Effect of rutin on diabetic‐induced erectile dysfunction: Possible involvement of testicular biomarkers in male rats

The present study aimed to investigate effects of rutin on diabetic‐induced impairments of sexual behaviour, spermatogenesis and oxidative testicular damage. Diabetes was induced by a single injection of STZ (65 mg/kg) in male adult Wistar rats. Two weeks later, rutin (50 and 100 mg kg−1 day−1) was...

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Veröffentlicht in:Andrologia 2017-10, Vol.49 (8), p.e12737-n/a
Hauptverfasser: Al‐Roujeaie, A. S., Abuohashish, H. M., Ahmed, M. M., Alkhamees, O. A.
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container_issue 8
container_start_page e12737
container_title Andrologia
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creator Al‐Roujeaie, A. S.
Abuohashish, H. M.
Ahmed, M. M.
Alkhamees, O. A.
description The present study aimed to investigate effects of rutin on diabetic‐induced impairments of sexual behaviour, spermatogenesis and oxidative testicular damage. Diabetes was induced by a single injection of STZ (65 mg/kg) in male adult Wistar rats. Two weeks later, rutin (50 and 100 mg kg−1 day−1) was treated to normal and diabetic rats for 5 weeks. Sexual behaviour of the animals was observed by taking stimulus females. At the end of the study, sperm count, motility and viability were recorded. Serum levels of glucose, inflammatory markers and testosterone were also estimated. In penile tissue, cGMP levels were measured, while lipid peroxidation and antioxidant molecules and enzyme activities were determined. Finally, histopathological changes were evaluated in a cross‐section of testis. Diabetic‐induced alterations in male sexual behaviour and sperm count, motility and viability were markedly corrected following 5 weeks of rutin treatment to the diabetic animals. Rutin also attenuated the inhibited serum testosterone and penile cGMP content, while improved diabetic‐associated inflammation and testicular lipid peroxidation and oxidative stress. Histopathological evaluation revealed damaged testicular tissues in diabetic rats, which was protected following rutin treatment. In conclusion, treatment with rutin improved sexual functionality and also protects against diabetic‐induced testicular damage.
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S. ; Abuohashish, H. M. ; Ahmed, M. M. ; Alkhamees, O. A.</creator><creatorcontrib>Al‐Roujeaie, A. S. ; Abuohashish, H. M. ; Ahmed, M. M. ; Alkhamees, O. A.</creatorcontrib><description>The present study aimed to investigate effects of rutin on diabetic‐induced impairments of sexual behaviour, spermatogenesis and oxidative testicular damage. Diabetes was induced by a single injection of STZ (65 mg/kg) in male adult Wistar rats. Two weeks later, rutin (50 and 100 mg kg−1 day−1) was treated to normal and diabetic rats for 5 weeks. Sexual behaviour of the animals was observed by taking stimulus females. At the end of the study, sperm count, motility and viability were recorded. Serum levels of glucose, inflammatory markers and testosterone were also estimated. In penile tissue, cGMP levels were measured, while lipid peroxidation and antioxidant molecules and enzyme activities were determined. Finally, histopathological changes were evaluated in a cross‐section of testis. Diabetic‐induced alterations in male sexual behaviour and sperm count, motility and viability were markedly corrected following 5 weeks of rutin treatment to the diabetic animals. Rutin also attenuated the inhibited serum testosterone and penile cGMP content, while improved diabetic‐associated inflammation and testicular lipid peroxidation and oxidative stress. Histopathological evaluation revealed damaged testicular tissues in diabetic rats, which was protected following rutin treatment. 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S.</creatorcontrib><creatorcontrib>Abuohashish, H. M.</creatorcontrib><creatorcontrib>Ahmed, M. M.</creatorcontrib><creatorcontrib>Alkhamees, O. A.