(2021) Systemic inflammation and oxidative stress induced by inhaled paraquat in rat improved by carvacrol, possible role of PPARγ receptors. BioFactors. pp. 778-787. ISSN 09516433 (ISSN)
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Abstract
Control rats were exposed to saline aerosol, two groups were exposed to paraquat (PQ), 27 (PQ-L) and 54 (PQ-H) mg/m3 aerosols and six groups were treated with carvacrol, 20 (C-L) and 80 (C-H) mg/kg/day, pioglitazone, 5 (Pio-L) and 10 (Pio-H) mg/kg/day, C-L+Pio-L and dexamethasone, 0.03 mg/kg/day, for 16 days after the end of exposure to PQ-H. Different variables were measured after the end of treatment period. Total and differential white blood cells counts, nitrite, malondialdehyde, interleukin (IL)-10, and interferon-gamma levels were significant increased, but thiol, superoxide dismutase, catalase, IL-17, and tumor necrosis factor alpha were decreased in the blood due to both doses of PQ (p < 0.05-p < 0.001). Most measured parameters were significantly improved in treated groups with both doses of carvacrol, pioglitazone, the combination of C-L+Pio-L and dexamethasone compared to PQ-H group (p < 0.05-p < 0.001). Treatment with C-L+Pio-L showed significantly higher effects compared to each one alone (p < 0.05-p < 0.001). Systemic oxidative stress and inflammation due to inhaled PQ were improved by carvacrol and pioglitazone. Higher effects of C-L+Pio-L than each one alone suggests carvacrol modulating PPAR-γ receptors.
Item Type: | Article |
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Keywords: | Keywords: PPAR-γ agonist; carvacrol; oxidative stress; paraquat; systemic inflammation. |
Divisions: | Research Vice-Chancellor Department > Non-Communicable Diseases Research Center Research Vice-Chancellor Department > Physiology-Pharmacology Research Center |
Page Range: | pp. 778-787 |
Journal or Publication Title: | BioFactors |
Journal Index: | Pubmed |
Volume: | 47 |
Number: | 5 |
Identification Number: | https://doi.org/10.1002/biof.1761 |
ISSN: | 09516433 (ISSN) |
Depositing User: | خانم مهتاب اکبری |
URI: | http://eprints.rums.ac.ir/id/eprint/29187 |
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