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      Intranasal Flunisolide Suppresses Pathological Alterations Caused by Silica Particles in the Lungs of Mice

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          Abstract

          Silicosis is an occupational disease triggered by the inhalation of fine particles of crystalline silica and characterized by inflammation and scarring in the form of nodular lesions in the lungs. In spite of the therapeutic arsenal currently available, there is no specific treatment for the disease. Flunisolide is a potent corticosteroid shown to be effective for controlling chronic lung inflammatory diseases. In this study, the effect of flunisolide on silica-induced lung pathological changes in mice was investigated. Swiss-Webster mice were injected intranasally with silica particles and further treated with flunisolide from day 21 to 27 post-silica challenge. Lung function was assessed by whole body invasive plethysmography. Granuloma formation was evaluated morphometrically, collagen deposition by Picrus sirius staining and quantitated by Sircol. Chemokines and cytokines were evaluated using enzyme-linked immunosorbent assay. The sensitivity of lung fibroblasts was also examined in in vitro assays. Silica challenge led to increased leukocyte numbers (mononuclear cells and neutrophils) as well as production of the chemokine KC/CXCL-1 and the cytokines TNF-α and TGF-β in the bronchoalveolar lavage. These alterations paralleled to progressive granuloma formation, collagen deposition and impairment of lung function. Therapeutic administration of intranasal flunisolide inhibited granuloma and fibrotic responses, noted 28 days after silica challenge. The upregulation of MIP-1α/CCL-3 and MIP-2/CXCL-2 and the cytokines TNF-α and TGF-β, as well as deposition of collagen and airway hyper-reactivity to methacholine were shown to be clearly sensitive to flunisolide, as compared to silica-challenge untreated mice. Additionally, flunisolide effectively suppressed the responses of proliferation and MCP-1/CCL-2 production from IL-13 stimulated lung fibroblasts from silica- or saline-challenged mice. In conclusion, we report that intranasal treatment with the corticosteroid flunisolide showed protective properties on pathological features triggered by silica particles in mice, suggesting that the compound may constitute a promising strategy for the treatment of silicosis.

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          Silicosis.

          Silicosis is a fibrotic lung disease caused by inhalation of free crystalline silicon dioxide or silica. Occupational exposure to respirable crystalline silica dust particles occurs in many industries. Phagocytosis of crystalline silica in the lung causes lysosomal damage, activating the NALP3 inflammasome and triggering the inflammatory cascade with subsequent fibrosis. Impairment of lung function increases with disease progression, even after the patient is no longer exposed. Diagnosis of silicosis needs carefully documented records of occupational exposure and radiological features, with exclusion of other competing diagnoses. Mycobacterial diseases, airway obstruction, and lung cancer are associated with silica dust exposure. As yet, no curative treatment exists, but comprehensive management strategies help to improve quality of life and slow deterioration. Further efforts are needed for recognition and control of silica hazards, especially in developing countries. Copyright © 2012 Elsevier Ltd. All rights reserved.
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            Some new, simple and efficient stereological methods and their use in pathological research and diagnosis.

            Stereology is a set of simple and efficient methods for quantitation of three-dimensional microscopic structures which is specifically tuned to provide reliable data from sections. Within the last few years, a number of new methods has been developed which are of special interest to pathologists. Methods for estimating the volume, surface area and length of any structure are described in this review. The principles on which stereology is based and the necessary sampling procedures are described and illustrated with examples. The necessary equipment, the measurements, and the calculations are invariably simple and easy.
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              Glucocorticoids induce differentiation of a specifically activated, anti-inflammatory subtype of human monocytes.

              Monocytes and macrophages may either promote or down-regulate inflammatory reactions depending on their state of activation. The effects of glucocorticoids (GCs), the most widely used immunosuppressive drugs, on monocytes are currently not well defined. By analyzing the GC-induced expression pattern in human monocytes by microarray technology, we identified for the first time GC-dependent regulation of 133 genes, including anti-inflammatory molecules such as adenosine A3 receptor, CD1d, and IL-1 receptor II. The results were independently confirmed by real-time polymerase chain reaction (PCR) and flow cytometry. Functional clustering of GC-regulated genes indicated induction of monocytic properties such as phagocytosis and motility as well as repression of adhesion, apoptosis, and oxidative burst. These predictions were confirmed by independent functional assays. GCs up-regulate fMLP receptors and specifically promote chemotaxis to this chemoattractant. Furthermore, GCs promote survival of an anti-inflammatory monocytic phenotype in inflammatory reactions, probably by inhibition of apoptosis because of oxidative stress. GCs limit tissue damage because of induction of antioxidative properties and high capacity for phagocytosis of proinflammatory agents. Thus, GC treatment did not cause a global suppression of monocytic effector functions but results in differentiation of a specific anti-inflammatory phenotype which seems to be actively involved in resolution of inflammatory reactions.
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                Author and article information

                Contributors
                URI : http://loop.frontiersin.org/people/313745/overview
                URI : http://loop.frontiersin.org/people/856739/overview
                URI : http://loop.frontiersin.org/people/857471/overview
                URI : http://loop.frontiersin.org/people/837134/overview
                URI : http://loop.frontiersin.org/people/327787/overview
                URI : http://loop.frontiersin.org/people/856721/overview
                URI : http://loop.frontiersin.org/people/451481/overview
                URI : http://loop.frontiersin.org/people/856711/overview
                URI : http://loop.frontiersin.org/people/857490/overview
                URI : http://loop.frontiersin.org/people/35654/overview
                URI : http://loop.frontiersin.org/people/47912/overview
                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                17 June 2020
                2020
                : 11
                : 388
                Affiliations
                [1] 1Laboratory of Inflammation, Oswaldo Cruz Institute, Oswaldo Cruz Foundation , Rio de Janeiro, Brazil
                [2] 2Department of Medicine, Cedars-Sinai Medical Center, Women's Guild Lung Institute , Los Angeles, CA, United States
                [3] 3Departments of Physiology and Pharmacology, and Medicine, Cumming School of Medicine, University of Calgary , Calgary, AB, Canada
                Author notes

                Edited by: Rachida Guennoun, Institut National de la Santé et de la Recherche Médicale (INSERM), France

                Reviewed by: Nils Lambrecht, VA Long Beach Healthcare System, United States; Ben Nephew, Worcester Polytechnic Institute, United States

                *Correspondence: Patrícia Machado Rodrigues e Silva patsilva1910@ 123456gmail.com

                This article was submitted to Neuroendocrine Science, a section of the journal Frontiers in Endocrinology

                †These authors have contributed equally to this work

                Article
                10.3389/fendo.2020.00388
                7311565
                6e54d39d-6813-4b70-a8f1-c0cb5126a1d5
                Copyright © 2020 Ferreira, Lima, Farias-Filho, Jannini de Sá, de Arantes, Guimarães, Carvalho, Hogaboam, Wallace, Martins and Silva.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 03 December 2019
                : 15 May 2020
                Page count
                Figures: 9, Tables: 0, Equations: 0, References: 51, Pages: 12, Words: 6606
                Categories
                Endocrinology
                Original Research

                Endocrinology & Diabetes
                lung,fibrosis,silica particles,therapy,flunisolide
                Endocrinology & Diabetes
                lung, fibrosis, silica particles, therapy, flunisolide

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