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Changes in the activity of sperm nitric oxide synthase in the oviductal reservoir during ovulation
Background: The oviductal isthmus is known to act as a sperm reservoir in several mammalian species including mice, but it is still unclear how sperm are released from the reservoir after ovulation. Recently, nitric oxide (NO) was reported to have important roles as a mediator in various sperm func...
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Published in: | Reproductive medicine and biology 2003-06, Vol.2 (2), p.75-81 |
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creator | Oh‐Oka, Tadasuke Saxena, Dinesh Kumar Tanii, Ichiro Yoshinaga, Kazuya Toshimori, Kiyotaka |
description | Background: The oviductal isthmus is known to act as a sperm reservoir in several mammalian species including mice, but it is still unclear how sperm are released from the reservoir after ovulation. Recently, nitric oxide (NO) was reported to have important roles as a mediator in various sperm functions, including hyperactivation and capacitation. Therefore, we have investigated the change of the activity of nitric oxide synthase (NOS) of sperm of the isthmus in relation to ovulation under in vivo fertilization conditions.
Methods and Results: The sperm were collected from the isthmus and uterus of the female mated before or after ovulation. The NOS activity change was evaluated by using the β‐nicotinamide adenine dinucleotide phosphate‐diaphorase staining method, and sperm NOS activity was quantified by using NIH image software. The results showed that, in the reservoir, the peak intensity of sperm NOS activity was higher after ovulation (135.5 ± 22.4) than before ovulation (102.7 ± 15.5; P ≤ 0.05). After ovulation, the number of free sperm in the isthmus increased, and these sperm expressed strong NOS activity.
Conclusion: The change of sperm NOS activity is related to their release from the epithelium of the oviductal reservoir. (Reprod Med Biol 2003; 2: 75–81) |
doi_str_mv | 10.1046/j.1445-5781.2003.00024.x |
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Methods and Results: The sperm were collected from the isthmus and uterus of the female mated before or after ovulation. The NOS activity change was evaluated by using the β‐nicotinamide adenine dinucleotide phosphate‐diaphorase staining method, and sperm NOS activity was quantified by using NIH image software. The results showed that, in the reservoir, the peak intensity of sperm NOS activity was higher after ovulation (135.5 ± 22.4) than before ovulation (102.7 ± 15.5; P ≤ 0.05). After ovulation, the number of free sperm in the isthmus increased, and these sperm expressed strong NOS activity.
Conclusion: The change of sperm NOS activity is related to their release from the epithelium of the oviductal reservoir. (Reprod Med Biol 2003; 2: 75–81)</description><identifier>ISSN: 1445-5781</identifier><identifier>EISSN: 1447-0578</identifier><identifier>DOI: 10.1046/j.1445-5781.2003.00024.x</identifier><identifier>PMID: 29699168</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Capacitation ; Epithelium ; Females ; Fertilization ; Infertility ; Localization ; Motility ; NADPH-diaphorase ; Nitric oxide ; Nitric-oxide synthase ; oviductal reservoir ; Ovulation ; Pathophysiology ; Physiology ; Sperm</subject><ispartof>Reproductive medicine and biology, 2003-06, Vol.2 (2), p.75-81</ispartof><rights>2003. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4144-4d1edc85fb3a2487ef45495f786b378935d69da0f2a415c71b5b073169c0fcc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3066202275/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3066202275?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1046%2Fj.1445-5781.2003.00024.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29699168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oh‐Oka, Tadasuke</creatorcontrib><creatorcontrib>Saxena, Dinesh Kumar</creatorcontrib><creatorcontrib>Tanii, Ichiro</creatorcontrib><creatorcontrib>Yoshinaga, Kazuya</creatorcontrib><creatorcontrib>Toshimori, Kiyotaka</creatorcontrib><title>Changes in the activity of sperm nitric oxide synthase in the oviductal reservoir during ovulation</title><title>Reproductive medicine and biology</title><addtitle>Reprod Med Biol</addtitle><description>Background: The oviductal isthmus is known to act as a sperm reservoir in several mammalian species including mice, but it is still unclear how sperm are released from the reservoir after ovulation. Recently, nitric oxide (NO) was reported to have important roles as a mediator in various sperm functions, including hyperactivation and capacitation. Therefore, we have investigated the change of the activity of nitric oxide synthase (NOS) of sperm of the isthmus in relation to ovulation under in vivo fertilization conditions.
Methods and Results: The sperm were collected from the isthmus and uterus of the female mated before or after ovulation. The NOS activity change was evaluated by using the β‐nicotinamide adenine dinucleotide phosphate‐diaphorase staining method, and sperm NOS activity was quantified by using NIH image software. The results showed that, in the reservoir, the peak intensity of sperm NOS activity was higher after ovulation (135.5 ± 22.4) than before ovulation (102.7 ± 15.5; P ≤ 0.05). After ovulation, the number of free sperm in the isthmus increased, and these sperm expressed strong NOS activity.
