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Traditional Chinese Medication Qiliqiangxin Protects Against Cardiac Remodeling and Dysfunction in Spontaneously Hypertensive Rats

机译:中药七里强新对自发性高血压大鼠心脏重塑和功能障碍的保护作用

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摘要

Qiliqiangxin (QLQX), a traditional Chinese herbs medication, exerted protective effect in chronic heart failure patients in a multicenter randomized double-blind study. QLQX has also been found to improve cardiac function and reduce cardiac fibrosis in spontaneously hypertension animal model. However, the effect of longterm treatment with QLQX in such a condition and the related molecular mechanisms remain largely unknown. In the present study, thirteen-week-old spontaneously hypertensive rats (SHRs) were treated by daily intragastric administration of QLQX or saline for one year. Echocardiography, electron microscopy, and Masson's trichrome staining were used to determine cardiac function, mitochondria ultrastructure, and cardiac fibrosis, respectively. Quantitative reverse transcription polymerase chain reactions (qRT-PCRs) and Western blotting were used to determine gene expressions. We found that QLQX significantly improved cardiac function and reduced gene markers of pathological hypertrophy including ANP, BNP, and Myh7. QLQX also attenuated cardiac fibrosis and apoptosis in SHRs as evidenced by downregulation of α-SMA, collagen I, collagen III, and TGF-β expressions and reduction of Bax to Bcl-2 ratio. Moreover, the damage of mitochondrial ultrastructure was greatly improved and the reduction of PPAR-α, PPAR-γ, and PGC-1α expression levels was significantly restored in SHRs by treatment with QLQX. In conclusion, longterm treatment with QLQX protects against cardiac remodeling and dysfunction in hypertension by increasing PPARs and PGC-1α.
机译:在一项多中心随机双盲研究中,中药七里强新(QLQX)对慢性心力衰竭患者具有保护作用。在自发性高血压动物模型中,还发现QLQX可改善心脏功能并减少心脏纤维化。然而,在这种情况下用QLQX进行长期治疗的效果以及相关的分子机制仍然未知。在本研究中,每天通过胃内给予QLQX或生理盐水治疗13周大的自发性高血压大鼠(SHR)一年。超声心动图,电子显微镜和Masson三色染色分别用于测定心脏功能,线粒体超微结构和心脏纤维化。定量逆转录聚合酶链反应(qRT-PCR)和蛋白质印迹法用于确定基因表达。我们发现QLQX可以显着改善心脏功能并减少包括ANP,BNP和Myh7在内的病理性肥大的基因标记。 QLQX还可以减轻SHRs的心脏纤维化和凋亡,这可以通过下调α-SMA,I型胶原,III型胶原和TGF-β的表达以及降低Bax与Bcl-2的比例来证明。此外,通过QLQX处理,SHRs中线粒体超微结构的损伤得到了极大的改善,PPAR-α,PPAR-γ和PGC-1α表达水平的降低得以显着恢复。总之,长期服用QLQX可以通过增加PPAR和PGC-1α来预防高血压的心脏重塑和功能障碍。

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