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The Journal of Neuroscience, April 1, 1998, 18(7):2685-2696

Corticosteroid Regulation of Ion Channel Conductances and mRNA Levels in Individual Hippocampal CA1 Neurons

Suresh M. Nair1, Taco R. Werkman3, Johanna Craig4, Richard Finnell4, Marian Joëls3, and James H. Eberwine1, 2

Departments of 1 Pharmacology and 2 Psychiatry, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania 19104, 3 Department of Experimental Zoology, University of Amsterdam, 1098 SM Amsterdam, The Netherlands, and 4 Department of Veterinary Anatomy and Public Health, College of Veterinary Medicine, Texas Agriculture and Mining University, College Station, Texas 77843-4458

Overexposure to corticosteroid hormones is harmful to hippocampal neuronal integrity, likely by perturbation of calcium homeostasis. To identify molecular mechanisms at the single-cell level, we characterized mRNA expression corresponding to voltage- and ligand-gated Ca channels in individual dissociated CA1 neurons in response to long-term corticosterone (CORT) exposure. Predominant mineralocorticoid receptor occupation (ADC-LO group) resulted in low levels of P/Q- and L-type Ca channel mRNAs, high levels of GluR-2 versus GluR-1, and a high ratio of NMDAR-2A to NMDAR-2B mRNA. Corresponding alterations in protein expression were consistent with the restriction of Ca influx. In contrast, additional glucocorticoid receptor occupation (ADC-HI group) altered the expression of these mRNAs in a manner consistent with enhanced Ca influx; interestingly, qualitatively similar alterations were seen in control ADX neurons. Electrophysiological data from the same neurons indicate that Ca current amplitudes also are modulated by CORT, although on a shorter time scale. Finally, principal components analysis (PCA) suggests that neuronal AMPA and NMDA receptor composition may be regulated by MR and GR activation in a complex manner. Therefore, our data implicate molecular events by which CORT may regulate Ca influx into CA1 hippocampal neurons.

Key words: corticosterone; dissociated CA1 Neurons; aRNA amplification; expression profile; mRNA; ion channels; hippocampus


Copyright © 1998 Society for Neuroscience  0270-6474/98/1872685-12$05.00/0


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