The mechanism of lack of hypocholesterolemic effects of pravastatin sodium, a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, in rats

• Published in: Biochimica et biophysica acta Vol. 1254; no. 1; pp. 7 - 12
• Main Authors: Fujioka, Tomoyuki, Nara, Futoshi, Tsujita, Yoshio, Fukushige, Junichiro, Fukami, Masaharu, Kuroda, Masao
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 03-01-1995
• Subjects: Animals; Cholesterol - analysis; Cholesterol - blood; Cholesterol metabolism; Cholesterol, VLDL - analysis; Hydroxymethylglutaryl CoA Reductases - analysis; Hydroxymethylglutaryl-CoA reductase; Hydroxymethylglutaryl-CoA reductase inhibitor; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Liver - drug effects; Liver - metabolism; Male; Pravastatin; Pravastatin - pharmacology; Rabbits; Rats; Rats, Wistar; Receptors, LDL - analysis; Species specificity; Triton WR-1339; Hydroxymethylglutaryl-CoA reductase inhibitor; Hydroxymethylglutaryl-CoA reductase; Species specificity; Pravastatin; Triton WR-1339; Cholesterol metabolism
• ISSN: 0005-2760; 0006-3002; 1879-145X
• DOI: 10.1016/0005-2760(94)00154-Q

In order to clarify the reason why pravastatin, a 3-hydroxy-3-methylglutaryl (HMG)-CoA reductase inhibitor, did not show hypocholesterolemic effects in rats, the changes of various parameters affecting the serum cholesterol levels by pravastatin were determined in rats and rabbits, as a comparison. In rabbits, pravastatin administration at 50 mg/kg for 14 days decreased serum and liver cholesterol by 40% and 8%, respectively. The hepatic LDL receptor activity was increased 1.7-fold, and VLDL cholesterol secretion was decreased. Cholesterol 7α-hydroxylase activity was not changed. In contrast, in rats, serum cholesterol was increased by 14% at 50 mg/kg and 27% at 250 mg/kg for 7 days, respectively. At 250 mg/kg, liver cholesterol was significantly increased by 11%. Under these conditions, neither the hepatic LDL receptor activity nor cholesterol 7α-hydroxylase was changed, and VLDL cholesterol secretion was increased. At 250 mg/kg, net cholesterol synthesis in rat liver was increased after 7 days of consecutive administration. These results imply that in rats, stimulated net cholesterol synthesis caused the increase of liver cholesterol followed by the increase of VLDL cholesterol secretion, and resulted in the raise of plasma cholesterol. Although hepatic HMG-CoA reductase was induced almost the same fold in both animals at 50 mg/kg, the induced HMG-CoA reductase activity in rats might overcome the inhibitory capability of pravastatin, resulting in an increase of net cholesterol synthesis, but not in rabbits. This overresponse to pravastatin in rats might cause the lack of hypocholesterolemic effects of this drug.