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Docosahexaenoic acid (DHA) ameliorates paraquat-induced pulmonary fibrosis in rats possibly through up-regulation of Smad 7 and SnoN
•DHA ameliorated the fibrotic alterations of lung induced by paraquat.•DHA inhibited paraquat-induced increase of TGF-β1 mRNA levels.•DHA reversed the decreases of Smad 7 and SnoN protein induced by paraquat. Paraquat (PQ) poisoning has caused a large number of human fatalities due to the progressiv...
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Published in: | Food and chemical toxicology 2013-07, Vol.57, p.330-337 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •DHA ameliorated the fibrotic alterations of lung induced by paraquat.•DHA inhibited paraquat-induced increase of TGF-β1 mRNA levels.•DHA reversed the decreases of Smad 7 and SnoN protein induced by paraquat.
Paraquat (PQ) poisoning has caused a large number of human fatalities due to the progressive and irreversible pulmonary fibrosis. Docosahexaenoic acid (DHA) is well-recognized as important modulators of multiple biological pathways that affect health and disease. A line of studies have shown that DHA supplementation is associated with the alleviation of some tissue fibrosis. In the current study, pulmonary fibrosis of rats was produced by a single oral dose of 50mg/kgbw PQ treatment. Daily 500mg/kgbw DHA supplementation was provided 7days before PQ treatment and lasted for consecutive 35days. DHA was found to ameliorate the pulmonary fibrotic alterations induced by PQ, which was evidenced by significant reduction of histological changes, hydroxyproline content and level of the transforming growth factor-β1 (TGF-β1) mRNA. Furthermore, the protein levels of Smad 7 and SnoN in the DHA supplemented rats were significantly increased compared with those in the rats of the PQ group. These results suggested that DHA ameliorated pulmonary fibrosis induced by PQ might be attributed to its enhancement of Smad 7 and SnoN expression. |
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ISSN: | 0278-6915 1873-6351 |
DOI: | 10.1016/j.fct.2013.03.045 |