Preliminary studies on cryopreservation of snakehead (Channa striata) embryos
This paper reports the findings of the ongoing studies on cryopreservation of the snakehead, Channa striata embryos. The specific objective of this study was to collect data on the sensitivity of C. striata embryo hatching rate to low temperatures at two different developmental stages in the presenc...
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Veröffentlicht in: | Cryobiology 2014-08, Vol.69 (1), p.1-9 |
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description | This paper reports the findings of the ongoing studies on cryopreservation of the snakehead, Channa striata embryos. The specific objective of this study was to collect data on the sensitivity of C. striata embryo hatching rate to low temperatures at two different developmental stages in the presence of four different cryoprotectants. Embryos at morula and heartbeat stages were selected and incubated in 1M dimethyl sulfoxide (Me2SO), 1M ethylene glycol (EG), 1M methanol (MeOH) and 0.1M sucrose solutions at different temperatures for a period of time. Embryos were kept at 24°C (control), 15°C, 4°C and −2°C for 5min, 1h and 3h. Following these treatments, the embryos were then transferred into a 24°C water bath until hatch to evaluate the hatching rate. The results showed that there was a significant decrease of hatching rate in both developmental stages following exposure to 4°C and −2°C at 1h and 3h exposure in each treatment. Heartbeat stage was more tolerant against chilling at −2°C for 3h exposure in Me2SO followed by MeOH, sucrose and EG. Further studies will be conducted to find the best method to preserve embryos for long term storage. |
doi_str_mv | 10.1016/j.cryobiol.2014.04.001 |
format | Article |
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The specific objective of this study was to collect data on the sensitivity of C. striata embryo hatching rate to low temperatures at two different developmental stages in the presence of four different cryoprotectants. Embryos at morula and heartbeat stages were selected and incubated in 1M dimethyl sulfoxide (Me2SO), 1M ethylene glycol (EG), 1M methanol (MeOH) and 0.1M sucrose solutions at different temperatures for a period of time. Embryos were kept at 24°C (control), 15°C, 4°C and −2°C for 5min, 1h and 3h. Following these treatments, the embryos were then transferred into a 24°C water bath until hatch to evaluate the hatching rate. The results showed that there was a significant decrease of hatching rate in both developmental stages following exposure to 4°C and −2°C at 1h and 3h exposure in each treatment. Heartbeat stage was more tolerant against chilling at −2°C for 3h exposure in Me2SO followed by MeOH, sucrose and EG. Further studies will be conducted to find the best method to preserve embryos for long term storage.</description><identifier>ISSN: 0011-2240</identifier><identifier>EISSN: 1090-2392</identifier><identifier>DOI: 10.1016/j.cryobiol.2014.04.001</identifier><identifier>PMID: 24726775</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Animals ; Channa striata ; Chilling experiment ; Cold Temperature ; Cryopreservation ; Cryopreservation - methods ; Cryoprotective Agents - pharmacology ; Dimethyl Sulfoxide - pharmacology ; Embryo, Nonmammalian ; Ethylene Glycol - pharmacology ; Fishes - embryology ; Methanol - pharmacology ; Morula - physiology ; Myocardial Contraction - drug effects ; Snakehead ; Sucrose - pharmacology</subject><ispartof>Cryobiology, 2014-08, Vol.69 (1), p.1-9</ispartof><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-da8648cd668b69c6ac9501b456f6bf93b06b319f496d44748551801f385f09713</citedby><cites>FETCH-LOGICAL-c438t-da8648cd668b69c6ac9501b456f6bf93b06b319f496d44748551801f385f09713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S001122401400073X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24726775$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohd Sharifuddin, M.</creatorcontrib><creatorcontrib>Siti Azizah, M.N.</creatorcontrib><title>Preliminary studies on cryopreservation of snakehead (Channa striata) embryos</title><title>Cryobiology</title><addtitle>Cryobiology</addtitle><description>This paper reports the findings of the ongoing studies on cryopreservation of the snakehead, Channa striata embryos. The specific objective of this study was to collect data on the sensitivity of C. striata embryo hatching rate to low temperatures at two different developmental stages in the presence of four different cryoprotectants. Embryos at morula and heartbeat stages were selected and incubated in 1M dimethyl sulfoxide (Me2SO), 1M ethylene glycol (EG), 1M methanol (MeOH) and 0.1M sucrose solutions at different temperatures for a period of time. Embryos were kept at 24°C (control), 15°C, 4°C and −2°C for 5min, 1h and 3h. Following these treatments, the embryos were then transferred into a 24°C water bath until hatch to evaluate the hatching rate. The results showed that there was a significant decrease of hatching rate in both developmental stages following exposure to 4°C and −2°C at 1h and 3h exposure in each treatment. Heartbeat stage was more tolerant against chilling at −2°C for 3h exposure in Me2SO followed by MeOH, sucrose and EG. Further studies will be conducted to find the best method to preserve embryos for long term storage.