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Molecular basis for the effects of zinc deficiency on spermatogenesis: An experimental study in the Sprague-dawley rat model
Introduction: The objective of this study is to investigate the molecular mechanisms underlying the effects of zinc deficiency on spermatogenesis in the Sprague-Dawley (SD) rat. Materials and Methods: Three groups of eight adult male SD rats were maintained for 4 weeks on a normal diet as control, z...
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Published in: | Indian journal of urology 2015-01, Vol.31 (1), p.57-64 |
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container_title | Indian journal of urology |
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creator | Omu, Alexander Al-Azemi, Majedah Al-Maghrebi, May Mathew, Chacko Omu, Florence Kehinde, Elijah Anim, Jehoram Oriowo, Mabayoje Memon, Anjum |
description | Introduction: The objective of this study is to investigate the molecular mechanisms underlying the effects of zinc deficiency on spermatogenesis in the Sprague-Dawley (SD) rat.
Materials and Methods: Three groups of eight adult male SD rats were maintained for 4 weeks on a normal diet as control, zinc deficient diet and zinc deficient diet with zinc supplementation of 28 mg zinc/kg body weight respectively. Using standard techniques, the following parameters were compared between the three groups of experimental animals at the end of 4 weeks: (a) Serum zinc, magnesium (Mg), copper (Cu), selenium (Se) and cadmium (Cd), (b) serum sex hormones, malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GPX), (c) interleukin-4 (IL-4), tumor necrosis factor-alpha (TNF-α), Bcl-2, Bax and caspase-3 expression in the testes, (d) assessment of apoptosis of testicular cells using electron microscopy and (e) testicular volume and histology using the orchidometer and Johnsen score, respectively.
Results: The zinc deficient group showed a reduction of testicular volume, serum concentrations of Zn, Cu, Se, Mg, SOD, GPX, IL-4, Bcl-2 and testosterone (P < 0.05), as well as increased levels of serum Cd, MDA and tissue TNF-α, Bax, caspase-3 and apoptosis of the germ cells (P < 0.05) compared with control and zinc supplementation groups.
Conclusion: Zinc deficiency is associated with impaired spermatogenesis because of reduced testosterone production, increased oxidative stress and apoptosis. These findings suggest that zinc has a role in male reproduction. |
doi_str_mv | 10.4103/0970-1591.139570 |
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Materials and Methods: Three groups of eight adult male SD rats were maintained for 4 weeks on a normal diet as control, zinc deficient diet and zinc deficient diet with zinc supplementation of 28 mg zinc/kg body weight respectively. Using standard techniques, the following parameters were compared between the three groups of experimental animals at the end of 4 weeks: (a) Serum zinc, magnesium (Mg), copper (Cu), selenium (Se) and cadmium (Cd), (b) serum sex hormones, malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GPX), (c) interleukin-4 (IL-4), tumor necrosis factor-alpha (TNF-α), Bcl-2, Bax and caspase-3 expression in the testes, (d) assessment of apoptosis of testicular cells using electron microscopy and (e) testicular volume and histology using the orchidometer and Johnsen score, respectively.
Results: The zinc deficient group showed a reduction of testicular volume, serum concentrations of Zn, Cu, Se, Mg, SOD, GPX, IL-4, Bcl-2 and testosterone (P < 0.05), as well as increased levels of serum Cd, MDA and tissue TNF-α, Bax, caspase-3 and apoptosis of the germ cells (P < 0.05) compared with control and zinc supplementation groups.
