Preoperative measurement of segmental liver volume of donors for living related liver transplantation

Seiji Kawasaki, Masatoshi Makuuchi, Hidetoshi Matsunami, Yasuhiko Hashikura, Toshihiko Ikegami, Hisanao Chisuwa, Tatsuo Ikeno, Terumasa Noike, Tadatoshi Takayama, Hideo Kawarazaki – 1 November 1993 – Segmental liver volume determination by computed tomographic scan was carried out preoperatively in nine donors for living related liver transplantation. The calculated volume was compared with the graft size actually obtained by three types of donor hepatectomy. The volume of the left lateral segment (175 to 241 ml) and the left lobe (310 to 490 ml) varied markedly among the donors.

Vasoactive effects of bile salts in cirrhotic rats: In vivo and In vitro studies

Jung‐Min Pak, Samuel S. Lee – 1 November 1993 – To clarify a possible pathogenic role for bile salts in the hyperdynamic circulation of cirrhosis, we studied the vasoactive effects of three different bile salts–tauroursodeoxycholic acid, taurochenodeoxycholic acid and taurodeoxycholic acid–in cirrhotic rats. Cirrhosis was induced with bile duct ligation; controls underwent sham surgery. In vivo, the bile salts were intravenously infused at one of three doses (1.2 × 10−7, 1.2 × 10−6 and 6.0 × 10−5 mol · 100 gm−1 · min−1) for 5 min.

True transport: One or more sodium‐dependent bile acid transporters?

Roger Lester, Piotr Zimniak – 1 November 1993 – Sodium‐dependent bile acid transport is a well‐established function of the sinusoidal segment of the hepatocyte plasma membrane. Evidence has been provided previously by the authors for the existence of a putative sinusoidal plasma membrane sodium‐dependent bile acid transporter with a mass of 49 kD. This protein has been partially characterized with a monoclonal antibody and by reconstitution in proteoliposomes. Further characterization is provided in the paper under discussion.

Bile acid–induced modifications in DNA synthesis by the regenerating perfused rat liver

Jose J. G. Marin, Emilio R. Barbero, Maria C. Herrera, Arantxa Tabernero, Maria J. Monte – 1 November 1993 – Liver cell proliferation is a complex process that can be affected by a large number of factors such as bile acids, which have been reported to be associated to the pathogenesis of liver cancer. In this work, bile acid–induced modifications in DNA synthesis by regenerating perfused rat liver were investigated. Two‐thirds hepatectomy was carried out 24 hr before perfusion of livers with recirculating, erythrocyte‐free Krebs‐Henseleit solution.

Modulators of the protein kinase C system influence biliary excretion of cationic drugs

Herman Steen, Hans Smit, Almar Nijholt, Marjolijn Merema, Dirk K. F. Meijer – 1 November 1993 – To investigate whether hepatobiliary transport of organic cations is under regulatory control, we studied transport of tri‐n‐butylmethylammonium in the isolated perfused rat liver and in isolated rat hepatocytes. Transport was investigated in the presence of modulators of the protein kinase C and the cyclic AMP second‐messenger system.

A new bile acid transporter?

Winita Hardikar, Frederick J. Suchy – 1 November 1993 – Transport systems involved in uptake and biliary secretion of bile salts have been extensively studied in rat liver; however, little is known about these systems in the human liver. In this study, we investigated taurocholate (TC) transport in canalicular and basolateral plasma membrane vesicles isolated from 15 human livers (donor age 6–64 yr). ATP stimulated the uptake of TC into both canalicular and basolateral human liver plasma membrane vesicles (cLPM and bILPM, respectively).

Hepatic blood volume responses and compliance in cats with long‐term bile duct ligation

Joshua Schafer, Mark S. D'Almeida, Harvey Weisman, W. Wayne Lautt – 1 October 1993 – Hepatic capacitance responses were compared in sham‐operated and 14‐day bile duct–ligated cats under pentobarbital anesthesia. Both groups were subjected to splenectomy and had the anterior hepatic nerve plexus sectioned to allow stimulation; the posterior plexus was intact. Blood volume compensation for hemorrhage was reduced in the bile duct ligation group compared with the control group: The liver compensated for 20.1% and 10.6% of blood loss, respectively.

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