Neuroprotective Effect of N-acetylcysteine Against Monocrotophos-Induced Oxidative Stress in Different Brain Regions of Rats.
Twinkle DhillonAmit KumarVijay KumarPublished in: Applied biochemistry and biotechnology (2022)
Monocrotophos (MCP) is systemic organophosphate insecticide used against crop pests. It is reported to cause mammalian toxicity through both acute and chronic exposure. In the present study, we have shown the protective role of N-acetylcysteine (NAC) against MCP-induced oxidative stress in frontal cortex, corpus striatum and hippocampus brain regions of rats. Male Albino Wistar rats were divided into control, NAC-treated, MCP and NAC + MCP-treated groups. An oral dose of MCP (0.9 mg/kg b.wt) and NAC (200 mg/kg b.wt) was administered for 28 days. Results showed an increase in lipid peroxidation (LPO) and protein oxidation followed by decreased antioxidant enzymes after 28 days of MCP exposure. Histopathological analysis showed that monocrotophos exposure caused neurodegenerative changes as evident by neurons with dystrophic changes in the form of shrunken hyperchromatic nuclei in all the regions of the rat brain. N-acetylcysteine supplementation to MCP-treated rats showed a reduction in oxidative stress and ameliorated cellular alterations in all of the three regions. The results of the study indicate that N-acetylcysteine offers neuroprotection by improving antioxidant response and decreasing oxidative stress in different regions of the rat brain.
Keyphrases
- oxidative stress
- transcription factor
- cerebral ischemia
- hydrogen peroxide
- functional connectivity
- resting state
- dna damage
- white matter
- ischemia reperfusion injury
- diabetic rats
- working memory
- genome wide analysis
- induced apoptosis
- newly diagnosed
- anti inflammatory
- liver failure
- intensive care unit
- zika virus
- blood brain barrier
- brain injury
- amino acid
- small molecule
- aedes aegypti