Pulmonary Protein Oxidation and Oxidative Stress Modulation by Lemna minor L. in Progressive Bleomycin-Induced Idiopathic Pulmonary Fibrosis.
Pulmonary Protein Oxidation and Oxidative Stress Modulation by Lemna minor L. in Progressive Bleomycin-Induced Idiopathic Pulmonary Fibrosis.
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DOI:
10.3390/antiox11030523
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发表时间:
2022-03-08
期刊:
影响因子:
--
通讯作者:
Nikolova G
中科院分区:
文献类型:
--
作者:
Karamalakova Y;Stefanov I;Georgieva E;Nikolova G
Bleomycin (BLM) administration is associated with multifunctional proteins inflammations and induction of idiopathic pulmonary fibrosis (IPF). Lemna minor L. extract, a free-floating monocot macrophyte possesses antioxidant and anti-inflammatory potential. The aim of the study was to examine the protective effect of L. minor extract on lung protein oxidation and oxidative stress modulation by BLM-induced pulmonary fibrosis in Balb/c mice. For this purpose, the protein carbonyl content, advanced glycation end product, nitroxide protein oxidation (5-MSL), and lipid peroxidation (as MDA and ROS), in lung cells were examined. The histological examinations, collagen deposition, and quantitative measurements of IL-1β, IL-6, and TNF in lung tissues and blood were investigated. Intraperitoneal, BLM administration (0.069 U/mL; 0.29 U/kg b.w.) for 33 days, caused IPF induction in Balb/c mice. Pulmonary combining therapy was administered with L. minor at dose 120 mg/mL (0.187 mg/kg b.w.). L. minor histologically ameliorated BLM induced IPF in lung tissues. L. minor significantly modulated (p < 0.05) BLM-alterations induced in lung hydroxyproline, carbonylated proteins, 5-MSL-protein oxidation. Oxidative stress decreased levels in antioxidant enzymatic and non-enzymatic systems in the lung were significantly regulated (p < 0.05) by L. minor. L. minor decreased the IL-1β, IL-6, and TNF-α expression in lung tissues and plasma. The L. minor improves the preventive effect/defense response in specific pulmonary protein oxidation, lipid peroxidation, ROS identifications, and cytokine modulation by BLM-induced chronic inflammations, and could be a good antioxidant, anti-inflammatory, and anti-fibrotic alternative or IPF prevention involved in their pathogenesis.
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影响因子:
6.4
作者:
Cha SI;Chang CS;Kim EK;Lee JW;Matthay MA;Golden JA;Elicker BM;Jones K;Collard HR;Wolters PJ
通讯作者:
Wolters PJ
影响因子:
5.8
作者:
Fois AG;Paliogiannis P;Sotgia S;Mangoni AA;Zinellu E;Pirina P;Carru C;Zinellu A
通讯作者:
Zinellu A
DOI:
10.1513/pats.201203-023aw
发表时间:
2012-07-01
期刊:
Proceedings of the American Thoracic Society
影响因子:
--
作者:
Fernandez, Isis E;Eickelberg, Oliver
通讯作者:
Eickelberg, Oliver
影响因子:
6.1
作者:
Garbuzenko, E;Nagler, A;Levi-Schaffer, F
通讯作者:
Levi-Schaffer, F
影响因子:
3.2
作者:
Baek G;Saeed M;Choi HK
通讯作者:
Choi HK