Accumulation of aluminium chloride results in damage to different brain regions, and has been used to model damage to the hippocampus which can be associated with various neurodegenerative diseases such as Alzheimer’s and Parkinson’s. The aim of this study was to assess the protective effects of eugenol on aluminium induced neurotoxicity in the hippocampus of adult Wistar rats. 30 adult Wistar rats were procured and divided into six groups with five animals in each group, namely: EGH (300 mg/kg eugenol), EGL (150 mg/kg eugenol), EGH+AL (300 mg/kg eugenol and 100 mg/kg AlCl3), EGL+AL (150 mg/kg eugenol and 100 mg/kg AlCl3), AL (100 mg/kg AlCl3) and CTRL (2 mL/kg distilled water). All Groups were treated orally for 21 days after which they were humanely sacrificed under 0.8 mL/kg ketamine as an anaesthetizing agent. Thereafter, brain tissues were removed and processed for histological demonstration, while the frontal lobe was homogenized and the resultant homogenate obtained was used to assay the levels of superoxide dismutase (SOD) activity. Rat body weights were measured before and after treatment. Aluminium resulted in a significant (p<0.05) reduction in SOD activities. There was alteration in the histology of hippocampal neurons (CA1) and a significant (p<0.01) reduction in body weight of animals. However, the administration of Eugenol was able to restore the activity of SOD. The use of Eugenol offers a promising prospect in the management of neurodegenerative diseases associated with aluminium toxicity.
Lead (Pb) is a widespread toxic metal found in the environment with potential danger to human health. It is used in the manufacture of batteries, metal products, paints and other domestic substances. This study investigated the effect of aqueous seed extract of Nigella sativa on leadinduced cerebral cortex toxicity in Long Evan's rats. Twenty five Long Evans rats divided into five groups of five animals were used for the study. Group I received Distilled water, group II received aqueous seed extract of Nigella sativa (1000mg/kg), group III received lead (60mg/kg), group IV received lead (60mg/kg) followed by aqueous seed extract of Nigella sativa (1000mg/kg) and group V received lead (60mg/kg) followed by aqueous seed extract of Nigella sativa (500mg/kg) via oral intubation. Elevated Plus Maze (EPM) was used to study anxiety-like behaviour. Activities on the elevated plus maze showed that there was no statistically significant decreased rate of anxiety across the groups (P>0.05). The histology of the cerebral cortex of long Evans rats in group IV that received Lead (60 mg/kg) followed by aqueous seed extract of Nigella sativa (1000mg/kg) showed mild neuronal damage while the histology of group V animals that received lead (60mg/kg) followed by aqueous seed extract of Nigella sativa (500mg/kg) showed severe neuronal damage. It can be concluded that aqueous seed extract of Nigella sativa at high dose have more therapeutic effect than at low dose.
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