Edna  F Pereira
 

Edna F Pereira Ph.D.

Academic Title: Assistant Professor
Primary Appointment: Pharmacology and Experimental Therapeutics
epereira@umaryland.edu
Location: Bressler Research Building, 4-002
Phone: (410) 706-3563

Personal History

In 1987, I finished a 5-year course in the School of Pharmacy at the Universidade Federal do Rio de Janeiro, in Brazil. In 1989, I earned a master's degree from the Departmento de Farmacologia Basica e Clinica at the same University. During my training, I received a broad and in-depth education in classical pharmacology, and conducted experimental research aimed at evaluating the antiinflamatory and anagesic properties of novel compounds designed and synthesized at the Departamento de Tecnologia Farmaceutica at the Universidade Federal do Rio de Janeiro. The results of my research were then published in peer-reviewed journals.
 
In 1989, I started a pre-doctoral training in electrophysiological techniques applied to the CNS at the Instituto de Biofisica Carlos Chagas Filho at the Universidade Federal do Rio de Janeiro. Under the guidance of Dr. Edson X. Albuquerque and Dr. Yasco Aracava, I assessed the effects of ethanol and drugs used to treat alcohol addiction on NMDA and nicotinic receptors in hippocampal neurons. At the end of one year, I moved to Dr. Albuquerque's laboratory at the Department of Pharmacology and Experimental Therapeutics, where I started pursuing my doctoral education in 1993.
 
During my Ph.D., I received training from Dr. Edson Albuquerque at the University of Maryland School of Medicine and Dr. Alfred Maelicke at the University of Mainz, Germany. Under their guidance, I studied the modulation of neuronal nicotinic receptors by compounds now referred to as "nicotinic allosteric potentiating ligands" and approved to treat Alzheimer's disease.
 
After finishing my Ph.D. in 1996, I developed post-doctoral work with Drs. Albuquerque and Maelicke and in 2001, I joined the faculty of the Department of Pharmacology and Experimental Therapeutics. Currently, I am pursuing a scientific career as an Assistant Professor in the Department.

Research Interests

Research in the laboratory has a strong translational component and is focused on nicotinic cholinergic systems in the brain. We examine, by means of electrophysiological, pharmacological and molecular biological techniques, how toxicants and clinically used drugs modify the function and structure of nicotinic cholinergic systems and their integration with other systems in the developing and mature brain of male and female rodents.
 
In the Department of Pharmacology and Experimental Therapeutics, I have ongoing collaborations with Dr. Edson X. Albuquerque and Dr. William Randall in studies of function and expression of nicotinic receptors, and with Drs. Laure Aurelian and Cynthia Smith in studies of cell signaling. I also collaborate with Dr. Harry L. June, a professor working in animal behavior and drug addiction in the Department of Psychiatry.

Lab Techniques and Equipment

Electrophysiology. Various modalities of the patch-clamp technique, including the cell attached, the whole cell and the outside out, are used to characterize pharmacologically and functionally the activity of different receptors in neurons of the central nervous system.  They are also used to study synaptic activity, integration and plasticity in preparations ranging from primary and organotypic cultures to fresh slices.
 
Molecular biology and biochemistry. Immunocytochemistry, western blots, binding and enzymatic assays are used primarily to complement the functional studies and to identify developmental or drug-induced changes in receptor expression and enzymatic activity associated with alterations in receptor function and synaptic integration.
 
Neuroimaging. Analyses of neuronal structures, including dendrites and dendritic spines, is performed in fresh slices and in whole brain using the Golgi technique, immunocytochemistry with Lucifer Yellow, or chemical processing of biocytin. The neurolucida software is used to reconstruct the image of the neurons and to quantify dendritic length and spines. 

Laboratory Personnel:

Iusta Caminha, MD. Graduate student, 2005-present.
Mabel Zelle, Research Assistant.
William P. Fawcett, Ph.D., Research Associate.

Publications

Pereira, E.F.R., Reinhardt-Maelicke, S., Schrattenholz, A., Maelicke, A., and Albuquerque, E.X. Identification and functional characterization of a new agonist site on nicotinic acetylcholine receptors of cultured hippocampal neurons. J. Pharmacol. Exp. Ther. 265:1474-1491, 1993.
 
Alkondon, M., Pereira, E.F.R., Eisenberg, H.M., and Albuquerque, E.X. Nicotinic receptor activation in human cerebral cortical interneurons: a mechanism for inhibition and disinhibition of neuronal networks. J. Neurosci. 20:66-75, 2000.
 
Hilmas, C., Pereira, E.F.R., Alkondon, M., Rassoulpour, A., Schwarcz, R., and Albuquerque E.X. The brain metabolite hynurenic acid inhibits alpha7 nicotinic receptor activity and increases non-alpha7 nicotinic receptor expression: Physiopathological implications. J. Neurosci. 21:7463-7473, 2001.
 
Pereira, E.F.R., Hilmas, C., Santos, M.D., Alkondon, M., Maelicke, A., and Albuquerque, E.X. Unconventional ligands and modulators of nicotinic receptors. J. Neurobiol. 53:479-500, 2002.
 
Santos, M.D., Pereira, E.F.R., Aracava, Y., Castro, N.G., Fawcett, W.P., Randall, W.R., and Albuquerque, E.X.  Low concentrations of pyridostigmine prevent soman-induced inhibition of GABAergic transmission in the central nervous system: Involvement of muscarinic receptors.  J. Pharmacol. Exp. Ther.  304:254-265, 2003.
 
Almeida, L.E.F., Pereira, E.F.R., Camara, A.L., Maelicke, A., and Albuquerque, E.X.  Sensitivity of neuronal nicotinic acetylcholine receptors to the opiate antagonists naltrexone and naloxone: receptor blockade and up-regulation.  Bioorg. Med. Chem. Lett. 14:1879-1887, 2004.
 
Alkondon, M., Pereira, E.F.R., Yu, P., Arruda, E.Z., Almeida, L.E.F., Guidetti, P., Fawcett, W.P., Sapko, M.T., Randall, W.R., Schwarcz, R., Tagle, D.A., and Albuquerque, E.X. Targeted deletion of the kynurenine aminotransferase II gene reveals a critical role of endogenous kynurenic acid in the regulation of synaptic transmission via alpha7 nicotinic receptors in the hippocampus. J. Neurosci. 24:4635-4648, 2004.
 
Aracava, Y., Pereira, E.F.R., Maelicke, A., and Albuquerque, E.X. Memantine blocks alpha7* nicotinic acetylcholine receptors more potently than NMDA receptors in rat hippocampal neurons. J. Pharmacol. Exp. Ther. 312:1195-1205, 2005.



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