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				Board A                            
				Board B                           
				Board C  
				   
				This is a set of three circuit boards, each 
				representing a short length of axon as a set of six identical 
				cylindrical compartments.  Each compartment is represented 
				by a high transmembrane resistance
				Rm 
				and capacitance Cm.  Each compartment is 
				separated from its neighbors by lower intracellular logitudinal resistances Ri.  The 
				extracellular longitudinal resistances are assumed to be 
				insignificant, hence the extracellular sides of all compartments 
				are simply shorted together to a common extracellular space.  
				Recording access to each compartment is provided by a pair of 
				simple machine screw posts - intracellular (red) and 
				extracellular (black).  
				   
				As 
				detailed in the diagram below, board A models a 
				small diameter axon.  Board B models a large 
				diameter axon, 10x the diameter of A, with a correspondingly 
				increased Cm 
				(10x) and decreased 
				Rm (.1x) and
				Ri 
				(.01x).  Board C models a small diameter 
				axon, but with the middle four compartments myelinated.  
				The outer two compartments and all intracellular resistances 
				Ri 
				match board A, but in the middle four myelinated compartments
				Cm 
				is decreased (.01x) and
				Rm 
				is increased (100x).     
				     
				As described in Laboratory 
				#8 of the BIO325 manual, this model is used with a 
				square-wave stimulus pulse (supplied by an electronic 
				stimulator) to study both capacitive rounding and spatial 
				amplitude decay with distance of a transient input signal.  
				This introduces the student to the concepts of the time constant
				tau 
				for capacitive rounding and the space constant lambda 
				for distance decay.  Students also discover that the large 
				diameter axon involves significantly greater current flow (i.e. 
				metabolic cost) than either small axon.  Finally, students 
				compare rise time to threshold at a recording site (node 5) 
				distant to the stimulating site (node 0) across the three axon 
				models.  This will ultimately be related to increased axon 
				diameter and myelination as alternative ways to speed action 
				potential propagation.     
				Printouts of the results of using this model as described in 
				laboratory #8 are available online in a
				poster (PowerPoint format) or upon request from
				
				brhoades@wesleyancollege.edu . |