Renal elimination of protein S-100β in pigs with acute encephalopathy
Protein S-100 beta is an established biochemical marker for cerebral injury in serum. For the further interpretation and possible use of S-100 beta serum measurements in acute hepatic encephalopathy, renal elimination of S-100 beta was measured in pigs with elevated S-100 beta levels due to hepatic...
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Published in | Scandinavian journal of clinical and laboratory investigation Vol. 61; no. 3; pp. 217 - 225 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oslo
Scandinavian University Press
01.05.2001
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Subjects | |
Online Access | Get full text |
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Summary: | Protein S-100 beta is an established biochemical marker for cerebral injury in serum. For the further interpretation and possible use of S-100 beta serum measurements in acute hepatic encephalopathy, renal elimination of S-100 beta was measured in pigs with elevated S-100 beta levels due to hepatic encephalopathy. Eighteen female Norwegian Landrace pigs were randomly allocated to either hepatic devascularization (n=13) or sham operation (n=5). Repeated samples from the common carotid artery, right renal vein, and urine were simultaneously drawn for S-100 beta analysis, using the Sangtec100 Liamat immunoassay. In hepatic devascularized pigs, arterial serum levels of S-100 beta increased from 0.96 0.04 mu g/L (mean SEM) at t=0h to 1.74 0.11 mu g/L (mean SEM) at t=5h. Urinary excretion increased simultaneously from 8.48 3.66ng/h (mean SEM) to 20.4 9.54ng/h (mean SEM), while renal arterial-venous fluxes for both kidneys increased 2444 590ng/h (mean SEM). Increased arterial S-100 beta levels in pigs with acute hepatic encephalopathy are not a result of decreased renal elimination. The large difference between the renal arterial-venous S-100 beta concentrations and the urinary excretion of S-100 beta indicate that renal metabolism is the major route of elimination. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0036-5513 1502-7686 |
DOI: | 10.1080/003655101300133658 |