IGF-I is an anabolic hormone which has been reported to increase bone forma
tion in several conditions of undernutrition. Advanced liver cirrhosis is a
ssociated with osteopenia and also with low serum levels of IGF-I. Previous
results showed that low doses of IGF-I increase osteoblastic activity and
decrease bone reabsoption in early liver cirrhosis. The aim of this study w
as to evaluate whether IGF-I-treatment also induces beneficial effect on os
teopenia associated with advanced cirrhosis. Rats with ascitic cirrhosis we
re divided into two groups: group CI (n=10) which received saline and group
CI+IGF (n=10) which were treated with IGP-I (2 mu g/100 g bw.day, sc, duri
ng 21 days). Healthy controls which received saline were studied in paralle
l (CO n=10). On the 22nd day, the animals were sacrificed, and bone paramet
ers were analyzed in femur. Posterior-anterior diameter was similar in all
groups. No significant differences were observed in bone content of calcium
, total proteins, collagen and hydroxyapatite in cirrhotic rats as compared
with controls. However, CI rats showed significant reductions in total bon
e density (-13.5%, p<0.001) assessed by densitometry and radiological study
. In CI+IGF rat bone density (assesed by densitometry) improved significant
ly as compared with CI animals. In summary, osteopenia characterized by los
s of bone mass and preserved bone composition was found in rats with advanc
ed cirrhosis induced by CCl4 and phenobarbital in drinking water. This bone
disorder is partially restored by treatment with low doses of IGF-I during
only three weeks. Thus, IGF-I could be considered as a possible therapy fo
r osteopenia associated with advanced liver cirrhosis.