Food restriction, ghrelin, its antagonist and obestatin control expression of ghrelin and its receptor in chicken hypothalamus and ovary

The purpose of the present study was to identify the role of age, nutritional state and some metabolic hormones in control of avian hypothalamic and ovarian ghrelin/ghrelin receptor system. We examined the effect of food restriction, administration of ghrelin 1–18, ghrelin antagonistic analogue (D-L...

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Veröffentlicht in:Comparative biochemistry and physiology. Part A, Molecular & integrative physiology Molecular & integrative physiology, 2013-01, Vol.164 (1), p.141-153
Hauptverfasser: Sirotkin, Alexander V., Pavlova, Silvia, Tena-Sempere, Manuel, Grossmann, Roland, Jiménez, Magdalena Romero, Rodriguez, Juan Manuel Castellano, Valenzuela, Francisco
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container_issue 1
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container_title Comparative biochemistry and physiology. Part A, Molecular & integrative physiology
container_volume 164
creator Sirotkin, Alexander V.
Pavlova, Silvia
Tena-Sempere, Manuel
Grossmann, Roland
Jiménez, Magdalena Romero
Rodriguez, Juan Manuel Castellano
Valenzuela, Francisco
description The purpose of the present study was to identify the role of age, nutritional state and some metabolic hormones in control of avian hypothalamic and ovarian ghrelin/ghrelin receptor system. We examined the effect of food restriction, administration of ghrelin 1–18, ghrelin antagonistic analogue (D-Lys-3)-GHRP-6, obestatin and combinations of them on the expression of ghrelin and ghrelin receptor (GHS-R1a) in hypothalamus and ovary of old (23months of age) and young (7months of age) chickens. Expression of mRNAs for ghrelin and GHS-R1a in both hypothalamus and largest ovarian follicle was measured by RT-PCR. It was observed that food restriction could promote the expression of ghrelin and GHS-R1a in hypothalamus and ovary of the old chickens, but in the young chickens it reduced expression of ghrelin and did not affect expression of GHS-R1a in the ovary. Administration of ghrelin 1–18 did not affect hypothalamic or ovarian ghrelin mRNA, but significantly increased the expression of GHS-R1a in hypothalamus, but not in ovary. (D-Lys-3)-GHRP-6, significantly stimulated accumulation of ghrelin, but not GHS-R1a mRNA in hypothalamus or ghrelin or GHS-R1a in the ovary. Ghrelin 1–18 and (D-Lys-3)-GHRP-6, when given together, were able either to prevent or to induce effect of these hormones. Obestatin administration increased expression of ghrelin gene in the hypothalamus, but not expression of hypothalamic GHS-R1a, ovarian ghrelin and GHS-R1a. Furthermore, obestatin was able to modify effect of both ghrelin and fasting on hypothalamic and ovarian mRNA for ghrelin GHS-R1a. Our results (1) confirm the existence of ghrelin and its functional receptors GHS-R1a in the chicken hypothalamus and ovary (2) confirm the age-dependent control of ovarian ghrelin by feeding, (3) demonstrate, that nutritional status can influence the expression of both ghrelin and GHS-R1a in hypothalamus and in the ovary (3) demonstrates for the first time, that ghrelin can promote generation of its functional receptor in the hypothalamus, but not in the ovary, (4) show that ghrelin1–18 and (D-Lys-3)-GHRP-6 could not only be antagonists in the action on chicken hypothalamus and ovaries, but also independent regulators and even agonists, and (5) provide first evidence for action of obestatin on hypothalamic ghrelin and on the response of hypothalamic and ovarian ghrelin/GHS-R1a system to food restriction. These data indicate the involvement of both hypothalamic and ovarian ghrelin/GHS-R1 systems i
