ABSTRACT
This study examines and compares the prophylactic role of aprotinin and Dextran 40 in acute pancreatitis. Experimental acute pancreatitis was induced in 70 male Wistar rats using the closed-duodenal-loop technique. The rats were randomly divided into four groups; sham operation, untreated acute pancreatitis, and therapy with aprotinin or Dextran 40. Samples of blood and urine were collected at the beginning and at the end of the 24-hr period for measurement of amylase and creatinine which allowed calculation of the amylase-creatinine clearance ratio (ACCR). Mortality in the aprotinin group was the same as the untreated rats (20%). Dextran 40 therapy was associated with a lower mortality rate (6.7%). Light microscopic examination confirmed that the histologic changes of acute pancreatitis were less severe in both the aprotinin- and Dextran 40-treated rats. The ACCR was elevated after Dextran 40 therapy, which was due mainly to high urinary amylase levels. These results suggest that Dextran 40 may have a prophylactic role in acute experimental pancreatitis but again emphasizes the high false-positive rate of the ACCR determination.
Subject(s)
Aprotinin/therapeutic use , Dextrans/therapeutic use , Pancreatitis/drug therapy , Acute Disease , Amylases/blood , Animals , Creatinine/blood , Male , Pancreas/pathology , Pancreatitis/blood , Pancreatitis/enzymology , Pancreatitis/pathology , Rats , Rats, Inbred StrainsABSTRACT
We have compared three analytical systems for the measurement of serum thyroxine: enzyme-linked immunoassay (EIA), fluorescent immunoassay (FIA) and a radioimmunoassay (RIA). These were evaluated with respect to their precision, accuracy, analytical sensitivity and sample throughput. The RIA is more sensitive than the EIA (10 microgram/L vs. 35 Ug/L. Both systems have excellent precision (X = 86 ug/L, C.V.RIA = C.V.EIA = 4.6%). Both the EIA and RIA demonstrate good accuracy with recovery of between 97-98% of added thyroxine. The FIA has an apparent sensitivity between that of the RIA and EIA (25 microgram/L), but a precision consistently lower than the other two systems (C.V. = 7.4%, X = 86 microgram/L). Patients' results by RIA compared well with those from EIA )r = 0.91, P less than 0.05), but a poor correlation was found with FIA (r = 0.865, P greater than 0.05). Although not fully automated, the EIA performed on the Abbott ABA-100 analyzer has a sample throughput equal to the automated RIA system (Micromedic, Concept 4).