnormalities of sperm, plasma malondialdehyde (MDA) levels and glutathione (GSH) levels, and GSH‐peroxidase (GSH‐Px), catalase (CAT) and superoxide dismutase (SOD) activities in erythrocytes, and testicular histopathological changes were examined. CP administration caused statistically significant increases in tail and total abnormality of sperm, plasma MDA level and erythrocyte SOD activity, and decreases in erythtocyte CAT activity, diameters of seminiferous tubules, germinal cell layer thickness and Johnsen’s Testicular Score along with degeneration, necrosis, immature germ cells, congestion and atrophy in testicular tissue. However, LC or EA treatments to CP‐treated rats markedly improved the CP‐induced lipid peroxidation, and normalized sperm morphology and testicular histopathology. In conclusion, CP‐induced lipid peroxidation leads to the structural damages in spermatozoa and testicular tissue of rats, and also LC or EA have a protective effect on these types of damage.</description><subject>Animals</subject><subject>Antineoplastic Agents, Alkylating - toxicity</subject><subject>Antioxidants - metabolism</subject><subject>Atrophy</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Carotenoids - therapeutic use</subject><subject>Catalase</subject><subject>Catalase - metabolism</subject><subject>Cyclophosphamide</subject><subject>Cyclophosphamide - toxicity</subject><subject>Degeneration</subject><subject>ellagic acid</subject><subject>Ellagic Acid - therapeutic use</subject><subject>Erythrocytes</subject><subject>Erythrocytes - metabolism</subject><subject>Germ cells</subject><subject>Glutathione</subject><subject>Glutathione - blood</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Lipid peroxidation</subject><subject>lycopene</subject><subject>Male</subject><subject>Malondialdehyde</subject><subject>Malondialdehyde - blood</subject><subject>Medical sciences</subject><subject>Necrosis</subject><subject>Oxidants - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Protective Agents - therapeutic use</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Seminiferous tubule</subject><subject>Sperm</subject><subject>Spermatozoa - drug effects</subject><subject>Spermatozoa - pathology</subject><subject>Statistical analysis</subject><subject>Superoxide dismutase</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Tails</subject><subject>Testes</subject><subject>Testis - drug effects</subject><subject>Testis - pathology</subject><issn>1742-7835</issn><issn>1742-7843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc9uEzEQxi0EoqXwCsgXxKVJ7fX-8R44JFGglYJaQThbrj1uHXnXi72B7I1H4CV4MZ4EbxLCFV88Hv_G83k-hDAlU5rW1WZKqzybVDxn04ykLCFFRae7J-j8dPH0FLPiDL2IcUNIVuWUPEdnGWEFyzk7R7_WfmcVXhoDqsfe4MWgnO8efeweZWM1YN_izx2EBn_0IeWdfxgu8Rpib9XWyYCvbez3WSxbjefOe41vd1bLtv_94-es7a0_nPBcOtkquNyDd8H3qaX9BviTdxDH3qtB-Q5a2ANL5-RDkjZTVr9Ez4x0EV4d9wv05f1yvbierG4_3Cxmq4nKGaETzkGZ-l5WFTUKjMoUI6aEHAjwstKKlnXBDaU6o6UuS1MVLKMciCnqNEVdswv09vBuF_zXbfqjaGxUkJS04LdRVEXO66LmPJH8QKrgYwxgRBdsI8MgKBGjR2IjxvGL0QoxeiT2HoldKn19bLK9b0CfCv-akoA3R0BGJZ0JaWo2_uMYqbOMkMS9O3DfrYPhvwWI-eJunSL2B_Awr_g</recordid><startdate>201009</startdate><enddate>201009</enddate><creator>Çeribaşi, Ali Osman</creator><creator>Türk, Gaffari</creator><creator>Sönmez, Mustafa</creator><creator>Sakin, Fatih</creator><creator>Ateşşahin, Ahmet</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>201009</creationdate><title>Toxic Effect of Cyclophosphamide on Sperm Morphology, Testicular Histology and Blood Oxidant‐Antioxidant Balance, and Protective Roles of Lycopene and Ellagic Acid</title><author>Çeribaşi, Ali Osman ; Türk, Gaffari ; Sönmez, Mustafa ; Sakin, Fatih ; Ateşşahin, Ahmet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4301-88ecf9ba771fcefc2c30f6e4e0e867dc16958f11d216d66f753218e0f59201d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Alkylating - toxicity</topic><topic>Antioxidants - metabolism</topic><topic>Atrophy</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Carotenoids - therapeutic use</topic><topic>Catalase</topic><topic>Catalase - metabolism</topic><topic>Cyclophosphamide</topic><topic>Cyclophosphamide - toxicity</topic><topic>Degeneration</topic><topic>ellagic acid</topic><topic>Ellagic Acid - therapeutic use</topic><topic>Erythrocytes</topic><topic>Erythrocytes - metabolism</topic><topic>Germ cells</topic><topic>Glutathione</topic><topic>Glutathione - blood</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Lipid peroxidation</topic><topic>lycopene</topic><topic>Male</topic><topic>Malondialdehyde</topic><topic>Malondialdehyde - blood</topic><topic>Medical sciences</topic><topic>Necrosis</topic><topic>Oxidants - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Protective Agents - therapeutic use</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Seminiferous tubule</topic><topic>Sperm</topic><topic>Spermatozoa - drug effects</topic><topic>Spermatozoa - pathology</topic><topic>Statistical analysis</topic><topic>Superoxide dismutase</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Tails</topic><topic>Testes</topic><topic>Testis - drug effects</topic><topic>Testis - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Çeribaşi, Ali Osman</creatorcontrib><creatorcontrib>Türk, Gaffari</creatorcontrib><creatorcontrib>Sönmez, Mustafa</creatorcontrib><creatorcontrib>Sakin, Fatih</creatorcontrib><creatorcontrib>Ateşşahin, Ahmet</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Basic &amp; clinical pharmacology &amp; toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Çeribaşi, Ali Osman</au><au>Türk, Gaffari</au><au>Sönmez, Mustafa</au><au>Sakin, Fatih</au><au>Ateşşahin, Ahmet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxic Effect of Cyclophosphamide on Sperm Morphology, Testicular Histology and Blood Oxidant‐Antioxidant Balance, and Protective Roles of Lycopene and Ellagic Acid</atitle><jtitle>Basic &amp; clinical pharmacology &amp; toxicology</jtitle><addtitle>Basic Clin Pharmacol Toxicol</addtitle><date>2010-09</date><risdate>2010</risdate><volume>107</volume><issue>3</issue><spage>730</spage><epage>736</epage><pages>730-736</pages><issn>1742-7835</issn><eissn>1742-7843</eissn><abstract>:  In this study, the toxic effect of cyclophosphamide (CP) on sperm morphology, testicular histology and blood oxidant–antioxidant balance, and protective roles of lycopene (LC) and ellagic acid (EA) were investigated. For this purpose, 48 healthy, adult, male Sprague‐Dawley rats were divided into six groups; eight animals in each group. The control group was treated with placebo. LC, EA and CP groups were given alone LC (10 mg/kg/every other day), EA (2 mg/kg/every other day) and CP (15 mg/kg/week) respectively. One of the last two groups received CP + LC, and the other treated with CP + EA. All treatments were maintained for 8 weeks. At the end of the treatment period, morphological abnormalities of sperm, plasma malondialdehyde (MDA) levels and glutathione (GSH) levels, and GSH‐peroxidase (GSH‐Px), catalase (CAT) and superoxide dismutase (SOD) activities in erythrocytes, and testicular histopathological changes were examined. CP administration caused statistically significant increases in tail and total abnormality of sperm, plasma MDA level and erythrocyte SOD activity, and decreases in erythtocyte CAT activity, diameters of seminiferous tubules, germinal cell layer thickness and Johnsen’s Testicular Score along with degeneration, necrosis, immature germ cells, congestion and atrophy in testicular tissue. However, LC or EA treatments to CP‐treated rats markedly improved the CP‐induced lipid peroxidation, and normalized sperm morphology and testicular histopathology. In conclusion, CP‐induced lipid peroxidation leads to the structural damages in spermatozoa and testicular tissue of rats, and also LC or EA have a protective effect on these types of damage.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20353483</pmid><doi>10.1111/j.1742-7843.2010.00571.x</doi><tpages>7</tpages></addata></record>
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subjects Animals
Antineoplastic Agents, Alkylating - toxicity
Antioxidants - metabolism
Atrophy
Biological and medical sciences
Blood
Carotenoids - therapeutic use
Catalase
Catalase - metabolism
Cyclophosphamide
Cyclophosphamide - toxicity
Degeneration
ellagic acid
Ellagic Acid - therapeutic use
Erythrocytes
Erythrocytes - metabolism
Germ cells
Glutathione
Glutathione - blood
Glutathione Peroxidase - metabolism
Lipid peroxidation
lycopene
Male
Malondialdehyde
Malondialdehyde - blood
Medical sciences
Necrosis
Oxidants - metabolism
Pharmacology. Drug treatments
Protective Agents - therapeutic use
Rats
Rats, Sprague-Dawley
Seminiferous tubule
Sperm
Spermatozoa - drug effects
Spermatozoa - pathology
Statistical analysis
Superoxide dismutase
Superoxide Dismutase - metabolism
Tails
Testes
Testis - drug effects
Testis - pathology
title Toxic Effect of Cyclophosphamide on Sperm Morphology, Testicular Histology and Blood Oxidant‐Antioxidant Balance, and Protective Roles of Lycopene and Ellagic Acid
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