Mostafa Fallah
1, Najmeh Moghble
1, Iraj Javadi
1, Hossein Bahadoran
2, Alireza Shahriary
3* 1 Department of Toxicology, Faculty of Pharmacy, Islamic Azad University, Shahreza Branch, Shahreza, Iran.
2 Department of Anatomy, Baqiyatallah University of Medical Sciences, Tehran, Iran.
3 Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Abstract
Background: Arsenic
is a toxic element that widely widespread in environment. Inflammation is now
considered as one of the major mechanisms implicated in arsenic poisoning.
Curcumin (Cur) and N-acetylcysteine (NAC) are potential antioxidants that
protect cells against inflammation. This study aimed to compare the protective
effect of Cur and NAC on brain histology and inflammatory factors, including
matrix metalloproteinases-2, -9 (MMP-2, 9) and tumor necrosis factor-α (TNF-α)
in rats exposed to single dose of arsenic.
Methods: Rats
were exposed to single dose of arsenic (20mg/kg, by gavage) for 30 days and
then treated with 300mg/kg NAC (by gavage) and 100mg/kg Cur (by gavage),
individually. Serum level of TNF-α was
measured using specific ELISA kits. MMP2
and MMP9 contents were measured using Gelatin Zymography method. Brain samples
were collected for histopathological and morphological examinations.
Results: Arsenic
treatment induced white matter lesions and cellular damages at hippocampal CA1
area of the brain. The number of hippocampal CA1 pyramidal cells was
significantly declined in arsenic exposed rats (p<0.05). Treatment with NAC
and Cur improved these abnormalities. The mean levels of MMP2, MMP9 and TNF-α
inflammatory biomarkers were slightly declined after treatment with NAC and Cur
(p>0.05).
Conclusion: NAC and
Cur play an important role in protecting the hippocampal CA1 cells injury
induced by arsenic.