Key result
Administration of a novel GH receptor antagonist (B2036-PEG) to adult mice for 7 days caused a dose-dependent decrease in circulating, hepatic, and renal IGF-I levels at the highest doses.
Why the study?
Does the growth hormone receptor antagonist B2036-PEG alter circulating, hepatic, and renal expression of the GH/IGF system in adult mice?
Does the growth hormone receptor antagonist B2036-PEG alter circulating, hepatic, and renal expression of the GH/IGF system in adult mice?
Administration of the GHRA B2036-PEG in adult mice dose-dependently decreases IGF-I levels and alters the hepatic and renal GH/IGF axis, providing mechanistic insights for future clinical applications.
The effects of growth hormone (GH) in regulating the expression of the hepatic and renal GH and insulin-like growth factor (IGF) system were studied by administering a novel GH receptor antagonist (GHRA) (B2036-PEG) at different doses (0, 1.25, 2.5, 5 and 10 mg/kg/day) to mice for 7 days. No differences were observed in the groups with respect to body weight, food consumption or blood glucose. However, a dose-dependent decrease was observed in circulating IGF-I levels and in hepatic and renal IGF-I levels at the highest doses. In contrast, in the 5 and 10 mg/kg/day GHRA groups, circulating and hepatic transcriptional IGF binding protein-3 (IGFBP-3) levels were not modified, likely resulting in a significantly decreased IGF-I/IGFBP-3 ratio. Hepatic GH receptor (GHR) and GH binding protein (GHBP) mRNA levels increased significantly in all GHRA dosage groups. Endogenous circulatory GH levels increased significantly in the 2.5 and 5 mg/kg/day GHRA groups. Remarkably, increased circulating IGFBP-4 and hepatic IGFBP-4 mRNA levels were observed in all GHRA administration groups. Renal GHR and GHBP mRNA levels were not modified by GHRA administration at the highest doses. Also, renal IGFBP-3 mRNA levels remained unchanged in most GHRA administration groups, whereas IGFBP-1, -4 and -5 mRNA levels were significantly increased in the 5 and 10 mg/kg/day GHRA administration groups. In conclusion, the effects of a specific GHR blockade on circulating, hepatic and renal GH/IGF axis reported here, may prove useful in the future clinical use of GHRAs.
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Neck et al. (2000) studied this question. Growth hormone receptor antagonist (B2036-PEG) vs. 0 mg/kg/day was evaluated on Circulating, hepatic and renal expression of the GH/IGF system. Administration of a novel GH receptor antagonist (B2036-PEG) to adult mice for 7 days caused a dose-dependent decrease in circulating, hepatic, and renal IGF-I levels at the highest doses.
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