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Nutritional Iron Deprivation Attenuates Kainate-Induced Neurotoxicity in Rats: Implications for Involvement of Iron in Neurodegeneration
aResearch Department, Herzog Hospital, Jerusalem, Israel bEve Topf and National Parkinson Foundation Centers for Neurodegenerative Diseases, Department of Pharmacology, Technion-Israel Institute of Technology, Haifa, Israel
Address for correspondence: Dr. Shai Shoham, Research Department, Herzog Hospital, Jerusalem 91351, Israel. Voice: +972-2-5316860; fax: +972-2-6536075. sshoham{at}md2.huji.ac.il Ann. N.Y. Acad. Sci. 1012: 94-114 (2004).
There is evidence suggesting that oxidative stress contributes to kainate neurotoxicity. Since iron promotes oxidative stress, the present study explores how change in nutritional iron content modulates kainate-induced neurotoxicity. Rats received an iron-deficient diet (ID) from 22 days of age for 4 weeks. One control group received the same diet supplemented with iron and another control group received standard rodent diet. Cellular damage after subcutaneous kainate (10 mg/kg) was assessed by silver impregnation and gliosis by staining microglia. ID reduced cellular damage in piriform and entorhinal cortex, in thalamus, and in hippocampal layers CA1-3. ID also attenuated gliosis, except in the hippocampal CA1 layer. Given involvement of zinc in hippocampal neurotransmission and in oxidative stress, we tested for a possible interaction of nutritional iron with nutritional zinc. Rats were made iron-deficient and then assigned to supplementation with iron, zinc, or iron + zinc. Controls were continued on ID diet. After 2 weeks, rats were treated with kainate. Iron supplementation abolished the protective effect of ID in piriform and entorhinal cortex. In hippocampal CA1 and dorsal thalamus, neither iron nor zinc supplementation alone abolished the protective effect of ID against cellular damage. Iron + zinc supplementation abolished ID protection in dorsal thalamus, but not in reuniens nucleus. Kainate-induced gliosis in CA1 remained unaffected by nutritional treatments. Thus, in piriform and entorhinal cortex, nutritional iron has a major impact on cellular damage and gliosis. In hippocampal CA1, gliosis may associate with synaptic plasticity not modulated by nutritional iron, while cellular damage is sensitive to nutritional iron and zinc.
Key Words: kainate • hippocampus • piriform cortex • thalamus • oxidative stress • neurodegeneration • iron • zinc • epilepsy • microglia This article has been cited by other articles:
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