Spinal Inputs to Reticulospinal Müller Cells During Locomotor
Activity
Doris Kim
Marquette University
Mentor: Dr. James Buchanan
Reticulospinal neurons make up the main descending pathway in lamprey,
involved in the control and initiation of locomotion in the spinal cord.
Via an ascending feedback pathway, these reticulospinal neurons receive
rhythmic ascending spinal input during locomotor activity. These ascending
inputs to the reticulospinal neurons can be characterized by the amplitude
and timing of membrane potential oscillations using intracellular electrodes.
In this experiment, ascending spinal inputs were recorded in 8 different
bilateral pairs of uniquely identifiable reticulospinal neurons, called
Müller cells, in sea lamprey (Petromyzon marinus) in order to determine
if different reticulospinal neurons receive inputs from different ascending
spinal neurons.
The experiments were performed on in vitro lamprey brainstem-spinal
cord preparations in which a Vaseline diffusion barrier was constructed
just caudal to the brainstem. Locomotor activity was induced in the spinal
cord with perfusion of D-glutamate (0.8mM) to the spinal cord bath. Polysynaptic
pathways in the brainstem were suppressed by elevating calcium and magnesium
in the brainstem bathing solution. Locomotor output was recorded with extracellular
electrodes on the ventral on each side of the spinal cord. Reticulospinal
Müller cells were impaled with sharp intracellular microelectrodes
and their membrane potential oscillations were recorded. For each cell,
the ventral root and intracellular recordings were averaged with respect
to the ventral root burst onsets and measured for average peak and trough
latencies and peak-to-trough amplitudes of potential oscillations. Locomotor
spinal inputs were statistically analyzed between and within cells based
on these measurements.
Results of these experiments demonstrated that Müller cells receive
direct rhythmic inputs from the spinal locomotor networks with significantly
different peak and trough timings of membrane potential oscillations. These
timing differences suggest that individual Müller cells receive ascending
locomotor input from different subsets of spinal neurons. Results also
show a strong inverse correlation between the distance of the Müller
cell body from the spinal cord and the oscillation amplitude.
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