Skip to main content
. Author manuscript; available in PMC: 2012 Nov 15.
Published in final edited form as: Bioorg Med Chem Lett. 2011 Sep 20;21(22):6746–6750. doi: 10.1016/j.bmcl.2011.09.048

Figure 3. In Vivo Characterizations of 4-MDM in Murine Intra-nasal Elastase-induced Pulmonary Emphysema.

Figure 3

Mouse lungs were assessed 28 days after either intra-nasal (IN) elastase or vehicle exposure with either daily intra-peritoneal (IP) injection of 4-MDM or vehicle treatment in WT mice at the ages of 6-8 weeks. All mice were sacrificed at the ages of 10-12 weeks. P=IN phosphate buffered saline vehicle, E=IN elastase; V=IP peanut oil drug vehicle; D=IP 4-MDM; horizontal line is the mean of each group; vertical bars are +/- SEM; and * indicates p < 0.05.

(A) Pre mortem lung compliance measurement with a Scireq Flexivent. As emphysema worsens, compliance increases.

(B) Representative pictures of the gross mouse lungs after harvested en block, inflated at a uniform 25cm water pressure, and fixed in paraformaldehyde for 18 hours. These are a representative pictures of the lungs used for lung volume measurement.

(C) Post mortem lung size measurement by volume displacement technique after inflating the lungs with a uniform 25cm water pressure. As emphysema worsens, the sizes of the lungs increase.

(D) Representative H&E histology pictures of the mice lungs used for the chord length measurement. Large holes are emphysematous alveoli. These pictures were taken at 5× magnification.

(E) Post mortem computerized measurement of average alveolar sizes. As emphysema worsens, lung loses elasticity, and therefore, alveolar sizes increase when inflated with a uniform 25 cm water pressure.