Wülfert E
Nouv Presse Med. 1980 Dec 22;9(49):3733-6.
In animal models and in man the lipid-lowering activity of fenofibrate is characterized by a reduction of the serum fraction that carries most of the circulating cholesterol. Pharmacological studies in rodents have shown that fenofibrate induces a "catabolic" state with decreased HDL-cholesterol in normal rats and decreased VLDL-cholesterol ester and liver cholesterol ester in hypercholesterolaemic rats. The mechanism of this enhanced elimination is still unknown. The relative increase in free cholesterol in relation to cholesterol ester might indirectly reduce HMG-CoA reductase activity. In addition, we have shown a direct inhibitory effect of fenofibrate on human liver microsomic enzyme activity in vitro. The blood levels of fenofibric acid in man would be sufficient to inhibit this enzyme in vivo.
在动物模型和人体中,非诺贝特的降脂活性表现为携带大部分循环胆固醇的血清组分减少。对啮齿动物的药理学研究表明,非诺贝特在正常大鼠中诱导出一种“分解代谢”状态,导致高密度脂蛋白胆固醇降低,在高胆固醇血症大鼠中导致极低密度脂蛋白胆固醇酯和肝脏胆固醇酯降低。这种增强的清除机制尚不清楚。游离胆固醇相对于胆固醇酯的相对增加可能间接降低羟甲基戊二酸单酰辅酶A还原酶活性。此外,我们已经证明非诺贝特在体外对人肝微粒体酶活性有直接抑制作用。人体中非诺贝特酸的血药浓度足以在体内抑制这种酶。