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Am J Physiol Regul Integr Comp Physiol 292: R2144-R2150, 2007. First published March 1, 2007; doi:10.1152/ajpregu.00903.2006
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APPETITE, OBESITY, DIGESTION, AND METABOLISM

Intestinotrophic effects of exogenous IGF-I are not diminished in IGF binding protein-5 knockout mice

Sangita G. Murali,1 Xiaowen Liu,1 David W. Nelson,1 Angela K. Hull,1 Michael Grahn,1 Murray K. Clayton,2 John E. Pintar,3 and Denise M. Ney1

1Department of Nutritional Sciences, 2Departments of Statistics and Plant Pathology, University of Wisconsin-Madison, Madison, Wisconsin; and 3Department of Neuroscience and Cell Biology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey

Submitted 27 December 2006 ; accepted in final form 27 February 2007

IGF binding protein-5 (IGFBP-5) modulates the availability of IGF-I to its receptor and potentiates the intestinotrophic action of IGF-I. Our aim was to test the hypothesis that stimulation of intestinal growth due to coinfusion of IGF-I with total parenteral nutrition (TPN) solution is dependent on increased expression of IGFBP-5 through conducting our studies in IGFBP-5 knockout (KO) mice. IGFBP-5 KO, heterozygote (HT) and wild type (WT) male and female mice were maintained with TPN or TPN plus coinfusion of IGF-I [recombinant human (rh)IGF-I; 2.5 mg·kg–1·day–1] for 5 days. The concentration of IGF-I in serum was 73% greater (P < 0.0001) in mice given TPN + IGF-I infusion compared with TPN alone. IGF-I attenuated the 2–3 g loss of body weight associated with TPN in WT mice, whereas KO and HT mice did not show improvement in body weight with IGF-I treatment. KO and HT mice had significantly greater levels of circulating IGF-I binding proteins (IGFBPs) compared with WT mice. Intestinal growth due to IGF-I was observed in all groups treated with IGF-I based on greater concentrations of protein and DNA in small intestine and colon and significantly greater crypt depth and muscularis thickness in jejunum. Jejunal expression of IGFBP-5 mRNA was greater in WT mice, whereas IGFBP-3 mRNA was greater in KO mice treated with IGF-I. In summary, the absence of the IGFBP-5 gene did not block the ability of IGF-I to stimulate intestinal growth, possibly because greater jejunal expression of IGFBP-3 compensates for the absence of IGFBP-5.

total parenteral nutrition; jejunum; IGF-binding proteins-3 and 5



Address for reprint requests and other correspondence: D. M. Ney, Univ. of Wisconsin-Madison, Dept. of Nutritional Sciences, 1415 Linden Dr., Madison, WI 53706 (e-mail: ney{at}nutrisci.wisc.edu)







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