No abstract available.
Female ; Humans ; Lipoma/*pathology ; Pharyngeal Neoplasms/*pathology

OBJECTIVES: Allergic rhinitis (AR) is a chronic upper respiratory tract disease that inflames the mucous membranes of the nose and occurs when circulating inflammatory cells including eosinophils and basophils migrate to and accumulate in the inflammation area by passing through the interstitium and capillary walls. To pass through these barriers, the inflammatory cells degrade extracellular matrix proteins. Matrix metalloproteinases (MMPs) released by inflammatory cells mediate the degradation of these proteins. MMPs have synthetic inhibitors and doxycycline, a tetracycline antibiotic, inhibits MMPs. This study investigated the efficiency of intranasal doxycycline in decreasing the symptoms and inflammatory cell infiltration in an animal model of AR. METHODS: AR was created in female Wistar rats by repeated intranasal challenge with ovalbumin by intraperitoneal injection. For 15 days, topical intranasal doxycycline was administered one hour before ovalbumin administration. Following intranasal administration, nasal symptoms were scored and the nasal mucosae of all rats were evaluated histopathologically. To investigate tissue changes, hematoxyline-eosin and Alcian blue/periodic acid Schiff stains were used. As well, cilia loss, goblet cell changes, vascular congestion, vascular proliferation, inflammatory cell infiltration, eosinophil infiltration and the degree of hypertrophy in chondrocytes were evaluated with light microscopy. RESULTS: Typical symptoms of AR were decreased by intranasal doxycycline administration. These effects were stable after repeated intranasal ovalbumin administration. Histological evaluation of doxycycline treated rats did not reveal typical inflammatory changes associated with AR. CONCLUSION: MMPs may have crucial functions in AR and topical intranasal doxycycline, which decreases inflammatory cell infiltration, may offer an alternative therapy for AR.
Administration, Intranasal ; Animals ; Basophils ; Capillaries ; Chondrocytes ; Cilia ; Coloring Agents ; Doxycycline* ; Eosinophils ; Estrogens, Conjugated (USP) ; Extracellular Matrix Proteins ; Female ; Goblet Cells ; Humans ; Hypertrophy ; Inflammation ; Injections, Intraperitoneal ; Matrix Metalloproteinase Inhibitors ; Matrix Metalloproteinases ; Microscopy ; Models, Animal ; Mucous Membrane ; Nasal Mucosa ; Nose ; Ovalbumin ; Rats* ; Rats, Wistar ; Respiratory Tract Diseases ; Rhinitis* ; Tetracycline