Literature DB >> 6182

Effect of phenobarbitone on plasma lipids in normal subjects.

P N Durrington, C J Roberts, L Jackson, R A Branch, M Hartog.   

Abstract

1. Phenobarbitone in a dose of 180 mg daily was administered to ten normal subjects for 3 weeks. There was a significant increase in total plasma cholesterol, plasma low-density-lipoprotein cholesterol, plasma low-density-lipoprotein (LDL) triglycerides and plasma LDL protein. The increase in plasma LDL cholesterol accounted for the increase in total plasma cholesterol. There was a significant reduction in the ratio of LDL cholesterol to LDL protein. 2. No significant changes were observed in total plasma triglycerides, plasma very-low-density-lipoprotein (VLDL) triglycerides, plasma VLDL cholesterol or plasma VLDL protein. 3. Evidence that drug-metabolizing enzymes were induced by phenobarbitone was provided by an increase in antipyrine clearance. No relationship was observed between changes in plasma cholesterol and changes in antipyrine clearance. Serum gamma-glutamyl transpeptidase was also increased after phenobarbitone administration, the increase being unrelated to changes in antipyrine clearance or plasma cholesterol.

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Year:  1976        PMID: 6182     DOI: 10.1042/cs0500349

Source DB:  PubMed          Journal:  Clin Sci Mol Med        ISSN: 0301-0538


  3 in total

1.  Hypertriglyceridaemia and abnormalities of triglyceride catabolism persisting after pancreatitis.

Authors:  P N Durrington; O P Twentyman; J M Braganza; J P Miller
Journal:  Int J Pancreatol       Date:  1986-10

2.  Relationship between lipid composition and drug metabolizing capacity of human liver.

Authors:  M J Savolainen; A J Arranto; I E Hassinen; P V Luoma; R O Pelkonen; E A Sotaniemi
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

3.  Effect of CAR activation on selected metabolic pathways in normal and hyperlipidemic mouse livers.

Authors:  Tadeja Rezen; Viola Tamasi; Anita Lövgren-Sandblom; Ingemar Björkhem; Urs A Meyer; Damjana Rozman
Journal:  BMC Genomics       Date:  2009-08-19       Impact factor: 3.969

  3 in total

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