Recombinant human IGF-I does not modify the ACTH and cortisol responses tohCRH and hexarelin, a peptidyl GH secretagogue, in humans

An inhibitory influence of insulin-like growth factor-I (IGF-I) on hypothal amus-pituitary-adrenal (HPA) axis has been hypothesized. In fact, it has be en reported that the rhGH (recombinant human GH)-induced IGF-I increase inh ibits both cortisol and GH response to MK-0677, a non-peptidyl GH secretago gue in animals. The aim of this study was to further clarify the inhibitory role, if any, of IGF-I on corticotroph function. We studied the effect of rhIGF-I (recombinant human IGF-I; 20 mug/kg sc at -180 min) or placebo on t he ACTH and cortisol responses to hCRH (human CRH; 2.0 mug/kg iv at 0 min) or hexarelin (HEX; 2.0 mug/kg iv at 0 min), a peptidyl GHS, in normal young women. The effect of rhIGF-I on the GH response to HEX was also studied. T he subjects were six normal young women [age: 26-35 yr; body mass index (BM I): 19-23 kg/m(2)] in their early follicular phase. The results showed that after sc rhIGF-I administration, circulating IGF-I revels increased approx imately 77%, peaking at -60 min and persisting similar up to +120 min.The m ean ACTH, cortisol and GH concentrations did not change from -180 to 0 min when evaluated after both placebo or rhIGF-I. CRH and HEX induced similar A CTH (peak vs baseline, mean+/-SE: 47.5+/- 10.9 vs 21.3+/- 3.0 pg/ml and 30. 3+/-6.9 vs 19.2+/-3.8 pg/ml, respectively; p <0.04) and cortisol responses (177.5+/-5.4 vs 109.3+/-10.3 mug/l and 149.4+/-12.3 vs 119.8+/-16.4 mug/l, respectively, p <0.04). RhIGF-I pretreatment did not modify the ACTH and co rtisol responses to hCRH (46.0+/-3.8 pg/ml and 181.1+/-16.9 mug/l, respecti vely) as well as those to HEX (28.8+/-5.0 pg/ml and 144.1+/-16.2 mug/l, res pectively). On the other hand, the GH response to HU was clearly reduced by rhIGF-I (23.9+/-4.7 vs 64.7+/-14.8 mug/l, p <0.05). Our findings show that rhIGf-I-induced increase of circulating IGF-I levels exerts negative feedb ack action on somatotroph secretion, while it does not modify the corticotr oph and the adrenal responsiveness to CRH or hexarelin. (C) 2001, Editrice Kurtis.