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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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 & clinical pharmacology & toxicology, 2010-09, Vol.107 (3), p.730-736</ispartof><rights>2010 The Authors. Basic & Clinical Pharmacology & Toxicology © 2010 Nordic Pharmacological Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4301-88ecf9ba771fcefc2c30f6e4e0e867dc16958f11d216d66f753218e0f59201d93</citedby><cites>FETCH-LOGICAL-c4301-88ecf9ba771fcefc2c30f6e4e0e867dc16958f11d216d66f753218e0f59201d93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1742-7843.2010.00571.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1742-7843.2010.00571.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23092200$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20353483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Çeribaşi, Ali Osman</creatorcontrib><creatorcontrib>Türk, Gaffari</creatorcontrib><creatorcontrib>Sönmez, Mustafa</creatorcontrib><creatorcontrib>Sakin, Fatih</creatorcontrib><creatorcontrib>Ateşşahin, Ahmet</creatorcontrib><title>Toxic Effect of Cyclophosphamide on Sperm Morphology, Testicular Histology and Blood Oxidant‐Antioxidant Balance, and Protective Roles of Lycopene and Ellagic Acid</title><title>Basic & clinical pharmacology & toxicology</title><addtitle>Basic Clin Pharmacol Toxicol</addtitle><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.</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 & clinical pharmacology & 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 & clinical pharmacology & 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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