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effects of osmolality on sperm quality in Jenynsia multidentata (Cyprinodontiformes: Anablepidae)
Sperm quality tests on fish are classically used for evaluating cryopreservation procedures, and they are also promising to assess aquatic toxicity and biomarkers of xenobiotic effects on reproduction. Osmotic shock from the storage medium is one of the main factors affecting sperm quality during ev...
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Published in: | Fish physiology and biochemistry 2016-02, Vol.42 (1), p.93-102 |
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container_title | Fish physiology and biochemistry |
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creator | da Silva, Janaína Camacho Varela Junior, Antonio Sergio Caldas, Jôsie Shwartz da Silva Freitas, Clarissa Botelho, Joziel Gonçalves Colares, Elton Pinto Corcini, Carine Dahl |
description | Sperm quality tests on fish are classically used for evaluating cryopreservation procedures, and they are also promising to assess aquatic toxicity and biomarkers of xenobiotic effects on reproduction. Osmotic shock from the storage medium is one of the main factors affecting sperm quality during evaluation. Thus, the objective of this study was to evaluate the effects of different osmolalities (240–460 mOsm/kg) for at least 4 days on the sperm quality parameters of the viviparous fish Jenynsia multidentata. The level of significance was (P |
doi_str_mv | 10.1007/s10695-015-0120-3 |
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Osmotic shock from the storage medium is one of the main factors affecting sperm quality during evaluation. Thus, the objective of this study was to evaluate the effects of different osmolalities (240–460 mOsm/kg) for at least 4 days on the sperm quality parameters of the viviparous fish Jenynsia multidentata. The level of significance was (P < 0.05). The plasma osmolality of J. multidentata is 326 ± 3.9 mOsm/kg. The motility of fresh semen was higher in osmolalities of 280 and 300 mOsm/kg but did not differ between osmolalities from 240 to 320 mOsm/kg. Above 380 mOsm/kg, the motility observed was 0 %. Over the time period studied motility increased with increasing osmolality, and the most constant and long-lasting rates were between 300 and 320 mOsm/kg. On the 4th day of evaluation, higher membrane integrity rates were observed between 280 and 360 mOsm/kg, higher mitochondrial membrane potential was observed between 300 and 460 mOsm/kg, and higher DNA integrity rates were observed between 260 and 380 mOsm/kg. Moreover, osmolalities ≥460 and ≤240 resulted in the lowest motility and DNA integrity levels. Over 4 days, the plasma membrane integrity was significantly lower at ≤260 and ≥400 mOsm/kg, and the mitochondrial membrane potential was significantly lower only in osmolalities ≤240 mOsm/kg. Therefore, we conclude that for sperm quality preservation in J. multidentata, an osmolality of 300–320 mOsm/kg of the most suitable diluent is necessary. Furthermore, we conclude that the storage of sperm in a hyposmotic (<260 mOsm/kg) or hyperosmotic (>400 mOsm/kg) solution affects not only motility but also other sperm quality parameters.</description><identifier>ISSN: 0920-1742</identifier><identifier>EISSN: 1573-5168</identifier><identifier>DOI: 10.1007/s10695-015-0120-3</identifier><identifier>PMID: 26342693</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Animal Biochemistry ; Animal Physiology ; Animals ; Biomarkers ; Biomedical and Life Sciences ; Cell Membrane ; College campuses ; Cryopreservation ; Cyprinodontiformes - physiology ; Deoxyribonucleic acid ; DNA ; fish ; Freshwater & Marine Ecology ; Histology ; Jenynsia multidentata ; Life Sciences ; Male ; membrane potential ; Membrane Potential, Mitochondrial ; Membranes ; mitochondrial membrane ; Morphology ; Motility ; osmolality ; Osmolar Concentration ; osmotic stress ; plasma membrane ; reproduction ; semen ; Specimen Handling ; Sperm ; Sperm Motility ; spermatozoa ; Spermatozoa - physiology ; Toxicity ; Zoology</subject><ispartof>Fish physiology and biochemistry, 2016-02, Vol.42 (1), p.93-102</ispartof><rights>Springer Science+Business Media Dordrecht 2015</rights><rights>Springer Science+Business Media Dordrecht 