Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/114408
Title: An aqueous pomegranate peel extract (Punica granatum) protect against Elastase-induced pulmonary emphysema in Sprague Dawley rats model
Authors: Fatma, Z
Martín Barrasa, José Luis 
Espinosa De Los Monteros, A. 
Santana Reyes, Laura
Herráez Thomas, Pedro 
González Martín, Jesús María
Ramos Nuez, Ángela
Bachoual, Rafik
UNESCO Clasification: 310801 Bacterias
Keywords: Punica granatum
Rat
Elastase
Lung inflammation
Lung oedema, et al
Issue Date: 2021
Journal: Brazilian Journal of Pharmaceutical Sciences 
Abstract: We investigated the effect of Punica granatum peel aqueous extract (PGE), on pulmonary inflammation and alveolar degradation induced by intratracheal administration of Elastase in Sprague Dawley rats. Lung inflammation was induced in rats by intratracheal instillation of Elastase. On day 1 and 2, animals received an intraperitoneal injection of PGE (200 mg/mL), three hours later, they were intratracheally instilled with 25U/kg pancreatic porcine Elastase. Animals were sacrificed 7 days later. Bronchoalveolar lavage (BAL) were collected and cellularity, histology and mRNA expression of Monocyte chemotactic protein 1(MCP-1), Tumor Necrosis Factor-Alpha (TNF-α), Interleukin 6 (IL-6), and Matrix Metalloproteinase-2 (MMP-2) were studied. In addition, activity of TNF-α, IL-6 and MCP-1 on BAL were also analyzed by ELISA Kit. Elastase administration increased: BAL cellularity, neutrophils recruitment and BAL MCP-1, IL-6 expressions. It also increased lung TNF-α, MCP-1, MMP-2 expressions, platelets recruitment, histological parameters at 7th day of elastase treatment. Intraperitoneal injection of 200 mg/kg of PGE reduced, significantly, BAL cellularity, and neutrophils recruitment. However, in animal treated with PGE, MCP-1, MMP-2 and IL-6 on day 7, were similar to the Sham group. Treatment with PGE (200 mg/ kg) also significantly reduced lung TNF-α, and MCP-1 expression. This study reveals that PGE Punica granatum protects against elastase lung inflammation and alveolar degradation induced in rats.
URI: http://hdl.handle.net/10553/114408
ISSN: 1984-8250
DOI: 10.1590/s2175-97902020000418972
Source: Brazilian Journal of Pharmaceutical Sciences [ISSN 1984-8250], n. 57
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