Troglitazone, a PPAR-γ agonist, decreases LTC 4 concentration in mononuclear cells in patients with asthma
Autor: | Daria Luczynska, Ewa Pniewska, Milena Sokolowska, Joanna Wieczfinska, Rafał Pawliczak, Emilia Luczak |
---|---|
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Pharmacology Eotaxin medicine.medical_specialty business.industry Troglitazone General Medicine medicine.disease Peripheral blood mononuclear cell 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Pharmacotherapy Endocrinology 030228 respiratory system Internal medicine Medicine Tumor necrosis factor alpha business Receptor Asthma medicine.drug Whole blood |
Zdroj: | Pharmacological Reports. 69:1315-1321 |
ISSN: | 1734-1140 |
DOI: | 10.1016/j.pharep.2017.05.006 |
Popis: | Background Asthma is an inflammatory disorder with multiple mediators involved in the inflammatory response. Despite several attempts, no new anti-inflammatory drugs have been registered for asthma treatment for several years. However, thiazolidinediones, peroxisome proliferator-activated receptor agonists, have demonstrated some anti-inflammatory properties in various experimental settings. The aim of this study was to assess the influence of troglitazone on LTC 4 and 15-HETE concentrations. It also evaluates TNF-induced eotaxin synthesis in peripheral blood mononuclear cells from 14 patients with mild asthma and 13 healthy controls. Methods PBMCs were isolated from the whole blood of the asthmatics and healthy subjects and pretreated with 0.1, 1 or 10 μM of Troglitazone. The cells were then exposed to 10 −6 M calcium jonophore or 10 ng/ml TNF. The production and release of LTC 4 , 15-HETE and eotaxin were then assessed. Results Troglitazone caused a dose-dependent inhibition in LTC 4 synthesis in both asthmatics and healthy subjects. Troglitazone did not influence 15-HETE or eotaxin production in either asthmatic patients or in healthy individuals. Conclusion Due to its inhibition of LTC 4 synthesis, troglitazone therapy is an interesting potential therapeutic approach in asthma and other LTC 4 related inflammatory disorders. |
Databáze: | OpenAIRE |
Externí odkaz: |