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-5e692a174b6bb56083f123b16903979e25588ade1b9bfe0ee09e14adcd1e5d503</citedby><cites>FETCH-LOGICAL-c433t-5e692a174b6bb56083f123b16903979e25588ade1b9bfe0ee09e14adcd1e5d503</cites><orcidid>0000-0001-5683-7801</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26342693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>da Silva, Janaína Camacho</creatorcontrib><creatorcontrib>Varela Junior, Antonio Sergio</creatorcontrib><creatorcontrib>Caldas, Jôsie Shwartz</creatorcontrib><creatorcontrib>da Silva Freitas, Clarissa</creatorcontrib><creatorcontrib>Botelho, Joziel Gonçalves</creatorcontrib><creatorcontrib>Colares, Elton Pinto</creatorcontrib><creatorcontrib>Corcini, Carine Dahl</creatorcontrib><title>effects of osmolality on sperm quality in Jenynsia multidentata (Cyprinodontiformes: Anablepidae)</title><title>Fish physiology and biochemistry</title><addtitle>Fish Physiol Biochem</addtitle><addtitle>Fish Physiol Biochem</addtitle><description>Sperm quality tests on fish are classically used for evaluating cryopreservation procedures, and they are also promising to assess aquatic toxicity and biomarkers of xenobiotic effects on reproduction. Osmotic shock from the storage medium is one of the main factors affecting sperm quality during evaluation. Thus, the objective of this study was to evaluate the effects of different osmolalities (240–460 mOsm/kg) for at least 4 days on the sperm quality parameters of the viviparous fish Jenynsia multidentata. The level of significance was (P < 0.05). The plasma osmolality of J. multidentata is 326 ± 3.9 mOsm/kg. The motility of fresh semen was higher in osmolalities of 280 and 300 mOsm/kg but did not differ between osmolalities from 240 to 320 mOsm/kg. Above 380 mOsm/kg, the motility observed was 0 %. Over the time period studied motility increased with increasing osmolality, and the most constant and long-lasting rates were between 300 and 320 mOsm/kg. On the 4th day of evaluation, higher membrane integrity rates were observed between 280 and 360 mOsm/kg, higher mitochondrial membrane potential was observed between 300 and 460 mOsm/kg, and higher DNA integrity rates were observed between 260 and 380 mOsm/kg. Moreover, osmolalities ≥460 and ≤240 resulted in the lowest motility and DNA integrity levels. Over 4 days, the plasma membrane integrity was significantly lower at ≤260 and ≥400 mOsm/kg, and the mitochondrial membrane potential was significantly lower only in osmolalities ≤240 mOsm/kg. Therefore, we conclude that for sperm quality preservation in J. multidentata, an osmolality of 300–320 mOsm/kg of the most suitable diluent is necessary. Furthermore, we conclude that the storage of sperm in a hyposmotic (<260 mOsm/kg) or hyperosmotic (>400 mOsm/kg) solution affects not only motility but also other sperm quality parameters.</description><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Animal Physiology</subject><subject>Animals</subject><subject>Biomarkers</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Membrane</subject><subject>College campuses</subject><subject>Cryopreservation</subject><subject>Cyprinodontiformes - physiology</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>fish</subject><subject>Freshwater & Marine Ecology</subject><subject>Histology</subject><subject>Jenynsia multidentata</subject><subject>Life Sciences</subject><subject>Male</subject><subject>membrane potential</subject><subject>Membrane Potential, Mitochondrial</subject><subject>Membranes</subject><subject>mitochondrial membrane</subject><subject>Morphology</subject><subject>Motility</subject><subject>osmolality</subject><subject>Osmolar Concentration</subject><subject>osmotic stress</subject><subject>plasma membrane</subject><subject>reproduction</subject><subject>semen</subject><subject>Specimen Handling</subject><subject>Sperm</subject><subject>Sperm Motility</subject><subject>spermatozoa</subject><subject>Spermatozoa - physiology</subject><subject>Toxicity</subject><subject>Zoology</subject><issn>0920-1742</issn><issn>1573-5168</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kE9P3DAQxa2qqCy0H6CXYokLHEJn7NiJuaEVf4XUQ8vZcjZjFJTYi50c9tuTVWjFqYfRSKP33jz9GPuOcIEA1c-MoI0qAPcjoJCf2ApVJQuFuv7MVmDmI1alOGRHOb8AgKk0fmGHQstSaCNXzJH3tBkzj57HPMTe9d244zHwvKU08NdpOXSBP1DYhdw5Pkz92LUURjc6frbebVMXYhvD2PmYBsqX_Cq4pqdt1zo6_8oOvOszfXvfx-zp5vrP-q54_HV7v756LDallGOhSBvh5rKNbhqloZYehWxQG5CmMiSUqmvXEjam8QREYAhL125aJNUqkMfsdMndpvg6UR7tS5xSmF9arLSQZS2ralbhotqkmHMib-f2g0s7i2D3UO0C1c5Q7R6qlbPnx3vy1AzU_nP8pTgLxCLIexTPlD68_k_qyWLyLlr3nLpsn34LQA2AIJVG-Qadyoum</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>da