Pa. King et Jj. Betts, INSULIN AND NA-DEPENDENT ALANINE TRANSPORT IN SKELETAL-MUSCLE OF OBESE ZUCKER (FA FA) RATS/, American journal of physiology. Regulatory, integrative and comparative physiology, 36(6), 1994, pp. 180001606-180001610
Obese Zucker (fa/fa) rat skeletal muscle is characterized by a reduced
rate of muscle protein deposition possibly due to alterations in amin
o acid transport. The purpose of the present study was to investigate
alanine transport in plasma membrane vesicles from skeletal muscle of
lean and obese Zucker rats, facilitating the study of alanine transpor
t independent of cellular metabolism. Initial rates of alanine transpo
rt were measured in the presence and absence of Na using a rapid filtr
ation technique, and the properties of membranes from control and maxi
mally insulin-treated lean and obese Zucker rats were studied. For lea
n rats, the maximal stimulation (V-max) for Na-dependent alanine trans
port was 207 pmol.mg(-1).s(-1), and the half-maximal affinity constant
(K-1/2) was 2.3 mM. Insulin treatment increased the V-max to 387 pmol
.mg(-1).s(-1) with no changes in K-1/2. For the obese rats, the V-max
for Na-dependent alanine transport was 248 pmol.mg(-1).s(-1), and the
K-1/2 was 2.8 mM. These values were not changed by insulin treatment.
Thus Na-dependent alanine transport in obese rat skeletal muscle is re
sistant to stimulation by insulin; this alteration may contribute to t
he abnormal muscle protein metabolism observed in these animals.