Effects of silver nanoparticles–polysaccharide on bleomycin-induced pulmonary fibrosis in rats

博莱霉素 马森三色染色 肺纤维化 化学 H&E染色 病理 羟脯氨酸 肿瘤坏死因子α 纤维化 医学 内科学 染色 化疗
作者
Amal I. Hassan,Amer Samir,Hanan Youssef,Sahar S. Mohamed,Mohsen S. Asker,Manal G. Mahmoud
出处
期刊:Journal of Pharmacy and Pharmacology [Oxford University Press]
卷期号:73 (11): 1503-1512 被引量:5
标识
DOI:10.1093/jpp/rgab037
摘要

Abstract Objectives The first goal of this study was to synthesize the silver nanoparticles Alcaligenes xylosoxidans exopolysaccharide (Ag-AXEPS). The second objective was to analyse the role of Ag-AXEPS nanoparticles (NPS) in treating bleomycin (BLM)-induced lung fibrosis. Methods Intratracheal bleomycin (2.5 U/kg) was administered to prompt pulmonary fibrosis in rats, and pulmonary fibrosis was treated with Ag-AXEPS nanoparticles (100 ppm/twice a week for four weeks). Key findings Ag-AXEPS nanoparticles significantly decreased the diversity of pulmonary inflammatory agents in rats with BLM-induced fibrosis. Reduced levels of respiratory tumor necrosis factor-alpha, monocyte chemotactic protein-1, matrix metalloproteinases (MMP-2 and MMP-9) were observed on treatment with synthesized Ag-AXEPS. Similarly, the treatment decreased IL-12, mRNA levels of BAX and plasma fibrosis markers like N-terminal procollagen III propeptide and transforming growth factor-β1. On the other hand, the treatment increased mRNA BCL2 and total antioxidant capacity. It also lowered the level of fibrosis, as was shown by a quantified pathologic study of hematoxylin–eosin-stained lung parts. The treatment, however, ensured that lung collagen was restored, as assessed by Masson’s trichrome stain, and that overall survival was increased and enhanced. Conclusions Our work showed that nanoparticles could be obtained at 37°C and may be a possible pulmonary fibrosis therapeutic agent.
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