Gemfibrozil, a hypolipidemic drug mainly used in the treatment of hype
rtriglyceridemic states, strongly inhibits the rat hepatic microsomal
fatty acid chain elongation system in vitro. The inhibition is indepen
dent on the reducing cofactor used in the assay. Furthermore, gemfibro
zil seems to act by inhibiting the rate-limiting step of the elongatio
n process, the condensing reaction, without discriminating among the p
roposed three different condensing enzymes, devoted to condensation of
saturated, mono-unsaturated and polyunsaturated acyl-CoA substrates.