Conclusion: Zinc deficiency is associated with impaired spermatogenesis because of reduced testosterone production, increased oxidative stress and apoptosis. These findings suggest that zinc has a role in male reproduction.</description><identifier>ISSN: 0970-1591</identifier><identifier>EISSN: 1998-3824</identifier><identifier>DOI: 10.4103/0970-1591.139570</identifier><identifier>PMID: 25624578</identifier><language>eng</language><publisher>India: Medknow Publications</publisher><subject>Animal research models ; Animal spermatogenesis ; Antioxidants ; Apoptosis ; Genetic aspects ; Kinases ; Original ; oxidative stress ; Physiological aspects ; Risk factors ; Rodents ; sex hormones ; spermatogenesis ; Studies ; Zinc ; Zinc deficiency diseases</subject><ispartof>Indian journal of urology, 2015-01, Vol.31 (1), p.57-64</ispartof><rights>COPYRIGHT 2015 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications & Media Pvt Ltd Jan-Mar 2015</rights><rights>Copyright: © Indian Journal of Urology 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c653a-93e2d0d66ad7dad79568e4ed494edfc839e07a6f89ed19fef6340272118439b83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1642669561/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1642669561?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4023,25752,27457,27922,27923,27924,37011,37012,44589,53790,53792,74997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25624578$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Omu, Alexander</creatorcontrib><creatorcontrib>Al-Azemi, Majedah</creatorcontrib><creatorcontrib>Al-Maghrebi, May</creatorcontrib><creatorcontrib>Mathew, Chacko</creatorcontrib><creatorcontrib>Omu, Florence</creatorcontrib><creatorcontrib>Kehinde, Elijah</creatorcontrib><creatorcontrib>Anim, Jehoram</creatorcontrib><creatorcontrib>Oriowo, Mabayoje</creatorcontrib><creatorcontrib>Memon, Anjum</creatorcontrib><title>Molecular basis for the effects of zinc deficiency on spermatogenesis: An experimental study in the Sprague-dawley rat model</title><title>Indian journal of urology</title><addtitle>Indian J Urol</addtitle><description>Introduction: The objective of this study is to investigate the molecular mechanisms underlying the effects of zinc deficiency on spermatogenesis in the Sprague-Dawley (SD) rat.
Materials and Methods: Three groups of eight adult male SD rats were maintained for 4 weeks on a normal diet as control, zinc deficient diet and zinc deficient diet with zinc supplementation of 28 mg zinc/kg body weight respectively. Using standard techniques, the following parameters were compared between the three groups of experimental animals at the end of 4 weeks: (a) Serum zinc, magnesium (Mg), copper (Cu), selenium (Se) and cadmium (Cd), (b) serum sex hormones, malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GPX), (c) interleukin-4 (IL-4), tumor necrosis factor-alpha (TNF-α), Bcl-2, Bax and caspase-3 expression in the testes, (d) assessment of apoptosis of testicular cells using electron microscopy and (e) testicular volume and histology using the orchidometer and Johnsen score, respectively.
Results: The zinc deficient group showed a reduction of testicular volume, serum concentrations of Zn, Cu, Se, Mg, SOD, GPX, IL-4, Bcl-2 and testosterone (P < 0.05), as well as increased levels of serum Cd, MDA and tissue TNF-α, Bax, caspase-3 and apoptosis of the germ cells (P < 0.05) compared with control and zinc supplementation groups.
Conclusion: Zinc deficiency is associated with impaired spermatogenesis because of reduced testosterone production, increased oxidative stress and apoptosis. These findings suggest that zinc has a role in male reproduction.</description><subject>Animal research models</subject><subject>Animal spermatogenesis</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Genetic aspects</subject><subject>Kinases</subject><subject>Original</subject><subject>oxidative stress</subject><subject>Physiological aspects</subject><subject>Risk factors</subject><subject>Rodents</subject><subject>sex hormones</subject><subject>spermatogenesis</subject><subject>Studies</subject><subject>Zinc</subject><subject>Zinc deficiency diseases</subject><issn>0970-1591</issn><issn>1998-3824</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt1v0zAUxSMEYmPwzhOyxAsvKf6KY_OAVE18TBriAXi2XPu6S5faxU5WivjjcdetrKiKEkvXv3NyfX2q6iXBE04we4tVi2vSKDIhTDUtflSdEqVkzSTlj6vT_fZJ9SznBcacSCqeVie0EZQ3rTyt_nyJPdixNwnNTO4y8jGh4QoQeA92yCh69LsLFjnwne0g2A2KAeUVpKUZ4hwCFNU7NA0IfpVit4QwmB7lYXQb1IVbr2-rZOYj1M6se9igZAa0jA7659UTb_oML-7Ws-rHxw_fzz_Xl18_XZxPL2srGmZqxYA67IQwrnXlVY2QwMFxVT7eSqYAt0Z4qcAR5cELxjFtKSGSMzWT7Ky62Pm6aBZ6VZo0aaOj6fRtIaa5NmnobA9aGjyjkraMeOCYSEmMFI4pZo3gXoni9X7ntRpnS3C2HDeZ_sD0cCd0V3oebzRnGDctLwZv7gxS_DlCHvSyyxb63gSIY9ZENJRTJXhT0Nf_oYs4plBGVShOhSiTIP-ouSkH6IKP5b92a6qnrHQsWqlooeoj1Pb-SpMxlNst5QN-coQvj4NlZ48K8E5gU8w5gd_PhGC9TavexlFv46h3aS2SVw9nuRfcx7MA0x2wjv0AKV_34xqSLux1iOsD4_qBsW5afZ9r9hc8lvkU</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Omu, Alexander</creator><creator>Al-Azemi, Majedah</creator><creator>Al-Maghrebi, May</creator><creator>Mathew, Chacko</creator><creator>Omu, Florence</creator><creator>Kehinde, Elijah</creator><creator>Anim, Jehoram</creator><creator>Oriowo, Mabayoje</creator><creator>Memon, Anjum</creator><general>Medknow Publications</general><general>Medknow Publications and Media Pvt. 