Histological evidence supporting the inferior olive as the major source of cerebellar climbing fibers in the rat

1974 ◽  
Vol 77 (3) ◽  
pp. 365-384 ◽  
Author(s):  
Jean C. Desclin
2006 ◽  
Vol 95 (4) ◽  
pp. 2342-2351 ◽  
Author(s):  
Beerend Winkelman ◽  
Maarten Frens

The climbing fibers (CFs) that project from the dorsal cap of the inferior olive (IO) to the flocculus of the cerebellar cortex have been reported to be purely sensory, encoding “retinal slip.” However, a clear oculomotor projection from the nucleus prepositus hypoglossi (NPH) to the IO has been shown. We therefore studied the sensorimotor information that is present in the CF signal. We presented rabbits with visual motion noise stimuli to break up the tight relation between instantaneous retinal slip and eye movement. Strikingly, the information about the motor behavior in the CF signal more than doubled that of the sensory component and was time-locked more tightly. The contribution of oculomotor signals was independently confirmed by analysis of spontaneous eye movements in the absence of visual input. The motor component of the CF code is essential to distinguish unexpected slip from self-generated slip, which is a prerequisite for proper oculomotor learning.


1974 ◽  
Vol 52 (6) ◽  
pp. 1212-1217 ◽  
Author(s):  
J. Courville ◽  
F. Faraco-Cantin ◽  
N. Diakiw

The olivo–cerebellar projection has been demonstrated by injections of small volumes of tritiated l-leucine in the inferior olive. A strictly contralateral projection to the cerebellar cortex has been found. Labelling of terminal fibers in the molecular layer is restricted to the paravermian and lateral regions of cortex after an injection of the central region of the olive. The distribution presents a very striking feature: the label is distributed along sagittal bands about 0.4 mm wide interrupted by empty spaces of the same width. It is suggested that an extra-olivary source provides the climbing fibers distributed in these spaces.


1981 ◽  
Vol 24 (1) ◽  
pp. 103-108 ◽  
Author(s):  
E. Chung Hwang ◽  
A. Plaitakis ◽  
I. Magnussen ◽  
M.H. Van Woert

2003 ◽  
Vol 90 (4) ◽  
pp. 2349-2357 ◽  
Author(s):  
Daniel A. Nicholson ◽  
John H. Freeman

The development of synaptic interconnections between the cerebellum and inferior olive, the sole source of climbing fibers, could contribute to the ontogeny of certain forms of motor learning (e.g., eyeblink conditioning). Purkinje cell complex spikes are produced exclusively by climbing fibers and exhibit short- and long-latency activity in response to somatosensory stimulation. Previous studies have demonstrated that evoked short- and long-latency complex spikes generally occur on separate trials and that this response segregation is regulated by inhibitory feedback to the inferior olive. The present experiment tested the hypothesis that complex spikes evoked by periorbital stimulation are regulated by inhibitory feedback from the cerebellum and that this feedback develops between postnatal days (PND) 17 and 24. Recordings from individual Purkinje cell complex spikes in urethan-anesthetized rats indicated that the segregation of short- and long-latency evoked complex spike activity emerges between PND17 and PND24. In addition, infusion of picrotoxin, a GABAA-receptor antagonist, into the inferior olive abolished the response pattern segregation in PND24 rats, producing evoked complex spike response patterns similar to those characteristic of younger rats. These data support the view that cerebellar feedback to the inferior olive, which is exclusively inhibitory, undergoes substantial changes in the same developmental time window in which certain forms of motor learning emerge.


1980 ◽  
Vol 43 (1) ◽  
pp. 182-206 ◽  
Author(s):  
N. H. Barmack ◽  
J. I. Simpson

1. Discrete, unilateral, electrolytic lesions of the dorsal cap of the inferior olive were made in rabbits in an attempt to assess the effect on eye movements of removal of a visual climbing fiber input to the fluocculus. The position of the lesioning electrode within the dorsal cap was adjusted on the basis of the field potential evoked by flash stimulation of the contralateral eye. 2. Electrophysiological and anatomical evidence confirmed that the microlesions of the dorsal cap destroyed 10-80% of olivary cells, but cause only slight damage to the olivocerebellar pathway originating from the contralateral dorsal cap. 3. The immediate effect of the microlesions was a spontaneous, conjugate drift of the eyes to the side contralateral to the lesion. The effects of the microlesions on eye movements were further examined using reflexes evoked by vestibular and optokinetic stimulation. 4. Postoperatively, the vestibuloocular reflex (VOR) gain was not modified, but there was a marked VOR velocity bias to the contralateral side. This velocity bias was most pronounced at low stimulus frequencies (0.02-0.05 Hz, +/- 10 degrees) and was minimal at stimulus frequencies above 0.5 Hz. 5. Monocular, sinusoidal optokinetic stimulation with a large contrast-rich visual target evokes, in normal rabbits, a conjugate asymmetric following response with a higher eye velocity for target movement from posterior to anterior. Following damage to the dorsal cap, the asymmetry of this optokinetic reflex was reversed when the target was presented to the eye contralateral to the lesion. With monocular, constant-velocity optokinetic stimulation delivered to the contralateral eye, the optokinetic gain for movement in the posterior to anterior direction was decreased. 6. These data suggest that visual climbing fibers are part of a feedback loop that reduces retinal slip of low velocity. The relatively low discharge rate of climbing fibers would seem appropriate to ecode continuously retinal slip of low velocity and to influence low-velocity eye movements.


2008 ◽  
Vol 100 (2) ◽  
pp. 1032-1040 ◽  
Author(s):  
Shahin Hakimian ◽  
Scott A. Norris ◽  
Bradley Greger ◽  
Jeffrey G. Keating ◽  
Charles H. Anderson ◽  
...  

A number of studies have been interpreted to support the view that the inferior olive climbing fibers send periodic signals to the cerebellum to time and pace behavior. In a direct test of this hypothesis in macaques performing nonperiodic tasks, we analyzed continuous recordings of complex spikes from the lateral cerebellar hemisphere. We found no periodicity outside of a 100-ms relative refractory period.


1983 ◽  
Vol 271 (1) ◽  
pp. 135-140 ◽  
Author(s):  
Nathan K. Blank ◽  
Fredrick J. Seil ◽  
Arnold L. Leiman

2008 ◽  
Vol 507 (3) ◽  
pp. 1409-1427 ◽  
Author(s):  
Hao-Gang Xue ◽  
Chun-Ying Yang ◽  
Naoyuki Yamamoto

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