RESEARCH 2006
RESEARCH 2005
RESEARCH 2004
RESEARCH 2003
> Dr. James Anderson
> Dr. James Buchanan
> Dr. James Courtright
> Dr. Jane E. Dorweiler
> Dr. Stephen Downs
> Dr. Robert Fitts
> Dr. James Maki
   - Alissa R. DeHaan
   - Jenny Strickland
> Dr. Michael Schläppi 
> Dr. Rosemary A. Stuart
> Dr. Gail Waring
> Dr. Pinfen Yang
   - Zagum Bhatti
   - Jennifer Dienes
   - Susan R. Hupp

RESEARCH 2002
RESEARCH 2001
RESEARCH 2000

 

 

Electrophysiological Study of Spinobulbar Neuron Distribution in Lampreys

Wai Hong Leong
Marquette University
Milwaukee, WI
Faculty Mentor: Dr. James Buchanan

Locomotor behaviors, such as swimming, flying, and walking, have been studied in many animals to understand the neurobiological basis of rhythmic motor activity. The basic motor pattern for locomotion is generated by centrally located neuronal circuits, known as a central pattern generators (CPG). However, the basic pattern produced by the CPG is usually modified by sensory information from peripheral receptors and signals from other regions of the central nervous system, such as reticulospinal cells. Ascending spinal neurons that terminate in the brain stem (ie, spinobulbar cells) transmit sensory and motor information about the environment and the internal state of the spinal cord to the brain in order to modulate the activity of several groups of descending brain neurons, which in turn regulate the locomotor CPG.

Previous anatomical studies of the spinobulbar cells in lampreys have shown that the majority of these neurons are located in the rostral spinal cord. The present study was aimed at determining whether spinobulbar neurons activated during locomotor activity have a similar distribution in the spinal cord. Our hypothesis is that the functional distribution of spinobulbar cells is similar to the anatomical distribution. 

Lamprey, the most primitive living vertebrate, is used as the experimental model in this study due the relative simplicity of its nervous system compared to higher vertebrates and the capability of the isolated spinal cord to remain viable for several days in cold physiological solution. Spinal cord activity was examined in an in vitro preparation and the spinal locomotor networks were activated by applying 0.5 mM D-glutamate to three spinal pools separately: rostral, middle and caudal, each consisting of about 16 spinal segments. The rhythmic activity induced in the spinal cord by D-glutamate is referred to as “fictive swimming”. The spiking frequency and spiking activity amplitude of spinobulbar cell axons recorded at the rostral end of the cord were measured and analyzed.

In all five preparations, the spiking frequency and spiking amplitude of the cord were found to be highest when fictive swimming was induced in the rostral spinal pool, followed by the middle pool and lastly the caudal pool. In addition, we found that the spiking activity is often rhythmic indicating that the ascending signal is composed in part of locomotor signals from the CPG. However, the rhythmic activity in the cord was relatively weak compared to ventral roots. This could possibly due to the smearing effect of rhythmic bursting activity coming from a number of segments and the overlap of ipsilateral and contralateral signals, which are active in an alternating pattern.

Our functional distribution matches closely a previous anatomical study in which the spinolbulbar cells were found to be mostly distributed in the rostral spinal cord. This leads us to suggest that the rostral compartment of the spinal cord is more important in conveying information to the brain about the internal state of the network activity during locomotion. 


 

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