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      Combination of losartan with pirfenidone: a protective anti-fibrotic against pulmonary fibrosis induced by bleomycin in rats

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          Abstract

          Pirfenidone (PFD), one acceptable medication for treating idiopathic pulmonary fibrosis (IPF), is not well tolerated by patients at full doses. Hence, employing of some approaches such as combination therapy may be applicable for increasing therapeutic efficacy of PFD. Losartan (LOS), an angiotensin II receptor antagonist, could be a suitable candidate for combination therapy because of its stabilizing effect on the pulmonary function of IPF patients. Therefore, this study aimed to investigate the effects of LOS in combination with PFD on bleomycin (BLM)-induced lung fibrosis in rats. BLM-exposed rats were treated with LOS alone or in combination with PFD. The edema, pathological changes, level of transforming growth factor-β (TGF-β1), collagen content, and oxidative stress parameters were assessed in the lung tissues. Following BLM exposure, the inflammatory response, collagen levels, and antioxidant markers in rat lung tissues were significantly improved by PFD, and these effects were improved by combination with LOS. The findings of this in vivo study suggest that the combined administration of PFD and LOS may provide more potent protection against IPF than single therapy through boosting its anti-inflammatory, anti-fibrotic, and anti-oxidant effects. These results hold promise in developing a more effective therapeutic strategy for treating of lung fibrosis.

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          Idiopathic Pulmonary Fibrosis

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            Pulmonary fibrosis and COVID-19: the potential role for antifibrotic therapy

            Summary In December, 2019, reports emerged from Wuhan, China, of a severe acute respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). By the end of April, 2020, over 3 million people had been confirmed infected, with over 1 million in the USA alone, and over 215 000 deaths. The symptoms associated with COVID-19 are diverse, ranging from mild upper respiratory tract symptoms to severe acute respiratory distress syndrome. The major risk factors for severe COVID-19 are shared with idiopathic pulmonary fibrosis (IPF), namely increasing age, male sex, and comorbidities such as hypertension and diabetes. However, the role of antifibrotic therapy in patients with IPF who contract SARS-CoV-2 infection, and the scientific rationale for their continuation or cessation, is poorly defined. Furthermore, several licensed and potential antifibrotic compounds have been assessed in models of acute lung injury and viral pneumonia. Data from previous coronavirus infections such as severe acute respiratory syndrome and Middle East respiratory syndrome, as well as emerging data from the COVID-19 pandemic, suggest there could be substantial fibrotic consequences following SARS-CoV-2 infection. Antifibrotic therapies that are available or in development could have value in preventing severe COVID-19 in patients with IPF, have the potential to treat severe COVID-19 in patients without IPF, and might have a role in preventing fibrosis after SARS-CoV-2 infection.
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              Idiopathic pulmonary fibrosis

              Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive lung disease characterized by progressive lung scarring and the histological picture of usual interstitial pneumonia (UIP). It is associated with increasing cough and dyspnoea and impaired quality of life. IPF affects ∼3 million people worldwide, with incidence increasing dramatically with age. The diagnostic approach includes the exclusion of other interstitial lung diseases or overlapping conditions and depends on the identification of the UIP pattern, usually with high-resolution CT; lung biopsy might be required in some patients. The UIP pattern is predominantly bilateral, peripheral and with a basal distribution of reticular changes associated with traction bronchiectasis and clusters of subpleural cystic airspaces. The biological processes underlying IPF are thought to reflect an aberrant reparative response to repetitive alveolar epithelial injury in a genetically susceptible ageing individual, although many questions remain on how to define susceptibility. Substantial progress has been made in the understanding of the clinical management of IPF, with the availability of two pharmacotherapeutic agents, pirfenidone and nintedanib, that decrease physiological progression and likely improve progression-free survival. Current efforts are directed at identifying IPF early, potentially relying on combinations of biomarkers that include circulating factors, demographics and imaging data.
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                Author and article information

                Contributors
                Alimandegary@yahoo.com
                Mehrnaz.mehrabani@yahoo.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                16 April 2024
                16 April 2024
                2024
                : 14
                : 8729
                Affiliations
                [1 ]Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, ( https://ror.org/02kxbqc24) Kerman, Iran
                [2 ]Department of Toxicology and Pharmacology, Faculty of Pharmacy, Kerman University of Medical Sciences, ( https://ror.org/02kxbqc24) Kerman, Iran
                [3 ]Pharmaceutics Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, ( https://ror.org/02kxbqc24) Kerman, Iran
                [4 ]Department of Pathology, Pathology and Stem Cell Research Center, Faculty of Medicine, Kerman University of Medical Sciences, ( https://ror.org/02kxbqc24) Kerman, Iran
                [5 ]Department of Dental Biomaterials, School of Dentistry, Shahid Beheshti University of Medical Sciences, ( https://ror.org/034m2b326) Tehran, Iran
                [6 ]Herbal and Traditional Medicines Research Center, Kerman University of Medical Sciences, ( https://ror.org/02kxbqc24) Kerman, Iran
                [7 ]GRID grid.412505.7, ISNI 0000 0004 0612 5912, Department of Toxicology and Pharmacology, Faculty of Pharmacy, , Shahid Sadoughi University of Medical Sciences, ; Yazd, Iran
                Article
                59395
                10.1038/s41598-024-59395-8
                11018867
                38622264
                b91992c8-8d96-4837-9e4d-29d4112c52b1
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 2 June 2023
                : 10 April 2024
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004621, Kerman University of Medical Sciences;
                Award ID: 98000071
                Award Recipient :
                Categories
                Article
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                © Springer Nature Limited 2024

                Uncategorized
                idiopathic pulmonary fibrosis,oxidative stress,combination therapy,bleomycin,pirfenidone,losartan,respiratory tract diseases,transforming growth factor beta

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