Source:http://linkedlifedata.com/resource/pubmed/id/10746655
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2000-4-11
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pubmed:abstractText |
The actions of insulin-like growth factor-I (IGF-I) are modulated by IGF binding proteins (IGFBPs). The effects of IGFBP-1 in vivo are insufficiently known, with respect to inhibitory or stimulatory actions on IGF-induced growth of specific organs. Therefore, we studied the effects of IGFBP-1 on IGF-I-induced somatic and organ growth in pituitary-deficient Snell dwarf mice. Human GH, IGF-I, IGFBP-1, and a preequilibrated combination of equimolar amounts of IGF-I and IGFBP-1 were administered sc during 4 weeks. Treatment with IGF-I alone induced a significant increase in body length (108% of control) and weight (112%) as well as an increase in weight of the submandibular salivary glands (135%), kidneys (124%), femoral muscles (111%), testes (129%), and spleen (126%) compared with saline-treated controls. IGFBP-1 alone induced a significant increase in weight of the kidneys (152% of control). Coadministration of IGF-I with IGFBP-1 neutralized the stimulating effects of IGF-I on body length and weight as well as on the femoral muscles and testes. In contrast, the weights of the submandibular salivary glands (143%) were not significantly different from those of IGF-I-treated animals, whereas the weights of the kidneys (171%) and spleen (156%) were significantly increased compared with IGF-I-treated mice. The effect of IGFBP-1 plus IGF-I on kidney weight was not significantly greater than the effect of IGFBP-1 alone. Western ligand blotting showed induction of the IGFBP-3 doublet as well as IGFBPs with molecular masses of 24 kDa, most probably IGFBP-4, by human GH, IGF-I alone, and IGF-I in combination with IGFBP-1. Our data show that coadministration of IGFBP-1 inhibits IGF-I-induced body growth of GH-deficient mice but significantly stimulates the growth promoting effects of IGF-I on the kidneys and the spleen. These data warrant further investigation because differences in concentrations of IGFBP-1 occurring in vivo may influence IGF-I-induced anabolic processes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor Binding...,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor Binding...,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I,
http://linkedlifedata.com/resource/pubmed/chemical/Somatomedins
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0013-7227
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pubmed:author |
pubmed-author:BloemenR JRJ,
pubmed-author:DropS LSL,
pubmed-author:GresnigtM GMG,
pubmed-author:HoogerbruggeC MCM,
pubmed-author:KoedamJ AJA,
pubmed-author:KosterJ GJG,
pubmed-author:Lindenbergh-KortleveD JDJ,
pubmed-author:Van Buul-OffersS CSC,
pubmed-author:Van KleffensMM,
pubmed-author:Van NeckJ WJW
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pubmed:issnType |
Print
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pubmed:volume |
141
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1493-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:10746655-Animals,
pubmed-meshheading:10746655-Blood Glucose,
pubmed-meshheading:10746655-Body Weight,
pubmed-meshheading:10746655-Dwarfism,
pubmed-meshheading:10746655-Endocrine Glands,
pubmed-meshheading:10746655-Humans,
pubmed-meshheading:10746655-Insulin-Like Growth Factor Binding Protein 1,
pubmed-meshheading:10746655-Insulin-Like Growth Factor Binding Proteins,
pubmed-meshheading:10746655-Insulin-Like Growth Factor I,
pubmed-meshheading:10746655-Kidney,
pubmed-meshheading:10746655-Mice,
pubmed-meshheading:10746655-Mice, Mutant Strains,
pubmed-meshheading:10746655-Somatomedins
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pubmed:year |
2000
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pubmed:articleTitle |
Human insulin-like growth factor (IGF) binding protein-1 inhibits IGF-I-stimulated body growth but stimulates growth of the kidney in snell dwarf mice.
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pubmed:affiliation |
Department of Pediatric Endocrinology, University Medical Center Utrecht, The Netherlands. s.vanbuul@wkz.az.nl
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pubmed:publicationType |
Journal Article
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