Source:http://linkedlifedata.com/resource/pubmed/id/11668024
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2001-10-22
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pubmed:abstractText |
Rats maintained with parenteral nutrition following 60% jejunoileal resection plus cecectomy exhibit minimal adaptive growth in the residual jejunum but a dramatic adaptive growth in the residual colon. Coinfusion of insulin-like growth factor I (IGF-I) with parenteral nutrition induces jejunal growth but has minimal effects in the colon. Our objective was to study the role of the endogenous IGF-I system in the differential responses of jejunum and colon to resection and/or IGF-I during parenteral nutrition. We measured concentrations of immunoreactive IGF-I in plasma, jejunum, and colon, IGF-I receptor binding, and levels of IGF receptor, IGF-I, IGF binding protein (IGFBP)-3 and IGFBP-5 mRNA in residual jejunum and colon 7 days after resection and/or IGF-I treatment. IGF-I receptor number was increased (74-99%) in jejunum and colon due to resection; IGF-I mRNA was increased 5-fold in jejunum and 15-fold in colon due to resection. Resection increased circulating IGFBPs but did not alter plasma IGF-I concentration. Resection induced colonic growth in association with significantly greater colonic IGFBP-5 mRNA and significantly lower colonic immunoreactive IGF-I. IGF-I treatment had no significant effect on IGF-I mRNA or IGF-I receptor number. Concentrations of plasma and jejunal immunoreactive IGF-I were significantly increased in rats given IGF-I in association with jejunal growth. IGF-I treatment significantly increased IGFBP-5 mRNA in the jejunum, which also correlated with jejunal growth. Thus resection upregulated IGF-I receptor number and IGF-I mRNA in residual jejunum and colon, but differential adaptation of these segments correlated with differential regulation of IGFBP-5 mRNA.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
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 Binding...,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, IGF Type 1
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0193-1857
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
281
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
G1158-68
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11668024-Anastomosis, Surgical,
pubmed-meshheading:11668024-Animals,
pubmed-meshheading:11668024-Body Weight,
pubmed-meshheading:11668024-Colon,
pubmed-meshheading:11668024-Insulin-Like Growth Factor Binding Protein 3,
pubmed-meshheading:11668024-Insulin-Like Growth Factor Binding Protein 5,
pubmed-meshheading:11668024-Insulin-Like Growth Factor Binding Proteins,
pubmed-meshheading:11668024-Insulin-Like Growth Factor I,
pubmed-meshheading:11668024-Intestinal Mucosa,
pubmed-meshheading:11668024-Jejunum,
pubmed-meshheading:11668024-Male,
pubmed-meshheading:11668024-Organ Size,
pubmed-meshheading:11668024-Parenteral Nutrition,
pubmed-meshheading:11668024-RNA, Messenger,
pubmed-meshheading:11668024-Rats,
pubmed-meshheading:11668024-Rats, Sprague-Dawley,
pubmed-meshheading:11668024-Receptor, IGF Type 1,
pubmed-meshheading:11668024-Up-Regulation
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pubmed:year |
2001
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pubmed:articleTitle |
Resection upregulates the IGF-I system of parenterally fed rats with jejunocolic anastomosis.
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pubmed:affiliation |
Department of Nutritional Sciences, University of Wisconsin-Madison, 53706, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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