Adipose tissue beta-adrenergic and A1 adenosine receptors in suckling pigs

During the first few weeks after birth, major changes occur in porcine adipocyte lipid metabolism. Two of the important receptors controlling lipid metabolism in adipocytes are the beta-adrenergic receptors (betaAR) and the A1 adenosine receptors (A1R). To gain insight into the role of these recepto...

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Veröffentlicht in:Journal of animal science 1997-12, Vol.75 (12), p.3161-3168
Hauptverfasser: Mersmann, H.J, Carey, G.B, Smith, E.O
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Carey, G.B
Smith, E.O
description During the first few weeks after birth, major changes occur in porcine adipocyte lipid metabolism. Two of the important receptors controlling lipid metabolism in adipocytes are the beta-adrenergic receptors (betaAR) and the A1 adenosine receptors (A1R). To gain insight into the role of these receptors in modulating neonatal adipocyte lipid metabolism, we measured receptor affinity and number in suckling pigs. Adipose tissue from crossbred (X-Bred) and genetically obese suckling pigs at 0, 3, 10, and 17 d of age was used to prepare crude membranes. The betaAR and A1R number and affinity were measured in membranes by equilibrium saturation binding with radioligands. Obese pigs were smaller than X-Bred pigs (average weight = 1.62 and 2.43 kg for obese and X-Bred, respectively; P .01). Osmium-fixed adipocytes were larger in obese pigs than in X-Bred pigs (average cell diameter 330 pM at younger ages; age effect P .01). The pattern for the betaAR number was complex; the lowest receptor number was at 10 d of age in obese and XBred pigs (average number 65 fmol/mg protein at older and younger ages; age effect P = .03). The higher betaAR Kd and the lower receptor number in younger animals suggest less regulation by physiologic concentrations of epinephrine and norepinephrine. This would allow greater anabolic lipid metabolism to proceed during the neonatal period, when adipocytes increase four- to sixfold in volume. There were no measurable A1R at any of these early ages; thus, adenosine control mechanisms to counteract the betaAR and provide negative controls to lipid accretion are not operable in suckling pigs
doi_str_mv 10.2527/1997.75123161x
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Two of the important receptors controlling lipid metabolism in adipocytes are the beta-adrenergic receptors (betaAR) and the A1 adenosine receptors (A1R). To gain insight into the role of these receptors in modulating neonatal adipocyte lipid metabolism, we measured receptor affinity and number in suckling pigs. Adipose tissue from crossbred (X-Bred) and genetically obese suckling pigs at 0, 3, 10, and 17 d of age was used to prepare crude membranes. The betaAR and A1R number and affinity were measured in membranes by equilibrium saturation binding with radioligands. Obese pigs were smaller than X-Bred pigs (average weight = 1.62 and 2.43 kg for obese and X-Bred, respectively; P .01). Osmium-fixed adipocytes were larger in obese pigs than in X-Bred pigs (average cell diameter 330 pM at younger ages; age effect P .01). The pattern for the betaAR number was complex; the lowest receptor number was at 10 d of age in obese and XBred pigs (average number 65 fmol/mg protein at older and younger ages; age effect P = .03). The higher betaAR Kd and the lower receptor number in younger animals suggest less regulation by physiologic concentrations of epinephrine and norepinephrine. This would allow greater anabolic lipid metabolism to proceed during the neonatal period, when adipocytes increase four- to sixfold in volume. There were no measurable A1R at any of these early ages; thus, adenosine control mechanisms to counteract the betaAR and provide negative controls to lipid accretion are not operable in suckling pigs</description><identifier>ISSN: 0021-8812</identifier><identifier>EISSN: 1525-3163</identifier><identifier>EISSN: 0021-8812</identifier><identifier>DOI: 10.2527/1997.75123161x</identifier><identifier>PMID: 