Dipartimento di Scienze dell'Uomo e dell'Ambiente, Unità di Biochimica Medica, University of Pisa, Pisa, Italy.
Mol Cell Biochem. 2011 Jun;352(1-2):301-7. doi: 10.1007/s11010-011-0766-9. Epub 2011 Mar 11.
We investigated whether acute and chronic administration of zofenopril, an angiotensin converting enzyme inhibitor, may modulate the expression of genes which are involved in the pathophysiology of myocardial ischemia and heart failure. We used an acute and a chronic model. In the former isolated rat hearts were perfused for 120 min in the presence or in the absence of 10 μM zofenoprilat, the active metabolite of zofenopril. In the chronic model one group of rats was treated with zofenopril (15.2 mg/Kg die per os) for 15 days, while control rats were treated with the same diet, except that zofenopril was omitted. Total RNA was extracted from hearts, and quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used to evaluate the expression of α myosin heavy chain, superoxide dismutase, heat shock protein 70 (HSP70), nitric oxide synthase 2 and 3 (NOS2, NOS3), heme oxygenase 1, atrial natriuretic peptide (ANP), muscle phosphofructokinase. Acute or chronic zofenopril administration did not produce any change in hemodynamic variables. qRT-PCR experiments showed that in the acute model ANP expression was slightly although not significantly increased. In the chronic model, significant changes in gene expression were detected: in particular, HSP70 was upregulated (1.06 ± 0.38 vs. 0.72 ± 0.20 arbitrary units, P = 0.025), while NOS3 was downregulated (0.66 ± 0.06 vs. 0.83 ± 0.18 arbitrary units, P = 0.007). In the chronic model, liver samples were also assayed, but no significant change in the expression of any gene was detected. We conclude that zofenopril can produce heart-specific effects on gene expression. Persistent changes were detected with regard to specific heat shock protein and nitric oxide synthase subtypes. This action might contribute to the therapeutical response, and particularly to the increased resistance to ischemia.
我们研究了血管紧张素转换酶抑制剂佐芬普利的急性和慢性给药是否可以调节参与心肌缺血和心力衰竭病理生理学的基因表达。我们使用了急性和慢性模型。在前者中,分离的大鼠心脏在存在或不存在 10μM 佐芬普利拉(佐芬普利的活性代谢物)的情况下进行 120 分钟的灌注。在慢性模型中,一组大鼠用佐芬普利(15.2mg/Kg 每天口服)治疗 15 天,而对照大鼠则用相同的饮食治疗,只是省略了佐芬普利。从心脏中提取总 RNA,并使用定量逆转录聚合酶链反应(qRT-PCR)评估α肌球蛋白重链、超氧化物歧化酶、热休克蛋白 70(HSP70)、一氧化氮合酶 2 和 3(NOS2、NOS3)、血红素加氧酶 1、心房利钠肽(ANP)、肌肉磷酸果糖激酶的表达。急性或慢性佐芬普利给药不会引起血流动力学变量的任何变化。qRT-PCR 实验表明,在急性模型中,ANP 的表达略有增加,但无统计学意义。在慢性模型中,检测到基因表达的显著变化:特别是,HSP70 上调(1.06 ± 0.38 对 0.72 ± 0.20 任意单位,P = 0.025),而 NOS3 下调(0.66 ± 0.06 对 0.83 ± 0.18 任意单位,P = 0.007)。在慢性模型中,还对肝组织样本进行了检测,但未检测到任何基因表达的显著变化。我们得出结论,佐芬普利可以对基因表达产生心脏特异性作用。检测到特定热休克蛋白和一氧化氮合酶亚型的持续变化。这种作用可能有助于治疗反应,特别是增加对缺血的耐受性。