Matthew McEchron
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Academic title Assistant Professor of Neural and Behavioral Sciences
College College of Medicine
Campuses Penn State Milton S. Hershey Medical Center
Department Neural and Behavioral Sciences
Graduate programs Integrative Biosciences
Neuroscience
Email Phone FAX
  mdm27@psu.edu
  717 531 7400
  717 531 6916
Educational background
  Ph.D., University of Miami, 1995
Postdoctoral Training, Northwestern University Medical School, 1995-1998
Research interests
 

Neural Networks of Learning and Memory; Nutrition and Hippocampal Development; Neurophysiology of Aging and Learning

The primary focus of my laboratory is to understand how neuronal networks process and store information during learning. Along these lines, we would also like to know how nutrition affects the early development of these networks. Much of this research concentrates on an area of the brain called the hippocampus. This is one of the most important brain areas for acquiring and processing new information for later long-term storage. To understand how neuronal networks within the hippocampus and other structures encode learned information, we use single neuron electrophysiological recording techniques. These techniques measure the firing of electrical impulses (i.e., action potentials) transmitted by the single neurons within these networks. This electrophysiological recording technique has been optimized so that electrical signals can be recorded simultaneously from approximately 10 to 100 single neurons from the hippocampus of a single rat. These electrical signals are recorded while the rat performs a learning task called trace fear conditioning. This learning task requires the association of an auditory conditioned stimulus (CS) and an aversive unconditioned stimulus (US). What is most important about this task is that each time the CS and US are presented they are separated by a silent 20-second trace interval. We have used these techniques to show that neurons in different subdivisions of the hippocampus exhibit different firing patterns during trace fear conditioning (Gilmartin & McEchron, 2005a). Another project has shown that single neurons in the medial prefrontal cortex may interact with the hippocampus to encode information during trace classical conditioning (Gilmartin & McEchron, 2005b).


Other projects in our laboratory are determining how developmental nutritional deficits impair the physiology of learning and memory areas of the brain. These projects show that the development of the hippocampus and learning ability can be severely compromised by early nutritional deficits in iron. Moreover, we have shown that rats that receive an iron deficient diet during early development later show altered synaptic efficacy in the hippocampus. These young iron deficient rats also show impairments in hippocampus-dependent learning ability. Specifically, the data below show that rats that receive an iron deficient diet during the perinatal period show impaired trace fear conditioning (McEchron et al., 2005). We also used an in-vitro brain slice preparation to show that pathways in the hippcoampus show reduced synaptic efficacy as the result of the perinatal iron deficient diet (McEchron & Paronish, 2005).

Graphic
  Graphic
  Panel A shows that developmental Iron deficiency irreversibly impairs trace fear conditioning (from McEchron et al., 2005). Heart rate (HR) changes from pre-CS baseline (in beats per min) were averaged across the first two CS-alone memory retrieval trials 72 hrs after trace or unpaired fear conditioning (gray symbols). Learned fear responses are shown as larger HR decelerations to the CS. The CS was presented for the duration of Bin 1. Panel B shows that slices from ID-diet rats showed reduced synaptic transmission in the CA1 hippocampus when compared with matched CN-diet controls (from McEchron & Paronish, 2005). These average input/output curves measure the voltage amplitude of the population spike from threshold to maximum amplitude for for CA1 slices. Insets shows population spikes from an exemplar CN slice from at one step above threshold (TH; Black) and at maximum (Max; Grey). Panel C shows a hippocampal brain slice diagram showing electrode arrangement used to stimulate (Stim) the Schaffer collateral pathway and record (Rec) somatic population spikes from CA1.
Areas of expertise
 
Biological Science DisciplinesNeurosciences
ElectrophysiologyAssociation Learning
LearningConditioning (Psychology)
Conditioning, ClassicalHippocampus
ElectrodesElectrodes, Implanted
MicroelectrodesNutritional Physiological Phenomena
AgingAction Potentials
FearNeurons
Pyramidal CellsConditioning, Eyelid
Brain MappingCerebral Cortex
Extinction, PsychologicalIron
Iron, DietaryNeuronal Plasticity
RabbitsSynapses
CorneaProto-Oncogene Proteins c-fos
Trigeminal Nucleus, SpinalAuditory Pathways
Geniculate BodiesAmygdala
Heart RateThalamic Nuclei
ArousalAttention
Memory, Short-TermMorphine
Serial LearningAvoidance Learning
Dentate GyrusAnimal Nutritional Physiological Phenomena
Prefrontal CortexPrenatal Nutritional Physiological Phenomena
Synaptic TransmissionCardiovascular System
Publication author name
  McEchron MD
Select publications
  McEchron MD. Bouwmeester H. Tseng W. Weiss C. Disterhoft JF. Hippocampectomy disrupts auditory trace fear conditioning and contextual fear conditioning in the rat. 1998. Hippocampus. 8(6):638-46.
National Institute on Aging
National Institute of Mental Health
Gilmartin MR. McEchron MD. Single neurons in the dentate gyrus and CA1 of the hippocampus exhibit inverse patterns of encoding during trace fear conditioning. 2005 Feb. Behav Neurosci. 119(1):164-79.
National Institute on Aging
National Institute of Mental Health
McEchron MD. Cheng AY. Liu H. Connor JR. Gilmartin MR. Perinatal nutritional iron deficiency permanently impairs hippocampus-dependent trace fear conditioning in rats. 2005 Jun. Nutr Neurosci. 8(3):195-206.
National Institute of Diabetes and Digestive and Kidney Diseases
Gilmartin MR. McEchron MD. Single neurons in the medial prefrontal cortex of the rat exhibit tonic and phasic coding during trace fear conditioning. 2005 Dec. Behav Neurosci. 119(6):1496-510.
National Institute on Aging
National Institute of Mental Health
McEchron MD. Paronish MD. Perinatal nutritional iron deficiency reduces hippocampal synaptic transmission but does not impair short- or long-term synaptic plasticity. 2005 Oct-Dec. Nutr Neurosci. 8(5-6):277-85.
National Institute of Diabetes and Digestive and Kidney Diseases

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