Subang M C, Stewart-Phillips J L, Gagnon R F
Department of Physiology, McGill University, Montreal, Canada.
Adv Perit Dial. 1992;8:381-4.
Using a mouse model of chronic renal failure (CRF), the possibility of using lovastatin to treat hypercholesterolemia associated with CRF was examined. Renal failure was induced in 5 week-old, C57BL/6J mice by electrocoagulation of the right kidney surface followed by left nephrectomy 2 weeks later. Five weeks post-nephrectomy, BUN and serum total cholesterol levels were assessed and lovastatin treatment commenced. Upon sacrifice 4 weeks later, BUN, serum total cholesterol levels and hepatic HMG-CoA reductase activity were measured. Results showed that CRF induced significant increases in serum total cholesterol levels and enzyme activity. Treatment with lovastatin led to a dose-dependent reduction in serum total cholesterol levels without affecting the enzyme activity. These results suggest that the hyper-cholesterolemia in CRF is partly due to an increase in de novo cholesterol synthesis in the liver and that the lipid-lowering effect of lovastatin is mediated by an action other than the direct reduction of hepatic HMG-CoA reductase activity.
利用慢性肾衰竭(CRF)小鼠模型,研究了使用洛伐他汀治疗与CRF相关的高胆固醇血症的可能性。通过电凝5周龄C57BL/6J小鼠右肾表面,2周后切除左肾来诱导肾衰竭。肾切除术后5周,评估血尿素氮(BUN)和血清总胆固醇水平,并开始洛伐他汀治疗。4周后处死小鼠,测量BUN、血清总胆固醇水平和肝脏HMG-CoA还原酶活性。结果显示,CRF导致血清总胆固醇水平和酶活性显著升高。洛伐他汀治疗导致血清总胆固醇水平呈剂量依赖性降低,而不影响酶活性。这些结果表明,CRF中的高胆固醇血症部分归因于肝脏中胆固醇从头合成增加,且洛伐他汀的降脂作用是通过直接降低肝脏HMG-CoA还原酶活性以外的作用介导的。