9419989</identifier><language>eng</language><publisher>Savoy, IL: Am Soc Animal Sci</publisher><subject>Adipocytes - chemistry ; Adipocytes - metabolism ; Adipocytes - pathology ; Adipose Tissue - metabolism ; Adipose Tissue - physiopathology ; ADIPOSE TISSUES ; Aging - metabolism ; Aging - physiology ; Animal productions ; Animals ; Animals, Suckling - metabolism ; Animals, Suckling - physiology ; BETA-ADRENERGIC RECEPTORS ; Biological and medical sciences ; BIOLOGICAL DIFFERENCES ; Body fat ; BODY WEIGHT ; Body Weight - physiology ; CELL MEMBRANES ; CELLS ; CELLULE ; CELULAS ; DIFERENCIAS BIOLOGICAS ; DIFFERENCE BIOLOGIQUE ; Female ; Fundamental and applied biological sciences. Psychology ; Hogs ; HORMONE RECEPTORS ; Iodocyanopindolol ; LECHON ; LINE DIFFERENCES ; LIPID METABOLISM ; Lipids ; Male ; MEMBRANAS CELULARES ; MEMBRANE CELLULAIRE ; Metabolism ; METABOLISME DES LIPIDES ; METABOLISMO DE LIPIDOS ; Models, Biological ; Obesity ; Obesity - genetics ; Obesity - metabolism ; Obesity - veterinary ; OVERWEIGHT ; PESO CORPORAL ; PIGLETS ; Pindolol - analogs &amp; derivatives ; Pindolol - metabolism ; POIDS CORPOREL ; PORCELET ; RECEPTEUR D'HORMONE ; RECEPTORES DE HORMONAS ; Receptors, Adrenergic, beta - analysis ; Receptors, Adrenergic, beta - metabolism ; Receptors, Adrenergic, beta - physiology ; Receptors, Purinergic P1 - analysis ; Receptors, Purinergic P1 - metabolism ; Receptors, Purinergic P1 - physiology ; SOBREPESO ; SURPOIDS ; Swine - metabolism ; Swine - physiology ; Swine Diseases - genetics ; Swine Diseases - metabolism ; Swine Diseases - physiopathology ; TEJIDO ADIPOSO ; Terrestrial animal productions ; TISSU ADIPEUX ; Vertebrates</subject><ispartof>Journal of animal science, 1997-12, Vol.75 (12), p.3161-3168</ispartof><rights>1998 INIST-CNRS</rights><rights>Copyright American Society of Animal Science Dec 1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-6c6ce2be81d163352546e71ba0d871b3a1f6487d531494eedffcd19f3b219d353</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2100923$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9419989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mersmann, H.J</creatorcontrib><creatorcontrib>Carey, G.B</creatorcontrib><creatorcontrib>Smith, E.O</creatorcontrib><title>Adipose tissue beta-adrenergic and A1 adenosine receptors in suckling pigs</title><title>Journal of animal science</title><addtitle>J Anim Sci</addtitle><description>During the first few weeks after birth, major changes occur in porcine adipocyte lipid metabolism. Two of the important receptors controlling lipid metabolism in adipocytes are the beta-adrenergic receptors (betaAR) and the A1 adenosine receptors (A1R). To gain insight into the role of these receptors in modulating neonatal adipocyte lipid metabolism, we measured receptor affinity and number in suckling pigs. Adipose tissue from crossbred (X-Bred) and genetically obese suckling pigs at 0, 3, 10, and 17 d of age was used to prepare crude membranes. The betaAR and A1R number and affinity were measured in membranes by equilibrium saturation binding with radioligands. Obese pigs were smaller than X-Bred pigs (average weight = 1.62 and 2.43 kg for obese and X-Bred, respectively; P .01). Osmium-fixed adipocytes were larger in obese pigs than in X-Bred pigs (average cell diameter 330 pM at younger ages; age effect P .01). The pattern for the betaAR number was complex; the lowest receptor number was at 10 d of age in obese and XBred pigs (average number 65 fmol/mg protein at older and younger ages; age effect P = .03). The higher betaAR Kd and the lower receptor number in younger animals suggest less regulation by physiologic concentrations of epinephrine and norepinephrine. This would allow greater anabolic lipid metabolism to proceed during the neonatal period, when adipocytes increase four- to sixfold in volume. There were no measurable A1R at any of these early ages; thus, adenosine control mechanisms to counteract the betaAR and provide negative controls to lipid accretion are not operable in suckling pigs</description><subject>Adipocytes - chemistry</subject><subject>Adipocytes - metabolism</subject><subject>Adipocytes - pathology</subject><subject>Adipose Tissue - metabolism</subject><subject>Adipose Tissue - physiopathology</subject><subject>ADIPOSE TISSUES</subject><subject>Aging - metabolism</subject><subject>Aging - physiology</subject><subject>Animal productions</subject><subject>Animals</subject><subject>Animals, Suckling - metabolism</subject><subject>Animals, Suckling - physiology</subject><subject>BETA-ADRENERGIC RECEPTORS</subject><subject>Biological and medical sciences</subject><subject>BIOLOGICAL DIFFERENCES</subject><subject>Body fat</subject><subject>BODY WEIGHT</subject><subject>Body Weight - physiology</subject><subject>CELL MEMBRANES</subject><subject>CELLS</subject><subject>CELLULE</subject><subject>CELULAS</subject><subject>DIFERENCIAS BIOLOGICAS</subject><subject>DIFFERENCE BIOLOGIQUE</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hogs</subject><subject>HORMONE RECEPTORS</subject><subject>Iodocyanopindolol</subject><subject>LECHON</subject><subject>LINE DIFFERENCES</subject><subject>LIPID METABOLISM</subject><subject>Lipids</subject><subject>Male</subject><subject>MEMBRANAS CELULARES</subject><subject>MEMBRANE CELLULAIRE</subject><subject>Metabolism</subject><subject>METABOLISME DES LIPIDES</subject><subject>METABOLISMO DE LIPIDOS</subject><subject>Models, Biological</subject><subject>Obesity</subject><subject>Obesity - genetics</subject><subject>Obesity - metabolism</subject><subject>Obesity - veterinary</subject><subject>OVERWEIGHT</subject><subject>PESO CORPORAL</subject><subject>PIGLETS</subject><subject>Pindolol - analogs &amp; derivatives</subject><subject>Pindolol - metabolism</subject><subject>POIDS CORPOREL</subject><subject>PORCELET</subject><subject>RECEPTEUR D'HORMONE</subject><subject>RECEPTORES DE HORMONAS</subject><subject>Receptors, Adrenergic, beta - analysis</subject><subject>Receptors, Adrenergic, beta - metabolism</subject><subject>Receptors, Adrenergic, beta - physiology</subject><subject>Receptors, Purinergic P1 - analysis</subject><subject>Receptors, Purinergic P1 - metabolism</subject><subject>Receptors, Purinergic P1 - physiology</subject><subject>SOBREPESO</subject><subject>SURPOIDS</subject><subject>Swine - metabolism</subject><subject>Swine - physiology</subject><subject>Swine Diseases - genetics</subject><subject>Swine Diseases - metabolism</subject><subject>Swine Diseases - physiopathology</subject><subject>TEJIDO ADIPOSO</subject><subject>Terrestrial animal productions</subject><subject>TISSU ADIPEUX</subject><subject>Vertebrates</subject><issn>0021-8812</issn><issn>1525-3163</issn><issn>0021-8812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkM2P0zAQxS0EWsrClRtShBCcUjx2HMfHasWnVuIAe7Yce5J1SZPgSbTw3-OqVZE4jUbze2-eHmMvgW-FEvo9GKO3WoGQUMPvR2wDSqgyL_Ix23AuoGwaEE_ZM6I95yCUUVfsylRZ15gN-7oLcZ4IiyUSrVi0uLjShYQjpj76wo2h2EHhAo4TxRGLhB7nZUpUxLGg1f8c4tgXc-zpOXvSuYHwxXles7uPH37cfC5vv336crO7Lb0EtZS1rz2KFhsIOaTMaasaNbSOhyYP6aCrq0YHJaEyFWLoOh_AdLIVYIJU8pq9PfnOafq1Ii32EMnjMLgRp5WsNpWplaoz-Po_cD-taczZrIBcSiW5yND2BPk0ESXs7JziwaU_Frg9NmyPDdtLw1nw6uy6tgcMF_xcab6_Od8deTd0yY0-0gUTwLkRMmPvTth97O8fYkJLBzcM2RTs3pFWFoQ9fvz3sHOTdX3KZnffj6G4Bt1o-RdD45eG</recordid><startdate>199712</startdate><enddate>199712</enddate><creator>Mersmann, H.J</creator><creator>Carey, G.B</creator><creator>Smith, E.O</creator><general>Am Soc Animal Sci</general><general>American Society of Animal Science</general><general>Oxford University Press</general><scope>FBQ</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>3V.