Both lovastatin (a fungal product) and a tocotrienol rich fraction (TRF25, a mixture of tocols isolated from stabilized and heated rice bran containing desmethyl [d-P-21-T3] and didesmethyl [d-P-25-T3] tocotrienols) are potent hypocholesterolemic agents, although they suppress cholesterol biosynthesis by different mechanisms. To determine additive and/or synergistic effects of both agents, chickens were fed diets supplemented with 50 ppm TRF25 or d-P-25-T3 in combination with 50 ppm lovastatin for 4 weeks. Combinations of d-P-25-T3 With lovastatin were found most effective in reducing serum total cholesterol and low-density lipoprotein (LDL) cholesterol compared to the control diet or individual supplements. The mixture of TRF25 + lovastatin inhibited the activity of beta -hydroxy-beta -methylglutaryl coenzymeA reductase (21%) compared to lovastatin alone, which did not change its activity. Cholesterol 7 alpha -hydroxylase activity was increased by lovastatin (11%,) and by lovastatin plus TRF25 (19%). TRF25 + lovastatin decreased levels of serum total cholesterol (22%). LDL cholesterol (42%), apolipoprotein B (13-38%). triglycerides (19%), thromboxane B-2 (34%) and platelet factor 4 (26%), although high-density lipoprotein (HDL) cholesterol. and apolipoprotein Al levels were unaffected. The mixture of TRF25 + lovastatin showed greater effects than did the individual treatments alone, reflecting possible additive pharmacological actions. The effects, however, of the d-P-25-T3/lovastatin combination were no greater than that of d-P-25-T3 alone, possibly indicating that d-P-25-T3 produced a maximum cholesterol lowering effect at the concentration used. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.