In vitro analysis of optimal stimuli for phase-locking and time-delayed modulation of firing in avian nucleus laminaris neurons.

Neurons of the avian nucleus laminaris (NL) provide a neural substrate for azimuthal sound localization. We examined the optimal stimuli for NL neurons to maintain high discharge rates, reliable phase-locking, and sensitivity to time-delayed stimuli. Whole-cell recordings were performed in chick [embryonic days 19-21 (E19-E21)] NL neurons using an in vitro slice preparation. Variation of membrane properties along the tonotopic axis was examined. Computer-controlled intracellular current injection was used to mimic postsynaptic currents or conductances (PSCs) generated in NL neurons by the firing of nucleus magnocellularis (NM) neurons during acoustic stimulation. At various stimulus frequencies, the effects of varying the number of NM cells and PSC amplitudes on firing rate and phase-locking were examined. During high-frequency stimulation, the greatest firing rate and phase-locking occurred when the protocol contained few NM cells that generated large PSCs. Because the stimulus-evoked unitary PSCs are small, we propose that NM cells fire in synchrony to generate large PSCs. To mimic the arrival of PSCs during binaural stimulation, two stimulus trains were summed at different delays before injection. The firing rate of NL neurons was greatest with zero delay. A delay of half the stimulus period evoked firing that was less than that evoked with a single train. Neurons lacking strong outward rectification exhibited neither reliable phase-locking during high-frequency stimulation nor sensitivity to stimulus delays. These findings suggest that the firing responses of NL neurons are determined primarily by their membrane properties.

A depolarizing inhibitory response to GABA in brainstem auditory neurons of the chick.

Neurons in the brainstem auditory nuclei, n. magnocellularis and n. laminaris, of the chick are contacted by terminals containing the inhibitory neurotransmitter gamma-aminobutyric acid (GABA). In this report we describe the physiological response of these neurons to GABA using an in vitro slice preparation. In brainstem auditory neurons, GABA produced a depolarization of up to 20 mV and an associated decrease in input resistance. This depolarization was inhibitory; action potentials generated by orthodromic synaptic drive, antidromic stimulation and intracellular current injection were prevented by GABA application. The GABA response still occurred when synaptic transmission was prevented by perfusing the slice with a medium containing low Ca2+ and high Mg2+ concentrations. Thus, the effects of GABA were directly on the postsynaptic neuron and not via an interneuron. Whole-cell voltage clamp of neurons revealed that the reversal potential of the inward current was approximately -45 mV, suggesting that the channel responsible for this response is not selective for Cl- or K+. Pharmacological analyses suggest that this GABA receptor has properties distinct from those typical of either GABAa or GABAb receptors. Although a similar response was observed with the GABAa agonist, muscimol, it was not blocked by the GABAa antagonist, bicuculline. The response was not evoked by the GABAb agonist, baclofen, and was not blocked by the GABAb antagonist phaclofen. This unusual depolarizing response is not a common feature of all brainstem neurons. Neurons located in the neighboring medial vestibular nucleus show a more traditional response to GABA application. At resting potential, these neurons show a hyperpolarizing or biphasic response associated with a decrease in input resistance and inhibition of their spontaneous activity. GABA-induced responses in the medial vestibular nucleus are blocked by bicuculline. These results suggest that an unusual form of the GABA receptor is present in the brainstem auditory system of the chick. It is possible that this form of GABA receptor provides an efficient mechanism for inhibiting the relatively powerful EPSPs received by brainstem auditory neurons, or it may play a trophic role in the afferent regulation of neuronal integrity in this system.

Membrane properties underlying the firing of neurons in the avian cochlear nucleus.

Neurons of the avian nucleus magnocellularis (NM) relay auditory information from the VIIIth nerve to other parts of the auditory system. To examine the cellular properties that permit NM neurons to transmit reliably the temporal characteristics of the acoustic stimulus, we performed whole-cell recordings in neurons of the chick NM using an in vitro thin slice preparation. NM neurons exhibited strong outward rectification near resting potential; the voltage responses to depolarizing current steps were substantially smaller than to equivalent hyperpolarizing steps. Suprathreshold current steps evoked only a single action potential at the start of the step. In contrast, stimulation with trains of brief current pulses evoked repetitive firing that was phase-locked to the stimulus cycle. The number of action potentials evoked by the pulses during the train decreased with increasing stimulus rate. Voltage-clamp experiments revealed a rapidly activating, slowly inactivating, outward current with a threshold near -65 mV. During depolarizing voltage steps, the outward current rose sigmoidally to a peak and then decayed slowly, reaching steady state within 5 sec. Application of 200 microM 4-aminopyridine (4-AP) reduced the peak of the outward current by 84%, leaving a small, persistent component. Under current clamp, application of 200 microM 4-AP reduced the outward rectification and increased the amplitude and duration of the action potentials. Moreover, NM neurons could no longer sustain firing during high rates of stimulation with the current pulses: increased temporal summation of the potentials caused sufficient depolarization to inactivate the sodium conductance underlying the action potential. These results suggest that the outward current is necessary for NM neurons to transmit well-timed events reliably for the duration of an acoustic stimulus.

