Consequences of Nitric Oxide Synthase Inhibition During Bovine Oocyte Maturation on Meiosis and Embryo Development

The importance of nitric oxide synthase (NOS) in bovine oocyte maturation was investigated. Oocytes were in vitro matured with the NOS inhibitor Nw- l-nitro-arginine methyl-ester (10⁻⁷, 10⁻⁵ and 10⁻³ m l-NAME) and metaphase II (MII) rates and embryo development and quality were assessed. The effect...

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Veröffentlicht in:Reproduction in domestic animals 2010-02, Vol.45 (1), p.75-80
Hauptverfasser: Schwarz, KRL, Pires, PRL, de Bem, THC, Adona, PR, Leal, CLV
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container_title Reproduction in domestic animals
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creator Schwarz, KRL
Pires, PRL
de Bem, THC
Adona, PR
Leal, CLV
description The importance of nitric oxide synthase (NOS) in bovine oocyte maturation was investigated. Oocytes were in vitro matured with the NOS inhibitor Nw- l-nitro-arginine methyl-ester (10⁻⁷, 10⁻⁵ and 10⁻³ m l-NAME) and metaphase II (MII) rates and embryo development and quality were assessed. The effect of l-NAME (10⁻⁷ m) during pre-maturation and/or maturation on embryo development and quality was also assessed. l-NAME decreased MII rates (78-82%, p < 0.05) when compared with controls without l-NAME (96%). Cleavage (77-88%, p > 0.05), Day 7 blastocyst rates (34-42%, p > 0.05) and total cell numbers in blastocysts were similar for all groups (146-171 cells, p > 0.05). Day 8 blastocyst TUNEL positive cells (3-4 cells) increased with l-NAME treatment (p < 0.05). For oocytes cultured with l-NAME during pre-maturation and/or maturation, Day 8 blastocyst development (26-34%) and Day 9 hatching rates (15-22%) were similar (p > 0.05) to controls pre-matured and matured without NOS inhibition (33 and 18%, respectively), while total cell numbers (Day 9 hatched blastocysts) increased (264-324 cells, p < 0.05) when compared with the controls (191 cells). TUNEL positive cells increased when NOS was inhibited only during the maturation period (8 cells, p < 0.05) when compared with the other groups (3-4 cells). NO may be involved in meiosis progression to MII and its deficiency during maturation increases apoptosis in embryos produced in vitro. Nitric oxide synthase inhibition during pre-maturation and/or maturation affects embryo quality.
doi_str_mv 10.1111/j.1439-0531.2008.01242.x
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Oocytes were in vitro matured with the NOS inhibitor Nw- l-nitro-arginine methyl-ester (10⁻⁷, 10⁻⁵ and 10⁻³ m l-NAME) and metaphase II (MII) rates and embryo development and quality were assessed. The effect of l-NAME (10⁻⁷ m) during pre-maturation and/or maturation on embryo development and quality was also assessed. l-NAME decreased MII rates (78-82%, p &lt; 0.05) when compared with controls without l-NAME (96%). Cleavage (77-88%, p &gt; 0.05), Day 7 blastocyst rates (34-42%, p &gt; 0.05) and total cell numbers in blastocysts were similar for all groups (146-171 cells, p &gt; 0.05). Day 8 blastocyst TUNEL positive cells (3-4 cells) increased with l-NAME treatment (p &lt; 0.05). For oocytes cultured with l-NAME during pre-maturation and/or maturation, Day 8 blastocyst development (26-34%) and Day 9 hatching rates (15-22%) were similar (p &gt; 0.05) to controls pre-matured and matured without NOS inhibition (33 and 18%, respectively), while total cell numbers (Day 9 hatched blastocysts) increased (264-324 cells, p &lt; 0.05) when compared with the controls (191 cells). TUNEL positive cells increased when NOS was inhibited only during the maturation period (8 cells, p &lt; 0.05) when compared with the other groups (3-4 cells). NO may be involved in meiosis progression to MII and its deficiency during maturation increases apoptosis in embryos produced in vitro. Nitric oxide synthase inhibition during pre-maturation and/or maturation affects embryo quality.</description><identifier>ISSN: 0936-6768</identifier><identifier>EISSN: 1439-0531</identifier><identifier>DOI: 10.1111/j.1439-0531.2008.01242.x</identifier><identifier>PMID: 20137060</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Animal reproduction ; Animals ; apoptosis ; Biological and medical sciences ; blastocyst ; Blastocyst - cytology ; Blastocyst - drug effects ; Blastocyst - physiology ; Cattle ; Cell Count ; Chemical synthesis ; embryogenesis ; Embryonic Development - drug effects ; Embryos ; enzyme inhibition ; enzyme inhibitors ; Enzyme Inhibitors - pharmacology ; Female ; Fertilization in Vitro - veterinary ; Fundamental and applied biological sciences. Psychology ; hatching ; In Situ Nick-End Labeling ; in vitro fertilization ; Male ; Mammalian reproduction. General aspects ; meiosis ; Meiosis - drug effects ; metaphase ; Metaphase - drug effects ; NG-Nitroarginine Methyl Ester - pharmacology ; Nitric oxide ; nitric oxide synthase ; Nitric Oxide Synthase - antagonists &amp; inhibitors ; oocytes ; Oocytes - cytology ; Oocytes - physiology ; Vertebrates: reproduction</subject><ispartof>Reproduction in domestic animals, 2010-02, Vol.45 (1), p.75-80</ispartof><rights>2008 The Authors. 