EFFECTS OF GROWTH-HORMONE ADMINISTRATION AND DIETARY-PROTEIN INTAKE ON INSULIN-LIKE GROWTH-FACTOR-I AND GROWTH-HORMONE RECEPTOR MESSENGER-RNA EXPRESSION IN PORCINE LIVER, SKELETAL-MUSCLE, AND ADIPOSE-TISSUE
Jm. Brameld et al., EFFECTS OF GROWTH-HORMONE ADMINISTRATION AND DIETARY-PROTEIN INTAKE ON INSULIN-LIKE GROWTH-FACTOR-I AND GROWTH-HORMONE RECEPTOR MESSENGER-RNA EXPRESSION IN PORCINE LIVER, SKELETAL-MUSCLE, AND ADIPOSE-TISSUE, Journal of animal science, 74(8), 1996, pp. 1832-1841
The effects of growth hormone (GH) and dietary protein on expression o
f IGF-I and GH receptor (GHR) genes in liver, muscle, and fat of pigs
were investigated. Forty-eight intact male Large White x Landrace pigs
were allotted to eight treatment groups (four diets with or without G
H). The pigs were restriction-fed one of four diets, which differed on
ly in their protein content (9.9, 13.1, 16.2, and 19.4%, as-fed basis)
, for a total of 3 wk. The pigs were then injected intramuscularly wit
h either porcine GH (50 mu g . kg(-1). d(-1) of rpST) or vehicle for t
he last 7 d. Pigs were slaughtered 4 h after the final injection. Tota
l RNA was extracted from all tissues and then RNase protection assays
were performed to measure expression of IGF-I and GHR genes. Expressio
n of IGF-I mRNA was found to be GH responsive in the liver, semitendin
osus (ST), and adipose tissue (P < .01) but not in longissimus muscle
(LD). Dietary protein increased IGF-I expression only in the adipose t
issue (P < .01). Expression of class 2 transcripts of IGF-I were obser
ved only in the livers of GH-treated pigs, with no effect of dietary p
rotein. Expression of GHR mRNA was found to increase with GH administr
ation in liver and skeletal muscle (LD and ST, P < .05) but not in adi
pose tissue. There were diet x GH interactions on GHR expression in li
ver, ST, and adipose tissue, resulting in the highest GHR expression b
eing in the high protein-fed, GH-treated group for liver, but in the l
ow protein-fed, GH-treated group for muscle and adipose tissue. This s
tudy demonstrates tissue-specific control of expression of the two gen
es and also tissue-specific promoter usage (IGF-I exon 2 in liver) in
response to GH administration.