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Fuzi and Banxia Combination Eighteen Antagonisms in Chinese Medicine Aggravates Adriamycin-Induced Cardiomyopathy Associated with PKA/β2AR-Gs Signaling

机译:夫子与半夏联用中药十八种拮抗作用加重阿霉素诱导的心肌病与PKA /β2AR-Gs信号传导的关系

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摘要

Aconite Lateralis Radix Praeparata (Fuzi) and Pinelliae Rhizoma (Banxia) are a combination often used to treat cardiovascular diseases in ancient and modern clinical practice. However, eighteen antagonisms based on traditional Chinese medicine (TCM) theory often abided against such combination therapy. Therefore, exploring whether coadministration of the two herbs can be used in adriamycin- (ADR-) induced cardiomyopathy and clarifying the potential mechanism could help to guide its clinical application. Echocardiography experiments revealed that either Fuzi, Banxia, or their combination had effect on ADR-induced heart dysfunction, while high dose Fuzi exerted positive inotropic effect associated with restored PKA levels. Moreover, low dose Fuzi significantly reduced QT/QTc prolongation, inhibited cardiac apoptosis, and upregulated protein expression of PKA. However, combination of Fuzi and Banxia greatly aggravated QT/QTc prolongation and cardiomyocyte apoptosis in ADR rats compared with each drug alone, which was accompanied by a marked decrease in PKA, pSer346 levels. Similarly, Banxia alone treatment promoted cardiac apoptosis and downregulated protein levels of PKA and pSer346. Additionally, high dose Fuzi treatment also produced proapoptotic effect. Taken together, our study has provided the first direct evidence that combination of Fuzi, a positive inotropic agent, with Banxia promoted cardiac apoptosis in an ADR induced rat model of cardiomyopathy, which may be associated with suppression of PKA/β2AR-Gs signaling. This study also provides scientific language for better understanding of the risks and limitations of combination of Fuzi and Banxia in clinical applications.
机译:黑附子(附子)和半夏(半夏)是在古代和现代临床实践中经常用于治疗心血管疾病的组合。然而,基于中医理论的十八种拮抗作用经常反对这种联合疗法。因此,探索两种药物的共同给药是否可用于阿霉素-(ADR-)诱发的心肌病,并阐明其潜在机制可有助于指导其临床应用。超声心动图实验显示,富滋,半夏或其组合对ADR引起的心脏功能障碍均具有影响,而高剂量富滋则具有与恢复的PKA水平相关的正性肌力作用。此外,低剂量富滋显着降低QT / QTc延长,抑制心脏凋亡和上调PKA蛋白表达。然而,与单独使用每种药物相比,伏子和半夏的组合大大加重了ADR大鼠的QT / QTc延长和心肌细胞凋亡,并伴有PKA,pSer346水平的显着降低。同样,半夏单独治疗可促进心脏凋亡并下调PKA和pSer346的蛋白质水平。另外,高剂量的富滋治疗也产生了促凋亡作用。综上所述,我们的研究提供了第一个直接证据,即正性肌力药Fuzi与半夏的组合可在ADR诱发的心肌病大鼠模型中促进心脏凋亡,这可能与抑制PKA /β2AR-Gs信号传导有关。这项研究还提供了科学的语言,可以更好地了解伏子和半夏组合在临床应用中的风险和局限性。

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