Urinary excretion of lithocholic acid and its conjugates by the bile duct–ligated rat

Joanna M. Little, Piotr Zimniak, Anna Radominska, Roger Lester, Paul Lehman – 1 October 1991 – The 3‐O‐glucuronide of lithocholic acid has been shown to be a potent cholestatic agent in rats. However, even after the onset of lithocholic acid glucuronide–induced cholestasis, little of the administered material was recovered in urine.

Dietary fish oil effects on biliary lipid secretion and cholesterol gallstone formation in the African green monkey

Martin W. Scobey, Fred L. Johnson, John S. Parks, Lawrence L. Rudel – 1 October 1991 – We studied two groups of adult male African green monkeys to assess the effects of dietary fish oil on biliary lipid secretion and cholesterol gallstone formation. One group was fed 0.8 mg cholesterol/kcal and 42% of calories as fat with half of the fat calories derived from lard; the other group was fed a similar diet except for the isocaloric substitution of menhaden oil for lard. After 21/2 to 3 yr, necropsies were performed and the presence of gallstones was determined.

Estrogen and progesterone receptors in the gallbladders from patients with gallstones

Franco O. Ranelletti, Mauro Piantelli, Everardo Zanella, Arnaldo Capelli, Attilio M. Farinon – 1 October 1991 – Cytosolic receptors for estrogen and progesterone were assayed in 50 gallbladders from 29 women and 21 men who had cholecystectomies because of choleithiasis. High‐affinity (equilibrium dissociation constant, KD = 0.46 ± 0.23 nmol/L of 24 cases) estrogen receptors were detected in 20 of 29 gallbladders from women (range = 1.6 to 32 fmol/mg protein; mean ± S.D. = 10.9 ± 8.1), whereas in men only 4 of 21 specimens contained detectable estrogen receptors.

Effects of single ethanol administration on hepatic ornithine decarboxylase induction and polyamine metabolism

Takashi Tanaka, Yoshihiro Sukegawa, Shuhei Nishiguchi, Tetsuo Kuroki, Kenzo Kobayashi, Isao Matsui‐Yuasa, Shuzo Otani, Takashi Toda, Takeyuki Monna – 1 October 1991 – The effects of a single ethanol administration on ornithine decarboxylase induction, polyamine metabolism and DNA synthesis in rat liver after partial hepatectomy were studied. Ethanol given 1 hr before partial hepatectomy at the dose of 2, 3 or 5 gm/kg body wt inhibited the increase in ornithine decarboxylase activity and that in the putrescine level in the liver 4 hr after partial hepatectomy.

Effect of cyclosporine and steroids on canine bile flow

John J. Brems, Jeffery Reese, Robert Kane, Donald L. Kaminski – 1 September 1991 – Cyclosporine and hydrocortisone are the main immunosuppressants used in transplant surgery. The purpose of this study was to determine the effect of intravenous administration of cyclosporine and hydrocortisone on bile flow in dogs. Cyclosporine in doses of 0.5, 1.0 and 1.5 mg · kg−1 · hr−1 and hydrocortisone in doses of 1.25, 2.5 and 5 mg · kg−1 · hr−1 were administered along with 18 μmol/min intravenous sodium taurocholate to dogs with chronic biliary and gastric fistulas.

Localization of hepatocyte growth factor in human and rat tissues: An immunohistochemical study

Helmut K. Wolf, Reza Zarnegar, George K. Michalopoulos – 1 September 1991 – Hepatocyte growth factor is a protein growth factor with a strong mitogenic effect on hepatocytes. Recently, hepatocyte growth factor and hepatocyte growth factor messenger RNA have been extracted from several organs of humans, rats and rabbits. This study was undertaken to comprehensively define and compare the cellular localization of hepatocyte growth factor in human and rat tissues in detail.

Structure‐function relationship of immunosuppressive drugs: A cautionary tale

Laurence A. Turka, Craig B. Thompson – 1 September 1991 – The immunosuppressants FK506 and rapamycin bind to the same immunophilin, FK506 binding protein (FKBP), and inhibit distinct signal transduction pathways in T lymphocytes. A nonnatural immunophilin ligand, 506BD, which contains only the common structural elements of FK506 and rapamycin, was synthesized and found to be a high‐affinity ligand of FKBP and a potent inhibitor of FKBP rotamase activity. Whereas 506BD does not interfere with T cell activation, it does block the immunosuppressive effects of both FK506 and rapamycin.

Vanadate inhibits glucose output from isolated perfused rat liver

Rafael Bruck, Haia Prigozin, Zipora Krepel, Paul Rotenberg, Yoram Shechter, Simon Bar‐Meir – 1 September 1991 – Previous studies have demonstrated that vanadate ions mimic many of the actions of insulin in in vitro systems. Also, vanadate administered to diabetic hyperglycemic rats lowers their blood glucose levels to normal values. In this study we demonstrate that vanadate inhibits glucose output in the isolated perfused rat liver. Glucose production was suppressed maximally (about 50% to 60%), on addition of extremely low vanadate ion concentrations (0.5 to 1 μmol/L).

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