GROWTH AND METABOLISM OF FETAL AND MATERNAL MUSCLES OF ADOLESCENT SHEEP ON ADEQUATE OR HIGH FEED INTAKES - POSSIBLE ROLE OF PROTEIN-KINASE-C-ALPHA IN FETAL MUSCLE GROWTH
Rm. Palmer et al., GROWTH AND METABOLISM OF FETAL AND MATERNAL MUSCLES OF ADOLESCENT SHEEP ON ADEQUATE OR HIGH FEED INTAKES - POSSIBLE ROLE OF PROTEIN-KINASE-C-ALPHA IN FETAL MUSCLE GROWTH, British Journal of Nutrition, 79(4), 1998, pp. 351-357
From days 4-104 of pregnancy, adolescent sheep, weighing 43.7 (SE 0.87
) kg were offered a complete diet at two different intakes (approximat
ely 5 or 15 kg/week) designed to meet slightly, or well above, materna
l maintenance requirements. The fetal and maternal muscles were taken
on day 104 of pregnancy and analysed for total DNA, RNA and protein. E
wes offered a high intake to promote rapid maternal weight gain, weigh
ed more (76.5 (SE 4.5) v. 50.0 (SE 1.7)kg) and had muscles with a grea
ter fresh weight, whilst their fetuses had smaller muscles, than those
fed at a lower intake. Plantaris muscle of the ewes fed at the high i
ntake contained more RNA and protein; again the opposite situation was
found in the fetal muscle. On the higher maternal intakes, the DNA, R
NA and protein contents of the fetal plantaris muscle were less than i
n fetuses of ewes fed at the lower intake. To investigate the possible
mechanisms involved in this decrease in fetal muscle mass, cytosolic
and membrane-associated muscle proteins were subjected to Western immu
noblotting with antibodies to nine isoforms of protein kinase C (PKC),
a family of enzymes known to play an important role in cell growth. F
ive PKC isoforms (alpha, epsilon, theta, mu and zeta) were identified
in fetal muscle. One of these, PKC-alpha, was located predominantly in
the cytosolic compartment in the smaller fetuses of the ewes fed at a
high plane of nutrition, but was present to a greater extent in the m
embranes of the more rapidly growing fetuses of the ewes fed at the lo
wer intake. This was the only isoform to demonstrate nutritionally rel
ated changes in its subcellular compartmentation suggesting that it ma
y mediate some aspects of the change in fetal growth rate.