THE EFFECTS OF ACUTE ADMINISTRATION OF ETHANOL ON JEJUNAL PROTEIN-SYNTHESIS AND CIRCULATING INSULIN-LIKE GROWTH-FACTOR (IGF)-1 AND IGF BINDING-PROTEINS IN AD-LIBITUM FED AND NUTRITIONALLY RESTRICTED RATS

Citation
Jp. Miell et al., THE EFFECTS OF ACUTE ADMINISTRATION OF ETHANOL ON JEJUNAL PROTEIN-SYNTHESIS AND CIRCULATING INSULIN-LIKE GROWTH-FACTOR (IGF)-1 AND IGF BINDING-PROTEINS IN AD-LIBITUM FED AND NUTRITIONALLY RESTRICTED RATS, Addiction biology, 1(4), 1996, pp. 371-378
Citations number
28
Categorie Soggetti
Substance Abuse",Biology
Journal title
ISSN journal
13556215
Volume
1
Issue
4
Year of publication
1996
Pages
371 - 378
Database
ISI
SICI code
1355-6215(1996)1:4<371:TEOAAO>2.0.ZU;2-R
Abstract
The effects of acute ethanol administration (75 mmol/kg body weight) t o male Wistar rats (either ad libitum fed or nutritionally restricted) on fractional rates of protein synthesis in the jejunum was assessed together with the changes in IGF-1 and IGF binding protein concentrati ons. Acute administration of ethanol resulted in significant decreases in fractional rates of protein synthesis in the whole jejunum and jej unal seromuscular layers of both the ad libitum fed and nutritionally restricted animals. The synthesis rate per unit RNA (k(RNA), mg protei n/day/mg RNA) in whole jejunum was reduced by 29% and 24% in the nutri tionally restricted and ad libitum fed animals, respectively. Mean IGF -1 levels were lower in the nutritionally restricted group (871 +/- 36 .9 mu g/l) than the ad libitum animals (960 +/- 27.3 mu g/l) although this did not reach significance. In contrast, administration of alcoho l to both groups markedly reduced circulating IGF-1 levels (ad libitum : 518 +/- 19.8 mu g/l, nutritionally restricted: 417 +/- 33.7 mu g/l). Furthermore, ethanol treatment resulted in a three-fold increase in t he intensity of a 30 kDa IGF binding protein (IGFBP) in the ad libitum fed animals and a fourfold increase in both 30 and 32 kDa IGFBP bands in the nutritionally restricted group as visualized by Western ligand blotting. Decreases in levels of IGF-1 allied with increased circulat ing small molecular weight IGFBPs may contribute to the reduction in f ractional rates of protein synthesis in the gastrointestinal tract of ethanol-treated rats.