Advanced glycation end products accumulate in the reproductive tract of men with diabetes
Summary Light microscopic studies comparing sperm parameters show little association between diabetes and male fertility. However, with the introduction of new analytical techniques, evidence is now emerging of previously undetectable effects of diabetes on sperm function. Specifically, a recent stu...
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Veröffentlicht in: | International journal of andrology 2009-08, Vol.32 (4), p.295-305 |
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creator | Mallidis, C. Agbaje, I. M. Rogers, D. A. Glenn, J. V. Pringle, R. Atkinson, A. B. Steger, K. Stitt, A. W. McClure, N. |
description | Summary
Light microscopic studies comparing sperm parameters show little association between diabetes and male fertility. However, with the introduction of new analytical techniques, evidence is now emerging of previously undetectable effects of diabetes on sperm function. Specifically, a recent study has found a significantly higher sperm nuclear DNA fragmentation in diabetic men. As advanced glycation end products (AGEs) are important instigators of oxidative stress and cell dysfunction in numerous diabetic complications, we hypothesized that these compounds could also be present in the male reproductive tract. The presence and localization of the most prominent AGE, carboxymethyl‐lysine (CML), in the human testis, epididymis and sperm was determined by immunohistochemistry. Parallel ELISA and Western blot analyses were performed to ascertain the amount of CML in seminal plasma and sperm from 13 diabetic and nine non‐diabetic subjects. CML immunoreactivity was found throughout the seminiferous epithelium, the nuclei of spermatogonia and spermatocytes, in the basal and principle cells cytoplasm and nuclei of the caput epididymis and on most sperm tails, mid pieces and all cytoplasmic droplets. The acrosomal cap, especially the equatorial band, was prominently stained in diabetic samples only. The amount of CML was significantly higher (p = 0.004) in sperm from non‐diabetic men. Considering the known detrimental actions of AGEs in other organs, the presence, location and quantity of CML, particularly the increased expression found in diabetic men, suggest that these compounds may play a hitherto unrecognized role in male infertility. |
doi_str_mv | 10.1111/j.1365-2605.2007.00849.x |
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Light microscopic studies comparing sperm parameters show little association between diabetes and male fertility. However, with the introduction of new analytical techniques, evidence is now emerging of previously undetectable effects of diabetes on sperm function. Specifically, a recent study has found a significantly higher sperm nuclear DNA fragmentation in diabetic men. As advanced glycation end products (AGEs) are important instigators of oxidative stress and cell dysfunction in numerous diabetic complications, we hypothesized that these compounds could also be present in the male reproductive tract. The presence and localization of the most prominent AGE, carboxymethyl‐lysine (CML), in the human testis, epididymis and sperm was determined by immunohistochemistry. Parallel ELISA and Western blot analyses were performed to ascertain the amount of CML in seminal plasma and sperm from 13 diabetic and nine non‐diabetic subjects. CML immunoreactivity was found throughout the seminiferous epithelium, the nuclei of spermatogonia and spermatocytes, in the basal and principle cells cytoplasm and nuclei of the caput epididymis and on most sperm tails, mid pieces and all cytoplasmic droplets. The acrosomal cap, especially the equatorial band, was prominently stained in diabetic samples only. The amount of CML was significantly higher (p = 0.004) in sperm from non‐diabetic men. Considering the known detrimental actions of AGEs in other organs, the presence, location and quantity of CML, particularly the increased expression found in diabetic men, suggest that these compounds may play a hitherto unrecognized role in male infertility.</description><identifier>ISSN: 0105-6263</identifier><identifier>EISSN: 1365-2605</identifier><identifier>DOI: 10.1111/j.1365-2605.2007.00849.x</identifier><identifier>PMID: 18217985</identifier><identifier>CODEN: IJANDP</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; AGEs ; Biological and medical sciences ; Blotting, Western ; Case-Control Studies ; diabetes ; Diabetes Complications - etiology ; Diabetes Complications - metabolism ; Diabetes Mellitus - metabolism ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Enzyme-Linked Immunosorbent Assay ; epididymis ; Epididymis - chemistry ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Fundamental and applied biological sciences. Psychology ; Glycation End Products, Advanced - analysis ; Gynecology. Andrology. Obstetrics ; Humans ; Immunohistochemistry ; Infertility, Male - etiology ; Infertility, Male - metabolism ; Lysine - analogs & derivatives ; Lysine - analysis ; Male ; Male genital diseases ; Mammalian male genital system ; Medical sciences ; Semen - chemistry ; spermatozoa ; Spermatozoa - chemistry ; testis ; Testis - chemistry ; Vertebrates: reproduction</subject><ispartof>International journal of andrology, 2009-08, Vol.32 (4), p.295-305</ispartof><rights>2008 The Authors. Journal compilation © 2008 European Academy of Andrology</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4859-f55a21f63ac9c67935b4c61ac6f255305072bb5ade2b8bb42b834e24040af62f3</citedby><cites>FETCH-LOGICAL-c4859-f55a21f63ac9c67935b4c61ac6f255305072bb5ade2b8bb42b834e24040af62f3</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.1365-2605.2007.00849.