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Al-Maghrebi, May ; Mathew, Chacko ; Omu, Florence ; Kehinde, Elijah ; Anim, Jehoram ; Oriowo, Mabayoje ; Memon, Anjum</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c653a-93e2d0d66ad7dad79568e4ed494edfc839e07a6f89ed19fef6340272118439b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animal research models</topic><topic>Animal spermatogenesis</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Genetic aspects</topic><topic>Kinases</topic><topic>Original</topic><topic>oxidative stress</topic><topic>Physiological aspects</topic><topic>Risk factors</topic><topic>Rodents</topic><topic>sex hormones</topic><topic>spermatogenesis</topic><topic>Studies</topic><topic>Zinc</topic><topic>Zinc deficiency diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Omu, Alexander</creatorcontrib><creatorcontrib>Al-Azemi, Majedah</creatorcontrib><creatorcontrib>Al-Maghrebi, May</creatorcontrib><creatorcontrib>Mathew, Chacko</creatorcontrib><creatorcontrib>Omu, Florence</creatorcontrib><creatorcontrib>Kehinde, Elijah</creatorcontrib><creatorcontrib>Anim, Jehoram</creatorcontrib><creatorcontrib>Oriowo, Mabayoje</creatorcontrib><creatorcontrib>Memon, Anjum</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Research Library China</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals (Open Access)</collection><jtitle>Indian journal of urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Omu, Alexander</au><au>Al-Azemi, Majedah</au><au>Al-Maghrebi, May</au><au>Mathew, Chacko</au><au>Omu, Florence</au><au>Kehinde, Elijah</au><au>Anim, Jehoram</au><au>Oriowo, Mabayoje</au><au>Memon, Anjum</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular basis for the effects of zinc deficiency on spermatogenesis: An experimental study in the Sprague-dawley rat model</atitle><jtitle>Indian journal of urology</jtitle><addtitle>Indian J Urol</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>31</volume><issue>1</issue><spage>57</spage><epage>64</epage><pages>57-64</pages><issn>0970-1591</issn><eissn>1998-3824</eissn><abstract>Introduction: The objective of this study is to investigate the molecular mechanisms underlying the effects of zinc deficiency on spermatogenesis in the Sprague-Dawley (SD) rat.
Materials and Methods: Three groups of eight adult male SD rats were maintained for 4 weeks on a normal diet as control, zinc deficient diet and zinc deficient diet with zinc supplementation of 28 mg zinc/kg body weight respectively. Using standard techniques, the following parameters were compared between the three groups of experimental animals at the end of 4 weeks: (a) Serum zinc, magnesium (Mg), copper (Cu), selenium (Se) and cadmium (Cd), (b) serum sex hormones, malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GPX), (c) interleukin-4 (IL-4), tumor necrosis factor-alpha (TNF-α), Bcl-2, Bax and caspase-3 expression in the testes, (d) assessment of apoptosis of testicular cells using electron microscopy and (e) testicular volume and histology using the orchidometer and Johnsen score, respectively.
Results: The zinc deficient group showed a reduction of testicular volume, serum concentrations of Zn, Cu, Se, Mg, SOD, GPX, IL-4, Bcl-2 and testosterone (P < 0.05), as well as increased levels of serum Cd, MDA and tissue TNF-α, Bax, caspase-3 and apoptosis of the germ cells (P < 0.05) compared with control and zinc supplementation groups.
Conclusion: Zinc deficiency is associated with impaired spermatogenesis because of reduced testosterone production, increased oxidative stress and apoptosis. These findings suggest that zinc has a role in male reproduction.</abstract><cop>India</cop><pub>Medknow Publications</pub><pmid>25624578</pmid><doi>10.4103/0970-1591.139570</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal research models Animal spermatogenesis Antioxidants Apoptosis Genetic aspects Kinases Original oxidative stress Physiological aspects Risk factors Rodents sex hormones spermatogenesis Studies Zinc Zinc deficiency diseases |
title | Molecular basis for the effects of zinc deficiency on spermatogenesis: An experimental study in the Sprague-dawley rat model |
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