Literature DB >> 2985659

Functional organization in cortical barrels of normal and vibrissae-damaged mice: a (3H) 2-deoxyglucose study.

D Durham, T A Woolsey.   

Abstract

The large mystacial vibrissae on the faces of rodents have punctate representations in all stations in the central trigeminal pathway, including layer IV of the somatosensory cortex (SmI). The cortical whisker correlates, multicellular units termed barrels, are not present at birth, and damage to the vibrissae during the first postnatal week results in altered adult cytoarchitectonics. The anatomical effects of vibrissae damage in the cortex have been well documented; here, we investigated the functional organization of altered SmI barrels with a high-resolution 2-deoxyglucose (2-DG) technique (Durham et al., '81, J. Neurosci. 1:519). The middle row of vibrissae was cauterized in 1-, 2-, 3-, 4-, or 5-day-old mice, and the animals were allowed to survive to sexual maturity. Various combinations of vibrissae were clipped acutely 24 hours prior to injection of 2-4 mCi of (3H)2-DG. Mice actively explored an empty cage for 60 minutes, stimulating the remaining vibrissae. The mice then were perfused and their brains prepared for paraffin histology and emulsion autoradiography. In tangential sections through layer IV, patterns of neuropil and cell body labeling were analyzed with respect to barrel cytoarchitecture in normal and vibrissae-damaged mice. In both control and experimental animals, patterns of neuropil and cell somata label corresponded exactly to barrel boundaries, whether normal or altered by vibrissae damage. Only those barrels for which vibrissae were intact had high levels of label, with anterior barrels more heavily labeled. Many neurons in the septa between these barrels and the adjacent barrels were labeled also. We found slightly higher neuropil label in the cortical zone corresponding to the damaged zone on the face in animals lesioned at any time. These data indicate that physiological somatotopy in vibrissae-damaged animals matches the anatomical cytoarchitecture.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2985659     DOI: 10.1002/cne.902350108

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


  8 in total

1.  GABAA receptor immunoreactivity in adult and developing monkey sensory-motor cortex.

Authors:  G W Huntley; A L de Blas; E G Jones
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

2.  Beta 2-adrenergic receptors are colocalized and coregulated with "whisker barrels" in rat somatosensory cortex.

Authors:  P Vos; D Kaufmann; P J Hand; B B Wolfe
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

3.  Is areal extent in sensory cerebral cortex determined by peripheral innervation density?

Authors:  E Welker; H Van der Loos
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

4.  Passive vs. active touch-induced activity in the developing whisker pathway.

Authors:  Tony Mosconi; Thomas A Woolsey; Mark F Jacquin
Journal:  Eur J Neurosci       Date:  2010-09-16       Impact factor: 3.386

5.  Local axonal trajectories in mouse barrel cortex.

Authors:  K L Bernardo; J S McCasland; T A Woolsey
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

6.  Connections and synaptic function in the posteroventral cochlear nucleus of deaf jerker mice.

Authors:  Xiao-Jie Cao; Matthew J McGinley; Donata Oertel
Journal:  J Comp Neurol       Date:  2008-09-20       Impact factor: 3.215

7.  Single vibrissal cortical column in the mouse labeled with 2-deoxyglucose.

Authors:  J Chmielowska; M Kossut; M Chmielowski
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

8.  Repetitive transcranial magnetic stimulation recovers cortical map plasticity induced by sensory deprivation due to deafferentiation.

Authors:  Ellen Kloosterboer; Klaus Funke
Journal:  J Physiol       Date:  2019-06-18       Impact factor: 5.182

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.