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We examined the effect of food restriction, administration of ghrelin 1–18, ghrelin antagonistic analogue (D-Lys-3)-GHRP-6, obestatin and combinations of them on the expression of ghrelin and ghrelin receptor (GHS-R1a) in hypothalamus and ovary of old (23months of age) and young (7months of age) chickens. Expression of mRNAs for ghrelin and GHS-R1a in both hypothalamus and largest ovarian follicle was measured by RT-PCR. It was observed that food restriction could promote the expression of ghrelin and GHS-R1a in hypothalamus and ovary of the old chickens, but in the young chickens it reduced expression of ghrelin and did not affect expression of GHS-R1a in the ovary. Administration of ghrelin 1–18 did not affect hypothalamic or ovarian ghrelin mRNA, but significantly increased the expression of GHS-R1a in hypothalamus, but not in ovary. (D-Lys-3)-GHRP-6, significantly stimulated accumulation of ghrelin, but not GHS-R1a mRNA in hypothalamus or ghrelin or GHS-R1a in the ovary. Ghrelin 1–18 and (D-Lys-3)-GHRP-6, when given together, were able either to prevent or to induce effect of these hormones. Obestatin administration increased expression of ghrelin gene in the hypothalamus, but not expression of hypothalamic GHS-R1a, ovarian ghrelin and GHS-R1a. Furthermore, obestatin was able to modify effect of both ghrelin and fasting on hypothalamic and ovarian mRNA for ghrelin GHS-R1a. Our results (1) confirm the existence of ghrelin and its functional receptors GHS-R1a in the chicken hypothalamus and ovary (2) confirm the age-dependent control of ovarian ghrelin by feeding, (3) demonstrate, that nutritional status can influence the expression of both ghrelin and GHS-R1a in hypothalamus and in the ovary (3) demonstrates for the first time, that ghrelin can promote generation of its functional receptor in the hypothalamus, but not in the ovary, (4) show that ghrelin1–18 and (D-Lys-3)-GHRP-6 could not only be antagonists in the action on chicken hypothalamus and ovaries, but also independent regulators and even agonists, and (5) provide first evidence for action of obestatin on hypothalamic ghrelin and on the response of hypothalamic and ovarian ghrelin/GHS-R1a system to food restriction. 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Part A, Molecular &amp; integrative physiology</title><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><description>The purpose of the present study was to identify the role of age, nutritional state and some metabolic hormones in control of avian hypothalamic and ovarian ghrelin/ghrelin receptor system. We examined the effect of food restriction, administration of ghrelin 1–18, ghrelin antagonistic analogue (D-Lys-3)-GHRP-6, obestatin and combinations of them on the expression of ghrelin and ghrelin receptor (GHS-R1a) in hypothalamus and ovary of old (23months of age) and young (7months of age) chickens. Expression of mRNAs for ghrelin and GHS-R1a in both hypothalamus and largest ovarian follicle was measured by RT-PCR. It was observed that food restriction could promote the expression of ghrelin and GHS-R1a in hypothalamus and ovary of the old chickens, but in the young chickens it reduced expression of ghrelin and did not affect expression of GHS-R1a in the ovary. Administration of ghrelin 1–18 did not affect hypothalamic or ovarian ghrelin mRNA, but significantly increased the expression of GHS-R1a in hypothalamus, but not in ovary. (D-Lys-3)-GHRP-6, significantly stimulated accumulation of ghrelin, but not GHS-R1a mRNA in hypothalamus or ghrelin or GHS-R1a in the ovary. Ghrelin 1–18 and (D-Lys-3)-GHRP-6, when given together, were able either to prevent or to induce effect of these hormones. Obestatin administration increased expression of ghrelin gene in the hypothalamus, but not expression of hypothalamic GHS-R1a, ovarian ghrelin and GHS-R1a. Furthermore, obestatin was able to modify effect of both ghrelin and fasting on hypothalamic and ovarian mRNA for ghrelin GHS-R1a. Our results (1) confirm the existence of ghrelin and its functional receptors GHS-R1a in the chicken hypothalamus and ovary (2) confirm the age-dependent control of ovarian ghrelin by feeding, (3) demonstrate, that nutritional status can influence the expression of both ghrelin and GHS-R1a in hypothalamus and in the ovary (3) demonstrates for the first time, that ghrelin can promote generation of its functional receptor in the hypothalamus, but not in the ovary, (4) show that ghrelin1–18 and (D-Lys-3)-GHRP-6 could not only be antagonists in the action on chicken hypothalamus and ovaries, but also independent regulators and even agonists, and (5) provide first evidence for action of obestatin on hypothalamic ghrelin and on the response of hypothalamic and ovarian ghrelin/GHS-R1a system to food restriction. These data indicate the involvement of both hypothalamic and ovarian ghrelin/GHS-R1 systems in mediating the effects of nutritional status, ghrelin and obestatin on reproductive processes.