Silva, Janaína Camacho</creator><creator>Varela Junior, Antonio Sergio</creator><creator>Caldas, Jôsie Shwartz</creator><creator>da Silva Freitas, Clarissa</creator><creator>Botelho, Joziel 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of osmolality on sperm quality in Jenynsia multidentata (Cyprinodontiformes: Anablepidae)</title><author>da Silva, Janaína Camacho ; Varela Junior, Antonio Sergio ; Caldas, Jôsie Shwartz ; da Silva Freitas, Clarissa ; Botelho, Joziel Gonçalves ; Colares, Elton Pinto ; Corcini, Carine Dahl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-5e692a174b6bb56083f123b16903979e25588ade1b9bfe0ee09e14adcd1e5d503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Animal Physiology</topic><topic>Animals</topic><topic>Biomarkers</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Membrane</topic><topic>College campuses</topic><topic>Cryopreservation</topic><topic>Cyprinodontiformes - physiology</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>fish</topic><topic>Freshwater & Marine 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sperm quality in Jenynsia multidentata (Cyprinodontiformes: Anablepidae)</atitle><jtitle>Fish physiology and biochemistry</jtitle><stitle>Fish Physiol Biochem</stitle><addtitle>Fish Physiol Biochem</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>42</volume><issue>1</issue><spage>93</spage><epage>102</epage><pages>93-102</pages><issn>0920-1742</issn><eissn>1573-5168</eissn><abstract>Sperm quality tests on fish are classically used for evaluating cryopreservation procedures, and they are also promising to assess aquatic toxicity and biomarkers of xenobiotic effects on reproduction. Osmotic shock from the storage medium is one of the main factors affecting sperm quality during evaluation. Thus, the objective of this study was to evaluate the effects of different osmolalities (240–460 mOsm/kg) for at least 4 days on the sperm quality parameters of the viviparous fish Jenynsia multidentata. The level of significance was (P < 0.05). The plasma osmolality of J. multidentata is 326 ± 3.9 mOsm/kg. The motility of fresh semen was higher in osmolalities of 280 and 300 mOsm/kg but did not differ between osmolalities from 240 to 320 mOsm/kg. Above 380 mOsm/kg, the motility observed was 0 %. Over the time period studied motility increased with increasing osmolality, and the most constant and long-lasting rates were between 300 and 320 mOsm/kg. On the 4th day of evaluation, higher membrane integrity rates were observed between 280 and 360 mOsm/kg, higher mitochondrial membrane potential was observed between 300 and 460 mOsm/kg, and higher DNA integrity rates were observed between 260 and 380 mOsm/kg. Moreover, osmolalities ≥460 and ≤240 resulted in the lowest motility and DNA integrity levels. Over 4 days, the plasma membrane integrity was significantly lower at ≤260 and ≥400 mOsm/kg, and the mitochondrial membrane potential was significantly lower only in osmolalities ≤240 mOsm/kg. Therefore, we conclude that for sperm quality preservation in J. multidentata, an osmolality of 300–320 mOsm/kg of the most suitable diluent is necessary. Furthermore, we conclude that the storage of sperm in a hyposmotic (<260 mOsm/kg) or hyperosmotic (>400 mOsm/kg) solution affects not only motility but also other sperm quality parameters.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>26342693</pmid><doi>10.1007/s10695-015-0120-3</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5683-7801</orcidid></addata></record> |
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subjects | Animal Anatomy Animal Biochemistry Animal Physiology Animals Biomarkers Biomedical and Life Sciences Cell Membrane College campuses Cryopreservation Cyprinodontiformes - physiology Deoxyribonucleic acid DNA fish Freshwater & Marine Ecology Histology Jenynsia multidentata Life Sciences Male membrane potential Membrane Potential, Mitochondrial Membranes mitochondrial membrane Morphology Motility osmolality Osmolar Concentration osmotic stress plasma membrane reproduction semen Specimen Handling Sperm Sperm Motility spermatozoa Spermatozoa - physiology Toxicity Zoology |
title | effects of osmolality on sperm quality in Jenynsia multidentata (Cyprinodontiformes: Anablepidae) |
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