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- Publisher Website: 10.1016/S0015-0282(99)00637-8
- Scopus: eid_2-s2.0-0034069417
- PMID: 10731525
- WOS: WOS:000086043700003
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Article: Effects of human follicular fluid on the capacitation and motility of human spermatozoa
Title | Effects of human follicular fluid on the capacitation and motility of human spermatozoa |
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Authors | |
Keywords | Acrosome reaction Capacitation Human follicular fluid Motility Spermatozoa |
Issue Date | 2000 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/fertnstert |
Citation | Fertility And Sterility, 2000, v. 73 n. 4, p. 680-686 How to Cite? |
Abstract | Objective: To investigate the capacitation and motility kinetics of spermatozoa treated with human follicular fluid (FF). Design: Controlled, experimental laboratory study.Setting: University-based gynecology unit. Patient(s): Human FF was collected from women undergoing assisted reproductive treatment. Semen samples were obtained from men visiting subfertility clinics. Intervention(s): Spermatozoa were incubated with human FF under various experimental conditions. Spermatozoa incubated with Earle's balanced salt solution were used as the control. Main Outcome Measure(s): Chlortetracycline staining patterns and sperm motility parameters. Result(s): The rate of capacitation in the human FF-treated spermatozoa was significantly higher than that in the control spermatozoa after 1 hour and 3 hours of treatment. The percentage of acrosome-reacted spermatozoa also was significantly higher after human FF treatment than after control treatment. These effects of human FF were dose-dependent. Human FF-treated spermatozoa maintained their velocities at the zero-hour level for 5 hours, whereas the velocities of the control spermatozoa decreased significantly after 1 hour. Human FF treatment significantly increased the beat cross-frequency above the rate at zero hour for 5 hours. The hyperactivation of the human FF-treated spermatozoa remained stable for 3 hours, whereas that of the control spermatozoa decreased significantly after 1 hour of incubation. Significantly more human FF-treated spermatozoa underwent hyperactivation than did control spermatozoa after 1 hour and 3 hours of treatment. The effects of human FF on beat cross-frequency and hyperactivation were dose-dependent. Conclusion(s): Human FF promotes capacitation and the acrosome reaction within a short period. It also stimulates or maintains various sperm motility parameters. Copyright (C) 2000 American Society for Reproductive Medicine. |
Persistent Identifier | http://hdl.handle.net/10722/87051 |
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 1.858 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Yao, YQ | en_HK |
dc.contributor.author | Ho, PC | en_HK |
dc.contributor.author | Yeung, WSB | en_HK |
dc.date.accessioned | 2010-09-06T09:24:41Z | - |
dc.date.available | 2010-09-06T09:24:41Z | - |
dc.date.issued | 2000 | en_HK |
dc.identifier.citation | Fertility And Sterility, 2000, v. 73 n. 4, p. 680-686 | en_HK |
dc.identifier.issn | 0015-0282 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/87051 | - |
dc.description.abstract | Objective: To investigate the capacitation and motility kinetics of spermatozoa treated with human follicular fluid (FF). Design: Controlled, experimental laboratory study.Setting: University-based gynecology unit. Patient(s): Human FF was collected from women undergoing assisted reproductive treatment. Semen samples were obtained from men visiting subfertility clinics. Intervention(s): Spermatozoa were incubated with human FF under various experimental conditions. Spermatozoa incubated with Earle's balanced salt solution were used as the control. Main Outcome Measure(s): Chlortetracycline staining patterns and sperm motility parameters. Result(s): The rate of capacitation in the human FF-treated spermatozoa was significantly higher than that in the control spermatozoa after 1 hour and 3 hours of treatment. The percentage of acrosome-reacted spermatozoa also was significantly higher after human FF treatment than after control treatment. These effects of human FF were dose-dependent. Human FF-treated spermatozoa maintained their velocities at the zero-hour level for 5 hours, whereas the velocities of the control spermatozoa decreased significantly after 1 hour. Human FF treatment significantly increased the beat cross-frequency above the rate at zero hour for 5 hours. The hyperactivation of the human FF-treated spermatozoa remained stable for 3 hours, whereas that of the control spermatozoa decreased significantly after 1 hour of incubation. Significantly more human FF-treated spermatozoa underwent hyperactivation than did control spermatozoa after 1 hour and 3 hours of treatment. The effects of human FF on beat cross-frequency and hyperactivation were dose-dependent. Conclusion(s): Human FF promotes capacitation and the acrosome reaction within a short period. It also stimulates or maintains various sperm motility parameters. Copyright (C) 2000 American Society for Reproductive Medicine. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/fertnstert | en_HK |
dc.relation.ispartof | Fertility and Sterility | en_HK |
dc.rights | Fertility and Sterility. Copyright © Elsevier Inc. | en_HK |
dc.subject | Acrosome reaction | en_HK |
dc.subject | Capacitation | en_HK |
dc.subject | Human follicular fluid | en_HK |
dc.subject | Motility | en_HK |
dc.subject | Spermatozoa | en_HK |
dc.title | Effects of human follicular fluid on the capacitation and motility of human spermatozoa | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0015-0282&volume=73&issue=4&spage=680&epage=686&date=2000&atitle=Effects+of+human+follicular+fluid+on+the+capacitation+and+motility+of+human+spermatozoa | en_HK |
dc.identifier.email | Ho, PC:pcho@hku.hk | en_HK |
dc.identifier.email | Yeung, WSB:wsbyeung@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ho, PC=rp00325 | en_HK |
dc.identifier.authority | Yeung, WSB=rp00331 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/S0015-0282(99)00637-8 | en_HK |
dc.identifier.pmid | 10731525 | en_HK |
dc.identifier.scopus | eid_2-s2.0-0034069417 | en_HK |
dc.identifier.hkuros | 49685 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034069417&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 73 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 680 | en_HK |
dc.identifier.epage | 686 | en_HK |
dc.identifier.isi | WOS:000086043700003 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yao, YQ=7403567431 | en_HK |
dc.identifier.scopusauthorid | Ho, PC=7402211440 | en_HK |
dc.identifier.scopusauthorid | Yeung, WSB=7102370745 | en_HK |
dc.identifier.issnl | 0015-0282 | - |