Literature DB >> 3571508

Spatial distribution of axon collaterals of single inferior olive neurons.

A Rosina, L Provini.   

Abstract

The aim of this study was to define the overall distribution pattern of the axon collaterals of single inferior olive (IO) neurons in relation to the multiple somatotopic maps defined by the climbing fiber (CF) input through the cerebellar cortex. In a previous study (Rosina and Provini: Brain Res. 289:45-63, '83), it was shown that the IO neurons supply interlobar collaterals to pairs of somatotopically related areas in the intermediate part of the anterior lobe (PIAL), in the paramedian lobule (PML), in crus II, and in the simple lobule, within strips C1 to D2. The residual branches then could either distribute within single folia or to adjacent folia within each somatotopically defined cerebellar area or both. We studied whether or not the IO axons branch over neighboring folia of the face-forelimb (FL) areas of PIAL and PML and how this interfolial branching relates to the interlobar collateralization by using the multiple fluorescent retrograde tracing technique. The main results of the study were as follows: the axons from neurons in IO subdivisions that are related to strips C1-C3 give off two interfolial branches in the FL area of PIAL and practically no interfolial collaterals are given in the FL area of PML; and the neurons that give off interfolial collaterals also give interlobar branches. From these data we have inferred the general branching pattern of the IO neurons that convey FL information to PIAL and PML. Each neuron gives off two interlobar collaterals: the branch directed to PIAL splits again into two interfolial collaterals, while each of these three collaterals should give off about three branches within each target folium to account for the ten collaterals estimated to be present in the cat. The distribution pattern of IO axon collaterals proposed here suggests that the same CF-relayed information may interact, at the Purkinje cell level, with different sets of mossy fiber inputs. The effect of this interaction would be to modulate the motor commands forwarded to specific muscle groups in relation to the different conditions under which a given movement is executed.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3571508     DOI: 10.1002/cne.902560302

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  5 in total

1.  The entire trajectories of single olivocerebellar axons in the cerebellar cortex and their contribution to Cerebellar compartmentalization.

Authors:  I Sugihara; H S Wu; Y Shinoda
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

2.  Gating of transmission in climbing fibre paths to cerebellar cortical C1 and C3 zones in the rostral paramedian lobule during locomotion in the cat.

Authors:  R Apps; S Lee
Journal:  J Physiol       Date:  1999-05-01       Impact factor: 5.182

3.  A study of branching in the projection from the inferior olive to the x and lateral c1 zones of the cat cerebellum using a combined electrophysiological and retrograde fluorescent double-labelling technique.

Authors:  R Apps; J R Trott; E Dietrichs
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

4.  Progressive limb ataxia following inferior olive lesions.

Authors:  K M Horn; A Deep; A R Gibson
Journal:  J Physiol       Date:  2012-10-01       Impact factor: 5.182

5.  Structure-function relations of two somatotopically corresponding regions of the rat cerebellar cortex: olivo-cortico-nuclear connections.

Authors:  Joanne Pardoe; Richard Apps
Journal:  Cerebellum       Date:  2002-07       Impact factor: 3.847

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.