Genomics Inform.  2010 Mar;8(1):41-49.

Gene Expression Analysis for Statin-induced Cytotoxicity from Rat Primary Hepatocytes

Affiliations
  • 1National Institution of Food and Drug Safety Evaluation, Seoul 122-704, Korea, Korea Food and Drug Administration, Seoul 122-704, Korea. hosa33@korea.kr

Abstract

Statins are competitive inhibitors of hydroxy-3-methyl glutaryl coenzyme A (HMG-CoA) reductase and used most frequently to reduce plasma cholesterol levels and to decrease cardiovascular events. However, statins also have been reported to have undesirable side effects such as myotoxicity and hepatotoxicity associated with their intrinsic efficacy mechanisms. Clinical studies recurrently reported that statin therapy elevated the level of liver enzymes such as ALT and AST in patients suggesting possible liver toxicity due to statins. This observation has been drawn great attention since statins are the most prescribed drugs and statin-therapy was extended to a larger number of high-risk patients. Here we employed rat primary hepatocytes and microarray technique to understand underlying mechanism responsible for statin-induced liver toxicity on cell level. We isolated genes whose expressions were commonly modulated by statin treatments and examined their biological functions. It is of interest that those genes have function related to response to stress in particular immunity and defense in cells. Our study provided the basic information on cellular mechanism of statin-induced cytotoxicity and may serve for finding indicator genes of statin-induced toxicity in rat primary hepatocytes.

Keyword

cytotoxicity; gene expression; hepatocyte; microarray; statin

MeSH Terms

Animals
Cholesterol
Coenzyme A
Gene Expression
Hepatocytes
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Liver
Oxidoreductases
Plasma
Rats
Cholesterol
Coenzyme A
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Oxidoreductases
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