Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation

Orexins are peptides controlling feeding, sleep, and neuroendocrine functions. They are synthesized by the hypothalamus with projections throughout the brain. Orexins and their orexin 1 (OX1) and orexin 2 receptors (OX2) are present outside the central nervous system. Here the expression of preproor...

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Autores principales: Silveyra, P., Lux-Lantos, V., Libertun, C.
Formato: JOUR
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rat
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_01931849_v293_n4_pE977_Silveyra
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spelling todo:paper_01931849_v293_n4_pE977_Silveyra2023-10-03T15:09:15Z Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation Silveyra, P. Lux-Lantos, V. Libertun, C. Orexin 1 and orexin 2 receptor antagonists Ovary cetrorelix gonadotropin jnj 10397049 orexin orexin 1 receptor orexin 2 receptor pentobarbital preproorexin receptor blocking agent sb 334867 a unclassified drug animal experiment animal tissue article bleeding controlled study estrus cycle female food intake gonadotropin blood level histology hyperemia light dark cycle nonhuman ovulation priority journal proestrus protein expression quantitative assay rat real time polymerase chain reaction reverse transcription polymerase chain reaction Sprague Dawley rat Animals Benzoxazoles Dioxanes Eating Estrous Cycle Female Gene Expression Regulation Gonadotropin-Releasing Hormone Gonadotropins Intracellular Signaling Peptides and Proteins Neuropeptides Ovary Ovulation Pentobarbital Phenylurea Compounds Rats Rats, Sprague-Dawley Receptors, G-Protein-Coupled Receptors, Neuropeptide RNA, Messenger Urea Orexins are peptides controlling feeding, sleep, and neuroendocrine functions. They are synthesized by the hypothalamus with projections throughout the brain. Orexins and their orexin 1 (OX1) and orexin 2 receptors (OX2) are present outside the central nervous system. Here the expression of preproorexin (PPO), OX1, and OX2 was studied in rat ovaries. PPO, OX1, and OX2 were determined by quantitative real-time RT-PCR in ovaries of cycling Sprague-Dawley rats on all days of the cycle. Serum hormones and food consumption were determined. Ovarian OX1 and OX2 expression was then studied after ovulation blockade with Cetrorelix or Nembutal. Finally, proestrous rats were treated at 1400 and 1900 with a selective OX1 antagonist (SB-334867-A) and/or a selective OX2 antagonist (JNJ-10397049), and hormone levels, ovulation, and ovarian histology were studied. Both receptors' expression increased in the ovary between 1700 and 2300 of proestrus exclusively, in coincidence with hormone peaks, but not with the dark-light cycle or food intake. PPO was not detected. Cetrorelix or Nembutal prevented the increases of OX1 and OX2 while blunting gonadotropin peaks. SB-334867-A and JNJ-10397049, alone or combined, decreased serum gonadotropins and reduced ova number the following morning; ovaries showed a bloody (hyperemic and/or hemorrhagic) reaction with more preovulatory follicles and less corpora lutea. Here we demonstrate for the first time an increased ovarian expression of both OX1 and OX2, only during proestrous afternoon, and its hormone dependence but not dependence on the dark-light cycle. Two new receptor antagonists reduced proestrous gonadotropins and/or ova number while producing ovarian structural changes. Copyright © 2007 the American Physiological Society. Fil:Silveyra, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01931849_v293_n4_pE977_Silveyra
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Orexin 1 and orexin 2 receptor antagonists
Ovary
cetrorelix
gonadotropin
jnj 10397049
orexin
orexin 1 receptor
orexin 2 receptor
pentobarbital
preproorexin
receptor blocking agent
sb 334867 a
unclassified drug
animal experiment
animal tissue
article
bleeding
controlled study
estrus cycle
female
food intake
gonadotropin blood level
histology
hyperemia
light dark cycle
nonhuman
ovulation
priority journal
proestrus
protein expression
quantitative assay
rat
real time polymerase chain reaction
reverse transcription polymerase chain reaction
Sprague Dawley rat
Animals
Benzoxazoles
Dioxanes
Eating
Estrous Cycle
Female
Gene Expression Regulation
Gonadotropin-Releasing Hormone
Gonadotropins
Intracellular Signaling Peptides and Proteins
Neuropeptides
Ovary
Ovulation
Pentobarbital
Phenylurea Compounds
Rats
Rats, Sprague-Dawley
Receptors, G-Protein-Coupled
Receptors, Neuropeptide
RNA, Messenger
Urea
spellingShingle Orexin 1 and orexin 2 receptor antagonists
Ovary
cetrorelix
gonadotropin
jnj 10397049
orexin
orexin 1 receptor
orexin 2 receptor
pentobarbital
preproorexin
receptor blocking agent
sb 334867 a
unclassified drug
animal experiment
animal tissue
article
bleeding
controlled study
estrus cycle
female
food intake
gonadotropin blood level
histology
hyperemia
light dark cycle
nonhuman
ovulation
priority journal
proestrus
protein expression
quantitative assay
rat
real time polymerase chain reaction
reverse transcription polymerase chain reaction
Sprague Dawley rat
Animals
Benzoxazoles
Dioxanes
Eating
Estrous Cycle
Female
Gene Expression Regulation
Gonadotropin-Releasing Hormone
Gonadotropins
Intracellular Signaling Peptides and Proteins
Neuropeptides
Ovary
Ovulation
Pentobarbital
Phenylurea Compounds
Rats
Rats, Sprague-Dawley
Receptors, G-Protein-Coupled
Receptors, Neuropeptide
RNA, Messenger
Urea
Silveyra, P.
