Lin Shan, Chu Jianfeng, Zhang Ling, Chen Daxin, Xiao Fei, Chen Hongwei, Lin Jiumao, Chen Youqin, Zhu Yuling, Peng Jun
Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian 350122, P.R. China.
Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Mol Med Rep. 2017 Sep;16(3):3125-3132. doi: 10.3892/mmr.2017.6963. Epub 2017 Jul 13.
Shexiang Tongxin Dropping Pill (STP) is an established traditional Chinese medicine that is widely used for the treatment of ischemic heart disease (IHD), although its mechanisms remain unclear. The present study investigated the protective effects of STP following pituitrin (PTT)‑induced myocardial ischemia in rats. ST‑segment elevation, blood rheology, and the serum levels of creatine kinase‑MB (CK‑MB) and lactate dehydrogenase (LDH) were measured. Following heart excision, histological analysis using hematoxylin and eosin and terminal deoxynucleotidyl transferase dUTP nick end labeling were performed. The mRNA expression levels of B‑cell lymphoma 2 (Bcl‑2) and Bcl‑2‑associated X protein (Bax) were determined using reverse transcription‑quantitative polymerase chain reaction, and their protein expression was detected using immunohistochemistry. The results demonstrated that STP treatment protected against ST elevation, lowered whole blood viscosity, and reduced the serum levels of CK‑MB and LDH following acute myocardial ischemia. In addition, STP treatment restored the histopathological change following PTT‑induced myocardial ischemia, and resulted in downregulated expression of Bax and upregulated expression of Bcl‑2 in myocardial tissue. The present study demonstrates the cardioprotective ability of STP in a rat model of myocardial ischemic injury, which may be attributed to its anti‑apoptotic properties. The cardioprotective properties of STP require further investigation to determine whether it may be used for the clinical treatment of IHDs.
麝香通心滴丸(STP)是一种已被认可的传统中药,广泛用于治疗缺血性心脏病(IHD),但其作用机制尚不清楚。本研究探讨了STP对垂体后叶素(PTT)诱导的大鼠心肌缺血的保护作用。测量了ST段抬高、血液流变学以及肌酸激酶同工酶MB(CK-MB)和乳酸脱氢酶(LDH)的血清水平。心脏切除后,进行苏木精-伊红染色和末端脱氧核苷酸转移酶介导的dUTP缺口末端标记的组织学分析。使用逆转录-定量聚合酶链反应测定B细胞淋巴瘤2(Bcl-2)和Bcl-2相关X蛋白(Bax)的mRNA表达水平,并使用免疫组织化学检测其蛋白表达。结果表明,STP治疗可预防急性心肌缺血后的ST段抬高,降低全血粘度,并降低CK-MB和LDH的血清水平。此外,STP治疗可恢复PTT诱导的心肌缺血后的组织病理学变化,并导致心肌组织中Bax表达下调和Bcl-2表达上调。本研究证明了STP在大鼠心肌缺血损伤模型中的心脏保护能力,这可能归因于其抗凋亡特性。STP的心脏保护特性需要进一步研究,以确定其是否可用于IHD的临床治疗。