Related Experiment Videos
Keratinocyte growth factor transiently alters pulmonary function in rats
Jens M Hohlfeld1, Heinz G Hoymann, Thomas Tschernig
1Department of Respiratory Medicine, Hannover Medical School, D-30625 Hannover, Germany. hohlfeld.jens@mh-hannover.de
Journal of Applied Physiology (Bethesda, Md. : 1985)
|October 21, 2003
Summary
Keratinocyte growth factor (KGF) administration causes lung epithelial cell proliferation in rats. This leads to temporary changes in lung function, including restrictive and obstructive patterns.
Area of Science:
- Pulmonary Medicine
- Cell Biology
- Respiratory Physiology
Background:
- Keratinocyte growth factor (KGF) is a known mitogen for pulmonary epithelial cells.
- KGF administration stimulates alveolar epithelial type II and bronchiolar epithelial cell proliferation.
- The functional consequences of KGF-induced lung cell proliferation on lung function remain largely unknown.
Purpose of the Study:
- To investigate the impact of intratracheal KGF administration on pulmonary function in adult rats.
- To correlate histological changes with functional alterations in the lungs.
Main Methods:
- Adult rats received intratracheal recombinant human KGF (rHuKGF) or vehicle.
- Pulmonary function was assessed using body plethysmography before and after treatment (days 3 and 7).
- Lung histology was quantified to assess epithelial cell proliferation and hyperplasia.
Main Results:
- rHuKGF induced transient proliferation of alveolar and bronchiolar epithelial cells.
- Increased type II cell hyperplasia correlated with reduced tidal volume and increased breathing frequency.
- KGF treatment resulted in transitory restrictive lung disorder (decreased compliance, TLC, VC) and obstructive changes (reduced expiratory flow, increased FRC).
Conclusions:
- KGF-induced pulmonary epithelial cell proliferation is associated with moderate, transient changes in lung function.
- Both restrictive and obstructive lung function patterns were observed.
- These functional consequences should be considered when evaluating the therapeutic potential of KGF.