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中药舒脉汤对减轻心肌缺血大鼠肿瘤坏死因子α诱导的心肌纤维化的作用。

Effect of traditional Chinese medicine Shu-Mai-Tang on attenuating TNFalpha-induced myocardial fibrosis in myocardial ischemia rats.

作者信息

Yin Hui-Qiu, Wang Bo, Zhang Ji-Dong, Lin Hai-Qing, Qiao Yun, Wang Rong, Liu Fen-Ye

机构信息

Department of Traditional Chinese Medicine, Qilu Hospital Affiliated to Shandong University, Jinan, Shandong, PR China.

出版信息

J Ethnopharmacol. 2008 Jun 19;118(1):133-9. doi: 10.1016/j.jep.2008.03.022. Epub 2008 Apr 10.

Abstract

Shu-Mai-Tang (SMT) is a traditional Chinese medicine for treatment of ischemic heart disease. The effect of SMT on inflammation-induced myocardial fibrosis, left ventricular (LV) remodeling, and the potential mechanism in myocardial ischemia (MI) rats were investigated. Rats with ligated left anterior descending coronary artery (MI model) were randomly divided into three groups (SMTL, SMTH, and MIR). A group undergoing Sham operation (Sham; n=16) was also included. SMT (342 or 1710 mg/kg for SMTL or SMTH groups, respectively) was orally administered daily for 1 and 6 weeks. Cardiac function, myocardial fibrosis, serum tumor necrosis factor-alpha (TNFalpha) concentration, the cardiac expressions of phosphorylated p38 MAPK and tissue inhibitor of matrix metalloproteinase (TIMP)-1 and TNFalpha were examined by echocardiography, histological staining, radioimmunoassay, western blot, respectively. In the present study, significant reduced myocardial fibrosis, as well as decreased phospho-p38 MAPK, TIMP-1, and TNFalpha proteins, and serum TNFalpha level, accompanied by improved cardiac function in the SMT-treated rats in a dose-dependent manner as compared with the MIR. These results suggested that SMT could anti-inflammation-induced myocardial fibrosis and reverse LV remodeling in MI rats, and the mechanism may be related to the effect of SMT on inhibiting p38 MAPK signaling pathway.

摘要

舒脉汤(SMT)是一种用于治疗缺血性心脏病的中药。本研究探讨了舒脉汤对炎症诱导的心肌纤维化、左心室(LV)重构的影响以及在心肌缺血(MI)大鼠中的潜在机制。将结扎左冠状动脉前降支的大鼠(MI模型)随机分为三组(SMTL、SMTH和MIR)。还纳入一组接受假手术的大鼠(假手术组;n = 16)。分别以342或1710 mg/kg的剂量给SMTL组和SMTH组大鼠每日口服舒脉汤,持续1周和6周。分别通过超声心动图、组织学染色、放射免疫分析、蛋白质印迹法检测心功能、心肌纤维化、血清肿瘤坏死因子-α(TNFα)浓度、磷酸化p38丝裂原活化蛋白激酶(MAPK)、基质金属蛋白酶组织抑制剂(TIMP)-1的心脏表达以及TNFα。在本研究中,与MIR组相比,舒脉汤治疗的大鼠心肌纤维化显著减轻,磷酸化p38 MAPK、TIMP-1和TNFα蛋白以及血清TNFα水平降低,且心功能改善呈剂量依赖性。这些结果表明,舒脉汤可抗炎症诱导的心肌纤维化并逆转MI大鼠的左心室重构,其机制可能与舒脉汤抑制p38 MAPK信号通路的作用有关。

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