Objective:

2

To determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats.

Methods:

2

Wistar rats were exposed orally to doses of 100 and 500 ppm lead acetate for 1 and 2 months to develop subchronic and chronic lead poisening models

respectively. For treatment

BBR (50 mg/kg daily) was injected intraperitoneally to rats poisoned with lead. At the end of the experiment

the spatial learning and memory of rats were assessed using the Morris water maze test. Hippocampal tissue changes were examined by hematoxylin and eosin staining. The activity of antioxidant enzymes catalase

superoxide dismutase

glutathione peroxidase

and malondialdehyde levels as parameters of oxidative stress and antioxidant status of the hippocampus were evaluated.

Results:

2

BBR reduced cognitive impairment in rats exposed to lead (

P

<

0.05 or

P

<

0.01). The resulting biochemical changes included a decrease in the activity of antioxidants and an increase in lipid peroxidation of the hippocampus of lead-exposed rats (

P

<

0.05 or

P

<

0.01)

which were significantly modified by BBR (

P

<

0.05). BBR also increased the density of healthy cells in the hippocampus of lead-exposed rats (

P

<

0.05). Significant changes in tissue morphology and biochemical factors of the hippocampus were observed in rats that received lead for 2 months (

P

<

0.05). Most of these changes were insignificant in rats that received lead for 1 month.

Conclusion:

2

BBR can improve oxidative tissue changes and hippocampal dysfunction in lead-exposed rats

which may be due to the strong antioxidant potential of BBR.