Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice

Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: S...

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Veröffentlicht in:American Journal of Physiology: Cell Physiology 2021-03, Vol.320 (3), p.C341-C354
Hauptverfasser: Fukuzaki, Silvia, Righetti, Renato Fraga, Santos, Tabata Maruyama Dos, Camargo, Leandro do Nascimento, Aristóteles, Luciana R C R B, Souza, Flavia C R, Garrido, Aurelio C, Saraiva-Romanholo, Beatriz Mangueira, Leick, Edna Aparecida, Prado, Carla Máximo, Martins, Mílton de Arruda, Tibério, Iolanda de Fátima Lopes Calvo
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container_end_page C354
container_issue 3
container_start_page C341
container_title American Journal of Physiology: Cell Physiology
container_volume 320
creator Fukuzaki, Silvia
Righetti, Renato Fraga
Santos, Tabata Maruyama Dos
Camargo, Leandro do Nascimento
Aristóteles, Luciana R C R B
Souza, Flavia C R
Garrido, Aurelio C
Saraiva-Romanholo, Beatriz Mangueira
Leick, Edna Aparecida
Prado, Carla Máximo
Martins, Mílton de Arruda
Tibério, Iolanda de Fátima Lopes Calvo
description Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. In conclusion, both treatments with anti-IL-17 contributed to improve most of parameters evaluated in inflammation and extracellular matrix remodeling in this model of lung injury.
doi_str_mv 10.1152/ajpcell.00017.2020
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We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. 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subjects Animals
Bronchoalveolar Lavage Fluid
Disease Models, Animal
Inflammation - metabolism
Interleukin-17 - metabolism
Lung - metabolism
Lung Injury - metabolism
Macrophages - metabolism
Male
Mice
Mice, Inbred C57BL
Neutrophils - metabolism
Nitric Oxide Synthase Type II - metabolism
Pancreatic Elastase - metabolism
Pulmonary Disease, Chronic Obstructive - metabolism
title Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice
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