N. Davies et al., EFFECTS OF OCTREOTIDE ON LIVER-REGENERATION AND TUMOR-GROWTH IN THE REGENERATING LIVER, Journal of gastroenterology and hepatology, 12(1), 1997, pp. 47-53
The ability of the liver to regenerate following resection is remarkab
le. However, there is evidence to suggest that tumour growth within th
e regenerating liver is significantly increased. As octreotide (a synt
hetic analogue of somatostatin) inhibits the growth and development of
hepatic tumour in rats, we have investigated its effects on liver reg
eneration, liver blood flow, hepatic reticuloendothelial system activi
ty and tumour growth in the rat following partial hepatectomy (PH). Oc
treotide significantly inhibited liver regeneration in the rat 1 and 2
weeks following PH when compared with controls (regeneration index: 1
.0 and 1.14 cf: 1.14 and 1.4, respectively). There was no significant
difference in hepatic arterial or portal venous blood flow following P
H in control or octreotide-treated rats. However, portal pressure was
significantly reduced in octreotide-treated rats. Hepatic reticuloendo
thelial system activity was significantly increased in octreotide-trea
ted rats compared with control animals 1 and 2 weeks after hepatectomy
(uptake of radiolabelled technetium-99m albumin colloid: 2.2 and 3.9
cf. 1 6 and 1.9). The growth of both HSN (fibrosarcoma) and K12-Tr (co
lonic adenocarcinoma) cells in the regenerating liver was significantl
y decreased by octreotide treatment compared with controls (median per
centage hepatic replacement: HSN control 71.3%, Octreotide 8.4%, K12-T
r Control 38.3%, Octreotide 4.5%). The results of the present study de
monstrate that octreotide inhibits both liver regeneration and tumour
growth following PH, possibly via a similar mechanism.