Objectives: To survey normal murine sinonasal anatomy and to create a mouse
model for chronic bacterial rhinosinusitis.
Design: Anatomic, histologic, and pathophysiologic study displaying normal
murine sinonasal anatomy and surgically created unilateral sinonasal inflam
mation.
Subjects: Twenty-one 6-week-old, male C57BL/6 mice.
Interventions: Animals that underwent unilateral maxillary sinus ostial obs
truction using Merocel nasal packing, animals with unilateral Bacteroides f
ragilis inoculation alone, and animals with both ostial obstruction and bac
terial inoculation were examined at 4 weeks for histologic evidence of chro
nic sinonasal inflammation. Experimental interventions were compared with c
ontralateral control sinuses within each animal and with normal and sham-op
erated controls.
Results: Normal mouse paranasal sinuses include maxillary sinuses, ethmoid
air cells, and respiratory-type epithelium. In experimental animals, the la
teral maxillary sinus wall, nasal septum, and superior turbinelle of the ma
xillary sinus were examined histologically. Epithelial thickening and disar
ray, goblet cell hyperplasia, inflammatory infiltrates, and sinonasal fibro
sis were present in the experimental sinuses of animals packed with Merocel
alone or Merocel with bacterial inoculation. Changes seen with Merocel and
bacteria were more dramatic than those with Merocel alone. Sham-operated c
ontrols and sinuses inoculated with bacteria alone did not differ significa
ntly from the sinuses of normal animals.
Conclusion: Unilateral maxillary sinus ostial obstruction using Merocel nas
al packing along with B fragilis inoculation results in a persistent, local
ized bacterial rhinosinusitis in mice.