Masoprocol decreases serum triglyceride concentrations in rats with fructose-induced hypertriglyceridemia

Historically, extracts of the creosote bush have been used by native healer s of the Southwest region of North America to treat symptoms of type 2 diab etes. More recently, we have shown that masoprocol (nordihydroguaiaretic ac id). a pure compound isolated from the creosote bush (Larrea tridentata), d ecreases serum glucose and triglyceride (TG) levels when administered orall y in rodent models of type 2 diabetes. The present studies were undertaken to determine if masoprocol also decreases TG concentrations in rats with fr uctose-induced hypertriglyceridemia (HTG), a nondiabetic model of HTG assoc iated with insulin resistance and hyperinsulinemia. Serum To levels, which were significantly higher after rats ate a fructose-enriched (60% by weight ) diet for 14 days as compared with chow-fed controls (411 v 155 mg/dL, P < .01). decreased in a stepwise fashion in fructose-fed rats treated orally with masoprocol for 4 to 8 days over a dose range of 10 to 80 mg/kg twice d aily. Using the nonionic detergent Triton WR 1339 to compare TG secretion r ates in masoprocol- and vehicle-treated rats, masoprocol at a dose of 40 or 80 mg/kg twice daily, significantly reduced hepatic TG secretion (P < .01) and liver TG content (P < .001). whereas lower doses of masoprocol decreas ed serum TG without an apparent reduction in hepatic TG secretion. Administ ration of Intralipid (a fat emulsion) showed that the half-time for removal of To from serum was also shorter in masoprocol-treated rats versus vehicl e-treated controls (31 v 64 minutes, P < .05). In addition adipose tissue l ipoprotein lipase (LPL) activity was increased in masoprocol-treated rats a nd adipose tissue hormone-sensitive lipase (HSL) activity was decreased. We conclude that masoprocol administration to rats with fructose-induced HTG results in lower serum TG levels associated with reduced hepatic TG secreti on and increased peripheral TG clearance. Copyright (C) 2000 by W.B. Saunde rs Company.