Radioprotective effect of diethylcarbamazine on radiation-induced acute lung injury and oxidative stress in mice.
Soghra FarzipourFereshteh Talebpour AmiriEhsan MihandoustFatemeh ShakiZohreh NoaparastArash GhasemiSeyed Jalal HosseinimehrPublished in: Journal of bioenergetics and biomembranes (2019)
The present study was designed to evaluate the radioprotective effect of diethylcarbamazine (DEC) against oxidative stress and acute lung injury induced by total body radiation (TBI) in mice. For study the optimum dose for radiation protection of DEC, mice were administrated with three dose of DEC (10, 50 and 100 mg/kg), once daily for eight consecutive days. Animals were exposed whole body to 5 Gy X-radiation on the 9 day. The radioprotective potential of DEC in lung tissues was assessed using oxidative stress examinations at 24 h after TBI and histopathological assay also was analyzed one week after TBI. Results from biochemical analyses demonstrated increased malonyldialdehyde (MDA), nitric oxide (NO) and protein carbonyl (PC) levels of lung tissues in only irradiated group. Histopathologic findings also showed an increase in the number of inflammatory cells and the acute lung injury in this group. DEC pretreatment significantly mitigated the oxidative stress biomarkers as well as histological damages in irradiated mice. The favorable radioprotective effect against lungs injury was observed at a dose of 10 mg/kg of DEC in mice as compared with two other doses (50 and 100 mg/kg). The data of this study showed that DEC at a dose of 10 mg/kg with having antioxidant and anti-inflammatory properties can be used as a therapeutic candidate for protecting the lung from radiation-induced damage.
Keyphrases
- oxidative stress
- radiation induced
- induced apoptosis
- traumatic brain injury
- nitric oxide
- high fat diet induced
- dna damage
- radiation therapy
- lipopolysaccharide induced
- ischemia reperfusion injury
- anti inflammatory
- diabetic rats
- lps induced
- gene expression
- type diabetes
- metabolic syndrome
- cell cycle arrest
- risk assessment
- high throughput
- binding protein
- severe traumatic brain injury
- endoplasmic reticulum stress
- skeletal muscle
- clinical trial
- machine learning
- randomized controlled trial
- hydrogen peroxide
- cell death
- deep learning
- climate change
- mild traumatic brain injury
- nitric oxide synthase