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      Cigarette smoke-induced hypercapnic emphysema in C3H mice is associated with increases of macrophage metalloelastase and substance P in the lungs.

      Experimental Lung Research
      Animals, Anoxia, etiology, Bronchoalveolar Lavage Fluid, cytology, Carbon Dioxide, blood, Female, Gene Expression Regulation, Hypercapnia, Lung, metabolism, pathology, Macrophages, Alveolar, Matrix Metalloproteinase 12, genetics, Mice, Mice, Inbred C3H, Oxygen, Pulmonary Disease, Chronic Obstructive, Pulmonary Emphysema, RNA, Messenger, Receptors, Neurokinin-1, Substance P, Tissue Inhibitor of Metalloproteinase-1, Tobacco Smoke Pollution, adverse effects

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          Abstract

          The authors tested whether macrophage metalloelastase (MMP-12) and substance P (SP) were increased in the cigarette smoke (CS)-exposed female C3H/HeN mice with hypercapnic emphysema. The authors found that as compared to control (filtered air), 16 weeks of CS exposure significantly up-regulated mRNA and protein levels of MMP-12, the ratio of MMP-12/tissue inhibitor of matrix metalloproteinase-1, and SP/preprotachykinin-A (a precursor to SP) in the lungs. Importantly, a significant correlation was found between MMP-12 and SP, and between MMP-12/SP and the degrees of hypoxemia/hypercapnia denoted in CS-exposed mice. These data suggest a possible involvement of SP and MMP-12 in the pathogenesis of severe COPD.

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