Organophosphate Induced Neurotoxic and Cardiotoxic Damages in Wistar Rats
Abstract:
Introduction: An estimated 300,000 deaths each year
are as a result of organophosphate toxicity. Organophosphate pesticides (OP’s) have
been used in large amounts in agricultural settings and homes, allowing intoxication.
This has been linked to the onset of neurotoxicity and cardiotoxicity.
Methods: Thirty-two adult wistar rats were grouped
and exposed to dichlorvos and chlorpyrifos, two widely used OP’s, for a period of
14 days. They underwent behavioural tests for anxiety-like behaviour and spatial
memory. The brain tissue was excised, and the amygdala and hippocampus were sectioned
out. These were put through biochemical tests for oxidative stress and Acetylcholinesterase
(AChE) activity. These parameters, along with the brain and body weight changes
were compared with those of a control group. Comparisons were analysed using one-way
analysis of variance (ANOVA) and subjected to post-hoc Bonferroni’s multiple comparison
test.
Results: There was a significant decrease (p≤0.05)
in the brain and body weights. In the behavioural tests for spatial working memory,
a significant defect (p≤0.05) was seen, shown by Morris water maze test. Anxiety-like
behaviours were also elevated, shown by changes (p≤0.05) in Open Field test and
Elevated Plus Maze test. AChE activity was markedly decreased (p≤0.05) in the amygdaloid
complex and the hippocampus. Oxidative stress markers, Nitric Oxide (NO) and Reactive
Oxygen Species (ROS) were also markedly increased (p≤0.05) in both brain regions.
A similar experiment, with cardiotoxicity focus showed atherogenic and atherosclerotic
indices and morphological damages, including a deterioration in plasma lipid profiles
and a rise in low density lipoprotein- cholesterol.
Conclusion: There is a significant increase in neurotoxic
and cardiotoxic profiles with OP exposure which can lead to neurodegenerative and
cardiovascular diseases.
Keywords: Organophosphates, Acetylcholinesterase,
Hippocampus, Amygdala, Atherogenic, Atherosclerotic.