Autor: |
Nuutinen, Hannu, Abei, Masato, Schwarzendrube, Jörg, Corradini, Stefano, Walsh, R., Kawczak, Paul, Holzbach, R. |
Zdroj: |
Digestive Diseases and Sciences; August 1995, Vol. 40 Issue: 8 p1786-1791, 6p |
Abstrakt: |
We recently identified a promoting glycoprotein in the concanavalin A-bound fraction of gallbladder bile as a biliary form ofα1-acid glycoprotein (AAG). The concentration of biliary AAG appears to exert an important promoting effect on the speed of cholesterol nucleation in many patients with cholesterol gallstone disease. In the current study, we provide information about the biliary concentration of AAG as well as the amount and comparative potency of its subfractions in patients with and without cholesterol gallstone disease. The amount of total biliary AAG and the amounts of its different isoforms separated by concanavalin A affinity chromatography were measured by ELISA. Estimates of absolute concentrations of AAG for each sample were normalized to the sample total protein content to give relative AAG values. The promoting activity (potency) of immunopurified biliary AAG from gallstone patients and gallstone-free controls on cholesterol crystallization was compared by a crystal growth assay. The mean absolute concentration of AAG in gallstone-free controls was not significantly different from multiple stone patients. The relative concentration of AAG (micrograms per milligram total protein) was significantly increased in patients with multiple stones when compared to controls (P<0.05), and both the absolute and relative concentrations of AAG (micrograms per milligram bile), were three- and to five fold higher in a number of these patients. The functional activity and distribution of AAG in different subfractions was similar in gallstone patients and gallstone-free controls. The relative concentration of biliary AAG is significantly greater in cholesterol gallstone patients with multiple stones than in gallstone-free controls. These observations suggest that raised levels of AAG may be of pathogenetic importance in a subgroup of patients with multiple gallstones. |
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