TY - JOUR
T1 - Inhibitory effects of somatostatin on growth and differentiation in cultured intestinal mucosa
AU - Stange, E. F.
AU - Schneider, A.
AU - Schusdziarra, V.
AU - Ditschuneit, H.
PY - 1984
Y1 - 1984
N2 - The effect of somatostatin on mucosal DNA, protein and brush border enzymes was studied in organ cultured rabbit jejunum and ileum. Compared to control cultures, somatostatin reduced the biopsy DNA and protein content in parallel in the jejunum, but was ineffective in the ileum. This was probably due to a direct growth inhibition, since DNA and brush border enzyme activity from desquamated cells in the postculture medium were unaffected. In addition, a direct inhibition of jejunal villous cell differentiation by somatostatin was reflected in a significant decrease of sucrase, maltase and alkaline phosphatase activity. In the ileum, only the specific activity of alkaline phosphatase was reduced. The key enzyme of cholesterol synthesis, HMG-CoA-reductase, was measured as an intracellular enzyme control and was not influenced by the hormone. The high somatostatin concentrations necessary to achieve the effects are not an artefact of hormone degradation during culture, as shown by radioimmunoassay, and suggest a local or 'paracrine' rather than systemic, inhibitory action of somatostatin on intestinal growth and differentiation.
AB - The effect of somatostatin on mucosal DNA, protein and brush border enzymes was studied in organ cultured rabbit jejunum and ileum. Compared to control cultures, somatostatin reduced the biopsy DNA and protein content in parallel in the jejunum, but was ineffective in the ileum. This was probably due to a direct growth inhibition, since DNA and brush border enzyme activity from desquamated cells in the postculture medium were unaffected. In addition, a direct inhibition of jejunal villous cell differentiation by somatostatin was reflected in a significant decrease of sucrase, maltase and alkaline phosphatase activity. In the ileum, only the specific activity of alkaline phosphatase was reduced. The key enzyme of cholesterol synthesis, HMG-CoA-reductase, was measured as an intracellular enzyme control and was not influenced by the hormone. The high somatostatin concentrations necessary to achieve the effects are not an artefact of hormone degradation during culture, as shown by radioimmunoassay, and suggest a local or 'paracrine' rather than systemic, inhibitory action of somatostatin on intestinal growth and differentiation.
UR - http://www.scopus.com/inward/record.url?scp=0021349085&partnerID=8YFLogxK
U2 - 10.1055/s-2007-1014701
DO - 10.1055/s-2007-1014701
M3 - Article
C2 - 6142852
AN - SCOPUS:0021349085
SN - 0018-5043
VL - 16
SP - 74
EP - 78
JO - Hormone and Metabolic Research
JF - Hormone and Metabolic Research
IS - 2
ER -