A. Don Murphy Lab, The University of Illinois at Chicago; Department of NeurobiologyGraduate School ApplicationsUIC Neurobiology GroupUIC Laboratory of Integrated NeuroscienceContact Don Murphy
buccal ganglia of Helisoma Whole mount of buccal ganglion of Helisoma trivolvis stained for SCPb immunoreactivity.
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Techniques and experimental approaches range from videomicroscopy of freely behaving intact animals through electrophysiological and pharmacological analyses of neural circuitry, and determination of mechanisms of action of specific neurotransmitters. Immunocytochemistry and a number of neuronal staining techniques are used to determine the morphology of physiologically characterized identifiable neurons.


Map of buccal neurons

The Murphy laboratory has focused pimarily on the neural circuitry underlying feeding and regurgitation in the pond snail, Helisoma trivolvis. The multifunctional CPG in the buccal ganglia has been extensively characterized. Its output can be modulated under experimental control to produce feeding and regurgitation behaviors. A model of the Helisoma CPG has been presented and hypothesized to serve as a "Universal Model" for buccal CPGs in rasping gastropods. 
 


Dopaminergic interneuron N1a

 

Dopaminergic interneuron N1a (A)

(A) Morphology of interneuron N1a as revealed by Lucifer yellow injections. A composite tracinc was made from projections of Ektachrome slides photographed at several different focal planes (B) The FaGlu histochemical technique indicated the presence of dopamine in interneuron N1a. An electrophysiologically characterized neuron N1a was injected with the dye, reactive red # 4, prior to processing the preparation for FaGlu histochemistry. 


Dopaminergic interneuron N1a (B)

FaGlu labelling of presumptive dopaminergic neuronal somata in the left buccal ganglion. The prominent bright soma near the left edge is interneuron N1a. The preparation was photographed using a filter combination designed for Lucifer Yellow.  The FaGlu-sensitive soma displayed dye that was injected into the electrophysiologically characterized interneuron N1a. The soma of only neuron N1a was visible when the preparation was photographed with a filter combination designed for rhodamine. Calibration bar = 100 mm. 
 

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Undergraduate Teaching: Biology of the Brain (intro. survey); Cell and Molecular Neurobiology; Cellular Neurobiology Laboratory; Comparitive Animal Behavior; Animal Physiology and Neurophysiology; Neuroetholgoy.  Quinlan, EM, Arnett, BC, and Murphy AD.  (1997). Feeding stimulants activate an identified dopaminergic interneuron that induces the feeding motor program in Helisoma. J. Neurophysiol.  78.(2): 812-824. 
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Murphy's Graduate Seminars: 
Model Neural Networks and Behavior; Neuropeptides and Behavior; Neural Control of Molluscan Feeding; Ion Channels and Neuronal Excitability; Neurobiology of Feeding and 
Appetite; Non-Classical Effects and Mechanisms 
of Action of Classical Neurotransmitters.
email: dmurphy@uic.edu
back to top Technical Contacts: Chris Brannen, University of Illinois at Chicago; Department of Biological Sciences (1999).
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