Rhythmic Motor Activity in Thin Transverse Slice Preparations of the Fetal Rat Spinal Cord

2004 ◽  
Vol 92 (1) ◽  
pp. 648-652 ◽  
Author(s):  
Kiyomi Nakayama ◽  
Hiroshi Nishimaru ◽  
Norio Kudo

Networks generating locomotor-like rhythmic motor activity are formed during the last week of the fetal period in the rat spinal cord. We investigated the coordinated rhythmic motor activity induced in transverse slice preparations of the lumbar spinal cord taken from fetal rats as early as embryonic day (E) 16.5. In slices as thin as 100 μm, bath-application of 5-hydroxytryptamine (5-HT) induced rhythmic [Ca2+]i elevations in motoneurons labeled with Calcium Green-1 dextran. The rhythmic [Ca2+]i elevations were similar in frequency to that in the intact lumbar spinal cord, although there was no temporal correlation between the activity in the left and right sides of 100-μm slices. Such rhythmic [Ca2+]i elevations were observed in the slices taken from all lumbar segments. Moreover, the rhythmic activity was abolished by simultaneous blockade of glutamate, glycine, and GABAA receptors, indicating that synaptic transmission mediated by these receptors is important for the generation of the rhythm in these slices. Synchronous rhythmic activity between the left-right sides was found in slices thicker than 200 μm taken from any segmental level of the lumbar spinal cord. In these preparations, commissural neurons were activated synchronously with ipsilateral motoneurons. These results indicate that the neuronal networks sufficient to generate coordinated rhythmic activity are contained in one-half of a single lumbar segment at E16.5. Such spinal cord slices are a promising experimental model to investigate the neuronal mechanisms and the development of rhythm generation in the spinal cord.

1995 ◽  
Vol 74 (3) ◽  
pp. 1109-1117 ◽  
Author(s):  
K. C. Cowley ◽  
B. J. Schmidt

1. The role of inhibitory amino acid transmission in the coordination and generation of rhythmic motor activity was examined with the use of an in vitro neonatal rat spinal cord preparation. Before adding gamma-aminobutyric acid (GABA) or glycine receptor agonists and antagonists, rhythmic motor activity was induced by bath application of acetylcholine (ACh), N-methyl-D,L-aspartate (NMA), or serotonin (5-HT) while monitoring bilateral ankle flexor and extensor electroneurograms (ENGs). The timing of rhythmic flexor and extensor discharge was consistent with that seen during overground locomotion in 27% of 84 bath applications of these substances (n = 65 preparations). 2. Subsequent addition of the GABAA receptor agonist muscimol, the GABAB receptor agonist baclofen, or glycine, abolished rhythmic activity in 95% of the tested applications. 3. GABAB receptor blockade did not disrupt alternating patterns of ENG discharge. However, addition of the GABAA receptor antagonist bicuculline, or the glycine receptor antagonist strychnine, transformed alternating flexor-extensor and left-right activity into patterns characterized by bilaterally synchronous rhythmic activation of all hindlimb ENGs. The onset of individual ENG bursts was more abrupt following bicuculline or strychnine. Strychnine also synchronized high-frequency (4-8 Hz) packets of rhythmic discharge within ENG bursts. 4. Some preparations developed synchronous, but unstable, rhythmic activity in the presence of bicuculline or strychnine alone. However, NMA, 5-HT, or ACh was usually required in addition to these antagonists to promote sustained rhythmic activity.(ABSTRACT TRUNCATED AT 250 WORDS)


Synapse ◽  
2011 ◽  
Vol 65 (12) ◽  
pp. 1282-1288 ◽  
Author(s):  
Christine G. Gerin ◽  
Kristin Smith ◽  
Seritta Hill ◽  
Angela Hill ◽  
Ikenna C. Madueke

2008 ◽  
Vol 436 (2) ◽  
pp. 91-95 ◽  
Author(s):  
Christine Gerin ◽  
Jean-Rene Teilhac ◽  
Kristin Smith ◽  
Alain Privat

2002 ◽  
Vol 87 (2) ◽  
pp. 1094-1105 ◽  
Author(s):  
Rezan Demir ◽  
Bao-Xi Gao ◽  
Meyer B. Jackson ◽  
Lea Ziskind-Conhaim

Neural networks capable of generating coordinated rhythmic activity form at early stages of development in the spinal cord. In this study, voltage-imaging techniques were used to examine the spatiotemporal pattern of rhythmic activity in transverse slices of lumbar spinal cord from embryonic and neonatal rats. Real-time images were recorded in slices stained with the voltage-sensitive fluorescent dye RH414 using a 464-element photodiode array. Fluorescence signals showed spontaneous voltage oscillations with a frequency of 3 Hz. Simultaneous recordings of fluorescence and extracellular field potential demonstrated that the two signals oscillated with the same frequency and had a distinct phase relationship, indicating that the fluorescence changes represented changes in transmembrane potentials. The oscillations were reversibly blocked by cobalt (1 mM), indicating a dependence on Ca2+ influx through voltage-gated Ca2+ channels. Extracellular field potentials revealed oscillations with the same frequency in both stained and unstained slices. Oscillations were apparent throughout a slice, although their amplitudes varied in different regions. The largest amplitude oscillations were produced in the lateral regions. To examine the spatial organization of rhythm-generating networks, slices were cut into halves and quarters. Each fragment continued to oscillate with the same frequency as intact slices but with smaller amplitudes. This finding suggested that rhythm-generating networks were widely distributed and did not depend on long-range projections. In slices from neonatal rats, the oscillations exhibited a complex spatiotemporal pattern, with depolarizations alternating between mirror locations in the right and left sides of the cord. Furthermore, within each side depolarizations alternated between the lateral and medial regions. This medial-lateral pattern was preserved in hemisected slices, indicating that pathways intrinsic to each side coordinated this activity. A different pattern of oscillation was observed in slices from embryos with synchronous 3-Hz oscillations occurring in limited regions. Our study demonstrated that rhythm generators were distributed throughout transverse sections of the lumbar spinal cord and exhibited a complex spatiotemporal pattern of coordinated rhythmic activity.


