• 1. Department of Respiratory Medicine, Jiangmen Central Hospital, Jiangmen, Guangdong, 529030, China;
  • 2. ;
HuangYanming, Email: huangyanmings@126.com
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Objective To explore the effects of simvastatin on the expression of matrix metalloproteinase (MMP) and inflammatory factors in rats with smoke-induced chronic obstructive pulmonary disease (COPD). Methods 40 male Wistar rats were randomly divided into four groups, including a normal group (group A), a simvastatin group (group B), a COPD model group (group C) and a simvastatin intervention group (group D). The COPD model of the group C and D were induced through exposing to the cigarette smoke repeatedly. At the same time, the rats of group B and D were given by gavage 5 mg/(kg·d) with simvastatin, and the other two groups were given with the same volume saline for 16 weeks. Pulmonary function tests and pathological examination of the lung tissue were performed after the induction of COPD model. Enzyme-linked immunosorbent assay (ELISA) method was used to measure the content of MMP-2, MMP-9, IL-6, IL-8, TNF-α in lung tissue homogenate. Results The airway resistance of group C and group D was significantly higher than the group A and group B (P<0.01), and the airway resistance of group D was significantly lower than group C (P<0.01). The degree of bronchial inflammation and emphysema of group C was more apparent than group D in the pathological section, and there were no bronchial inflammation and emphysema in group A and group B. The ELISA results showed that the contents of MMP-2, MMP-9, IL-6, IL-8, TNF-α in group C were all significantly higher than those in group D. Conclusion Simvastatin has inhibitory effect on pulmonary inflammation of COPD, and can reduce the expression of matrix metalloproteinase and inflammatory factors in the lung.

Citation: XiongPing, HuangYanming, ZuoWanli, ZhangChunlai, ZhouWei. The Effects of Simvastatin on Expression of Matrix Metalloproteinase and Inflammatory Factors in COPD Rats. Chinese Journal of Respiratory and Critical Care Medicine, 2015, 14(6): 541-545. doi: 10.7507/1671-6205.2015133 Copy

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