The influence of the somatostatin analogue angiopeptin on transplant a
rteriosclerosis was investigated using two aortic transplantation rat
models. One was characterized by ischemia/reperfusion-induced changes
in syngeneic transplants while immunologically induced changes dominat
ed in the other allogeneic model. Angiopeptin, 100 mu g/kg per day, wa
s administered continuously until the sacrifice of the rats after 8 we
eks. No. additional immunosuppression was used in either model. An ima
ge analysis system was used to quantify the intimal and medial thickne
sses of the grafts. In the syngeneic grafts, the intimal thickness was
less than 50 % of that of control grafts (P < 0.05), but no differenc
e was seen in the allogeneic model. The expression of selected cells,
TGF-beta s, and PDGF and PDGF alpha-receptors was detected immunohisto
chemically and displayed a similar picture in control and angiopeptin-
treated grafts in both models. We conclude that angiopeptin has no cle
ar immunosuppressive properties but may counteract ischemia-induced tr
ansplant arteriosclerosis.