Prostanoid secretion by rat hepatic sinusoidal endothelial cells and its regulation by exogenous adenosine triphosphate

Naoaki Hashimoto, Tsuyoshi Watanabe, Yasushi Shiratori, Yusei Ikeda, Hirokazu Kato, Katsuken Han, Haruki Yamada, Gotaro Toda, Kiyoshi Kurokawa – 1 June 1995 – We investigated the secretory profiles of prostanoids in two types of nonparenchymal cell from the rat liver, sinusoidal endothelial cells and Kupffer cells, in primary culture both under basal conditions and after stimulation with adenine nucleotides. Prostaglandin (PG) E2 was the main prostanoid secreted by both types of hepatic nonparenchymal cell in the basal and adenosine triphosphate (ATP)‐stimulated states.

Serial hemodynamic measurements in well‐differentiated hepatocellular carcinomas

Satoshi Saitoh, Kenji Ikeda, Isao Koida, Akihito Tsubota, Yasuji Arase, Kazuaki Chayama, Hiromitsu Kumada – 1 June 1995 – We performed serial hemodynamics in 15 patients with 21 well‐differentiated hepatocellular carcinomas. The total length of the observation period ranged from 129 to 678 days (median, 368). We investigated both arterial and portal blood flow at intervals of at least 4 months. Arterial blood flow was measured with carbon dioxide—enhanced ultrasonography (US), and portal blood flow was measured with computed tomographic arterial portography (CTAP).

Cytokine‐induced upregulation of hepatic intercellular adhesion molecule‐1 messenger RNA expression and its role in the pathophysiology of murine endotoxin shock and acute liver failure

Naeem A. Essani, Michael A. Fisher, Anwar Farhood, Anthony M. Manning, C. Wayne Smith, Hartmut Jaeschke – 1 June 1995 – Neutrophil‐induced liver injury during endotoxemia is dependent on the adhesion molecule Mac‐1 (CD11b/CD18) on neutrophils. The potential involvement of its counterreceptor, intercellular adhesion molecule—1 (ICAM‐1), in the pathogenesis was investigated after administration of 100 μg/kg Salmonella abortus equi endotoxin (ET) in galactosamine‐sensitized mice (Gal).

Different hepatocytes express the cholesterol 7α‐hydroxylase gene during its circadian modulation in vivo

Caryn M. Berkowitz, Cynthia S. Shen, Bahri M. Bilir, Edgardo Guibert, Jorge J. Gumucio – 1 June 1995 – Cholesterol 7α‐hydroxylase, the rate‐limiting enzyme in bile salt synthesis from cholesterol is a P450 enzyme (CYP7A). Its expression and activity are regulated by bile salts, cholesterol, hormones and a circadian modulator. Here we define the hepatocytes contributing to the expression of the rat CYP7A gene during its in vivo circadian variation.

Deletion of integrated hepatitis B virus genome and cellular flanking sequences in hepatocellular carcinoma cells in BALB/c Mice

Poa‐Chun Chang, Cheng‐Po Hu, Shu‐Hsia Chen, Sheng Wang‐Wuu, Chungming Chang – 1 June 1995 – We have previously reported the establishment of well‐differentiated BALB/c mouse liver (ML) cell lines. Transfection of these cell lines with hepatitis B virus (HBV) DNA led to the expression of HBV‐specific antigens and integration of HBV sequences in the cellular genome. Two cloned HBV‐transfected ML cell lines, ML‐2(HBV) and ML‐3(HBV), expressed viral antigens and were highly tumorigenic in nude mice. However, the tumorigenicity of the two cell lines was significantly reduced in BALB/c mice.

Regulation of human Gc (vitamin D — binding) protein levels: Hormonal and cytokine control of gene expression in vitro

Chandan Guha, Motoki Osawa, Phillip A. Werner, Robert M. Galbraith, Gary V. Paddock – 1 June 1995 – Studies were performed in Hep3B hepatocytes to better elucidate the mechanisms regulating circulating levels of human group—specific component (Gc). We measured changes in Gc messenger RNA (mRNA) synthesis and levels of secreted protein resulting from treatment of hepatocytes with cytokines and hormones known to influence synthesis of other proteins of hepatic origin. We particularly focused on compounds known to be prototypic stimulants during the acute phase response.

The frequency of 4977 base pair deletion of mitochondrial DNA in various types of liver disease and in normal liver

Shu Fukushima, Kazuo Honda, Masaaki Awane, Eiji Yamamoto, Ryouji Takeda, Ichiro Kaneko, Akira Tanaka, Taisuke Morimoto, Koichi Tanaka, Yoshio Yamaoka – 1 June 1995 – Using a polymerase chain reaction (PCR) method, we tested for the hepatic mitochondrial DNA (mtDNA) deletion in 40 hepatic tumors (28 hepatocellular carcinomas [HCCs], 9 other malignant tumors, and 3 benign tumors) and in the livers of 71 patients, including 16 pediatric patients with end‐stage liver disease who underwent living related donor liver transplantation and 16 liver donors.

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