Hepatic accumulation and intracellular binding of conjugated bilirubin.
نویسندگان
چکیده
After the intravenous injection of unconjugated [(3)H]bilirubin into normal Sprague-Dawley and Wistar R rats, radiolabeled bile pigments rapidly accumulated in the liver. By 1.5 min after injection, an average of 36% of the injected isotope was present in liver homogenates. Between 3 and 15 min, 37-64% of the total intrahepatic radiolabeled bilirubin was conjugated, as demonstrated by extraction of label into the polar phase of a solvent partition system. This indicates both rapid conjugation, and accumulation of conjugated bilirubin within the liver cell. Fluorometric determination of the dissociation constants of purified bilirubin and its mono- and diglucuronides for homogeneous preparations of two human and four rat glutathione S-transferases, including ligandin, revealed avid binding of all three bile pigments to this class of proteins. Hence, the observation that the intrahepatic bile pigment pool contains substantial amounts of conjugated bilirubin can be attributed to the high binding affinities observed. Thin-layer chromatographic analysis of the (3)H-pigments produced by p-iodoaniline diazotization of homogenates and cytosol demonstrated that the intrahepatic pool of conjugated bilirubin was almost exclusively monoglucuronide. Examination of radiolabeled bilirubin conjugates excreted in bile during the first 20 min after injection of [(3)H]bilirubin showed no preferential excretion of diglucuronide. These studies indicate that (a) both bilirubin and its monoglucuronide accumulate within the liver cell as ligands with the glutathione S-transferase; and (b) bilirubin diglucuronide does not significantly accumulate within the general intrahepatocellular pool of protein-bound bile pigments. The latter observation is compatible with the formation and excretion of bilirubin diglucuronide directly from the canalicular pool of the liver cell.
منابع مشابه
مقایسه تجویز مزمن میکرو و نانوذره اکسید منگنز بر شاخصهای عملکرد کبدی در موش نر بزرگ آزمایشگاهی
Background and Objective: Increased production and industrial application of manganese oxide (MnO2) nano and microparticles have led to increased human contact with these particles. In this study, the biodistribution of manganese in rat liver was studied after chronic administration of two MnO2 particles. Also, the effect of these particles was studied on body weight gain and liver fun...
متن کاملSilver Resistance In Acinetobacter baumannii BL54 Occurs Through Binding to a Ag-Binding Protein
The mechanism of plasmid mediated silver (Ag) resistance was investigated in Acinetobacter baumanniiBL54. The intracellular accumulation of Ag in both original strain BL54 and Escherichia coli K12transconjugant containing plasmid pUPI276 began immediately and reached a maximum within 60 minutes.This initial accumulation was followed by net loss of Ag which reached a maximum wi...
متن کاملThe Etiology of Neonatal Hyperbilirubinemia
Etiology of Physiologic Neonatal Hyperbilirubinemia. Every newborn infant develop·s hyperbilirubinemia during the first week of life which is called "physiologic". There are several factors responsible for the development of physiologic hyperbilirubinemia, as follows: 1. Increased bilirubin production, due to a - Increased blood volume. b - Decreased R.B.C. survival time. c - Increased in...
متن کاملHepatic intracellular distribution of tritium-labeled unconjugated and conjugated bilirubin in normal and Gunn rats.
متن کامل
Implication of trans-11,trans-13 conjugated linoleic acid in the development of hepatic steatosis
SCOPE Conjugated linoleic acids are linoleic acid isomers found in the diet that can also be produced through bacterial metabolism of polyunsaturated fatty acids. Our objective was to evaluate the contribution of fatty acid metabolites produced from polyunsaturated fatty acids by the gut microbiota in vivo to regulation of hepatic lipid metabolism and steatosis. METHODS AND RESULTS In mice wi...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The Journal of clinical investigation
دوره 61 1 شماره
صفحات -
تاریخ انتشار 1978