BILE SECRETION

被引:18
作者
ERLINGER, S [1 ]
机构
[1] HOP BEAJON,INSERM,U24,UNITE RECH PHYSIOPATHOL HEPAT,CLICHY,FRANCE
关键词
D O I
10.1093/oxfordjournals.bmb.a072582
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bile is an isotonic aqueous solution of bile acids, cholesterol, phospholipids, bile pigments and inorganic electrolytes. It is secreted by the hepatocytes into the bile canaliculi and modified in the bile ductules or ducts. The three main processes identified in the generation of bile flow are: 1. Active transport of bile acids from blood into bile canaliculi. This is responsible of the bile acid-dependent canalicular bile flow. Coupling between water flow and bile acid secretion is probably effected mainly through an osmotic mechanism. There is evidence that water flows (at least in part) through the interhepatocytic junctions. The bile acid-dependent flow accounts for 30 to 60% of spontaneous basal bile flow. 2. A canalicular, bile acid-independent secretion, probably due to transport into bile of organic solutes (glutathione) and inorganic electrolytes. This fraction of bile flow is stimulated by phenobarbital. It represents 30 to 60% of basal bile flow. Normal canalicular bile flow also depends on the integrity of intracellular cytoskeletal organelles, mostly microfilaments. 3. Reabsorption and secretion of fluid and inorganic electrolytes by the ductules and ducts. Secretion chiefly occurs in response to secretin and represents 30% of basal bile flow. Although several ion transport systems have been identified on the biliary epithelial cells (in particular a Na+/H+ exchange, a Na+:HCO3- symport and a Cl-/HCO3- exchange), the cellular mechanism of secretion is not known. Abnormalities of bile duct function may account for the liver disease of cystic fibrosis, but these abnormalities have not been characterized.
引用
收藏
页码:860 / 876
页数:17
相关论文
共 38 条
[1]   BILE SECRETORY FUNCTION OF INTRAHEPATIC BILIARY EPITHELIUM IN THE RAT [J].
ALPINI, G ;
LENZI, R ;
ZHAI, WR ;
SLOTT, PA ;
LIU, MH ;
SARKOZI, L ;
TAVOLONI, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (01) :G124-G133
[2]   BILIARY PHYSIOLOGY IN RATS WITH BILE DUCTULAR CELL HYPERPLASIA - EVIDENCE FOR A SECRETORY FUNCTION OF PROLIFERATED BILE DUCTULES [J].
ALPINI, G ;
LENZI, R ;
SARKOZI, L ;
TAVOLONI, N .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (02) :569-578
[3]   GALLSTONES IN CYSTIC-FIBROSIS - A CRITICAL REAPPRAISAL [J].
ANGELICO, M ;
GANDIN, C ;
CANUZZI, P ;
BERTASI, S ;
CANTAFORA, A ;
DESANTIS, A ;
QUATTRUCCI, S ;
ANTONELLI, M .
HEPATOLOGY, 1991, 14 (05) :768-775
[4]   RELATION BETWEEN BILIARY GLUTATHIONE EXCRETION AND BILE ACID-INDEPENDENT BILE-FLOW [J].
BALLATORI, N ;
TRUONG, AT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (01) :G22-G30
[5]  
BASS S, 1983, GASTROENTEROLOGY, V84, P1592
[6]   CYTOCHEMICAL-LOCALIZATION OF NA+, K+-ATPASE IN RAT HEPATOCYTE [J].
BLITZER, BL ;
BOYER, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1978, 62 (05) :1104-1108
[7]   SECRETIN EMPTIES BILE-DUCT CELL CYTOPLASM OF VESICLES WHEN IT INITIATES DUCTULAR HCO3-SECRETION IN THE PIG [J].
BUANES, T ;
GROTMOL, T ;
LANDSVERK, T ;
RAEDER, MG .
GASTROENTEROLOGY, 1988, 95 (02) :417-424
[8]   EFFECTS OF URSODEOXYCHOLIC ACID TREATMENT ON NUTRITION AND LIVER-FUNCTION IN PATIENTS WITH CYSTIC-FIBROSIS AND LONGSTANDING CHOLESTASIS [J].
COTTING, J ;
LENTZE, MJ ;
REICHEN, J .
GUT, 1990, 31 (08) :918-921
[9]  
CRAWFORD JM, 1988, J LIPID RES, V29, P144
[10]  
DUMONT M, 1980, GASTROENTEROLOGY, V79, P82