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2605.2007.00849.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21674255$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18217985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mallidis, C.</creatorcontrib><creatorcontrib>Agbaje, I. M.</creatorcontrib><creatorcontrib>Rogers, D. A.</creatorcontrib><creatorcontrib>Glenn, J. V.</creatorcontrib><creatorcontrib>Pringle, R.</creatorcontrib><creatorcontrib>Atkinson, A. B.</creatorcontrib><creatorcontrib>Steger, K.</creatorcontrib><creatorcontrib>Stitt, A. W.</creatorcontrib><creatorcontrib>McClure, N.</creatorcontrib><title>Advanced glycation end products accumulate in the reproductive tract of men with diabetes</title><title>International journal of andrology</title><addtitle>Int J Androl</addtitle><description>Summary
Light microscopic studies comparing sperm parameters show little association between diabetes and male fertility. However, with the introduction of new analytical techniques, evidence is now emerging of previously undetectable effects of diabetes on sperm function. Specifically, a recent study has found a significantly higher sperm nuclear DNA fragmentation in diabetic men. As advanced glycation end products (AGEs) are important instigators of oxidative stress and cell dysfunction in numerous diabetic complications, we hypothesized that these compounds could also be present in the male reproductive tract. The presence and localization of the most prominent AGE, carboxymethyl‐lysine (CML), in the human testis, epididymis and sperm was determined by immunohistochemistry. Parallel ELISA and Western blot analyses were performed to ascertain the amount of CML in seminal plasma and sperm from 13 diabetic and nine non‐diabetic subjects. CML immunoreactivity was found throughout the seminiferous epithelium, the nuclei of spermatogonia and spermatocytes, in the basal and principle cells cytoplasm and nuclei of the caput epididymis and on most sperm tails, mid pieces and all cytoplasmic droplets. The acrosomal cap, especially the equatorial band, was prominently stained in diabetic samples only. The amount of CML was significantly higher (p = 0.004) in sperm from non‐diabetic men. Considering the known detrimental actions of AGEs in other organs, the presence, location and quantity of CML, particularly the increased expression found in diabetic men, suggest that these compounds may play a hitherto unrecognized role in male infertility.</description><subject>Adult</subject><subject>AGEs</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Case-Control Studies</subject><subject>diabetes</subject><subject>Diabetes Complications - etiology</subject><subject>Diabetes Complications - metabolism</subject><subject>Diabetes Mellitus - metabolism</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>epididymis</subject><subject>Epididymis - chemistry</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycation End Products, Advanced - analysis</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Infertility, Male - etiology</subject><subject>Infertility, Male - metabolism</subject><subject>Lysine - analogs & derivatives</subject><subject>Lysine - analysis</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Mammalian male genital system</subject><subject>Medical sciences</subject><subject>Semen - chemistry</subject><subject>spermatozoa</subject><subject>Spermatozoa - chemistry</subject><subject>testis</subject><subject>Testis - chemistry</subject><subject>Vertebrates: reproduction</subject><issn>0105-6263</issn><issn>1365-2605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtv1DAURi0EosPAX0DewC7B7yQLFsMISquqsABRVpbj3FAPebS20878exwmGrZ4YVu657PvPQhhSnKa1rtdTrmSGVNE5oyQIiekFFW-f4JWp8JTtCKUyEwxxc_QixB2hBBecvocndGS0aIq5Qr93DQPZrDQ4F_dwZroxgHD0OA7PzaTjQEba6d-6kwE7AYcbwF7WIruAXD0xkY8triHAT-6eIsbZ2qIEF6iZ63pArxazjX6_unjt-3n7OrL-cV2c5VZUcoqa6U0jLaKG1tZVVRc1sIqaqxqmZScSFKwupamAVaXdS3SzgUwQQQxrWItX6O3x3dTV_cThKh7Fyx0nRlgnIJWhSRE8CKB5RG0fgzBQ6vvvOuNP2hK9KxV7_RsT8_29KxV_9Wq9yn6evljqnto_gUXjwl4swAmWNO1Pjl14cQxqgoxj7NG74_co-vg8N8N6IvLzXW6pXx2zLsQYX_KG_87zckLqX9cn-sPW17eXN581RX_A9nnoq0</recordid><startdate>200908</startdate><enddate>200908</enddate><creator>Mallidis, C.</creator><creator>Agbaje, I. M.</creator><creator>Rogers, D. A.</creator><creator>Glenn, J. V.</creator><creator>Pringle, R.</creator><creator>Atkinson, A. B.</creator><creator>Steger, K.</creator><creator>Stitt, A. W.</creator><creator>McClure, N.