J. Schole et al., THE TOTAL ANABOLIC ACTIVITY OF THE BLOOD AS A CONNECTING LINK BETWEENTHE INTESTINAL-FLORA THEORY AND THE INTERMEDIARY ACTION OF GROWTH PROMOTORS, Journal of animal physiology and animal nutrition, 71(3), 1994, pp. 156-168
Endocrine movements in rats induced by feeding of growth promoters, as
well as in germ-free animals, were established in three experimental
series. The following results were obtained: 1. In a preceding experim
ent it was demonstrated that growth promoters, which were hither to pr
esumed to influence only the intestinal flora (Toyocerin, fumaric acid
, formic acid), have a direct anabolic effect on the liver. The effect
ive concentrations are about 10-fold higher than those of other growth
-promoting compounds; 2. After feeding of all the tested growth promot
ers (Carbadox, Aureomycin, Flavomycin, CuSO4, Toyocerin, fumaric acid,
formic acid) both to experimental and control animals, a statisticall
y valid increase of anabolic regulators in the blood could be detected
in parallel to a significant higher daily weight gain. The same resul
ts were obtained after parenteral treatment with bovine somatotropin.
Somatomedin C (insulin-like growth factor 1) levels, analysed in paral
lel, were significantly increased in germ-free animals only; 3. Levels
of catabolic regulators (corticosterone, thyroid hormones (T3/T4)) af
ter feeding of growth promoters showed no statistically valid differen
ces (time of feeding 28 days). A tendency in endocrine movements compa
rable with those occurring at normal stress adaptation have been demon
strated, e.g., with CuSO4: in the growth phase, decreasing corticoster
one levels occurred simultaneously with increasing levels of T3 and T4
. This phase was followed by an increase in corticosteroids, normaliza
tion of T3/T4 levels, and a decrease in daily weight gain; 4. It is di
scussed whether growth promotion-independent of the method of inductio
n-is always connected with an increase of anabolic endocrine regulator
s. Growth promoters are reactive, but non-toxic, compounds which reach
the cell and the cell nucleus-unlike somatotropin and somatomedins-wi
thout receptors. Here, they cause a decrease in the concentrations of
radicals and an increase in the redox potential resulting in the start
of anabolic reaction sequences and-to ensure anabolism-in induction o
f cell-specific anabolic peptides.