Sexual dysfunction in men with chronic liver disease

1 March 1988 – Men with liver disease are hypogonadal and feminised. European workers consider the liver disease itself to be the major factor but American workers blame alcohol consumption. We studied sexual dysfunction and sex hormones in three matched groups of men; controls (n = 22), those with alcoholic liver disease (n = 21), and those with non‐alcoholic liver disease (n = 21). Men with alcoholic liver disease had more sexual dysfunction.

Large granular lymphocytes in the liver

Stephen P. James – 1 March 1988 – Considerable numbers of large granular lymphocytes (LGL) were isolated from rat liver by a simple method consisting of sinusoidal lavage at elevated (50 cm water column) perfusion pressure. This method gave a yield comparable with the enzymatic dissociation method commonly used for the isolation of nonparenchymal liver cells, but was shorter in time and had the advantage of avoiding the potentially harmful effects of the dissociating enzymes.

Phenobarbital induction of cytochrome p‐450 b,e genes is dependent on protein synthesis

Jose Chianale, Leyna Mulholland, Peter G. Traber, Jorge J. Gumucio – 1 March 1988 – Phenobarbital induces liver cytochrome P‐450 b,e proteins mainly by increasing the rate of transcription of these genes. The mechanism responsible for the phenobarbital increment in the rate of transcription of cytochrome P‐450 b,e genes is unknown. The objective of this study was to assess whether active protein synthesis was needed for phenobarbital to induce the liver cytochrome P‐450 b,e genes.

Regulation of bile acid synthesis. I. Effects of conjugated ursodeoxycholate and cholate on bile acid synthesis in chronic bile fistula rat

Douglas M. Heuman, Carmen R. Hernandez, Philip B. Hylemon, William M. Kubaska, Constance Hartman, Z. Reno Vlahcevic – 1 March 1988 – Bile acid synthesis is thought to be regulated by a negative feedback mechanism which is presumably dependent upon the flux of bile acids in the enterohepatic circulation.

Prognostic indicators in alcoholic cirrhotic men

Christian Gluud, Jens H. Henriksen, The Copenhagen Study Group for Liver Diseases – 1 March 1988 – The relationships between portal pressure, liver function and clinical variables on one hand and development of variceal hemorrhage and death on the other were investigated in 58 men with newly diagnosed alcoholic cirrhosis. Portal pressure was determined during hepatic vein catheterization as wedged minus free hepatic vein pressure, and median pressure was 14 mm Hg (range = 3 to 26 mm Hg).

Tissue localization and kinetics of pit cells or large granular lymphocytes in the liver of rats treated with biological response modifiers

Luc Bouwens, Eddie Wisse – 1 January 1988 – The numbers of Kupffer cells (macrophages) and pit cells (large granular lymphocytes) were counted by light and electron microscopy in perfusion‐fixed liver sinusoids. After a single intravenous injection of the biological response modifiers zymosan, Propionibacterium acnes and OK‐432, a 4‐ to 6‐fold increase in the number of pit cells and a 2‐ to 4‐fold increase in the number of Kupffer cells were observed within a period of 4 to 7 days.

IgA deposition and synthesis in alcoholic liver injury

D. R. Triger – 1 January 1988 – Immunoglobulin deposition in alcoholic and non‐alcoholic liver disease was studied using an indirect immunoperoxidase technique. A continuous pattern of IgA deposition, with IgA outlining the sinusoids, was shown to be a specific and sensitive marker for liver disease caused by alcohol in both cirrhotic and non‐cirrhotic livers. The sensitivity was lowest in cases of alcoholic disease showing fatty change alone.

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