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Azza EL-Medany

Azza EL-Medany

King Saud University, Saudi Arabia

Title: Green tea extract: Its potential protective effect on Bleomycin induced lung injuries in rats

Biography

Biography: Azza EL-Medany

Abstract

Lung fibrosis is a common side effect of the chemotherapeutic agent, bleomycin. Current evidence suggests that reactive oxygen species may play a key role in the development of lung fibrosis. The present work studied the effect of green tea extract on bleomycin induced lung fibrosis in rats. Animals were divided into three groups: Saline Control Group, Bleomycin Group in which rats were injected with bleomycin (15 mg/kg, i.p.) three times a week for four weeks and Bleomycin and Green Tea Group in which green tea extract was given to rats (100 mg/kg/day, p.o) a week prior to bleomycin and daily during bleomycin injections for 4 weeks until the end of the experiment. Bleomycin induced pulmonary injury and lung fibrosis that was indicated by increased lung hydroxyproline content, elevated nitric oxide synthase, myeoloperoxidase (MPO), platelet activating factor (PAF), tumor necrosis factor α (TNF-α ), transforming growth factor 1β ( TGF1β ) and angiotensin converting enzyme (ACE) activity in lung tissues. On the other hand, bleomycin induced a reduction in reduced glutathione concentration (GSH). Moreover, bleomycin resulted in severe histological changes in lung tissues revealed as lymphocytes and neutrophils infiltration, increased collagen deposition and fibrosis. Co-administration of bleomycin and green tea extract reduced bleomycin induced lung injury as evaluated by the significant reduction in hydroxyproline content, nitric oxide synthase activity, levels of MPO, PAF & TNF-α & ACE in lung tissues. Furthermore, green tea extracts ameliorated bleomycin induced reduction in GSH concentration. Finally, histological evidences supported the ability of green tea extract to attenuate bleomycin induced lung fibrosis and consolidation. Thus, the finding of the present study provides that green tea may serve as a novel target for potential therapeutic treatment of lung fibrosis.