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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1987-3-4
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pubmed:abstractText |
Immunoreactive insulin-like growth factor I (IGF-I) has recently been demonstrated in multiple tissues, including liver, kidney, lung, testes, and brain. Tissue IGF-I levels in hypophysectomized rats are elevated by GH. To examine whether tissue IGF-I production is regulated by local as well as systemic influences, we studied rat kidney IGF-I gene expression in renal compensatory hypertrophy occurring after unilateral nephrectomy. Northern analysis of kidney poly(A) RNA probed with [32P]IGF-I mouse cDNA revealed the presence of a mRNA species 1.3 kilobases in size. Dot hybridization of kidney poly(A) RNA showed that IGF-I mRNA was induced 5- to 6-fold in the kidneys of nephrectomized animals relative to levels in control sham-operated rats. This induction was present 24 h after surgery and continued for at least 7 days after the operation. Kidney radioimmunoassayable IGF-I content was also increased 73% in nephrectomized animals, although this was only apparent on the fourth day after surgery. In contrast, liver IGF-I mRNA levels were comparable in both experimental and control animals, suggesting that the IGF-I induction was specific to the tissue undergoing compensatory growth. Serum IGF-I and GH levels were not altered in nephrectomized and control animals for the duration of the experiments. These studies, therefore, confirm that IGF-I is synthesized in the kidney, and that kidneys undergoing compensatory growth have increased levels of IGF-I mRNA. This phenomenon occurs independently of changes in GH secretion, indicating that paracrine or autocrine factors are involved in the control of renal IGF-I production.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0013-7227
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
120
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
718-24
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3803301-Animals,
pubmed-meshheading:3803301-Hypertrophy,
pubmed-meshheading:3803301-Insulin-Like Growth Factor I,
pubmed-meshheading:3803301-Kidney,
pubmed-meshheading:3803301-Kinetics,
pubmed-meshheading:3803301-Male,
pubmed-meshheading:3803301-Nephrectomy,
pubmed-meshheading:3803301-Nucleic Acid Hybridization,
pubmed-meshheading:3803301-RNA, Messenger,
pubmed-meshheading:3803301-Rats,
pubmed-meshheading:3803301-Rats, Inbred Strains,
pubmed-meshheading:3803301-Somatomedins
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pubmed:year |
1987
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pubmed:articleTitle |
Relative increase in insulin-like growth factor I messenger ribonucleic acid levels in compensatory renal hypertrophy.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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