The overall goal of this revised R01 application is to define the relative contributions of sex steroids, GH, and IGF-1 to anabolic protein and calcium balance during puberty and in adults. To accomplish these goals, two specific aims are proposed. The first specific aim will study the tissue interactions among GH, IGF-1, and sex steroids in two models, GH- deficient youngsters and in GnRH agonist treated (hypogonadal adults). In the first series of experiments, GH deficient, prepubertal youngsters will be selectively primed with appropriate sex steroids and later treated with either hGH or rhIGF-1 for 1 month. Clinical endpoints will be obtained before sex steroid replacement, after steroid treatment and after hGH or rhIGF-1 replacement. These endpoints will include assessment of changes in whole body protein degradation, oxidation, and synthesis as well as calcium absorption, retention, and bone accretion and resorption. A second series of experiments will be carried out in a similar fashion in GnRH agonist treated adults. In these subjects, GH secretory dynamics will also be determined as well. In the third series of experiments, the effects of dihydrotestosterone (DHT), a nonaromatizable androgen, on GH pulsatility will be determined in prepubertal boys to determine if anabolic effects of androgens are direct or mediated indirectly by aromatization to estrogens.
The second aim will determine the longterm effects of rhIGF-1 on measures of whole body protein, calcium kinetics, and carbohydrate metabolism in adults with GH deficiency. These studies should help define therapeutic roles for GH, IGF-1, and sex steroids in treatment of growth disorders and in diseases with increased protein-catabolic states.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK051360-01
Application #
2152446
Study Section
Reproductive Endocrinology Study Section (REN)
Project Start
1995-09-25
Project End
1999-08-31
Budget Start
1995-09-25
Budget End
1996-08-31
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Nemours Children's Clinic
Department
Type
DUNS #
City
Jacksonville
State
FL
Country
United States
Zip Code
32207
Mauras, Nelly; Haymond, Morey W (2005) Are the metabolic effects of GH and IGF-I separable? Growth Horm IGF Res 15:19-27
Mauras, Nelly; Rini, Annie; Welch, Susan et al. (2003) Synergistic effects of testosterone and growth hormone on protein metabolism and body composition in prepubertal boys. Metabolism 52:964-9
Mauras, Nelly; George, Donald; Evans, Jonathan et al. (2002) Growth hormone has anabolic effects in glucocorticosteroid-dependent children with inflammatory bowel disease: a pilot study. Metabolism 51:127-35
Hayes, V Y; Urban, R J; Jiang, J et al. (2001) Recombinant human growth hormone and recombinant human insulin-like growth factor I diminish the catabolic effects of hypogonadism in man: metabolic and molecular effects. J Clin Endocrinol Metab 86:2211-9
Mauras, N (2001) Growth hormone and sex steroids. Interactions in puberty. Endocrinol Metab Clin North Am 30:529-44
Mauras, N; Martinez, V; Rini, A et al. (2000) Recombinant human insulin-like growth factor I has significant anabolic effects in adults with growth hormone receptor deficiency: studies on protein, glucose, and lipid metabolism. J Clin Endocrinol Metab 85:3036-42
Mauras, N; O'Brien, K O; Welch, S et al. (2000) Insulin-like growth factor I and growth hormone (GH) treatment in GH-deficient humans: differential effects on protein, glucose, lipid, and calcium metabolism. J Clin Endocrinol Metab 85:1686-94
Mauras, N; O'Brien, K O; Klein, K O et al. (2000) Estrogen suppression in males: metabolic effects. J Clin Endocrinol Metab 85:2370-7
Mauras, N; Walton, P; Nicar, M et al. (2000) Growth hormone stimulation testing in both short and normal statured children: use of an immunofunctional assay. Pediatr Res 48:614-8
Mauras, N; Hayes, V; O'Brien, K O (2000) Estrogen treatment and estrogen suppression: metabolic effects in adolescence. J Pediatr Endocrinol Metab 13 Suppl 6:1431-7

Showing the most recent 10 out of 15 publications