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Published Online First: 20 February 2007. doi:10.1136/thx.2006.068353
Thorax 2007;62:706-713
Copyright © 2007 BMJ Publishing Group Ltd & British Thoracic Society

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CHRONIC OBSTRUCTIVE PULMONARY DISEASE

Effect of an MMP-9/MMP-12 inhibitor on smoke-induced emphysema and airway remodelling in guinea pigs

Andrew Churg1, Rona Wang1, Xiaoshan Wang1, Per-Ola Onnervik2, Kerstin Thim2, Joanne L Wright1

1 Department of Pathology, University of British Columbia, Vancouver, BC, Canada
2 AstraZeneca R&D, Lund, Sweden

Correspondence to:
Correspondence to:
Dr Andrew Churg
Department of Pathology, University of British Columbia, 2211 Wesbrook Mall, Vancouver, BC, Canada V6T 2B5; achurg{at}interchange.ubc.ca

Background: Matrix metalloproteases (MMPs) are believed to be important in the pathogenesis of cigarette smoke-induced emphysema, but this hypothesis has only been proved in the mouse and its applicability to other species, particularly humans, is uncertain. The role of MMPs in smoke-induced small airway remodelling is unknown.

Methods: The effects of a dual MMP-9/MMP-12 inhibitor, AZ11557272, on the development of anatomical and functional changes of chronic obstructive pulmonary disease (COPD) in guinea pigs exposed daily to cigarette smoke for up to 6 months were examined.

Results: At all times, smoke-induced increases in lavage inflammatory cells, lavage desmosine (a marker of elastin breakdown) and serum tumour necrosis factor {alpha} (TNF{alpha}) were completely abolished by AZ11557272. At 6 months there was an increase in lung volumes and airspace size. AZ11557272 returned the pressure- volume curve to control levels, decreased smoke-induced increases in total lung capacity, residual volume and vital capacity by about 70%, and also reversed smoke-induced airspace enlargement by about 70%. There was a very strong correlation between surface to volume ratio and both lavage desmosine and serum TNF{alpha} levels. AZ11557272 protected against smoke-mediated increases in small airway wall thickness but did not prevent smoke-induced increases in mean pulmonary artery pressure.

Conclusions: An MMP-9/MMP-12 inhibitor can substantially ameliorate morphological emphysema, small airway remodelling and the functional consequences of these lesions in a non-murine species. These findings strengthen the idea that MMPs are important mediators of the anatomical changes behind COPD in humans, and suggest that MMP-9 and MMP-12 may be potential intervention targets.


Abbreviations: COPD, chronic obstructive pulmonary disease; Lm, mean airspace size; MMP, matrix metalloprotease; Sv, surface to volume ratio; TGFß, transforming growth factor ß; TNF{alpha}, tumour necrosis factor {alpha}


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