Han Li-Na, Li Tie-Ling, Zhang Ya-Jing, Yang Ting-Shu, Ding Yu
The First Department of Cardiovascular Internal Medicine, Chinese PLA General Hospital, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2011 Nov;27(4):452-6.
To investigate the inhibitor of matrix metalloproteinase-2 (MMP-2) (2R)-2-[5-[4-[ ethyl-methylamino] phenyl [thiophene-2-sulfonylamino]-3-methylbutyric acid (TISAM) therapeutic effect on experimental autoimmune myocarditis (EAM) in Lewis rats.
Treatment protocol of oral administration of 5 mg/kg TISAM once a day for 14 days was performed on EAM Lewis rats. EAM Lewis rats were divided into 3 groups: treatment in early, middle and later stage respectively (n = 20). After experiment at the designate time point, the rats were euthanatized and hearts were harvested. Cardiac inflammatory score, fibrosis score and content, and infiltration of macrophages and T lyminflammatory score, fibrosis score and content, and infiltration of macrophages and T lymphocytes, message RNA (mRNA) expression of matrix metalloproteinase (MMP)-2 and MMP-9 and protein activity of gelatinase were determined.
TISAM treatment in early phase was invalid (treatment started from the creation of the model), treatment in middle and later phase was effective (treatment started from 7 and 14 day after the creation of the model).
Inhibitor of MMP-2 can block ventricular remodeling in middle stage in EAM Lewis rats. The mechanism maybe alleviate the inflammatory cell cardiac infiltration, decrease the mRNA expression of MMP-2 at transcript level and downregulate gelatinase activity at protein level.
研究基质金属蛋白酶-2(MMP-2)抑制剂(2R)-2-[5-[4-[乙基甲基氨基]苯基][噻吩-2-磺酰氨基]-3-甲基丁酸(TISAM)对Lewis大鼠实验性自身免疫性心肌炎(EAM)的治疗作用。
对EAM Lewis大鼠实施每日口服5 mg/kg TISAM、连续14天的治疗方案。将EAM Lewis大鼠分为3组:分别为早期、中期和后期治疗组(n = 20)。在指定时间点进行实验后,对大鼠实施安乐死并摘取心脏。测定心脏炎症评分、纤维化评分及含量,以及巨噬细胞和T淋巴细胞浸润情况,基质金属蛋白酶(MMP)-2和MMP-9的信使核糖核酸(mRNA)表达及明胶酶的蛋白活性。
早期治疗无效(从模型建立开始治疗),中期和后期治疗有效(从模型建立后第7天和第14天开始治疗)。
MMP-2抑制剂可阻断EAM Lewis大鼠中期的心室重塑。其机制可能是减轻炎症细胞的心脏浸润,在转录水平降低MMP-2的mRNA表达,并在蛋白水平下调明胶酶活性。