Gonadotropin-releasing hormone increases cleavage rates of bovine oocytes fertilized in vitro
Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p 0.01) in med...
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Published in: | Biology of reproduction Vol. 53; no. 3; pp. 541 - 545 |
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Language: | English |
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Madison, WI
Society for the Study of Reproduction
01-09-1995
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Abstract | Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p 0.01) in media containing 0.8 micrograms/ml GnRH (68%) than in controls (59%) and were consistent across three bulls. In a second experiment, two GnRH agonists also increased cleavage rates. A dose response for GnRH was demonstrated in a third experiment with a low-fertility bull (p 0.09): cleavage rates were 37, 36, 43, 48, and 47% for 0, 0.16, 0.8, 4, and 20 micrograms/ml GnRH, respectively. A GnRH antagonist was also shown to abolish the enhancing effect of GnRH on cleavage rates. No significant (p 0.10) effect on percentage blastocysts per cleaved ovum was detected in any experiment. No specific binding of a GnRH analog to sperm was detected in radioreceptor assays. However, mRNA for the GnRH receptor was detected in matured cumulus-oocyte complexes by means of reverse transcription-polymerase chain reaction and was verified by Southern hybridization with cDNA for the ovine GnRH receptor. In summary, GnRH and GnRH agonists enhance bovine in vitro fertilization, and detection of mRNA for the GnRH receptor in cumulus-oocyte complexes is suggestive that GnRH may act through its receptor |
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AbstractList | Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p 0.01) in media containing 0.8 micrograms/ml GnRH (68%) than in controls (59%) and were consistent across three bulls. In a second experiment, two GnRH agonists also increased cleavage rates. A dose response for GnRH was demonstrated in a third experiment with a low-fertility bull (p 0.09): cleavage rates were 37, 36, 43, 48, and 47% for 0, 0.16, 0.8, 4, and 20 micrograms/ml GnRH, respectively. A GnRH antagonist was also shown to abolish the enhancing effect of GnRH on cleavage rates. No significant (p 0.10) effect on percentage blastocysts per cleaved ovum was detected in any experiment. No specific binding of a GnRH analog to sperm was detected in radioreceptor assays. However, mRNA for the GnRH receptor was detected in matured cumulus-oocyte complexes by means of reverse transcription-polymerase chain reaction and was verified by Southern hybridization with cDNA for the ovine GnRH receptor. In summary, GnRH and GnRH agonists enhance bovine in vitro fertilization, and detection of mRNA for the GnRH receptor in cumulus-oocyte complexes is suggestive that GnRH may act through its receptor Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p < 0.01) in media containing 0.8 microgram/ml GnRH (68%) than in controls (59%) and were consistent across three bulls. In a second experiment two GnRH agonists also increased cleavage rates. A dose response for GnRH was demonstrated in a third experiment with a low-fertility bull (p < 0.09): cleavage rates were 37, 36, 43, 48, and 47% for 0, 0.16, 0.8, 4, and 20 micrograms/ml GnRH, respectively. A GnRH antagonist was also shown to abolish the enhancing effect of GnRH on cleavage rates. No significant (p > 0.10) effect on percentage blastocysts per cleaved ovum was detected in any experiment. No specific binding of a GnRH analog to sperm was detected in radioreceptor assays. However, mRNA for the GnRH receptor was detected in matured cumulus-oocyte complexes by means of reverse transcription-polymerase chain reaction and was verified by Southern hybridization with cDNA for the ovine GnRH receptor. In summary, GnRH and GnRH agonists enhance bovine in vitro fertilization, and detection of mRNA for the GnRH receptor in cumulus-oocyte complexes is suggestive that GnRH may act through its receptor. Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p < 0.01) in media containing 0.8 microgram/ml GnRH (68%) than in controls (59%) and were consistent across three bulls. In a second experiment two GnRH agonists also increased cleavage rates. A dose response for GnRH was demonstrated in a third experiment with a low-fertility bull (p < 0.09): cleavage rates were 37, 36, 43, 48, and 47% for 0, 0.16, 0.8, 4, and 20 micrograms/ml GnRH, respectively. A GnRH antagonist was also shown to abolish the enhancing effect of GnRH on cleavage rates. No significant (p > 0.10) effect on percentage blastocysts per cleaved ovum was detected in any experiment. No specific binding of a GnRH analog to sperm was detected in radioreceptor assays. However, mRNA for the GnRH receptor was detected in matured cumulus-oocyte complexes by means of reverse transcription-polymerase chain reaction and was verified by Southern hybridization with cDNA for the ovine GnRH receptor. In summary, GnRH and GnRH agonists enhance bovine in vitro fertilization, and detection of mRNA for the GnRH receptor in cumulus-oocyte complexes is suggestive that GnRH may act through its receptor. Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p < 0.01) in media containing 0.8 pg/ml GnRH (68%) than in controls (59%) and were consistent across three bulls. In a second experiment, two GnRH agonists also increased cleavage rates. A dose response for GnRH was demonstrated in a third experiment with a low-fertility bull (p < 0.09): cleavage rates were 37, 36, 43, 48, and 47% for 0, 0.16, 0.8, 4, and 20 mu g/ml GnRH, respectively. A GnRH antagonist was also shown to abolish the enhancing effect of GnRH on cleavage rates. No significant (p > 0.10) effect on percentage blastocysts per cleaved ovum was detected in any experiment. No specific binding of a GnRH analog to sperm was detected in radioreceptor assays. However, mRNA for the GnRH receptor was detected in matured cumulus-oocyte complexes by means of reverse transcription-polymerase chain reaction and was verified by Southern hybridization with cDNA for the ovine GnRH receptor. In summary, GnRH and GnRH agonists enhance bovine in vitro fertilization, and detection of mRNA for the GnRH receptor in cumulus-oocyte complexes is suggestive that GnRH may act through its receptor. Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro fertilization media to study effects on cleavage rates of bovine oocytes obtained from slaughterhouse ovaries. Cleavage rates were higher (p < 0.01) in media containing 0.8 microgram/ml GnRH (68%) than in controls (59%) and were consistent across three bulls. In a second experiment two GnRH agonists also increased cleavage rates. A dose response for GnRH was demonstrated in a third experiment with a low-fertility bull (p < 0.09): cleavage rates were 37, 36, 43, 48, and 47% for 0, 0.16, 0.8, 4, and 20 micrograms/ml GnRH, respectively. A GnRH antagonist was also shown to abolish the enhancing effect of GnRH on cleavage rates. No significant (p > 0.10) effect on percentage blastocysts per cleaved ovum was detected in any experiment. No specific binding of a GnRH analog to sperm was detected in radioreceptor assays. However, mRNA for the GnRH receptor was detected in matured cumulus-oocyte complexes by means of reverse transcription-polymerase chain reaction and was verified by Southern hybridization with cDNA for the ovine GnRH receptor. In summary, GnRH and GnRH agonists enhance bovine in vitro fertilization, and detection of mRNA for the GnRH receptor in cumulus-oocyte complexes is suggestive that GnRH may act through its receptor. |
Author | Seidel, G.E. Jr Funston, R.N. (Colorado State University, Fort Collins, CO.) |
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Keywords | Agonist Bovine Gonadotropin RH Germinal cell Fecundation In vitro Hypothalamic hormone Reproduction Vertebrata Mammalia Female Artiodactyla Hormone releasing factor Mechanism of action Ungulata Oocyte Hormonal receptor |
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Snippet | Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro... Because a direct effect of GnRH on spermatozoa has been implied in clinical studies with subfertile bulls and stallions, we added GnRH to in vitro... |
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SubjectTerms | AGONISTAS AGONISTE Animal productions Animals ANTAGONISTAS DE LAS HORMONAS ANTAGONISTE D'HORMONE ARN MENSAJERO ARN MESSAGER Base Sequence Biological and medical sciences Blastocyst - drug effects Blastocyst - physiology Blotting, Southern BOVIN Cattle Cleavage Stage, Ovum - drug effects CULTIVO DE EMBRIONES CULTURE D'EMBRYON DIVISION CELLULAIRE DIVISION CELULAR Embryo, Mammalian - drug effects Embryo, Mammalian - physiology ESPERMATOZOO EXPERIMENTACION IN VITRO EXPERIMENTATION IN VITRO FECONDATION FECUNDACION Female Fertilization in Vitro Fundamental and applied biological sciences. Psychology GANADO BOVINO GONADOLIBERINE Gonadotropin-Releasing Hormone - agonists Gonadotropin-Releasing Hormone - pharmacology HORMONA LIBERADORA DE GONADOTROPINA Male Molecular Sequence Data Oocytes - drug effects Ovary - cytology OVULE OVULO Polymerase Chain Reaction Radioligand Assay RECEPTEUR D'HORMONE RECEPTORES DE HORMONAS Spermatozoa - drug effects Spermatozoa - physiology SPERMATOZOIDE Terrestrial animal productions Vertebrates |
Title | Gonadotropin-releasing hormone increases cleavage rates of bovine oocytes fertilized in vitro |
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