Effect of bemegride on root potentials of the frog spinal cord

The effect of the convulsant bemegride (β-ethyl-β-methylglutarimide) on spinal-root potentials was investigated in frogs. After intravenous injection in subconvulsant doses (5–12 mg/kg) bemegride caused rapid depression of the dorsal-root potentials evoked by stimulation of the neighboring dorsal or ventral root. Their amplitude fell by 55–67% 3–6 min after bemegride injection. The action of bemegride was reversible and the amplitude of the dorsal-root potentials returned to its initial level within 1 h. Ventral-root potentials showed greater fluctuations of amplitude after injection of bemegride than in the control. Bemegride is evidently an effective agent blocking depolarization of primary afferents in the frog spinal cord.     

Participation of the GABA B receptors in presynaptic inhibition of the spinal cord descending projections fibers in the frog Rana ridibunda

(-)-Baclophen was found to depress in a dose-dependent and reversible way the excitatory post-synaptic potentials (EPSPS) of motor neurons and the ventral root potentials evoked by stimulation of fibres of the ipsi- and contralateral ventral columns. The (-)-baclophen depressing effect could be eliminated with saclophen. Picrotoxin eliminated the depressing effect of the GABA on the descending EPSPS. Depressing effects of (-)-baclophen and GABA upon the ventral root potentials were also shown. The data obtained in pharmacological analysis corroborate to a certain extent existence of the GABAB receptor presynaptic inhibition in descending fibres monosynaptically corrected with the spinal cord motor neurons in the frog Rana ridibunda.     

Electrophysiological study of the effects of cardiodilatin 1-16 on the frog spinal cord in vitro

Using the isolated spinal cord of the frog, hemisected and further divided into two distinct quadrants, we studied electrophysiological changes produced by peptides present in the atrial natriuretic factor (ANF) preprohormone. ANF and related peptides (atriopeptin I and atriopeptin III) did not affect the frog spinal cord. The 1-16 fragment from cardiodilatin (10(-5) M) induced slow depolarization in ventral and dorsal nerve stumps. The depolarization was associated with an increase of the evoked dorsal root potentials and depression of the fast component of the reflex responses. When depolarization approached its maximum value, spontaneous slow potentials appeared progressively similar to the evoked potentials, and became rhythmic until they reached a frequency of one potential every 15-20 seconds. The effects of cardiodilatin 1-16 are localized at dorsal horn level. It is suggested that this substance exerts a modulatory effect on frog cord physiology.     

Transmission of amplitude-modulated signals in the presynaptic inhibition system of the cat spinal cord

In experiments with cats under the hexenal anesthesia it has been found that the transmission of information in multineuronic reflex ring carries out by frequency-dependent way. The optimum frequency subrange corresponds to each meaning of the modulation depth. Appearing signal distortions are accompanied by the phase lead of dorsal potentials with maximum on "resonance" frequency. The mechanism of presynaptic inhibition serves as control command amplifier. For all this the information signal amplitude grows, signal relation to noise increases, noise immunity of information transmission through the neuronic communication channel of multineuronic reflex ring improves considerably.     

The effect of SHF waves on the evoked potentials in the cat spinal cord

In experiments with adult cats there revealed a pronounced effect of SHF radiation on the electrogenesis of spinal cord, the beam density being 15 mW/cm2 and time of exposure 10 min. The estimates of the induced somatosensory brain potentials indicate that there is a phase of a 20 per cent response inhibition with the effect reaching maximum 2-3 h following irradiation. Subsequently, potential characteristics are exponentially restored to be the same with the control values. The evidence is presented that the synaptic neuron contacts within the reflex arc are highly susceptible to SHF radiation.     

Neurochemical and ionic mechanisms of dorsal root potentials in the spinal cord of immature rats

Dorsal root potentials (DRPs) were recorded by a sucrose gap method in experiments on parasagittal slices of the isolated rat spinal cord. In most cases the DRP consisted of fast and slow waves. The fast wave of DRP was inhibited by the GABA antagonist picrotoxin and the blocker of GABA-activated chloride channels, furosemide, but it was potentiated by pentobarbital sodium. The slow wave of DRP disappeared if the extracellular K⁺ concentration was raised to 10 mM and it was depressed by tetraethylammonium and 4-aminopyridine, blockers of electrically excitable potassium channels. It is concluded that the fast wave of DRP and the initial components of the slow wave of DRP are GABA-ergic in origin; the slow wave of DRP, however, is linked with an increase in extracellular K⁺ concentration near the primary afferent terminals. The possible mechanisms of the increase in extracellular K⁺ concentration during dorsal root stimulation are discussed.A. M. Gor'kii Donetsk Medical Institute. Translated from Neirofiziologiya, Vol. 16, No. 6, pp. 796–800, November–December, 1984.     

