Bonetti Piero O, Wilson Stephanie H, Rodriguez-Porcel Martin, Holmes David R, Lerman Lilach O, Lerman Amir
Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
J Am Coll Cardiol. 2002 Aug 7;40(3):546-54. doi: 10.1016/s0735-1097(02)01985-x.
OBJECTIVES; This study was designed to assess the lipid-independent effects of simvastatin on myocardial perfusion (MP) and coronary microvascular permeability index (PI) at baseline and during episodes of increased cardiac demand in experimental hypercholesterolemia.
Simvastatin preserves coronary endothelial function in experimental hypercholesterolemia independent of its lipid-lowering effect. However, the functional significance of this observation is unknown.
Pigs were randomized to three groups: normal diet (N), high-cholesterol diet (HC) and HC diet plus simvastatin (HC+S) for 12 weeks. Subsequently, cardiac electron beam computed tomography was performed before and during intravenous infusion of adenosine and dobutamine, and MP and PI were calculated.
Total and low density lipoprotein cholesterol levels were similarly and significantly increased in HC and HC+S animals compared with N. Basal MP was similar in all groups. Myocardial perfusion significantly increased in response to either adenosine or dobutamine in N and HC+S animals. Dobutamine also significantly increased MP in HC animals. However, the changes of MP in response to either drug were significantly lower in the HC group compared with the other two groups (p < 0.01 for adenosine and p < 0.05 for dobutamine vs. N and HC+S). Basal PI was similar in all groups and was not altered by either drug in N and HC+S animals. In contrast, PI significantly increased in HC pigs during infusion of either adenosine (p < 0.001) or dobutamine (p < 0.05).
These findings demonstrate that chronic administration of simvastatin preserves myocardial perfusion response and coronary microvascular integrity during cardiac stress in experimental hypercholesterolemia independent of lipid lowering.
目的;本研究旨在评估辛伐他汀在实验性高胆固醇血症基线期及心脏需求增加发作期间对心肌灌注(MP)和冠状动脉微血管通透性指数(PI)的非脂质依赖性作用。
辛伐他汀在实验性高胆固醇血症中可保留冠状动脉内皮功能,与其降脂作用无关。然而,这一观察结果的功能意义尚不清楚。
将猪随机分为三组:正常饮食(N)组、高胆固醇饮食(HC)组和高胆固醇饮食加辛伐他汀(HC+S)组,为期12周。随后,在静脉输注腺苷和多巴酚丁胺之前及期间进行心脏电子束计算机断层扫描,并计算MP和PI。
与N组相比,HC组和HC+S组动物的总胆固醇和低密度脂蛋白胆固醇水平同样显著升高。所有组的基础MP相似。N组和HC+S组动物对腺苷或多巴酚丁胺的反应使心肌灌注显著增加。多巴酚丁胺也使HC组动物的MP显著增加。然而,与其他两组相比,HC组对任何一种药物的MP变化均显著降低(腺苷与N组和HC+S组相比,p<0.01;多巴酚丁胺与N组和HC+S组相比,p<0.05)。所有组的基础PI相似,N组和HC+S组动物的PI均未因任何一种药物而改变。相反,在HC猪中,输注腺苷(p<0.001)或多巴酚丁胺(p<0.05)期间PI显著增加。
这些发现表明,在实验性高胆固醇血症中,长期给予辛伐他汀可在心脏应激期间保留心肌灌注反应和冠状动脉微血管完整性,且与降脂无关。