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Oocytes were in vitro matured with the NOS inhibitor Nw- l-nitro-arginine methyl-ester (10⁻⁷, 10⁻⁵ and 10⁻³ m l-NAME) and metaphase II (MII) rates and embryo development and quality were assessed. The effect of l-NAME (10⁻⁷ m) during pre-maturation and/or maturation on embryo development and quality was also assessed. l-NAME decreased MII rates (78-82%, p &lt; 0.05) when compared with controls without l-NAME (96%). Cleavage (77-88%, p &gt; 0.05), Day 7 blastocyst rates (34-42%, p &gt; 0.05) and total cell numbers in blastocysts were similar for all groups (146-171 cells, p &gt; 0.05). Day 8 blastocyst TUNEL positive cells (3-4 cells) increased with l-NAME treatment (p &lt; 0.05). For oocytes cultured with l-NAME during pre-maturation and/or maturation, Day 8 blastocyst development (26-34%) and Day 9 hatching rates (15-22%) were similar (p &gt; 0.05) to controls pre-matured and matured without NOS inhibition (33 and 18%, respectively), while total cell numbers (Day 9 hatched blastocysts) increased (264-324 cells, p &lt; 0.05) when compared with the controls (191 cells). TUNEL positive cells increased when NOS was inhibited only during the maturation period (8 cells, p &lt; 0.05) when compared with the other groups (3-4 cells). NO may be involved in meiosis progression to MII and its deficiency during maturation increases apoptosis in embryos produced in vitro. Nitric oxide synthase inhibition during pre-maturation and/or maturation affects embryo quality.</description><subject>Animal reproduction</subject><subject>Animals</subject><subject>apoptosis</subject><subject>Biological and medical sciences</subject><subject>blastocyst</subject><subject>Blastocyst - cytology</subject><subject>Blastocyst - drug effects</subject><subject>Blastocyst - physiology</subject><subject>Cattle</subject><subject>Cell Count</subject><subject>Chemical synthesis</subject><subject>embryogenesis</subject><subject>Embryonic Development - drug effects</subject><subject>Embryos</subject><subject>enzyme inhibition</subject><subject>enzyme inhibitors</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Fertilization in Vitro - veterinary</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hatching</subject><subject>In Situ Nick-End Labeling</subject><subject>in vitro fertilization</subject><subject>Male</subject><subject>Mammalian reproduction. General aspects</subject><subject>meiosis</subject><subject>Meiosis - drug effects</subject><subject>metaphase</subject><subject>Metaphase - drug effects</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Nitric oxide</subject><subject>nitric oxide synthase</subject><subject>Nitric Oxide Synthase - antagonists &amp; inhibitors</subject><subject>oocytes</subject><subject>Oocytes - cytology</subject><subject>Oocytes - physiology</subject><subject>Vertebrates: reproduction</subject><issn>0936-6768</issn><issn>1439-0531</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV1v0zAUhiMEYmXwF8BCQlyl-COxnQsutnZfYluljYlLy3FPNpfULnaytf8eZy1F4grLsi35eY_ec94sQwSPSVpfFmNSsCrHJSNjirEcY0ILOl6_yEb7j5fZCFeM51xweZC9iXGBMSmlEK-zA4oJE5jjURYm3kX41YMzEJFv0LXtgjVotrZzQLcb1z3oCOjCPdjadtY7NO2Ddffo2D9aB2jmzaYDdKW7Pujn_7SvwPpoI9Jujk6Wddh4NIVHaP1qCa57m71qdBvh3e4-zO5OT75PzvPL2dnF5OgyN4UUNC8kJfNa16SSkvGyAeCmqCC5btJZGsbqhhFaNrWQhheNhBIbjedEE17xqmKH2edt3VXwqcHYqaWNBtpWO_B9VIIVmBZFQRL58R9y4fvgkjlF06BKzJlIkNxCJvgYAzRqFexSh40iWA2pqIUahq-G4ashFfWcilon6ftd_b5ewnwv_BNDAj7tAB2NbpugnbHxL0cZqQhhifu65Z5sC5v_NqBupkfDK-nzrd7GDtZ7vQ4_FRepUfXj-kyJ8tuNkByr88R_2PKN9krfh-Tp7nZwjYmgUnLOfgP3Hr-q</recordid><startdate>201002</startdate><enddate>201002</enddate><creator>Schwarz, KRL</creator><creator>Pires, PRL</creator><creator>de Bem, THC</creator><creator>Adona, PR</creator><creator>Leal, CLV</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201002</creationdate><title>Consequences of Nitric Oxide Synthase Inhibition During Bovine Oocyte Maturation on Meiosis and Embryo Development</title><author>Schwarz, KRL ; Pires, PRL ; de Bem, THC ; Adona, PR ; Leal, CLV</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4872-4821dbab1988365fee6c49e060f9e05c33bf3125fb78c64f8e50ca0d1a1696993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animal