Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Health, Shandong University Qilu Hospital, Shandong Province, China.
J Cell Mol Med. 2009 Nov-Dec;13(11-12):4444-52. doi: 10.1111/j.1582-4934.2008.00484.x.
Although peroxisome proliferator-activated receptor alpha (PPARalpha) is highly expressed in the heart, the effects of PPARalpha on cardiac remodelling and the underlying mechanisms are unclear. The present study was undertaken to test the hypothesis that PPARalpha activator fenofibrate plays a key role in left ventricular hypertrophic remodelling via the formation of c-fos/c-jun heterodimers in spontaneous hypertensive rats (SHRs). Twenty-four male 8-week-old SHRs were randomly divided into two groups, one group treated with oral saline (n= 10) and another treated with oral fenofibrate (60 mg.kg-1.d-1, n= 14). Ten same-aged Wistar-Kyoto (WKY) rats were selected as a normal control group. Using echocardiography, immunohistochemistry, co-immunoprecipitation, Western blot analysis and real-time RT-PCR, we showed that the left ventricular wall thickness and significantly reduced and left ventricular diastolic function improved in SHRs treated with fenofibrate compared with SHRs treated with saline. Similarly, the excessive collagen deposition and the up-regulation of collagen I, collagen III, c-fos and c-jun seen in SHRs receiving saline were significantly attenuated in SHRs receiving fenofibrate. In addition, fenofibrate markedly decreased the expression of AP-1 and c-fos/c-jun heterodimers (P < 0.01). These results demonstrated that PPARalpha activator fenofibrate may exert a protective effect on cardiac remodelling in SHRs by decreasing the expression of c-fos and c-jun and suppressing the formation of c-fos/c-jun heterodimers, which may further inhibit transcription of the downstream genes involved in the pathogenesis of left ventricular hypertrophy induced by hypertension.
虽然过氧化物酶体增殖物激活受体α(PPARα)在心脏中高度表达,但 PPARα 对心脏重塑的影响及其潜在机制尚不清楚。本研究旨在验证以下假设:PPARα 激活剂非诺贝特通过在自发性高血压大鼠(SHR)中形成 c-fos/c-jun 异二聚体,在左心室肥厚重塑中发挥关键作用。24 只 8 周龄雄性 SHR 被随机分为两组,一组给予口服生理盐水(n=10),另一组给予口服非诺贝特(60mg·kg-1·d-1,n=14)。选择 10 只同龄 Wistar-Kyoto(WKY)大鼠作为正常对照组。通过超声心动图、免疫组化、共免疫沉淀、Western blot 分析和实时 RT-PCR,我们发现与生理盐水处理的 SHR 相比,非诺贝特处理的 SHR 左心室壁厚度明显降低,左心室舒张功能改善。同样,在接受生理盐水的 SHR 中观察到的过度胶原沉积和胶原 I、胶原 III、c-fos 和 c-jun 的上调在接受非诺贝特的 SHR 中明显减弱。此外,非诺贝特显著降低了 AP-1 和 c-fos/c-jun 异二聚体的表达(P<0.01)。这些结果表明,PPARα 激活剂非诺贝特可能通过降低 c-fos 和 c-jun 的表达并抑制 c-fos/c-jun 异二聚体的形成,从而对 SHR 的心脏重塑发挥保护作用,进一步抑制高血压诱导的左心室肥厚相关下游基因的转录。