Ration size and protein intake affect circulating growth hormone concentration, hepatic growth hormone binding and plasma insulin-like growth factor-I immunoreactivity in a marine teleost, the gilthead sea bream (Sparus aurata)

J Nutr. 1995 Mar;125(3):546-52. doi: 10.1093/jn/125.3.546.

Abstract

The nutritional regulation of the growth hormone liver axis has been studied in gilthead sea bream (Sparus aurata). In a first study, fingerling fish were fed three experimental diets with varying proportions of protein (34, 45 and 55%). A 60% decrease in plasma growth hormone concentration was observed with the increase of specific growth rates and dietary protein levels. An opposite response was observed in hepatic growth hormone-binding sites and plasma insulin-like growth factor-I immunoreactivity that would reflect the insensitivity of liver to growth hormone action during relatively low protein intake. In a second study, fish were fed a commercial diet (55% protein) at different feeding levels (0, 1.2, 2.7 and 5.5 g/(100 g body wt.d). An 84% decrease in plasma growth hormone concentration was observed with the increase of specific growth rates and feeding levels from 0 to 2.7 g/(100 g body wt.d). However, significantly greater growth hormone concentration was found in fish fed 5.5 g/(100 g body wt.d) when compared with fish fed 2.7 g/(100 g body wt.d). Hepatic growth hormone-binding sites and plasma insulin-like growth factor-I immunoreactivity increased with the increase of feeding levels from 0 to 2.7 g/(100 g body wt.d), but these values were lower in fish-fed 5.5 g/(100 g body wt.d) than in those fed 2.7 g/(100 g body wt.d). The physiological importance of these results remains to be clarified, though probably it is a part of the mechanism that diminishes feed utilization for growth at high feeding levels.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Nutritional Physiological Phenomena
  • Animals
  • Dietary Proteins / administration & dosage*
  • Dietary Proteins / pharmacology
  • Energy Metabolism
  • Growth Hormone / blood*
  • Growth Hormone / metabolism
  • Insulin-Like Growth Factor I / metabolism*
  • Liver / metabolism*
  • Nitrogen / metabolism
  • Nutritional Status
  • Perciformes / blood
  • Perciformes / growth & development
  • Perciformes / metabolism*

Substances

  • Dietary Proteins
  • Insulin-Like Growth Factor I
  • Growth Hormone
  • Nitrogen