reproduction</topic><topic>Animals</topic><topic>apoptosis</topic><topic>Biological and medical sciences</topic><topic>blastocyst</topic><topic>Blastocyst - cytology</topic><topic>Blastocyst - drug effects</topic><topic>Blastocyst - physiology</topic><topic>Cattle</topic><topic>Cell Count</topic><topic>Chemical synthesis</topic><topic>embryogenesis</topic><topic>Embryonic Development - drug effects</topic><topic>Embryos</topic><topic>enzyme inhibition</topic><topic>enzyme inhibitors</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>Fertilization in Vitro - veterinary</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hatching</topic><topic>In Situ Nick-End Labeling</topic><topic>in vitro fertilization</topic><topic>Male</topic><topic>Mammalian reproduction. General aspects</topic><topic>meiosis</topic><topic>Meiosis - drug effects</topic><topic>metaphase</topic><topic>Metaphase - drug effects</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nitric oxide</topic><topic>nitric oxide synthase</topic><topic>Nitric Oxide Synthase - antagonists &amp; inhibitors</topic><topic>oocytes</topic><topic>Oocytes - cytology</topic><topic>Oocytes - physiology</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwarz, KRL</creatorcontrib><creatorcontrib>Pires, PRL</creatorcontrib><creatorcontrib>de Bem, THC</creatorcontrib><creatorcontrib>Adona, PR</creatorcontrib><creatorcontrib>Leal, CLV</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Reproduction in domestic animals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwarz, KRL</au><au>Pires, PRL</au><au>de Bem, THC</au><au>Adona, PR</au><au>Leal, CLV</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Consequences of Nitric Oxide Synthase Inhibition During Bovine Oocyte Maturation on Meiosis and Embryo Development</atitle><jtitle>Reproduction in domestic animals</jtitle><addtitle>Reprod Domest Anim</addtitle><date>2010-02</date><risdate>2010</risdate><volume>45</volume><issue>1</issue><spage>75</spage><epage>80</epage><pages>75-80</pages><issn>0936-6768</issn><eissn>1439-0531</eissn><abstract>The importance of nitric oxide synthase (NOS) in bovine oocyte maturation was investigated. Oocytes were in vitro matured with the NOS inhibitor Nw- l-nitro-arginine methyl-ester (10⁻⁷, 10⁻⁵ and 10⁻³ m l-NAME) and metaphase II (MII) rates and embryo development and quality were assessed. The effect of l-NAME (10⁻⁷ m) during pre-maturation and/or maturation on embryo development and quality was also assessed. l-NAME decreased MII rates (78-82%, p &lt; 0.05) when compared with controls without l-NAME (96%). Cleavage (77-88%, p &gt; 0.05), Day 7 blastocyst rates (34-42%, p &gt; 0.05) and total cell numbers in blastocysts were similar for all groups (146-171 cells, p &gt; 0.05). Day 8 blastocyst TUNEL positive cells (3-4 cells) increased with l-NAME treatment (p &lt; 0.05). For oocytes cultured with l-NAME during pre-maturation and/or maturation, Day 8 blastocyst development (26-34%) and Day 9 hatching rates (15-22%) were similar (p &gt; 0.05) to controls pre-matured and matured without NOS inhibition (33 and 18%, respectively), while total cell numbers (Day 9 hatched blastocysts) increased (264-324 cells, p &lt; 0.05) when compared with the controls (191 cells). TUNEL positive cells increased when NOS was inhibited only during the maturation period (8 cells, p &lt; 0.05) when compared with the other groups (3-4 cells). NO may be involved in meiosis progression to MII and its deficiency during maturation increases apoptosis in embryos produced in vitro. Nitric oxide synthase inhibition during pre-maturation and/or maturation affects embryo quality.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>20137060</pmid><doi>10.1111/j.1439-0531.2008.01242.x</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Animal reproduction
Animals
apoptosis
Biological and medical sciences
blastocyst
Blastocyst - cytology
Blastocyst - drug effects
Blastocyst - physiology
Cattle
Cell Count
Chemical synthesis
embryogenesis
Embryonic Development - drug effects
Embryos
enzyme inhibition
enzyme inhibitors
Enzyme Inhibitors - pharmacology
Female
Fertilization in Vitro - veterinary
Fundamental and applied biological sciences. Psychology
hatching
In Situ Nick-End Labeling
in vitro fertilization
Male
Mammalian reproduction. General aspects
meiosis
Meiosis - drug effects
metaphase
Metaphase - drug effects
NG-Nitroarginine Methyl Ester - pharmacology
Nitric oxide
nitric oxide synthase
Nitric Oxide Synthase - antagonists & inhibitors
oocytes
Oocytes - cytology
Oocytes - physiology
Vertebrates: reproduction
title Consequences of Nitric Oxide Synthase Inhibition During Bovine Oocyte Maturation on Meiosis and Embryo Development
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