Gao Yuan, Song Ge, Cao Ying-Jie, Yan Kui-Po, Li Bin, Zhu Xin-Feng, Wang You-Ping, Xing Zuo-Ying, Cui Lin, Wang Xiao-Xiao, Zhu Ming-Jun
First Affiliated Hospital, Henan University of Traditional Chinese Medicine, Zhengzhou, China.
Henan Province Hospital of Traditional Chinese Medicine, Zhengzhou, China.
Evid Based Complement Alternat Med. 2019 Jan 21;2019:1947465. doi: 10.1155/2019/1947465. eCollection 2019.
Guizhi Gancao Decoction (GGD) is a well-known traditional Chinese herbal medicine for the treatment of various cardiovascular diseases, such as myocardial ischemia-reperfusion (I/R) injury and arrhythmia. However, the mechanism by which GGD contributes to the amelioration of cardiac injury remains unclear. The aim of this study was to investigate the potential protective role of GGD against myocardial I/R injury and its possible mechanism. Consistent with the effect of the positive drug (Trimetazidine, TMZ), we subsequently validated that GGD could ameliorate myocardial I/R injury as evidenced by histopathological examination and triphenyltetrazolium chloride (TTC) staining. Moreover, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay demonstrated that GGD suppressed myocardial apoptosis, which may be related to the upregulation of Bcl-2, PPAR, and PPAR and downregulation of Bax, caspase-3, and caspase-9. Pretreatment with GGD attenuated the levels of proinflammatory cytokines including tumor necrosis factor- (TNF-), interleukin- (IL-) 6, and IL-1 in serum by inhibiting Toll-like receptor 4 (TLR4)/NF-B signaling pathway. These results indicated that GGD exhibits cardioprotective effects on myocardial I/R injury through inhibition of the TLR4/NF-B signaling pathway, which led to reduced inflammatory response and the subsequent cardiomyocyte apoptosis.
桂枝甘草汤(GGD)是一种治疗多种心血管疾病的著名传统中药,如心肌缺血再灌注(I/R)损伤和心律失常。然而,GGD改善心脏损伤的机制仍不清楚。本研究的目的是探讨GGD对心肌I/R损伤的潜在保护作用及其可能机制。与阳性药物(曲美他嗪,TMZ)的作用一致,我们随后通过组织病理学检查和氯化三苯基四氮唑(TTC)染色验证了GGD可改善心肌I/R损伤。此外,末端脱氧核苷酸转移酶dUTP缺口末端标记(TUNEL)分析表明,GGD抑制心肌细胞凋亡,这可能与Bcl-2、PPAR和PPAR的上调以及Bax、caspase-3和caspase-9的下调有关。GGD预处理通过抑制Toll样受体4(TLR4)/核因子-κB(NF-κB)信号通路降低了血清中包括肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1(IL-1)在内的促炎细胞因子水平。这些结果表明,GGD通过抑制TLR4/NF-κB信号通路对心肌I/R损伤发挥心脏保护作用,从而减少炎症反应和随后的心肌细胞凋亡。