Lux-Lantos, V.
Libertun, C.
Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation
topic_facet Orexin 1 and orexin 2 receptor antagonists
Ovary
cetrorelix
gonadotropin
jnj 10397049
orexin
orexin 1 receptor
orexin 2 receptor
pentobarbital
preproorexin
receptor blocking agent
sb 334867 a
unclassified drug
animal experiment
animal tissue
article
bleeding
controlled study
estrus cycle
female
food intake
gonadotropin blood level
histology
hyperemia
light dark cycle
nonhuman
ovulation
priority journal
proestrus
protein expression
quantitative assay
rat
real time polymerase chain reaction
reverse transcription polymerase chain reaction
Sprague Dawley rat
Animals
Benzoxazoles
Dioxanes
Eating
Estrous Cycle
Female
Gene Expression Regulation
Gonadotropin-Releasing Hormone
Gonadotropins
Intracellular Signaling Peptides and Proteins
Neuropeptides
Ovary
Ovulation
Pentobarbital
Phenylurea Compounds
Rats
Rats, Sprague-Dawley
Receptors, G-Protein-Coupled
Receptors, Neuropeptide
RNA, Messenger
Urea
description Orexins are peptides controlling feeding, sleep, and neuroendocrine functions. They are synthesized by the hypothalamus with projections throughout the brain. Orexins and their orexin 1 (OX1) and orexin 2 receptors (OX2) are present outside the central nervous system. Here the expression of preproorexin (PPO), OX1, and OX2 was studied in rat ovaries. PPO, OX1, and OX2 were determined by quantitative real-time RT-PCR in ovaries of cycling Sprague-Dawley rats on all days of the cycle. Serum hormones and food consumption were determined. Ovarian OX1 and OX2 expression was then studied after ovulation blockade with Cetrorelix or Nembutal. Finally, proestrous rats were treated at 1400 and 1900 with a selective OX1 antagonist (SB-334867-A) and/or a selective OX2 antagonist (JNJ-10397049), and hormone levels, ovulation, and ovarian histology were studied. Both receptors' expression increased in the ovary between 1700 and 2300 of proestrus exclusively, in coincidence with hormone peaks, but not with the dark-light cycle or food intake. PPO was not detected. Cetrorelix or Nembutal prevented the increases of OX1 and OX2 while blunting gonadotropin peaks. SB-334867-A and JNJ-10397049, alone or combined, decreased serum gonadotropins and reduced ova number the following morning; ovaries showed a bloody (hyperemic and/or hemorrhagic) reaction with more preovulatory follicles and less corpora lutea. Here we demonstrate for the first time an increased ovarian expression of both OX1 and OX2, only during proestrous afternoon, and its hormone dependence but not dependence on the dark-light cycle. Two new receptor antagonists reduced proestrous gonadotropins and/or ova number while producing ovarian structural changes. Copyright © 2007 the American Physiological Society.
format JOUR
author Silveyra, P.
Lux-Lantos, V.
Libertun, C.
author_facet Silveyra, P.
Lux-Lantos, V.
Libertun, C.
author_sort Silveyra, P.
title Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation
title_short Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation
title_full Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation
title_fullStr Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation
title_full_unstemmed Both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: Effects of orexin receptor antagonists on gonadotropins and ovulation
title_sort both orexin receptors are expressed in rat ovaries and fluctuate with the estrous cycle: effects of orexin receptor antagonists on gonadotropins and ovulation
url http://hdl.handle.net/20.500.12110/paper_01931849_v293_n4_pE977_Silveyra
work_keys_str_mv AT silveyrap bothorexinreceptorsareexpressedinratovariesandfluctuatewiththeestrouscycleeffectsoforexinreceptorantagonistsongonadotropinsandovulation
AT luxlantosv bothorexinreceptorsareexpressedinratovariesandfluctuatewiththeestrouscycleeffectsoforexinreceptorantagonistsongonadotropinsandovulation
AT libertunc bothorexinreceptorsareexpressedinratovariesandfluctuatewiththeestrouscycleeffectsoforexinreceptorantagonistsongonadotropinsandovulation
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