</creatorcontrib><title>Effect of rutin on diabetic‐induced erectile dysfunction: Possible involvement of testicular biomarkers in male rats</title><title>Andrologia</title><addtitle>Andrologia</addtitle><description>The present study aimed to investigate effects of rutin on diabetic‐induced impairments of sexual behaviour, spermatogenesis and oxidative testicular damage. Diabetes was induced by a single injection of STZ (65 mg/kg) in male adult Wistar rats. Two weeks later, rutin (50 and 100 mg kg−1 day−1) was treated to normal and diabetic rats for 5 weeks. Sexual behaviour of the animals was observed by taking stimulus females. At the end of the study, sperm count, motility and viability were recorded. Serum levels of glucose, inflammatory markers and testosterone were also estimated. In penile tissue, cGMP levels were measured, while lipid peroxidation and antioxidant molecules and enzyme activities were determined. Finally, histopathological changes were evaluated in a cross‐section of testis. Diabetic‐induced alterations in male sexual behaviour and sperm count, motility and viability were markedly corrected following 5 weeks of rutin treatment to the diabetic animals. Rutin also attenuated the inhibited serum testosterone and penile cGMP content, while improved diabetic‐associated inflammation and testicular lipid peroxidation and oxidative stress. Histopathological evaluation revealed damaged testicular tissues in diabetic rats, which was protected following rutin treatment. In conclusion, treatment with rutin improved sexual functionality and also protects against diabetic‐induced testicular damage.</description><subject>Androgens</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Antioxidants - therapeutic use</subject><subject>Cell Survival - drug effects</subject><subject>Cyclic GMP</subject><subject>Cyclic GMP - metabolism</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Experimental - complications</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Disease Models, Animal</subject><subject>Erectile dysfunction</subject><subject>Erectile Dysfunction - drug therapy</subject><subject>Erectile Dysfunction - etiology</subject><subject>Erectile Dysfunction - metabolism</subject><subject>Inflammation</subject><subject>Lipid peroxidation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Male</subject><subject>Motility</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Penis</subject><subject>Penis - drug effects</subject><subject>Penis - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rodents</subject><subject>Rutin</subject><subject>Rutin - pharmacology</subject><subject>Rutin - therapeutic use</subject><subject>Serum levels</subject><subject>Sexual behavior</subject><subject>Sexual Behavior, Animal - drug effects</subject><subject>Sperm</subject><subject>Sperm Count</subject><subject>Sperm Motility - drug effects</subject><subject>Spermatogenesis</subject><subject>Spermatozoa - drug effects</subject><subject>Spermatozoa - metabolism</subject><subject>streptozotocin</subject><subject>Testes</subject><subject>testicular damage</subject><subject>Testis - drug effects</subject><subject>Testis - metabolism</subject><subject>Testosterone</subject><subject>Testosterone - blood</subject><issn>0303-4569</issn><issn>1439-0272</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtOwzAQhi0EolXpggsgS6xYpLXjOE7ZVaU8pApYwDpykrHk0jrFToq64wickZMwfcCO2diyP_-e-Qg552zAsYbaVQMeK6GOSJcnYhSxWMXHpMsEE1Ei01GH9EOYM6xEKpUkp6QTK5XJTKRdsp4aA2VDa0N921hHa0crqwtobPn9-WVd1ZZQUfAI2QXQahNM63Bfu2v6XIdgCzy1bl0v1rAEt0tqIODzdqE9LWy91P4NfECILjXCXjfhjJwYvQjQP6w98no7fZncR7Onu4fJeBaVIstUFHMlpDasUCXPIEnBKEgqhVNJwQzHa54xXaRSgjE65SYFkEJpA5ynrBCiRy73uStfv7fYVj6vW-_wy5yPhIiliOMtdbWnSo8TeTD5yltse5Nzlm8l5yg530lG9uKQ2BZLqP7IX6UIDPfAB_ra_J-Ujx9v9pE__BqH7A</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Al‐Roujeaie, A. 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A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3887-21735af0b7c18e46ef7e4d7456530f1217180ab655effa61f6ee537afe1160b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Androgens</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Antioxidants - therapeutic use</topic><topic>Cell Survival - drug effects</topic><topic>Cyclic GMP</topic><topic>Cyclic GMP - metabolism</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus, Experimental - complications</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Disease Models, Animal</topic><topic>Erectile dysfunction</topic><topic>Erectile Dysfunction - drug therapy</topic><topic>Erectile Dysfunction - etiology</topic><topic>Erectile Dysfunction - metabolism</topic><topic>Inflammation</topic><topic>Lipid