Literature DB >> 8468400

Cerebellar nuclear projections from the basilar pontine nuclei and nucleus reticularis tegmenti pontis as demonstrated with PHA-L tracing in the rat.

G A Mihailoff1.   

Abstract

Small iontophoretic placements of the orthogradely transported axonal tracer Phaseolus vulgaris leucoagglutinin (PHA-L) were made in portions of the basilar pontine nuclei (BPN) or nucleus reticularis tegmenti pontis (NRTP) to determine if these cell groups provide projections to the cerebellar nuclei (CN) in the rat and if so, to visualize the morphology of the axons and terminals and illustrate any topographical organization in this system. Axons that originated from BPN or NRTP neurons and contained PHA-L were visualized by an immunohistochemical procedure that involved sequential incubation of tissue sections with goat anti-PHA-L antibody, biotinylated rabbit anti-goat immunoglobulin, and a biotin-avidin-peroxidase conjugate. Following injections of PHA-L restricted to ventral and medial portions of the BPN, labeled fibers were observed in the brachium pontis, the white matter dorsal to the CN, and to a lesser extent, in the white matter of the parafloccular stalk. Labeled preterminal axons entered the CN and gave rise to beaded axons that arborized primarily within dorsal portions of the lateral, interposed, and medial cerebellar nuclei. Injections of PHA-L restricted to either lateral portions of the BPN or ventrolateral regions of NRTP produced labeled fibers in the cerebellum that most frequently involved the parafloccular stalk and ventral portions of the CN. In contrast, dorsomedial NRTP injections resulted in the presence of labeled fibers both in the dorsal cerebellar white matter and the parafloccular stalk as well as dorsal and ventral portions of the CN. With the exception of the rostral and medial territory of interpositus anterior which received very sparse input, all portions of each CN subdivision seemed to exhibit some degree of terminal labeling. The density of labeled axon terminals in the CN appeared to be somewhat greater in the NRTP-injected cases compared to BPN-injected animals. These observations indicate that in the rat, both the BPN and NRTP contain neurons whose axons distribute to the CN. It is likely that most of the axons which project to the CN are collaterals of fibers that continue into the cerebellar cortex as mossy fibers but confirmation of this point must await further investigation. In light of the extensive projections from the cerebral cortex to the BPN and NRTP, this axonal system provides the cerebral cortex with a relatively direct route of access to the CN via one synapse in the BPN or NRTP.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8468400     DOI: 10.1002/cne.903300111

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


  20 in total

1.  Developmental changes in eyeblink conditioning and neuronal activity in the pontine nuclei.

Authors:  John H Freeman; Adam S Muckler
Journal:  Learn Mem       Date:  2003 Sep-Oct       Impact factor: 2.460

2.  Developmental changes in the neural mechanisms of eyeblink conditioning.

Authors:  John H Freeman; Daniel A Nicholson
Journal:  Behav Cogn Neurosci Rev       Date:  2004-03

Review 3.  The cerebellum in feeding control: possible function and mechanism.

Authors:  Jing-Ning Zhu; Jian-Jun Wang
Journal:  Cell Mol Neurobiol       Date:  2007-11-20       Impact factor: 5.046

4.  The fate of spontaneous synchronous rhythms on the cerebrocerebellar loop.

Authors:  Cornelius Schwarz
Journal:  Cerebellum       Date:  2010-03       Impact factor: 3.847

5.  Antidromal and synaptic activation of neurons of the associative parietal cortex of the cat brain elicited by spike activity from the intrinsic nuclei of the pons.

Authors:  E V Papoyan
Journal:  Neurosci Behav Physiol       Date:  1997 Nov-Dec

Review 6.  Consensus paper: current views on the role of cerebellar interpositus nucleus in movement control and emotion.

Authors:  Vincenzo Perciavalle; Richard Apps; Vlastislav Bracha; José M Delgado-García; Alan R Gibson; Maria Leggio; Andrew J Carrel; Nadia Cerminara; Marinella Coco; Agnès Gruart; Raudel Sánchez-Campusano
Journal:  Cerebellum       Date:  2013-10       Impact factor: 3.847

7.  Medial auditory thalamic nuclei are necessary for eyeblink conditioning.

Authors:  Hunter E Halverson; John H Freeman
Journal:  Behav Neurosci       Date:  2006-08       Impact factor: 1.912

8.  Eyeblink conditioning in rats using pontine stimulation as a conditioned stimulus.

Authors:  John H Freeman; Christine A Rabinak
Journal:  Integr Physiol Behav Sci       Date:  2004 Jul-Sep

Review 9.  Neural circuitry and plasticity mechanisms underlying delay eyeblink conditioning.

Authors:  John H Freeman; Adam B Steinmetz
Journal:  Learn Mem       Date:  2011-10-03       Impact factor: 2.460

10.  Inactivation of the interpositus nucleus blocks the acquisition of conditioned responses and timing changes in conditioning-specific reflex modification of the rabbit eyeblink response.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Neurobiol Learn Mem       Date:  2018-07-24       Impact factor: 2.877

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.