</description><subject>Age Factors</subject><subject>agonists</subject><subject>Animals</subject><subject>antagonists</subject><subject>Chicken</subject><subject>chickens</subject><subject>Chickens - genetics</subject><subject>Chickens - metabolism</subject><subject>fasting</subject><subject>Feeding</subject><subject>Female</subject><subject>Food Deprivation</subject><subject>Gene Expression Regulation, Developmental</subject><subject>genes</subject><subject>Ghrelin</subject><subject>Ghrelin - antagonists &amp; inhibitors</subject><subject>Ghrelin - metabolism</subject><subject>Ghrelin - pharmacology</subject><subject>Ghrelin receptor (GHS-R1a)</subject><subject>ghrelin receptors</subject><subject>Humans</subject><subject>Hypothalamus</subject><subject>Hypothalamus - cytology</subject><subject>Hypothalamus - drug effects</subject><subject>Hypothalamus - metabolism</subject><subject>messenger RNA</subject><subject>nutritional status</subject><subject>Obestatin</subject><subject>Oligopeptides - pharmacology</subject><subject>ovarian follicles</subject><subject>Ovary</subject><subject>Ovary - cytology</subject><subject>Ovary - metabolism</subject><subject>Receptors, Ghrelin - genetics</subject><subject>Receptors, Ghrelin - metabolism</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><issn>1095-6433</issn><issn>1531-4332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1TAQhS0Eoj_wAiwgSxZN8G98LbGpKgpIlVhA15bjTO71JTcOtm9F34DHZkJaluDNjKXvHM3MIeQVow2jrH23b3w3u4ZTxhuqG8roE3LKlGC1FII_xZ4aVbf4OSFnOe8pPsnkc3LC-UZrvVGn5Nd1jH2VIJcUfAlxuqi2uwRjwCaUXLmpuG2cQi7Y9lXskHQlTJWPU0lxrODnjOqMyioOj9o_7CJP4GEuMVWLYhf8d5iq3f0cy86N7nDMq-mdS_cvyLPBjRlePtRzcnv94dvVp_rmy8fPV5c3tZfalFqzjRNCdoobrqlmvemUwSpbo8WgKTUtgw1VPQjpOik9B8HNIHvmW98pJs7J29V3TvHHEbexh5A9jKObIB6zZZIZoQwT7f9RzqlopaYKUb6iPsWcEwx2TuGAa1lG7RKW3dslLLuEZam2GBaKXj_4H7sD9H8lj-kg8GYFBhet26aQ7e1XdFCUIoO2SLxfCcCT3QVINvsAk4c-4OmL7WP41wS_AaIwr2w</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Sirotkin, Alexander V.</creator><creator>Pavlova, Silvia</creator><creator>Tena-Sempere, Manuel</creator><creator>Grossmann, Roland</creator><creator>Jiménez, Magdalena Romero</creator><creator>Rodriguez, Juan Manuel Castellano</creator><creator>Valenzuela, Francisco</creator><general>Elsevier Inc</general><scope>FBQ</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>7X8</scope><scope>7TK</scope></search><sort><creationdate>201301</creationdate><title>Food restriction, ghrelin, its antagonist and obestatin control expression of ghrelin and its receptor in chicken hypothalamus and ovary</title><author>Sirotkin, Alexander V. ; Pavlova, Silvia ; Tena-Sempere, Manuel ; Grossmann, Roland ; Jiménez, Magdalena Romero ; Rodriguez, Juan Manuel Castellano ; Valenzuela, Francisco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-718a334b52927071d9b5907146973f700961e805de34ab44c2e329f4d1c6cb513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Age Factors</topic><topic>agonists</topic><topic>Animals</topic><topic>antagonists</topic><topic>Chicken</topic><topic>chickens</topic><topic>Chickens - genetics</topic><topic>Chickens - metabolism</topic><topic>fasting</topic><topic>Feeding</topic><topic>Female</topic><topic>Food Deprivation</topic><topic>Gene Expression Regulation, Developmental</topic><topic>genes</topic><topic>Ghrelin</topic><topic>Ghrelin - antagonists &amp; inhibitors</topic><topic>Ghrelin - metabolism</topic><topic>Ghrelin - pharmacology</topic><topic>Ghrelin receptor (GHS-R1a)</topic><topic>ghrelin receptors</topic><topic>Humans</topic><topic>Hypothalamus</topic><topic>Hypothalamus - cytology</topic><topic>Hypothalamus - drug effects</topic><topic>Hypothalamus - metabolism</topic><topic>messenger RNA</topic><topic>nutritional status</topic><topic>Obestatin</topic><topic>Oligopeptides - pharmacology</topic><topic>ovarian follicles</topic><topic>Ovary</topic><topic>Ovary - cytology</topic><topic>Ovary - metabolism</topic><topic>Receptors, Ghrelin - genetics</topic><topic>Receptors, Ghrelin - metabolism</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sirotkin, Alexander V.