Lo Shih-Hsiang, Hsu Chao-Tien, Niu Ho-Shan, Niu Chiang-Shan, Cheng Juei-Tang, Chen Zhih-Cherng
Division of Cardiology, Department of Internal Medicine, Zhongxing Branch of Taipei City Hospital, Taipei 10341, Taiwan.
Department of Nursing, Tzu Chi University of Science and Technology, Hualien 97041, Taiwan.
Int J Mol Sci. 2017 Jun 26;18(7):1364. doi: 10.3390/ijms18071364.
Ginsenoside Rh2 (Rh2) is an active principal ingredient contained in ginseng ( Meyer), a medicinal herb used to enhance health worldwide. The present study is designed to investigate the effect of Rh2 on myocardial fibrosis in diabetic rats. In a streptozotocin-induced model of type-1 diabetic rats (STZ-diabetic rats), the increased fasting blood glucose levels and heart weight/body weight (HW/BW) ratio were substantially alleviated by Rh2. Moreover, Rh2 improved cardiac performance in STZ-diabetic rats. Histological results from Masson staining showed that Rh2 attenuated cardiac fibrosis in STZ-diabetic rats. The effects of Rh2 were reversed by GSK0660 at a dose sufficient to inhibit peroxisome proliferator-activated receptor δ (PPARδ) in STZ-diabetic rats. The role of PPARδ was subsequently investigated in vitro. Rh2 restored the decreased PPARδ expression level in high glucose-cultured cardiomyocytes. Moreover, increased protein levels of fibrotic signals, including signal transducer and activator of transcription 3 (STAT3), connective tissue growth factor (CCN2) and fibronectin, were reduced by Rh2 in high glucose-cultured cardiomyocytes. These effects of Rh2 were reversed by GSK0660 or siRNA specific for PPARδ Taken together, PPARδ activation may inhibit STAT3 activation to reduce CCN2 and fibronectin expression in diabetic rats with cardiac fibrosis. Moreover, Rh2 improves cardiac function and fibrosis by increasing PPARδ signaling. Therefore, Rh2 is suitable to develop as an alternative remedy for cardiac fibrosis.
人参皂苷Rh2(Rh2)是人参(迈耶)中含有的一种活性主要成分,人参是一种在全球范围内用于增进健康的草药。本研究旨在探讨Rh2对糖尿病大鼠心肌纤维化的影响。在链脲佐菌素诱导的1型糖尿病大鼠模型(STZ糖尿病大鼠)中,Rh2显著减轻了空腹血糖水平的升高以及心脏重量/体重(HW/BW)比值。此外,Rh2改善了STZ糖尿病大鼠的心脏功能。Masson染色的组织学结果显示,Rh2减轻了STZ糖尿病大鼠的心脏纤维化。在STZ糖尿病大鼠中,GSK0660以足以抑制过氧化物酶体增殖物激活受体δ(PPARδ)的剂量逆转了Rh2的作用。随后在体外研究了PPARδ的作用。Rh2恢复了高糖培养心肌细胞中降低的PPARδ表达水平。此外,Rh2降低了高糖培养心肌细胞中包括信号转导和转录激活因子3(STAT3)、结缔组织生长因子(CCN2)和纤连蛋白在内的纤维化信号蛋白水平的升高。GSK0660或PPARδ特异性siRNA逆转了Rh2的这些作用。综上所述,PPARδ激活可能抑制STAT3激活,以降低糖尿病性心肌纤维化大鼠中CCN2和纤连蛋白的表达。此外,Rh2通过增加PPARδ信号改善心脏功能和纤维化。因此,Rh2适合开发成为治疗心脏纤维化的替代药物。