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>200908</creationdate><title>Advanced glycation end products accumulate in the reproductive tract of men with diabetes</title><author>Mallidis, C. ; Agbaje, I. M. ; Rogers, D. A. ; Glenn, J. V. ; Pringle, R. ; Atkinson, A. B. ; Steger, K. ; Stitt, A. W. ; McClure, N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4859-f55a21f63ac9c67935b4c61ac6f255305072bb5ade2b8bb42b834e24040af62f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>AGEs</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Case-Control Studies</topic><topic>diabetes</topic><topic>Diabetes Complications - etiology</topic><topic>Diabetes Complications - metabolism</topic><topic>Diabetes Mellitus - metabolism</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>epididymis</topic><topic>Epididymis - chemistry</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycation End Products, Advanced - analysis</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Infertility, Male - etiology</topic><topic>Infertility, Male - metabolism</topic><topic>Lysine - analogs & derivatives</topic><topic>Lysine - analysis</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Mammalian male genital system</topic><topic>Medical sciences</topic><topic>Semen - chemistry</topic><topic>spermatozoa</topic><topic>Spermatozoa - chemistry</topic><topic>testis</topic><topic>Testis - chemistry</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mallidis, C.</creatorcontrib><creatorcontrib>Agbaje, I. M.</creatorcontrib><creatorcontrib>Rogers, D. A.</creatorcontrib><creatorcontrib>Glenn, J. V.</creatorcontrib><creatorcontrib>Pringle, R.</creatorcontrib><creatorcontrib>Atkinson, A. B.</creatorcontrib><creatorcontrib>Steger, K.</creatorcontrib><creatorcontrib>Stitt, A. W.</creatorcontrib><creatorcontrib>McClure, N.</creatorcontrib><collection>Istex</collection><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>MEDLINE - Academic</collection><jtitle>International journal of andrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mallidis, C.</au><au>Agbaje, I. M.</au><au>Rogers, D. A.</au><au>Glenn, J. V.</au><au>Pringle, R.</au><au>Atkinson, A. B.</au><au>Steger, K.</au><au>Stitt, A. W.</au><au>McClure, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Advanced glycation end products accumulate in the reproductive tract of men with diabetes</atitle><jtitle>International journal of andrology</jtitle><addtitle>Int J Androl</addtitle><date>2009-08</date><risdate>2009</risdate><volume>32</volume><issue>4</issue><spage>295</spage><epage>305</epage><pages>295-305</pages><issn>0105-6263</issn><eissn>1365-2605</eissn><coden>IJANDP</coden><abstract>Summary
Light microscopic studies comparing sperm parameters show little association between diabetes and male fertility. However, with the introduction of new analytical techniques, evidence is now emerging of previously undetectable effects of diabetes on sperm function. Specifically, a recent study has found a significantly higher sperm nuclear DNA fragmentation in diabetic men. As advanced glycation end products (AGEs) are important instigators of oxidative stress and cell dysfunction in numerous diabetic complications, we hypothesized that these compounds could also be present in the male reproductive tract. The presence and localization of the most prominent AGE, carboxymethyl‐lysine (CML), in the human testis, epididymis and sperm was determined by immunohistochemistry. Parallel ELISA and Western blot analyses were performed to ascertain the amount of CML in seminal plasma and sperm from 13 diabetic and nine non‐diabetic subjects. CML immunoreactivity was found throughout the seminiferous epithelium, the nuclei of spermatogonia and spermatocytes, in the basal and principle cells cytoplasm and nuclei of the caput epididymis and on most sperm tails, mid pieces and all cytoplasmic droplets. The acrosomal cap, especially the equatorial band, was prominently stained in diabetic samples only. The amount of CML was significantly higher (p = 0.004) in sperm from non‐diabetic men. Considering the known detrimental actions of AGEs in other organs, the presence, location and quantity of CML, particularly the increased expression found in diabetic men, suggest that these compounds may play a hitherto unrecognized role in male infertility.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18217985</pmid><doi>10.1111/j.1365-2605.2007.00849.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult AGEs Biological and medical sciences Blotting, Western Case-Control Studies diabetes Diabetes Complications - etiology Diabetes Complications - metabolism Diabetes Mellitus - metabolism Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Enzyme-Linked Immunosorbent Assay epididymis Epididymis - chemistry Etiopathogenesis. Screening. Investigations. Target tissue resistance Fundamental and applied biological sciences. Psychology Glycation End Products, Advanced - analysis Gynecology. Andrology. Obstetrics Humans Immunohistochemistry Infertility, Male - etiology Infertility, Male - metabolism Lysine - analogs & derivatives Lysine - analysis Male Male genital diseases Mammalian male genital system Medical sciences Semen - chemistry spermatozoa Spermatozoa - chemistry testis Testis - chemistry Vertebrates: reproduction |
title | Advanced glycation end products accumulate in the reproductive tract of men with diabetes |
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