</creatorcontrib><creatorcontrib>Pavlova, Silvia</creatorcontrib><creatorcontrib>Tena-Sempere, Manuel</creatorcontrib><creatorcontrib>Grossmann, Roland</creatorcontrib><creatorcontrib>Jiménez, Magdalena Romero</creatorcontrib><creatorcontrib>Rodriguez, Juan Manuel Castellano</creatorcontrib><creatorcontrib>Valenzuela, Francisco</creatorcontrib><collection>AGRIS</collection><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><collection>Neurosciences Abstracts</collection><jtitle>Comparative biochemistry and physiology. 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Part A, Molecular &amp; integrative physiology</jtitle><addtitle>Comp Biochem Physiol A Mol Integr Physiol</addtitle><date>2013-01</date><risdate>2013</risdate><volume>164</volume><issue>1</issue><spage>141</spage><epage>153</epage><pages>141-153</pages><issn>1095-6433</issn><eissn>1531-4332</eissn><abstract>The purpose of the present study was to identify the role of age, nutritional state and some metabolic hormones in control of avian hypothalamic and ovarian ghrelin/ghrelin receptor system. We examined the effect of food restriction, administration of ghrelin 1–18, ghrelin antagonistic analogue (D-Lys-3)-GHRP-6, obestatin and combinations of them on the expression of ghrelin and ghrelin receptor (GHS-R1a) in hypothalamus and ovary of old (23months of age) and young (7months of age) chickens. Expression of mRNAs for ghrelin and GHS-R1a in both hypothalamus and largest ovarian follicle was measured by RT-PCR. It was observed that food restriction could promote the expression of ghrelin and GHS-R1a in hypothalamus and ovary of the old chickens, but in the young chickens it reduced expression of ghrelin and did not affect expression of GHS-R1a in the ovary. Administration of ghrelin 1–18 did not affect hypothalamic or ovarian ghrelin mRNA, but significantly increased the expression of GHS-R1a in hypothalamus, but not in ovary. (D-Lys-3)-GHRP-6, significantly stimulated accumulation of ghrelin, but not GHS-R1a mRNA in hypothalamus or ghrelin or GHS-R1a in the ovary. Ghrelin 1–18 and (D-Lys-3)-GHRP-6, when given together, were able either to prevent or to induce effect of these hormones. Obestatin administration increased expression of ghrelin gene in the hypothalamus, but not expression of hypothalamic GHS-R1a, ovarian ghrelin and GHS-R1a. Furthermore, obestatin was able to modify effect of both ghrelin and fasting on hypothalamic and ovarian mRNA for ghrelin GHS-R1a. Our results (1) confirm the existence of ghrelin and its functional receptors GHS-R1a in the chicken hypothalamus and ovary (2) confirm the age-dependent control of ovarian ghrelin by feeding, (3) demonstrate, that nutritional status can influence the expression of both ghrelin and GHS-R1a in hypothalamus and in the ovary (3) demonstrates for the first time, that ghrelin can promote generation of its functional receptor in the hypothalamus, but not in the ovary, (4) show that ghrelin1–18 and (D-Lys-3)-GHRP-6 could not only be antagonists in the action on chicken hypothalamus and ovaries, but also independent regulators and even agonists, and (5) provide first evidence for action of obestatin on hypothalamic ghrelin and on the response of hypothalamic and ovarian ghrelin/GHS-R1a system to food restriction. These data indicate the involvement of both hypothalamic and ovarian ghrelin/GHS-R1 systems in mediating the effects of nutritional status, ghrelin and obestatin on reproductive processes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22877785</pmid><doi>10.1016/j.cbpa.2012.07.010</doi><tpages>13</tpages></addata></record>
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subjects Age Factors
agonists
Animals
antagonists
Chicken
chickens
Chickens - genetics
Chickens - metabolism
fasting
Feeding
Female
Food Deprivation
Gene Expression Regulation, Developmental
genes
Ghrelin
Ghrelin - antagonists & inhibitors
Ghrelin - metabolism
Ghrelin - pharmacology
Ghrelin receptor (GHS-R1a)
ghrelin receptors
Humans
Hypothalamus
Hypothalamus - cytology
Hypothalamus - drug effects
Hypothalamus - metabolism
messenger RNA
nutritional status
Obestatin
Oligopeptides - pharmacology
ovarian follicles
Ovary
Ovary - cytology
Ovary - metabolism
Receptors, Ghrelin - genetics
Receptors, Ghrelin - metabolism
Recombinant Proteins - pharmacology
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - genetics
RNA, Messenger - metabolism
title Food restriction, ghrelin, its antagonist and obestatin control expression of ghrelin and its receptor in chicken hypothalamus and ovary
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