2019 ◽  
Vol 21 (2) ◽  
pp. 166-172
Author(s):  
S A Zhivolupov ◽  
N A Rashidov ◽  
L S Onishchenko ◽  
A Yu Kravchuk ◽  
O V Kostina ◽  
...  

Performing an experiment in which electronically microscopically studied the nature of reactive changes in the structural thin section of the spinal cord, as well as their dynamics during transcranial magnetic stimulation for 1 month after experimental neuromesis and after compression-ischemic neuropathy of the sciatic nerve. The reported development of compensatory-restorative processes in neurons, glial cells and the microvasculature of the lumbar spinal cord in rats that receive treatment with transcranial magnetic stimulation has been established. It was shown, that in all groups of rats changes in the structures of the lumbar thickening of the rat spinal cord developed in the form of depletion of the cytoplasm, destruction of organelles, changes in the nuclei and development of apoptosis of neurons and glial cells, destruction of the membranes and axial cylinders of myelin fibers. Moreover, these changes are more pronounced in groups after experimental neuromesis. However, in groups of rats, both after compression-ischemic neuropathy and after experimental neuromesis after treatment with transcranial magnetic stimulation, there were signs of the development of recovery processes in the form of intracellular repair of neurons, proliferation of oligodendrocytes, restoration of the structure of myelin fibers and capillaries, and the absence of free red blood cells in the extracellular space. The obtained morphological data confirm the effectiveness of treatment of transcranial magnetic stimulation of injuries of the peripheral nervous system in relation to neurons, glial cells, myelin and non-myelin fibers of the spinal cord.


2003 ◽  
Vol 89 (3) ◽  
pp. 1187-1195 ◽  
Author(s):  
Jun Ren ◽  
John J. Greer

Patterned spontaneous activity is generated in developing neuronal circuits throughout the CNS including the spinal cord. This activity is thought to be important for activity-dependent neuronal growth, synapse formation, and the establishment of neuronal networks. In this study, we examine the spatiotemporal distribution of motor patterns generated by rat spinal cord and medullary circuits from the time of initial axon outgrowth through to the inception of organized respiratory and locomotor rhythmogenesis during late gestation. This includes an analysis of the neuropharmacological control of spontaneous rhythms generated within the spinal cord at different developmental stages. In vitro spinal cord and medullary-spinal cord preparations isolated from rats at embryonic ages (E)13.5–E21.5 were studied. We found age-dependent changes in the spatiotemporal pattern, neurotransmitter control, and propensity for the generation of spontaneous rhythmic motor discharge during the prenatal period. The developmental profile of the neuropharmacological control of rhythmic bursting can be divided into three periods. At E13.5–E15.5, the spinal networks comprising cholinergic and glycinergic synaptic interconnections are capable of generating rhythmic activity, while GABAergic synapses play a role in supporting the spontaneous activity. At late stages (E18.5–E21.5), glutamate drive acting via non- N-methyl-d-aspartate (non-NMDA) receptors is primarily responsible for the rhythmic activity. During the middle stage (E16.5–E17.5), the spontaneous activity results from the combination of synaptic drive acting via non-NMDA glutamatergic, nicotinic acetylcholine, glycine, and GABAA receptors. The modulatory actions of chloride-mediated conductances shifts from predominantly excitatory to inhibitory late in gestation.


1999 ◽  
Vol 82 (6) ◽  
pp. 3563-3574 ◽  
Author(s):  
Matthew C. Tresch ◽  
Ole Kiehn

Several experiments have demonstrated that rostral segments of the vertebrate lumbar spinal cord produce a rhythmic motor output more readily and of better quality than caudal segments. Here we examine how this rostrocaudal gradient of rhythmogenic capability is reflected in the spike activity of neurons in the rostral (L2) and caudal (L5) lumbar spinal cord of the neonatal rat. The spike activity of interneurons in the ventromedial cord, a region necessary for the production of locomotion, was recorded intracellularly with patch electrodes and extracellularly with tetrodes during pharmacologically induced locomotion. Both L2 and L5 neurons tended to be active in phase with their homologous ventral root. L5 neurons, however, had a wider distribution of their preferred phases of activity throughout the locomotor cycle than L2 neurons. The strength of modulation of the activity of individual L2 neurons was also larger than that of L5 neurons. These differences resulted in a stronger rhythmic signal from the L2 neuronal population than from the L5 population. These results demonstrate that the rhythmogenic capability of each spinal segment was reflected in the activity of interneurons located in the same segment. In addition to paralleling the rostrocaudal gradient of rhythmogenic capability, these results further suggest a colocalization of motoneurons and their associated interneurons involved in the production of locomotion.


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