, 1989 and Maranhão et al., 2000). The measurements were performed three times by the same investigator in each animal at functional residual capacity. Special care was taken to perform the measurements at the same reference points and to avoid errors due to the soft tissue compressibility. Airway responsiveness was assessed 24 h after the last challenge with aerosolized methacholine in a FinePoint R/C Buxco Platform (Buxco Electronics, Sharon, CT, USA). Mice were anaesthetized with nembutal (60 mg/kg). Neuromuscular activity was blocked with bromide pancuronium
(1 mg/kg). Airflow and transpulmonary pressure were recorded using a Buxco Pulmonary Mechanics Processing System (Buxco Selleckchem VE-822 Electronics, Wilmington, NC, USA). This instrument was used to calculate airway resistance and dynamic
compliance (Cdyn). Analog signals from the computer were digitized using a Buxco analog to digital converter (Buxco Electronics). Mice were allowed to stabilize for 5 min and increasing concentrations of methacholine (3, 6 and 12 mg/mL) were aerosolized for 5 min each. Baseline resistance and Cdyn were assessed with aerosolized phosphate-buffered saline (PBS). The results were expressed as the mean absolute values of lung resistance and Cdyn responses recorded during 5 min after the administration of methacholine aerosol. A laparotomy was performed immediately after determination of the ventilatory variables, and heparin (1000 IU) was intravenously injected in the vena cava. The trachea was clamped AZD2014 solubility dmso at end-expiration (PEEP = 2 cmH2O), and the abdominal aorta and vena cava were sectioned, yielding a massive hemorrhage that quickly killed the animals. The right lung was then removed, fixed in 3% buffered formaldehyde and paraffin embedded. Four-μm-thick slices were cut and stained with hematoxylin–eosin. Lung morphometry
analysis was performed with an integrating eyepiece with a coherent system consisting of a grid with 100 points and 50 lines (known length) coupled to a conventional light microscope (Olympus BX51, Olympus Latin America-Inc., Brazil). Fraction areas of collapsed and those normal lung were determined by the point-counting technique (Hsia et al., 2010) across 10 random, non-coincident microscopic fields (Menezes et al., 2005 and Santos et al., 2006). Briefly, points falling on collapsed or normal pulmonary areas were counted and divided by the total number of points in each microscopic field. Airway bronchoconstriction index was determined by counting the points falling on the airway lumen and those falling on airway smooth muscle and on the epithelium, at a magnification of 400×. The perimeter of the airways was estimated by counting the intercepts of the lines of the integrating eyepiece with the epithelial basal membrane.
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