Sperm motility in fishes. I. Effects of temperature and pH: a review
Identifieur interne : 001578 ( Istex/Corpus ); précédent : 001577; suivant : 001579Sperm motility in fishes. I. Effects of temperature and pH: a review
Auteurs : Sayyed Mohammad Hadi Alavi ; Jacky CossonSource :
- Cell Biology International [ 1065-6995 ] ; 2005-02.
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Abstract
Sperm motility is a key factor in allowing us to determine semen quality and fertilizing capacity. Motility in semen is mainly controlled by K+ in salmonids, and probably also in sturgeons, and by osmotic pressure in other freshwater and seawater fish species, but other factors, such as concentration of surrounding metabolites and ions (Ca2+, Mg2+, etc.), pH and temperature also influence motility characteristics. In the present study, we have mainly reviewed and summarized the effects of temperature and pH on the motility of spermatozoa in three fish species: salmonids, cyprinids and sturgeons. Data in the literature show that motility, fertilizing ability and velocity of spermatozoa, as well as the duration of the motility period, depend on the temperature of the assay medium and also of that of the brood fish holding tank. In contrast, the pH of the swimming medium, and thus the intracellular pH of spermatozoa, has less influence on sperm motility parameters in cyprinids, salmonids and sturgeons.
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DOI: 10.1016/j.cellbi.2004.11.021
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Tel.: +33 493 763 790; fax: +33 493 763 792. <email normalForm="cosson@obs-vlfr.fr">cosson@obs‐vlfr.fr</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CBIN.CBIN1597.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received 17 November 2003; revised 15 October 2004; accepted 13 November 2004</unparsedEditorialHistory><countGroup><count type="referenceTotal" number="88"></count><count type="linksCrossRef" number="3"></count></countGroup><titleGroup><title type="main">Sperm motility in fishes. I. 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Motility in semen is mainly controlled by K<sup>+</sup> in salmonids, and probably also in sturgeons, and by osmotic pressure in other freshwater and seawater fish species, but other factors, such as concentration of surrounding metabolites and ions (Ca<sup>2+</sup>, Mg<sup>2+</sup>, etc.), pH and temperature also influence motility characteristics. In the present study, we have mainly reviewed and summarized the effects of temperature and pH on the motility of spermatozoa in three fish species: salmonids, cyprinids and sturgeons. Data in the literature show that motility, fertilizing ability and velocity of spermatozoa, as well as the duration of the motility period, depend on the temperature of the assay medium and also of that of the brood fish holding tank. 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Motility in semen is mainly controlled by K+ in salmonids, and probably also in sturgeons, and by osmotic pressure in other freshwater and seawater fish species, but other factors, such as concentration of surrounding metabolites and ions (Ca2+, Mg2+, etc.), pH and temperature also influence motility characteristics. In the present study, we have mainly reviewed and summarized the effects of temperature and pH on the motility of spermatozoa in three fish species: salmonids, cyprinids and sturgeons. Data in the literature show that motility, fertilizing ability and velocity of spermatozoa, as well as the duration of the motility period, depend on the temperature of the assay medium and also of that of the brood fish holding tank. In contrast, the pH of the swimming medium, and thus the intracellular pH of spermatozoa, has less influence on sperm motility parameters in cyprinids, salmonids and sturgeons.</abstract><subject lang="en"><genre>keywords</genre><topic>Beat frequency</topic><topic>Cyprinid</topic><topic>Fertilization</topic><topic>Spermatozoa motility</topic><topic>pH</topic><topic>Salmonid</topic><topic>Sturgeon</topic><topic>Temperature</topic></subject><relatedItem type="host"><titleInfo><title>Cell Biology International</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">1065-6995</identifier><identifier type="eISSN">1095-8355</identifier><identifier type="DOI">10.1002/(ISSN)1095-8355</identifier><identifier type="PublisherID">CBIN</identifier><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>29</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>101</start><end>110</end><total>10</total></extent></part></relatedItem><identifier type="istex">E8847ED320D9C491955FD012E529E7439EECAE4C</identifier><identifier type="DOI">10.1016/j.cellbi.2004.11.021</identifier><identifier type="ArticleID">CBIN1597</identifier><accessCondition type="use and reproduction" contentType="copyright">© The Author(s) Journal compilation © 2005 International Federation for Cell Biology</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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