Regulation of PSP/reg in rat pancreas: Immediate and steady-state adaptation to different diets

Citation
D. Bimmler et al., Regulation of PSP/reg in rat pancreas: Immediate and steady-state adaptation to different diets, PANCREAS, 19(3), 1999, pp. 255-267
Citations number
30
Categorie Soggetti
da verificare
Journal title
PANCREAS
ISSN journal
08853177 → ACNP
Volume
19
Issue
3
Year of publication
1999
Pages
255 - 267
Database
ISI
SICI code
0885-3177(199910)19:3<255:ROPIRP>2.0.ZU;2-5
Abstract
Pancreatic stone protein/reg protein (PSP/reg) is a secretory pancreatic pr otein of hitherto unknown function. It is precursor to a spontaneously prec ipitating peptide called pancreatic thread protein, which is found in prote in plugs within the pancreatic ductal system. Increasing PSP/reg concentrat ions in pancreatic juice might augment the risk of intraductal plug formati on and therefore be a condition predisposing to chronic pancreatitis. Malnu trition is associated with a high incidence of chronic pancreatitis in trop ical countries. In a diet study with rats, we tested the hypothesis that pr otein malnutrition leads to increased PSP/reg concentrations in pancreatic juice. A highly sensitive and reliable enzyme-linked immunosorbent assay (E LISA) for rat PSP/reg was newly established. Male Sprague-Dawley rats were allocated to three nearly isocaloric experimental diets, which contained 0, 45, or 82% casein, respectively, or to a control diet (22% casein). We eva luated PSP/reg expression under these four dietary conditions on the RNA an d on the protein level, performing a time-course study over a period of 28 days. Our results demonstrate that PSP/reg expression is not increased beca use of a protein deficient diet if investigated under steady-state conditio ns. After a temporary increase in PSP/reg levels due to a carbohydrate-defi cient high-protein diet, we could not find signs of a diet-dependent regula tion of this protein. The regulation of PSP/reg thus differs from that of m ost other pancreatic secretory proteins. Our findings contradict earlier re ports that had drawn conclusions based solely on messenger RNA levels.