Selective blockade of NMDA-activated channel currents may be implicated in learning deficits caused by lead. |
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Authors: | M Alkondon A C Costa V Radhakrishnan R S Aronstam E X Albuquerque |
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Affiliation: | Department of Pharmacology and Experimental Therapeutics, University of Maryland School of Medicine, Baltimore 21201. |
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Abstract: | The effect of Pb2+ on glutamate receptor activity in rat hippocampal neurons was investigated with a view of explaining the cognitive and learning deficits produced by this heavy metal. Pb2+ (2.5-50 microM) selectively inhibited N-methyl-D-aspartate (NMDA)-induced whole-cell and single-channel currents in a concentration-dependent but voltage-independent manner, without significantly altering currents induced by either quisqualate or kainate. The frequency of NMDA-induced channel activation was decreased by Pb2+. Neither glycine (10-100 microM), nor Ca2+ (10 mM) reversed the effect of Pb2+. Pb2+ also inhibited the [3H]MK-801 binding to rat hippocampal membranes in vitro. The elucidation of the actions of Pb2+ on the NMDA receptor ion channel complex provides important insights into the clinical and toxic effects of this cation. |
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