Arikan Meltem C, Shapiro Steven D, Mariani Thomas J
Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
J Cell Physiol. 2005 Jul;204(1):139-45. doi: 10.1002/jcp.20271.
The statins (including mevastatin and lovastatin) are a widely prescribed class of serum-cholesterol lowering drugs that function by inhibiting 3-hydroxymethylglutaryl coenzyme A (HMG CoA) reductase activity and cellular sterol synthesis. Statins are also widely being appreciated for their inhibitory effects upon inflammation, primarily mediated through direct regulation of inflammatory gene expression. Here we report that statins are also capable of increasing the expression of macrophage elastase (MMP-12). The induction of MMP-12 in mouse macrophages by statins is specific for HMG CoA reductase inhibition, rescued by mevalonate and not observed after inhibition of subsequent steps in the cholesterol biosynthetic pathway. Modulation of cholesterol metabolism may lead to changes in MMP-12 expression and subsequent impacts during physiological and pathophysiological states. We conclude that statins, in addition to their previously described anti-inflammatory properties, may promote the production of some proteinases from activated macrophages.
他汀类药物(包括美伐他汀和洛伐他汀)是一类广泛应用的降血脂药物,其作用机制是抑制3-羟基-3-甲基戊二酰辅酶A(HMG CoA)还原酶活性及细胞甾醇合成。他汀类药物还因其对炎症的抑制作用而受到广泛关注,这种抑制作用主要通过直接调节炎症基因表达来介导。在此我们报告,他汀类药物还能够增加巨噬细胞弹性蛋白酶(MMP-12)的表达。他汀类药物在小鼠巨噬细胞中诱导MMP-12的表达是HMG CoA还原酶抑制特异性的,可被甲羟戊酸挽救,且在胆固醇生物合成途径后续步骤被抑制后未观察到这种诱导现象。胆固醇代谢的调节可能导致MMP-12表达的变化以及在生理和病理生理状态下的后续影响。我们得出结论,他汀类药物除了具有先前描述的抗炎特性外,还可能促进活化巨噬细胞产生某些蛋白酶。