Two modes of interspike interval shortening by brief transient depolarizations in cat neocortical neurons.

1. The effects of small, brief depolarizing pulses and excitatory postsynaptic potentials (EPSPs) on neuronal firing were examined in layer V neurons in slices of cat sensorimotor cortex. During intracellular recording, brief depolarizing current pulses (duration, 0.5-2.0 ms; amplitude, 0.1-4.0 nA) were injected in neurons to produce pulse potentials (PPs) with a near-linear rise to a peak (0.08-3.6 mV; rise time = pulse duration) followed by an exponential decay. These PPs resembled EPSPs evoked by electrical stimulation of adjacent sites. When injected in neurons that were induced to discharge tonically, the PPs shortened the interspike intervals (ISIs) in two ways, depending on their time of arrival in the ISI. 2. Toward the end of the ISI, the PPs crossed a time-varying firing level, thereby directly evoking action potentials and shortening the ISIs. These directly evoked spikes occurred during the rise or peak of the PPs. The absolute firing level increased with the membrane trajectory during the latter part of the ISI. 3. PPs that appeared earlier in the ISI did not cross firing level directly but could nevertheless shorten the ISI by a slow regenerative process. The indirectly evoked spikes occurred after the peak of the PPs, at latencies whose magnitude and variability increased as the PPs appeared at successively earlier times in the ISI. PPs that occurred during the initial portion (approximately the 1st 3rd) of the ISI did not affect ISI duration. 4. Stimulus-evoked EPSPs shortened the ISIs in a manner similar to that of PPs. Like PPs, EPSPs caused direct crossings late in the ISI and indirect crossings earlier. Comparison of the mean and maximum ISI shortenings and the range of delays in which the PPs and EPSPs consistently produced ISI shortenings revealed no systematic differences. These similarities suggest that PPs may be used to simulate the ISI shortenings caused by EPSPs. 5. To characterize possible mechanisms underlying the ISI shortening, we examined the PP shapes at different times in the ISI. PPs immediately following a spike were smaller and decayed more rapidly than those evoked by the same current at rest. Late in the ISI, when the membrane potential was > 5 mV above rest, the PP height exceeded that of the PP at rest. This amplitude increase may be due to activation of the persistent sodium current.(ABSTRACT TRUNCATED AT 400 WORDS)

Effects of transient depolarizing potentials on the firing rate of cat neocortical neurons.

1. The effects of excitatory postsynaptic potentials (EPSPs) on interspike intervals (ISIs) of neocortical neurons can be mimicked by pulse potentials (PPs) produced by current injection. The present report documents the dependence of the ISI shortening on the amplitudes of PPs and EPSPs and on the firing rate of the affected neuron. 2. In rhythmically firing necortical neurons, the ISI shortenings caused by PPs arriving at specific times in the ISI can be described by a shortening-delay (S-D) curve. The S-D curve yields three measures of the PPs' ability to shorten the ISI: 1) the mean ISI shortening, S; 2) the maximum shortening, Smax; and 3) the effective interval, defined as the portion of the ISI in which the PP consistently shortens the ISI. For PPs ranging between 80 microV and 3.6 mV (and cells firing at 25 imp/s), the mean shortening increased with amplitude h as S (ms) = 1.2*h (mV)1.24 (r = 0.94; P < 0.01). Smax increased linearly with amplitude as 4.9 ms/mV (r = 0.86, P < 0.01). The effective interval (as a percentage of the ISI) increased slightly with PP amplitude and had a mean value of 65 +/- 21% (mean +/- SD). 3. S-D curves obtained with stimulus-evoked EPSPs varied with EPSP amplitude in a manner similar to those of PPs. The relations obtained for stimulus-evoked EPSPs were not statistically different from those obtained for PPs in the same cells. 4. To determine the effect of firing rate. PPs were applied while neurons fired at frequencies ranging from 8 to 71 imp/s. Both S and Smax were approximately inversely proportional to the baseline firing rate (fo) and could be described as: S or Smax = kfo-m. The mean value of the exponent m (+/- SD) was 0.96 +/- 0.25 for S and 1.2 +/- 0.4 for Smax. These values were not statistically different from a value of 1 (1 group, 2-tailed t test). The effective interval did not vary significantly with firing rate. 5. The dependence of S on PP amplitude and baseline firing rate was incorporated into an expression for the average change in firing rate (delta f) produced by PPs occurring at rate fs: delta f = 0.03 h1.24 fs. The delta f increased with PP amplitude but did not vary significantly with the baseline firing rate. The values of delta f calculated from the S-D curves matched the values that were computed directly from the spike trains.(ABSTRACT TRUNCATED AT 400 WORDS)

Root canal treatment in necrotic primary molars.

Fifty-three patients (27 boys and 26 girls) with necrotic primary teeth received root canal treatments with a paste consisting of KRI-1 paste and pure calcium hydroxide powder with one drop of formocresol. All cases were followed clinically, radiographically and some histologically at 6, 12 and 17 to 24 months postoperatively. All cases were clinically and radiographically successful.