Bandoh T, Mitani H, Niihashi M, Kusumi Y, Ishikawa J, Kimura M, Totsuka T, Sakurai I, Hayashi S
Department of Pharmacology, Sandoz Tsukuba Research Institute, Ibaraki, Japan.
Eur J Pharmacol. 1996 Nov 7;315(1):37-42. doi: 10.1016/s0014-2999(96)00573-0.
The anti-atherosclerotic effect of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors at doses insufficient to lower serum cholesterol was investigated in rabbit femoral artery denuded by balloon catheter. Fluvastatin and pravastatin were given orally at doses of 4 and 8 mg/kg per day, respectively, for 2 weeks after the catheterization. There was little change in serum cholesterol, triglyceride and phospholipid by chronic treatment with the drugs. The cross-sectional area of the intima, expressed as relative values to media (I/M ratio), was increased by the catheterization, showing intimal thickening in the denuded arteries. The I/M ratio was reduced by fluvastatin but not pravastatin: 0.327 +/- 0.060 for control, 0.116 +/- 0.035 for 4 mg/kg fluvastatin, 0.088 +/- 0.027 for 8 mg/kg fluvastatin and 0.22 +/- 0.069 for 8 mg/kg pravastatin. Fluvastatin (8 mg/kg)-induced effect on the I/M ratio, was prevented by the combined administration with 40 mg/kg per day mevalonate, a metabolite in the HMG-CoA reductase pathway. These results suggest that fluvastatin inhibits intimal thickening after catheterization-induced injury through percutaneous transluminal coronary angioplasty (PTCA) and that the inhibition is presumably attributed to reduced migration and proliferation of smooth muscle cells but not secondarily to a lowering of serum lipid.
在球囊导管剥脱的兔股动脉中,研究了剂量不足以降低血清胆固醇的3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂的抗动脉粥样硬化作用。导管插入术后,分别以每天4毫克/千克和8毫克/千克的剂量口服氟伐他汀和普伐他汀,持续2周。长期用药后,血清胆固醇、甘油三酯和磷脂几乎没有变化。内膜的横截面积以相对于中膜的相对值(I/M比值)表示,导管插入术后增加,显示剥脱动脉内膜增厚。氟伐他汀可降低I/M比值,而普伐他汀则不能:对照组为0.327±0.060,4毫克/千克氟伐他汀组为0.116±0.035,8毫克/千克氟伐他汀组为0.088±0.027,8毫克/千克普伐他汀组为0.22±0.069。每天联合给予40毫克/千克甲羟戊酸(HMG-CoA还原酶途径中的一种代谢产物)可阻止氟伐他汀(8毫克/千克)对I/M比值的影响。这些结果表明,氟伐他汀可抑制经皮腔内冠状动脉成形术(PTCA)导管插入术后损伤引起的内膜增厚,这种抑制作用可能归因于平滑肌细胞迁移和增殖的减少,而不是继发于血清脂质的降低。