</description><subject>Animals</subject><subject>Channa striata</subject><subject>Chilling experiment</subject><subject>Cold Temperature</subject><subject>Cryopreservation</subject><subject>Cryopreservation - methods</subject><subject>Cryoprotective Agents - pharmacology</subject><subject>Dimethyl Sulfoxide - pharmacology</subject><subject>Embryo, Nonmammalian</subject><subject>Ethylene Glycol - pharmacology</subject><subject>Fishes - embryology</subject><subject>Methanol - pharmacology</subject><subject>Morula - physiology</subject><subject>Myocardial Contraction - drug effects</subject><subject>Snakehead</subject><subject>Sucrose - pharmacology</subject><issn>0011-2240</issn><issn>1090-2392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUF1LwzAUDaK4Of0Lo4_zofWmTdL2TRl-wUQf9Dmk6S3L7MdM2sH-vSnbfBUOXLicD84hZE4hokDF3SbSdt8VpqujGCiLwAPoGZlSyCGMkzw-J1P_oWEcM5iQK-c2ACDShF2SSczSWKQpn5K3D4u1aUyr7D5w_VAadEHXBqP71qJDu1O98Y-uClyrvnGNqgwWy7VqW-UF1qhe3QbYFF7grslFpWqHN8c7I19Pj5_Ll3D1_vy6fFiFmiVZH5YqEyzTpRBZIXItlM450IJxUYmiypMCRJHQvGK5KBlLWcY5zYBWScYryFOazMji4Lu13c-ArpeNcRrrWrXYDU5SzpMUBOOpp4oDVdvOOYuV3FrT-LaSghynlBt5mlKOU0rwgDFjfswYigbLP9lpO0-4PxDQN90ZtNJpg63G0ljUvSw781_GL_auiB8</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Mohd Sharifuddin, M.</creator><creator>Siti Azizah, M.N.</creator><general>Elsevier Inc</general><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>20140801</creationdate><title>Preliminary studies on cryopreservation of snakehead (Channa striata) embryos</title><author>Mohd Sharifuddin, M. ; Siti Azizah, M.N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-da8648cd668b69c6ac9501b456f6bf93b06b319f496d44748551801f385f09713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Channa striata</topic><topic>Chilling experiment</topic><topic>Cold Temperature</topic><topic>Cryopreservation</topic><topic>Cryopreservation - methods</topic><topic>Cryoprotective Agents - pharmacology</topic><topic>Dimethyl Sulfoxide - pharmacology</topic><topic>Embryo, Nonmammalian</topic><topic>Ethylene Glycol - pharmacology</topic><topic>Fishes - embryology</topic><topic>Methanol - pharmacology</topic><topic>Morula - physiology</topic><topic>Myocardial Contraction - drug effects</topic><topic>Snakehead</topic><topic>Sucrose - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohd Sharifuddin, M.</creatorcontrib><creatorcontrib>Siti Azizah, M.N.</creatorcontrib><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>Cryobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohd Sharifuddin, M.</au><au>Siti Azizah, M.N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preliminary studies on cryopreservation of snakehead (Channa striata) embryos</atitle><jtitle>Cryobiology</jtitle><addtitle>Cryobiology</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>69</volume><issue>1</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>0011-2240</issn><eissn>1090-2392</eissn><abstract>This paper reports the findings of the ongoing studies on cryopreservation of the snakehead, Channa striata embryos. The specific objective of this study was to collect data on the sensitivity of C. striata embryo hatching rate to low temperatures at two different developmental stages in the presence of four different cryoprotectants. Embryos at morula and heartbeat stages were selected and incubated in 1M dimethyl sulfoxide (Me2SO), 1M ethylene glycol (EG), 1M methanol (MeOH) and 0.1M sucrose solutions at different temperatures for a period of time. Embryos were kept at 24°C (control), 15°C, 4°C and −2°C for 5min, 1h and 3h. Following these treatments, the embryos were then transferred into a 24°C water bath until hatch to evaluate the hatching rate. The results showed that there was a significant decrease of hatching rate in both developmental stages following exposure to 4°C and −2°C at 1h and 3h exposure in each treatment. Heartbeat stage was more tolerant against chilling at −2°C for 3h exposure in Me2SO followed by MeOH, sucrose and EG. Further studies will be conducted to find the best method to preserve embryos for long term storage.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>24726775</pmid><doi>10.1016/j.cryobiol.2014.04.001</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Channa striata Chilling experiment Cold Temperature Cryopreservation Cryopreservation - methods Cryoprotective Agents - pharmacology Dimethyl Sulfoxide - pharmacology Embryo, Nonmammalian Ethylene Glycol - pharmacology Fishes - embryology Methanol - pharmacology Morula - physiology Myocardial Contraction - drug effects Snakehead Sucrose - pharmacology |
title | Preliminary studies on cryopreservation of snakehead (Channa striata) embryos |
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