peroxidation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Male</topic><topic>Motility</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Penis</topic><topic>Penis - drug effects</topic><topic>Penis - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Rodents</topic><topic>Rutin</topic><topic>Rutin - pharmacology</topic><topic>Rutin - therapeutic use</topic><topic>Serum levels</topic><topic>Sexual behavior</topic><topic>Sexual Behavior, Animal - drug effects</topic><topic>Sperm</topic><topic>Sperm Count</topic><topic>Sperm Motility - drug effects</topic><topic>Spermatogenesis</topic><topic>Spermatozoa - drug effects</topic><topic>Spermatozoa - metabolism</topic><topic>streptozotocin</topic><topic>Testes</topic><topic>testicular damage</topic><topic>Testis - drug effects</topic><topic>Testis - metabolism</topic><topic>Testosterone</topic><topic>Testosterone - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Al‐Roujeaie, A. S.</creatorcontrib><creatorcontrib>Abuohashish, H. M.</creatorcontrib><creatorcontrib>Ahmed, M. M.</creatorcontrib><creatorcontrib>Alkhamees, O. A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>Andrologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al‐Roujeaie, A. S.</au><au>Abuohashish, H. M.</au><au>Ahmed, M. M.</au><au>Alkhamees, O. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of rutin on diabetic‐induced erectile dysfunction: Possible involvement of testicular biomarkers in male rats</atitle><jtitle>Andrologia</jtitle><addtitle>Andrologia</addtitle><date>2017-10</date><risdate>2017</risdate><volume>49</volume><issue>8</issue><spage>e12737</spage><epage>n/a</epage><pages>e12737-n/a</pages><issn>0303-4569</issn><eissn>1439-0272</eissn><abstract>The present study aimed to investigate effects of rutin on diabetic‐induced impairments of sexual behaviour, spermatogenesis and oxidative testicular damage. Diabetes was induced by a single injection of STZ (65 mg/kg) in male adult Wistar rats. Two weeks later, rutin (50 and 100 mg kg−1 day−1) was treated to normal and diabetic rats for 5 weeks. Sexual behaviour of the animals was observed by taking stimulus females. At the end of the study, sperm count, motility and viability were recorded. Serum levels of glucose, inflammatory markers and testosterone were also estimated. In penile tissue, cGMP levels were measured, while lipid peroxidation and antioxidant molecules and enzyme activities were determined. Finally, histopathological changes were evaluated in a cross‐section of testis. Diabetic‐induced alterations in male sexual behaviour and sperm count, motility and viability were markedly corrected following 5 weeks of rutin treatment to the diabetic animals. Rutin also attenuated the inhibited serum testosterone and penile cGMP content, while improved diabetic‐associated inflammation and testicular lipid peroxidation and oxidative stress. Histopathological evaluation revealed damaged testicular tissues in diabetic rats, which was protected following rutin treatment. In conclusion, treatment with rutin improved sexual functionality and also protects against diabetic‐induced testicular damage.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27785836</pmid><doi>10.1111/and.12737</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Androgens
Animals
Antioxidants
Antioxidants - pharmacology
Antioxidants - therapeutic use
Cell Survival - drug effects
Cyclic GMP
Cyclic GMP - metabolism
Diabetes
Diabetes mellitus
Diabetes Mellitus, Experimental - complications
Diabetes Mellitus, Experimental - metabolism
Disease Models, Animal
Erectile dysfunction
Erectile Dysfunction - drug therapy
Erectile Dysfunction - etiology
Erectile Dysfunction - metabolism
Inflammation
Lipid peroxidation
Lipid Peroxidation - drug effects
Male
Motility
Oxidative stress
Oxidative Stress - drug effects
Penis
Penis - drug effects
Penis - metabolism
Rats
Rats, Wistar
Rodents
Rutin
Rutin - pharmacology
Rutin - therapeutic use
Serum levels
Sexual behavior
Sexual Behavior, Animal - drug effects
Sperm
Sperm Count
Sperm Motility - drug effects
Spermatogenesis
Spermatozoa - drug effects
Spermatozoa - metabolism
streptozotocin
Testes
testicular damage
Testis - drug effects
Testis - metabolism
Testosterone
Testosterone - blood
title Effect of rutin on diabetic‐induced erectile dysfunction: Possible involvement of testicular biomarkers in male rats
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