Goldspink P H, McKinney R D, Kimball V A, Geenen D L, Buttrick P M
Department of Medicine, University of Illinois at Chicago, 60612, USA.
Mol Cell Biochem. 2001 Oct;226(1-2):83-8. doi: 10.1023/a:1012789819926.
Recently, the calcium-calmodulin-dependent calcineurin pathway has been defined as a central pathway for the induction of cardiac hypertrophy. The purpose of this study was to determine if cardiac hypertrophy in animals chronically treated with angiotensin II (AngII), could be prevented by blocking this pathway with cyclosporin A (CsA). Female Wistar rats were treated with AngII by subcutaneous infusion and injected twice a day with CsA (25 mg/kg) for 7 days. In the AngII treated group there was a 30% increase in the heart/body weight ratio (p < 0.05 vs. control). The increase in heart weight was blocked with CsA. Substantial increases in ANF and betaMHC gene expression were detected in the AngII treated animals, which were either attenuated or blocked with CsA treatment. Thus, this study demonstrates that CsA does prevent the development of cardiac hypertrophy in AngII treated rats, suggesting that the calcium-calmodulin-dependent calcineurin pathway is associated with angiotensin II induced hypertrophy in vivo.
最近,钙调神经磷酸酶(其活性依赖于钙调蛋白)信号通路已被确定为诱导心肌肥大的核心通路。本研究旨在确定,用环孢素A(CsA)阻断该信号通路是否能够预防长期接受血管紧张素II(AngII)治疗的动物发生心肌肥大。通过皮下输注对雌性Wistar大鼠进行AngII治疗,并每天两次注射CsA(25 mg/kg),持续7天。在AngII治疗组中,心脏/体重比增加了30%(与对照组相比,p < 0.05)。CsA能够阻止心脏重量增加。在接受AngII治疗的动物中,心房钠尿肽(ANF)和β-肌球蛋白重链(βMHC)基因表达显著增加,而CsA治疗可使其减弱或受到抑制。因此,本研究表明,CsA确实能够预防接受AngII治疗的大鼠发生心肌肥大,这表明钙调神经磷酸酶信号通路与体内血管紧张素II诱导的肥大有关。