Abstract

BackgroundThe brain is susceptible to methylmercury toxicity, which causes irreversible damage to neurons and glia and the leaf extract Dendropanax morbifera Léveille (DML) has various biological functions in the nervous system. In this study, we examined the effects of DML on mercury-induced proliferating cells and differentiated neuroblasts.MethodsDimethylmercury (5 μg/kg) and galantamine (5 mg/kg) was administered intraperitoneally and/or DML (100 mg/kg) was orally to 7-week-old rats every day for 36 days. One hour after the treatment, novel object recognition test was examined. In addition, spatial probe tests were conducted on the 6th day after 5 days of continuous training in the Morris swim maze. Thereafter, the rats were euthanized for immunohistochemical staining analysis with Ki67 and doublecortin and measurement for acetylcholinesterase (AChE) activity.ResultsDimethylmercury-treated rats showed reduced discrimination index in novel object recognition test and took longer to find the platform than did control group. Compared with dimethylmercury treatment alone, supplementation with DML or galatamine significantly ameliorated the reduction of discrimination index and reduced the time spent to find the platform. In addition, the number of platform crossings was lower in the dimethylmercury-treated group than in controls, while the administration of DML or galantamine significantly increased the number of crossings than did dimethylmercury treatment alone. Proliferating cells and differentiated neuroblasts, assessed by Ki67 and doublecortin immunohistochemical staining was significantly decreased in the dimethylmercury treated group versus controls. Supplementation with DML or galantamine significantly increased the number of proliferating cells and differentiated neuroblasts in the dentate gyrus. In addition, treatment with dimethylmercury significantly increased AChE activity in hippocampal homogenates, while treatment with dimethylmercury+DML or dimethylmercury+galantamine significantly ameliorated this increase.ConclusionsThese results suggest that DML may be a functional food that improves dimethylmercury-induced memory impairment and ameliorates dimethylmercury-induced reduction in proliferating cells and differentiated neuroblasts, and demonstrates corresponding activation of AChE activity in the dentate gyrus.

Highlights

  • The brain is susceptible to methylmercury toxicity, which causes irreversible damage to neurons and glia and the leaf extract Dendropanax morbifera Léveille (DML) has various biological functions in the nervous system

  • Rutin was most abundantly observed in the DML, while myricetin was lowest content in the DML

  • Effects of MeHg and DML on Morris water maze test In all groups, escape latency progressively decreased from days 1 to 5, the swimming speed did not show any significant differences among groups

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Summary

Introduction

The brain is susceptible to methylmercury toxicity, which causes irreversible damage to neurons and glia and the leaf extract Dendropanax morbifera Léveille (DML) has various biological functions in the nervous system. We examined the effects of DML on mercury-induced proliferating cells and differentiated neuroblasts. Heavy metals such as mercury, lead, and cadmium are hazardous because they are bioaccumulated and biomagnified as they ascend the food chain. Accumulated evidences demonstrated that Sprague-Dawley rats were most widely used animal models for MeHg toxicity in the brain. Treatment with MeHg impairs the cellular excitability and synaptic transmission by blocking the blocks calcium and sodium channels in rat hippocampal slices, while it does not affect the synaptic plasticity [9]. MeHg was found to reduce cell proliferation in the hippocampus at postnatal day 7 (P7), and significantly decrease granule cell layer population at P21 [6]

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