Effects of formoterol and ipratropium bromide on repeated cadmium inhalation -induced pulmonary inflammation and emphysema in rats; Fievez, Laurence ; et alin European Journal of Pharmacology (2010), 25(647), 178-187 Detailed reference viewed: 48 (9 ULg) Effects of formoterol,ipratropium and their combination on repeated cadmium inhalation-induced lung inflammation and airspace enlargement; Fievez, Laurence ; Cheu, Esteban et alin Fundamental & Clinical Pharmacology (2010), 10 Detailed reference viewed: 48 (15 ULg) Anti-inflammatory effects of formoterol and ipratropium bromide against acute cadmium-induced pulmonary inflammation in rats.; Fievez, Laurence ; Cheu, Esteban et alin European Journal of Pharmacology (2010), 628(1-3), 171-178 In this study, the anti-inflammatory properties of formoterol and ipratropium bromide, alone or in combination, were investigated in a rat model of acute pulmonary inflammation induced by cadmium ... [more ▼] In this study, the anti-inflammatory properties of formoterol and ipratropium bromide, alone or in combination, were investigated in a rat model of acute pulmonary inflammation induced by cadmium inhalation. Airway resistance and inflammatory responses, including matrix metalloproteinease-2 (MMP-2) and matrix metalloproteinease-9 (MMP-9) activities, were evaluated. Compared to values obtained in rats exposed to cadmium, pretreatment by bronchodilators administered alone significantly prevented the cadmium-induced increase of airway resistance. Formoterol elicited a significant decrease in total cell number, neutrophil and macrophage counts in bronchoalveolar lavage fluid, whereas ipratropium bromide reduced neutrophil numbers. The two compounds administered alone significantly attenuated the lung lesions associated with parenchyma inflammatory cell influx and congestion observed in the cadmium group. The increased MMP-9 activity was significantly attenuated. Although only formoterol induced a decrease protein concentration in bronchoalveolar lavage fluid, both compounds inhibited the pulmonary edema by reducing wet-to-dry weight ratio which returned to values similar to those recorded in the sham group. All the effects of formoterol on the cadmium-induced inflammatory responses were reversed by propranolol. Similar anti-inflammatory effects were obtained in rats pretreated with ilomastat which showed a significant reduction on inflammatory cell infiltration and MMP-9 activity in bronchoalveolar lavage fluid. Neither synergistic nor additive effects were obtained when the two bronchodilators were administered in combination. In conclusion, formoterol and ipratropium bromide partially protect the lungs against the inflammation by reducing neutrophilic infiltration. This protective effect is associated with reduced MMP-9 activity known to play an important pro-inflammatory role in acute inflammatory process. [less ▲] Detailed reference viewed: 70 (10 ULg) Anti-inflammatory effects of ipratropium bromide in rats with cadmium-induced acute pulmonary inflammation; Fievez, Laurence ; Cheu, Esteban et alin Proceedings of the 12th Annual Meeting of the French Society of Pharmacology and Therapeutics (2008) Detailed reference viewed: 19 (2 ULg) Anti-inflammatory effects of ipratropium bromide in rats with cadmium-induced acute pulmonary inflammationZhang, Yinghong ; Fievez, Laurence ; Cheu, Esteban et alin Fundamental & Clinical Pharmacology (2008), 22(1), 7 Detailed reference viewed: 42 (3 ULg) Anti-inflammatory effects of formoterol in rats after a single dose inhalation of nebulized cadmium; Fievez, Laurence ; Cheu, Esteban et alin Fundamental & Clinical Pharmacology (2007), 74 Detailed reference viewed: 27 (7 ULg) Effects of formoterol on repeated cadmium inhalation-induced lung inflammation and emphysema in rats; Fievez, Laurence ; Cheu, Esteban et alin Proceedings : Congrès de physiologie, de pharmacologie et de thérapeutique P2T (2007) Detailed reference viewed: 6 (3 ULg) Role of beta 2-receptors in the anti-inflammatory effects of formoterol in rats with cadmium-induced acute pulmonary inflammation; ; Fievez, Laurence et alin Proceedings: Autumn Meeting of the Belgian Society of Fundamental and Clinical Physiology and Pharmacology (2007) Detailed reference viewed: 3 (1 ULg) |
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