TY - JOUR
T1 - Studies of the Kinetics of Purified Conjugated Bilirubin‐3H in the Rat
AU - SHUPECK, MALCOLM
AU - WOLKOFF, ALLAN W.
AU - SCHARSCHMIDT, BRUCE F.
AU - WAGGONER, JEANNE C.
AU - BERK, PAUL D.
PY - 1978/9
Y1 - 1978/9
N2 - Radio‐labeled conjugated bilirubin was purified from rat bile by affinity chromatography. Following the intravenous injection of tracer does of this material, the initial fractional plasma disappearance rate of conjugated bilirubin‐3H in the normal Sprague‐Dawley rat was found to be approximately 50% faster than that for unconjugated bilirubin‐3H (0.51 ± 0.04 [SE] vs. 0.35 ± 0.02 min.−1; P > .001). Hepatic recovery studies in the rat indicated that, over the first four minutes after injection, disappearance of cholephilic anions from plasma is accounted for almost entirely by hepatic uptake. Hence, these studies demonstrate that hepatic uptake of conjugated bilirubin is substantially faster than that of unconjugated bilirubin. Net hepatic clearance of conjugated bilirubin in normal rates was three‐fold greater than that of unconjugated bilirubin (0.94 ± 0.16 vs. 0.30 ± 0.03 ml ./min./100gm. body weight; P > .001), presumably reflecting both the more rapid hepatic uptake and the ability of the formar pigment to by‐pass the conjugation step. Hepatic uptake of conjugated bilirubin was shown to be inhibited by uncojugated bilirubin, sulfobromophthalein and indocyanine green but not by glycocholate. These observations cannot be explained by simple diffusion and suggest that the hepatic uptake mechanism for conjugated bilirubin is the same as that for the unconjugated pigment.
AB - Radio‐labeled conjugated bilirubin was purified from rat bile by affinity chromatography. Following the intravenous injection of tracer does of this material, the initial fractional plasma disappearance rate of conjugated bilirubin‐3H in the normal Sprague‐Dawley rat was found to be approximately 50% faster than that for unconjugated bilirubin‐3H (0.51 ± 0.04 [SE] vs. 0.35 ± 0.02 min.−1; P > .001). Hepatic recovery studies in the rat indicated that, over the first four minutes after injection, disappearance of cholephilic anions from plasma is accounted for almost entirely by hepatic uptake. Hence, these studies demonstrate that hepatic uptake of conjugated bilirubin is substantially faster than that of unconjugated bilirubin. Net hepatic clearance of conjugated bilirubin in normal rates was three‐fold greater than that of unconjugated bilirubin (0.94 ± 0.16 vs. 0.30 ± 0.03 ml ./min./100gm. body weight; P > .001), presumably reflecting both the more rapid hepatic uptake and the ability of the formar pigment to by‐pass the conjugation step. Hepatic uptake of conjugated bilirubin was shown to be inhibited by uncojugated bilirubin, sulfobromophthalein and indocyanine green but not by glycocholate. These observations cannot be explained by simple diffusion and suggest that the hepatic uptake mechanism for conjugated bilirubin is the same as that for the unconjugated pigment.
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U2 - 10.1111/j.1572-0241.1978.tb00951.x
DO - 10.1111/j.1572-0241.1978.tb00951.x
M3 - Article
C2 - 717377
AN - SCOPUS:0018253688
SN - 0002-9270
VL - 70
SP - 259
EP - 264
JO - The American Journal of Gastroenterology
JF - The American Journal of Gastroenterology
IS - 3
ER -