</scope><scope>7RQ</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>199712</creationdate><title>Adipose tissue beta-adrenergic and A1 adenosine receptors in suckling pigs</title><author>Mersmann, H.J ; Carey, G.B ; Smith, E.O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-6c6ce2be81d163352546e71ba0d871b3a1f6487d531494eedffcd19f3b219d353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adipocytes - chemistry</topic><topic>Adipocytes - metabolism</topic><topic>Adipocytes - pathology</topic><topic>Adipose Tissue - metabolism</topic><topic>Adipose Tissue - physiopathology</topic><topic>ADIPOSE TISSUES</topic><topic>Aging - metabolism</topic><topic>Aging - physiology</topic><topic>Animal productions</topic><topic>Animals</topic><topic>Animals, Suckling - metabolism</topic><topic>Animals, Suckling - physiology</topic><topic>BETA-ADRENERGIC RECEPTORS</topic><topic>Biological and medical sciences</topic><topic>BIOLOGICAL DIFFERENCES</topic><topic>Body fat</topic><topic>BODY WEIGHT</topic><topic>Body Weight - physiology</topic><topic>CELL MEMBRANES</topic><topic>CELLS</topic><topic>CELLULE</topic><topic>CELULAS</topic><topic>DIFERENCIAS BIOLOGICAS</topic><topic>DIFFERENCE BIOLOGIQUE</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. 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Two of the important receptors controlling lipid metabolism in adipocytes are the beta-adrenergic receptors (betaAR) and the A1 adenosine receptors (A1R). To gain insight into the role of these receptors in modulating neonatal adipocyte lipid metabolism, we measured receptor affinity and number in suckling pigs. Adipose tissue from crossbred (X-Bred) and genetically obese suckling pigs at 0, 3, 10, and 17 d of age was used to prepare crude membranes. The betaAR and A1R number and affinity were measured in membranes by equilibrium saturation binding with radioligands. Obese pigs were smaller than X-Bred pigs (average weight = 1.62 and 2.43 kg for obese and X-Bred, respectively; P .01). Osmium-fixed adipocytes were larger in obese pigs than in X-Bred pigs (average cell diameter 330 pM at younger ages; age effect P .01). The pattern for the betaAR number was complex; the lowest receptor number was at 10 d of age in obese and XBred pigs (average number 65 fmol/mg protein at older and younger ages; age effect P = .03). The higher betaAR Kd and the lower receptor number in younger animals suggest less regulation by physiologic concentrations of epinephrine and norepinephrine. This would allow greater anabolic lipid metabolism to proceed during the neonatal period, when adipocytes increase four- to sixfold in volume. There were no measurable A1R at any of these early ages; thus, adenosine control mechanisms to counteract the betaAR and provide negative controls to lipid accretion are not operable in suckling pigs</abstract><cop>Savoy, IL</cop><pub>Am Soc Animal Sci</pub><pmid>9419989</pmid><doi>10.2527/1997.75123161x</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 0021-8812
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0021-8812
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Adipocytes - chemistry
Adipocytes - metabolism
Adipocytes - pathology
Adipose Tissue - metabolism
Adipose Tissue - physiopathology
ADIPOSE TISSUES
Aging - metabolism
Aging - physiology
Animal productions
Animals
Animals, Suckling - metabolism
Animals, Suckling - physiology
BETA-ADRENERGIC RECEPTORS
Biological and medical sciences
BIOLOGICAL DIFFERENCES
Body fat
BODY WEIGHT
Body Weight - physiology
CELL MEMBRANES
CELLS
CELLULE
CELULAS
DIFERENCIAS BIOLOGICAS
DIFFERENCE BIOLOGIQUE
Female
Fundamental and applied biological sciences. Psychology
Hogs
HORMONE RECEPTORS
Iodocyanopindolol
LECHON
LINE DIFFERENCES
LIPID METABOLISM
Lipids
Male
MEMBRANAS CELULARES
MEMBRANE CELLULAIRE
Metabolism
METABOLISME DES LIPIDES
METABOLISMO DE LIPIDOS
Models, Biological
Obesity
Obesity - genetics
Obesity - metabolism
Obesity - veterinary
OVERWEIGHT
PESO CORPORAL
PIGLETS
Pindolol - analogs & derivatives
Pindolol - metabolism
POIDS CORPOREL
PORCELET
RECEPTEUR D'HORMONE
RECEPTORES DE HORMONAS
Receptors, Adrenergic, beta - analysis
Receptors, Adrenergic, beta - metabolism
Receptors, Adrenergic, beta - physiology
Receptors, Purinergic P1 - analysis
Receptors, Purinergic P1 - metabolism
Receptors, Purinergic P1 - physiology
SOBREPESO
SURPOIDS
Swine - metabolism
Swine - physiology
Swine Diseases - genetics
Swine Diseases - metabolism
Swine Diseases - physiopathology
TEJIDO ADIPOSO
Terrestrial animal productions
TISSU ADIPEUX
Vertebrates
title Adipose tissue beta-adrenergic and A1 adenosine receptors in suckling pigs
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