Td. Etherton et al., MECHANISMS BY WHICH SOMATOTROPIN DECREASES ADIPOSE-TISSUE GROWTH, The American journal of clinical nutrition, 58(2), 1993, pp. 190000287-190000295
When growing pigs are treated daily with recombinantly derived porcine
somatotropin (pST) for 30-60 d there is a dose-dependent decrease in
lipid accretion. Maximal doses of pST can reduce lipid accretion by as
much as 70%. The reduction in lipid accretion occurs because of a mar
ked decrease in glucose transport and lipogenesis that is the result o
f a pST-dependent decrease in the ability of insulin to stimulate thes
e processes in the adipocyte; lipolysis is not affected. The decrease
in insulin sensitivity is not due to a decrease in insulin binding or
insulin receptor kinase activity. Little is understood about the somat
otropin (ST) intracellular signal pathway(s) that mediate the biologic
al effects of ST. These effects are chronic rather than acute as was p
reviously believed. This pattern likely reflects that ST decreases tra
nscription of important insulin-responsive genes such as the muscle-ad
ipose tissue transporter gene (GLUT4) and key lipogenic enzymes.