Plasma pancreatic-type
Poly-C specific ribonuclease (P-
RNase)-
enzyme activity increases in patients with
acute pancreatitis (AP) who develop
pancreatic necrosis and severe disease course. It is considered as a marker of pancreatic tissue destruction. The aim of this study was to estimate interrelations between major inflammatory
cytokines such as:
interleukin 6 (IL-6),
interleukin 8 (IL-8) and
tumor necrosis factor soluble receptors: sTNFR55 and sTNFR75 output, and plasma P-
RNase activity. The study was carried out in a group of 56 patients with AP, where 20 developed
pancreatic necrosis. It was found that serum P-
RNase concentration and levels of all studied inflammatory
cytokines significantly increase already in the first day from diagnose of the disease (2.5 folds for P-
RNase, 20 for IL-8, about 200 for IL-6 and 1.5 for receptors, respectively). In the first day from admission to hospital, P-
RNase activity significantly correlated with plasma concentration of studied inflammatory
cytokines. The most pronounced correlation was found for P-
RNase and
IL-6 in days 1-4 from diagnose, manifested by Pearson correlation r coefficients amounting to 0.86, 0.79, 0.60 and 0.57 respectively (p<0.001). Dividing the studied AP patients into two groups, varying in severity of disease a significant differences in P-
RNase and
IL-6,
IL-8 and sTNFR55/sTNFR75 were found. In patients with
acute necrotizing pancreatitis P-
RNase significantly correlate with levels of major inflammatory
cytokines. Carried out studies suggest that activity of P-
RNase reflects severity of inflammatory reaction, which is dependent on development of pancreatic injury and tissue
necrosis in AP.