Enkephalin but not morphine modulates the motor activity in the frog spinal cord in vitro

In the isolated frog spinal cord, methionine-enkephalin (ME, up to 3 X 10(-5) M) hyperpolarized the resting ventral and dorsal root potentials. These hyperpolarizations remained even under Ca2+-free conditions. ME depressed the fast component of the electrically stimulated spinal reflex and enlarged the following depolarizing component. Morphine (10(-4) M) had no apparent ME-like effects. ME may directly and indirectly affect the motoneuron and modulate the spinal motor activity in the frog spinal cord.     

Specific effects of alpha-D,L-aminoadipic acid on synaptic transmission in frog spinal cord

The sucrose gap technique was employed to investigate both synaptic and amino acid evoked responses from motoneurones or primary afferents of frog spinal cord. alpha-D,L-Aminoadipic acid (alpha-D,L-AAD) selectively antagonized responses to acidic amino acids, especially aspartate. The drug was most effective in antagonizing the polysynaptic components of synaptic potentials evoked by dorsal root or lateral column stimulation but had little effect on their monosynaptic components. The ventral root dorsal root potential which is thought to be mediated by a pathway that does not involve acidic amino acids was insensitive to alpha-D,L-AAD. These data, which were confirmed by intracellular recording from motoneurones, provided further evidence for the role of acidic amino acids in polysynaptic pathways in frog spinal cord.     

Influence of the stimulation of the dorsal hippocampus on the dorsal root potentials of the spinal cord in the cat

Rhythmic stimulation of the dorsal hippocampus causes a long-lasting (2–6 sec) depression of both the fast and the electrotonic dorsal root potentials. The depression depends on the intensity of the stimulation of the hippocampus and on the time interval between the stimulation of the hippocampus and the nerve. The sortest time interval producing the depression was within 15–20 msec. The action of afferent impulsation is depressed during both the ipsilateral and contralateral stimulation of the hippocampus. The stimulation of the fornix also exerts a depressing influence on the dorsal root potentials; however, it is not so prolonged as the stimulation of the hippocampus (500–600 msec).A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 1, No. 2, pp. 186–193, September–October, 1969.     

Effects of vasopressin and oxytocin on dorsal root potentials in perfused spinal cord isolated from newborn rats

Dorsal root potentials before and after adding vasopressin or oxytocin to the perfusing fluid were investigated during experiments on one or two perfused spinal cord segments isolated from 12- to 16-day-old rats. It was found that both neuropeptides reversibly inhibited the amplitude of dorsal root potentials produced by stimulating the adjoining dorsal root. The effect was dependent on concentration and time of peptide action on the brain. Both vasopressin and oxytocin were found to produce slow, reversible, dose-dependent depolarization at primary afferent fiber terminals. Depolarization persists when trans-synaptic transmission has been completely blocked owing to substitution of calcium by manganese ions in the perfusing solution. Synaptic contacts are thought to exist between peptidergic hypothalamospinal fibers and dorsal root afferent fiber terminals. The functional significance of these connections is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 6, pp. 757–763, November–December, 1988.     

Syntheses of spinal cord field potentials in the terrapin

A compartmental model of a terrapin motoneuron has been set up to compute membrane potential variations associated with synaptic input at different locations or with antidromic invasion. Membrane potential distributions obtained in that way were used to compute field potentials by means of a volume conduction formalism. The model was used to simulated field potentials measured in the spinal cord in response to stimulation of a muscle nerve with the intention to discriminate between different activation hypothesis for the generation of the spinal cord potential. Extracellular potentials calculated with an excitatory input distributed over the whole dorsal dendritic tree were found to give better reconstruction when compared with excitation restricted to the distal part of the dorsal dendrites, or with somatic inhibition.