Summary
The influence of insulin treatment in vivo and of insulin in vitro on the incorporation of amino acid into protein was studied in aorta of normal and
streptozotocin-diabetic rats. The incorporation of amino acid into protein was measured
by incubating aorta in vitro for 2-3 h in the presence of 14C-labelled L-leucine or L-phenylalanine and then determining the amount of radioactivity
incorporated into alkali-soluble protein.
After insulin treatment of diabetic rats for 48 h the incorporation of leucine-14C into aortic protein was increased, while insulin treatment for 12 or 24 h had no
effect. In non-diabetic rats insulin treatment for 24-72 h did not affect the incorporation
of leucine-14C or phenylalanine-14C into aortic protein.
Incubation of normal or diabetic rat aorta with insulin (0.1 U/ml) in vitro without serum for up to 48 h did not influence the leucine-14C incorporation. Addition of 5 % foetal bovine serum increased the incorporation of
leucine-14C into aortic protein, determined after 48 h. When the incubation medium was supplemented
with serum the leucine incorporation into protein in diabetic aorta was significantly
increased after 48 h by insulin added in a high concentration (0.1 U/ml), while insulin
at a physiological concentration had no demonstrable effect.
The absence of a direct effect of insulin in a physiological concentration in vitro on the amino acid incorporation in normal and diabetic aorta and the finding that
insulin treatment in vivo only stimulated the leucine-14C incorporation in diabetic aorta suggests that the effect of insulin administration
on the amino acid incorporation in diabetic aorta is due to the correction of the
diabetic state and not to a direct action on the aortic protein metabolism.
Key-Words
Rat Aorta - Vascular Smooth Muscle - Protein Metabolism - Diabetes Mellitus - Insulin
- Streptozotocin