EVIDENCE THAT PRETRANSLATIONAL AND TRANSLATIONAL DEFECTS DECREASE SERUM INSULIN-LIKE GROWTH FACTOR-I CONCENTRATIONS DURING DIETARY-PROTEIN RESTRICTION

被引:97
作者
THISSEN, JP [1 ]
TRIEST, S [1 ]
MOATSSTAATS, BM [1 ]
UNDERWOOD, LE [1 ]
MAUERHOFF, T [1 ]
MAITER, D [1 ]
KETELSLEGERS, JM [1 ]
机构
[1] CATHOLIC UNIV LOUVAIN,SCH MED,UNITE DIABETOL & NUTR,B-1200 BRUSSELS,BELGIUM
关键词
D O I
10.1210/endo-129-1-429
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dietary protein restriction causes GH resistance and decreases serum insulin-like growth factor-I (IGF-I) concentrations. To determine whether pretranslational or translational defects are involved in the decline of serum IGF-I concentrations during protein restriction, we measured hepatic IGF-I mRNA abundance together with the serum IGF-I peptide response to exogenous GH after 1 week of protein restriction (5% casein in diet; P5) in hypophysectomized rats. We compared these responses with those of hypophysectomized rats fed a protein-sufficient diet (15% casein in diet; P15) and given exogenous GH. A single injection of rat GH (200-mu-g/100 g BW) produced a comparable IGF-I mRNA increment in both groups (at 6 h, 7.8 +/- 1.1 arbitrary units in P5 vs. 8.2 +/- 1.1 in P15), but failed to raise serum IGF-I normally in the P5 group (at 6 h, 90 +/- 15 ng/ml in P5 vs. 216 +/- 63 in P15; P < 0.01). The post-GH decline of the 7.5-kilobase (kb) IGF-I mRNA abundance was faster in P5 than in P15 animals. In another experiment in intact rats subjected to protein restriction, injections of pharmacological doses of rat GH (400-mu-g/100 g BW.day) for 1 week restored liver IGF-I mRNA abundance to normal without normalization of serum IGF-I (403 +/- 91 vs. 713 +/- 53 ng/ml; P < 0.01). Our data suggest that 1) the machinery involved in the transcription of the liver IGF-I gene is intact in protein-restricted rats, because these animals retain the ability to muster normal IGF-I mRNA responses to high doses of exogenous GH; 2) the stability of the 7.5-kb IGF-I mRNA is probably decreased by the protein restriction, as suggested by the faster decline of the 7.5-kb transcript in P5 than in P15 hypophysectomized rats; and 3) the discrepancy between normal liver IGF-I mRNA abundance and low serum and liver IGF-I peptide concentrations suggests that translational stalling of the IGF-I mRNAs or increased serum IGF-I clearance is involved in the low serum IGF-I concentrations during dietary protein restriction.
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页码:429 / 435
页数:7
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