Classification by morphology of multipolar neurons of the human principal olivary nucleus

Author(s):  
Damjan Stojić ◽  
Dragana Radošević ◽  
Nemanja Rajković ◽  
Dušica L. Marić ◽  
Nebojša T. Milošević
Keyword(s):  
1985 ◽  
Vol 24 (7) ◽  
pp. 645-654 ◽  
Author(s):  
L.A. Barragan ◽  
N. Delhaye-Bouchaud ◽  
P. Laget

2018 ◽  
Vol 5 (1) ◽  
Author(s):  
Elan D. Louis ◽  
Daniel Trujillo Diaz ◽  
Sheng-Han Kuo ◽  
Shi-Rui Gan ◽  
Etty P. Cortes ◽  
...  

2008 ◽  
Vol 104 (5) ◽  
pp. 1351-1358 ◽  
Author(s):  
Jianguo Zhuang ◽  
Fadi Xu ◽  
Donald T. Frazier

Several studies have demonstrated that cerebellar deep nuclei, particularly the rostral fastigial nucleus (FNr), are involved in respiratory modulation. These nuclei receive inputs from the contralateral caudal inferior olivary nuclei of the medulla. The objectives of this study were to determine whether electrical and chemical activation of the vicinity of the caudal inferior olivary nuclei (vIOc) affected respiration and, if true, whether the FNr was involved in the vIOc stimulation-evoked ventilatory responses. Experiments were conducted in 30 anesthetized and spontaneously breathing rats. Our results showed that 1) electrical (25 or 100 μA at 10 or 20 Hz for 10 s) and chemical (1 or 100 mM, 25–50 nl N-methyl-d-aspartate) stimulation of the vIOc augmented ventilation predominantly via increasing tidal volume; 2) the responses to the electrical stimulation were almost eliminated by lesion of the contralateral FNr via microinjection of ibotenic acid; and 3) the respiratory responses to electrical stimulation in the vicinity of the rostral IO were 65–70% smaller compared with that evoked by vIOc stimulation. These findings strongly suggest that vIOc neurons play a significant role in modulation of respiratory activity, largely depending on their projections to the FNr.


1993 ◽  
Vol 70 (5) ◽  
pp. 2181-2186 ◽  
Author(s):  
I. Lampl ◽  
Y. Yarom

1. Subthreshold membrane potential oscillations have been observed in different types of CNS neurons. In this in vitro study, we examined the possible role of these oscillations by analyzing the responses of neurons from the inferior olivary nucleus to a combined stimulation of sine wave and synaptic potentials. 2. A nonlinear summation of the sine wave and the synaptic potential occurred in olivary neurons; a superlinear summation occurred when the synaptic potential was elicited at the trough of the sine wave or during the rising phase. On the other hand, a less than linear summation occurred when the synaptic potentials were evoked during the falling phase of the wave. 3. Significant changes in the delay of the synaptic responses were observed. As a result of these changes, the maximum amplitude of the response occurred at the peak of the sine wave, regardless of the exact time of stimulation. The output of the neuron was therefore synchronized with the sine wave and depended only partly on the input phase. 4. These data demonstrate that neurons from the inferior olivary nucleus are capable of operating as accurate synchronizing devices. Moreover, by affecting the delay line, they act as a logic gate that ensures that the information will be added to the system only at given times.


1983 ◽  
Vol 49 (6) ◽  
pp. 1410-1427 ◽  
Author(s):  
H. H. Zakon

In the frog, most neurons in the primary (dorsal medullary nucleus, DMN) and secondary (superior olivary nucleus, SO) auditory nuclei have V-shaped tuning curves, almost as narrowly tuned as those recorded in the nerve. Thus, the innervation pattern is such that if more than one excitatory afferent innervates a postsynaptic cell, they must all possess similar best frequencies (BFs). Similarly, binaural cells in these nuclei display matched frequency selectivities when acoustically stimulated via either ear. The VIIIth nerve was unilaterally severed and allowed to regenerate back into the DMN. At various postoperative intervals, extracellular single-unit recordings were made in the SO contralateral to the regenerated nerve, as that nucleus receives its dominant excitatory input (approximately 80%) from the contralateral side. Recordings were also made in the SO of a number of unoperated control animals. Functional reinnervation commenced between 4 and 5 wk postoperatively and by 6 wk, a normal innervation density, as judged by physiological criteria, was achieved. Single units of any best frequency represented within the frog's two auditory papillae could be recorded during earliest reinnervation. In general, the tuning curves of both monaural and binaural cells were V shaped in the 6 wk regenerates. Although many tuning curves were narrowly tuned (Q10dB greater than 1.0) as in unoperated animals, some were very broadly tuned (Q10dB less than 0.5). The mean Q10dB value for all contralaterally excited cells was 1.45 +/- 0.77 (SD), which was significantly lower than that of SO units in unoperated frogs (Q10dB = 1.66 +/- 0.52 (SD)). Binaural cells often had mismatched BFs and tuning curves. By 8 wk after nerve transection, tuning curves were as narrow as in unoperated animals (Q10dB = 1.64 +/- 0.68 (SD)), and the BFs of binaural cells evinced a greater match than at 6 wk. By 12 wk postoperatively, V-shaped tuning curves were still as narrow as in controls (Q10dB = 1.71 +/- 0.69 (SD)), and the tuning curves and BFs of binaural cells were well matched again. At all postoperative intervals, about 10% of the tuning curves in the SO of regenerates were W shaped. This was never seen in normal animals. The return of narrow V-shaped tuning curves in the majority of neurons and the recurrence of matched binaural cells in the SO are interpreted as evidence of specificity for potential postsynaptic targets in the DMN by regenerating auditory afferents.


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