Brefeldin A (BFA) inhibits transcytosis in the isolated perfused rat liver (IPRL) with no effect on bile flow and bile salt secretion

Hepatology ◽  
1993 ◽  
Vol 18 (4) ◽  
pp. A294
Author(s):  
D ALVARO
1992 ◽  
Vol 283 (2) ◽  
pp. 575-581 ◽  
Author(s):  
Y Hamada ◽  
A Karjalainen ◽  
B A Setchell ◽  
J E Millard ◽  
F L Bygrave

The effects were investigated of the choleretic bile salt glycoursodeoxycholate (G-UDCA) and of the cholestatic bile salt taurochenodeoxycholate (T-CDCA) on changes in perfusate Ca2+, glucose and oxygen and in bile calcium and bile flow induced by the administration of (a) vasopressin, (b) glucagon and (c) glucagon plus vasopressin together to the perfused rat liver [Hamada, Karjalainen, Setchell, Millard & Bygrave (1992) Biochem. J. 281, 387-392]. G-UDCA itself increased the secretion of calcium in the bile several-fold, but its principal effect was to augment each of the above-mentioned metabolic events except glucose and oxygen output; particularly noteworthy was its ability to augment the ‘transients’ in bile calcium and bile flow seen immediately after the administration of vasopressin with or without glucagon. T-CDCA, by contrast, produced opposite effects and attenuated all of the parameters measured, and in particular the transients in bile calcium and bile flow. The data provide evidence of a strong correlation between calcium fluxes occurring on both the sinusoidal and the bile-canalicular membranes and that all are modifiable by glucagon, Ca(2+)-mobilizing hormones and bile salts.


1992 ◽  
Vol 281 (3) ◽  
pp. 593-595 ◽  
Author(s):  
C Hallbrucker ◽  
F Lang ◽  
W Gerok ◽  
D Häussinger

The effects of aniso-osmotically and amino-acid-induced cell-volume changes on bile flow and biliary taurocholate excretion were studied in isolated perfused rat liver. With taurocholate (100 microM) in the influent perfusate, hypo-osmotic exposure (225 mosmol/l) increased taurocholate excretion into bile and bile flow by 42 and 27% respectively, whereas inhibition by 32 and 47% respectively was observed after hyperosmotic (385 mosmol/l) exposure. The effects of aniso-moticity on taurocholate excretion into bile was observed throughout aniso-osmotic exposure, even after completion of volume-regulatory ion fluxes and were fully reversible upon re-exposure to normo-osmotic media. Hypo-osmotic cell swelling (225 mosmol/l) increased the Vmax. of taurocholate translocation from the sinusoidal compartment into bile about 2-fold. Also, cell swelling induced by glutamine and glycine stimulated both bile flow and biliary taurocholate excretion. There was a close relationship between the aniso-osmotically and amino-acid-induced change of cell volume and taurocholate excretion into bile. The data suggest that liver cell volume plays an important role in regulating bile-acid-dependent bile flow and biliary taurocholate excretion.


Hepatology ◽  
1995 ◽  
Vol 21 (2) ◽  
pp. 450-459 ◽  
Author(s):  
Domenico Alvaro ◽  
Antonio Benedetti ◽  
Alessandro Gigliozzi ◽  
Adriano Bini ◽  
Sonia Furfaro ◽  
...  

1972 ◽  
Vol 50 (3) ◽  
pp. 276-278
Author(s):  
A. C. Nestruck ◽  
R. W. Furneaux

Isolated livers from fed rats were perfused for 1 h with a medium consisting of Krebs–Ringer bicarbonate buffer with added albumin and glucose. Rates of perfusate and bile flow, differences in [Formula: see text], [Formula: see text], and pH, and glucose and potassium efflux were measured. Rewarmed slices of liver taken before the surgical preparation and before the perfusion were found to be able to reverse a cation shift imposed by cold incubation. Slices of liver taken after one perfusion were not able to effect this expected cation transport. It is proposed that the perfusate used was not ideal as evidenced by the altered membrane function of slices after perfusion.


Pharmacology ◽  
1977 ◽  
Vol 15 (1) ◽  
pp. 57-64 ◽  
Author(s):  
Kaisu Nevasaari ◽  
Birgitta Alakare ◽  
Niilo T. Kärki

1968 ◽  
Vol 110 (2) ◽  
pp. 15P-16P
Author(s):  
T F Slater ◽  
B C Sawyer ◽  
V B Delaney ◽  
G Bullock

1994 ◽  
Vol 266 (2) ◽  
pp. G324-G329 ◽  
Author(s):  
A. Tanaka ◽  
K. Katagiri ◽  
M. Hoshino ◽  
T. Hayakawa ◽  
K. Tsukada ◽  
...  

The effects of endothelin (ET) on portal pressure and bile secretion were examined using isolated perfused rat liver and rat hepatocyte preparations. ET-1 raised portal pressure dose dependently; administration at a high dose (10(-9) mol) induced a > 200% increase along with reduced bile flow and decreased secretion of bile acid and phospholipids. However, a low dose (10(-10) mol) of ET-1 brought about a < 100% portal pressure rise, enhanced both bile flow and excretion of bile acid and phospholipids, and significantly increased transfer of preadministered horseradish peroxidase (HRP) into bile. In addition, values for Ca2+ concentrations, examined by indo 1 fluorescence, were elevated in isolated hepatocytes after administration of ET-1. Papaverine suppressed the low-dose ET-1 stimulation effects on both portal pressure and bile secretion. Moreover, it also reduced the HRP excretion and suppressed intracellular Ca2+ release. This study demonstrated that ET-1 stimulates vesicular transport, probably via promotion of intracellular Ca2+ release, and, as a result, increases bile acid-dependent bile flow.


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