Conclusion: The change of sperm NOS activity is related to their release from the epithelium of the oviductal reservoir. (Reprod Med Biol 2003; 2: 75–81)</description><subject>Capacitation</subject><subject>Epithelium</subject><subject>Females</subject><subject>Fertilization</subject><subject>Infertility</subject><subject>Localization</subject><subject>Motility</subject><subject>NADPH-diaphorase</subject><subject>Nitric oxide</subject><subject>Nitric-oxide synthase</subject><subject>oviductal reservoir</subject><subject>Ovulation</subject><subject>Pathophysiology</subject><subject>Physiology</subject><subject>Sperm</subject><issn>1445-5781</issn><issn>1447-0578</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNkV2L1DAUhoso7rr6FyTgjTetJ98NiKCDX7AiiF6HNE1nMnSSMWnHmX9vurO7qFde5cD7nIcc3qpCGBoMTLzaNpgxXnPZ4oYA0AYACGuOD6rLEsgaSvLwZj5DF9WTnLcAWCpGHlcXRAmlsGgvq261MWHtMvIBTRuHjJ38wU8nFAeU9y7tUPBT8hbFo-8dyqcwbUx2d3g8-H62kxlRctmlQ_QJ9XPyYV2ieTSTj-Fp9WgwY3bPbt-r6seH999Xn-rrrx8_r95e15aVj9asx663LR86aghrpRsYZ4oPshUdla2ivBeqNzAQwzC3Ene8A0mxUBYGawW9qt6cvfu52xWVC1Myo94nvzPppKPx-u8k-I1ex4PmChhveRG8vBWk-HN2edI7n60bRxNcnLMmQAlVChQt6It_0G2cUyjnaQpCECBELsL2TNkUc05uuP8MBr0Uqbd66UgvHemlSH1TpD6W1ed_HnO_eNdcAV6fgV9-dKf_FutvX96Vgf4GpGutsw</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Oh‐Oka, Tadasuke</creator><creator>Saxena, Dinesh Kumar</creator><creator>Tanii, Ichiro</creator><creator>Yoshinaga, Kazuya</creator><creator>Toshimori, Kiyotaka</creator><general>Blackwell Publishing Ltd</general><general>John Wiley & Sons, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200306</creationdate><title>Changes in the activity of sperm nitric oxide synthase in the oviductal reservoir during ovulation</title><author>Oh‐Oka, Tadasuke ; Saxena, Dinesh Kumar ; Tanii, Ichiro ; Yoshinaga, Kazuya ; Toshimori, Kiyotaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4144-4d1edc85fb3a2487ef45495f786b378935d69da0f2a415c71b5b073169c0fcc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Capacitation</topic><topic>Epithelium</topic><topic>Females</topic><topic>Fertilization</topic><topic>Infertility</topic><topic>Localization</topic><topic>Motility</topic><topic>NADPH-diaphorase</topic><topic>Nitric oxide</topic><topic>Nitric-oxide synthase</topic><topic>oviductal reservoir</topic><topic>Ovulation</topic><topic>Pathophysiology</topic><topic>Physiology</topic><topic>Sperm</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oh‐Oka, Tadasuke</creatorcontrib><creatorcontrib>Saxena, Dinesh Kumar</creatorcontrib><creatorcontrib>Tanii, Ichiro</creatorcontrib><creatorcontrib>Yoshinaga, Kazuya</creatorcontrib><creatorcontrib>Toshimori, Kiyotaka</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest - Publicly Available Content Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Reproductive medicine and biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Oh‐Oka, Tadasuke</au><au>Saxena, Dinesh Kumar</au><au>Tanii, Ichiro</au><au>Yoshinaga, Kazuya</au><au>Toshimori, Kiyotaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in the activity of sperm nitric oxide synthase in the oviductal reservoir during ovulation</atitle><jtitle>Reproductive medicine and biology</jtitle><addtitle>Reprod Med Biol</addtitle><date>2003-06</date><risdate>2003</risdate><volume>2</volume><issue>2</issue><spage>75</spage><epage>81</epage><pages>75-81</pages><issn>1445-5781</issn><eissn>1447-0578</eissn><abstract>Background: The oviductal isthmus is known to act as a sperm reservoir in several mammalian species including mice, but it is still unclear how sperm are released from the reservoir after ovulation. Recently, nitric oxide (NO) was reported to have important roles as a mediator in various sperm functions, including hyperactivation and capacitation. Therefore, we have investigated the change of the activity of nitric oxide synthase (NOS) of sperm of the isthmus in relation to ovulation under in vivo fertilization conditions.
Methods and Results: The sperm were collected from the isthmus and uterus of the female mated before or after ovulation. The NOS activity change was evaluated by using the β‐nicotinamide adenine dinucleotide phosphate‐diaphorase staining method, and sperm NOS activity was quantified by using NIH image software. The results showed that, in the reservoir, the peak intensity of sperm NOS activity was higher after ovulation (135.5 ± 22.4) than before ovulation (102.7 ± 15.5; P ≤ 0.05). After ovulation, the number of free sperm in the isthmus increased, and these sperm expressed strong NOS activity.
Conclusion: The change of sperm NOS activity is related to their release from the epithelium of the oviductal reservoir. (Reprod Med Biol 2003; 2: 75–81)</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>29699168</pmid><doi>10.1046/j.1445-5781.2003.00024.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Capacitation Epithelium Females Fertilization Infertility Localization Motility NADPH-diaphorase Nitric oxide Nitric-oxide synthase oviductal reservoir Ovulation Pathophysiology Physiology Sperm |
title | Changes in the activity of sperm nitric oxide synthase in the oviductal reservoir during ovulation |
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