Literature DB >> 3815072

The fibers which leave the Probst's longitudinal bundle seen in the brain of an acallosal mouse: a study with the horseradish peroxidase technique.

H S Ozaki, T H Murakami, T Toyoshima, M Shimada.   

Abstract

The congenital absence of the corpus callosum, a brain anomaly frequently noted in humans, has been recently found to occur in some mice of the ddN strain in our laboratory. In the brains of these mice, the Probst's longitudinal bundle is always present on both cerebral hemispheres and gives rise to some aberrant fibers toward the midline. In this research, the neuroanatomical features of these fibers were studied by iontophoretical injections of horseradish peroxidase (HRP) into the neocortex of acallosal mouse brains. The results revealed that the fibers which leave the Probst's longitudinal bundle are, at least, of 3 kinds: namely, the fibers that run out from the anterior portion of the bundle and take a U-turn ipsilaterally without crossing the midline through the septal tissue to go back again into the longitudinal bundle at the level where they have left it; the commissural fibers that leave the bundle from its middle portion and cross through a tiny bridge of tissue associated with the ventral hippocampal commissure to the opposite hemisphere; and the fibers that arise from the posterior portion of the bundle and accumulate as an anomalous fascicle below the cingulum. The observation that no labeled fibers were seen within the anterior commissure in the present HRP materials suggests that the axons from neocortex which are prevented from crossing the midline in mice with congenital absence of the corpus callosum cannot find an alternative pathway via the anterior commissure.

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Year:  1987        PMID: 3815072     DOI: 10.1016/0006-8993(87)90623-8

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  6 in total

1.  Diffusion tensor MR imaging visualizes the altered hemispheric fiber connection in callosal dysgenesis.

Authors:  Seung-Koo Lee; Susumu Mori; Dong Joon Kim; Sei Young Kim; Si Yeon Kim; Dong Ik Kim
Journal:  AJNR Am J Neuroradiol       Date:  2004-01       Impact factor: 3.825

Review 2.  Genetic and developmental defects of the mouse corpus callosum.

Authors:  D Wahlsten
Journal:  Experientia       Date:  1989-09-15

3.  Agenesis of the Corpus Callosum Due to Defective Glial Wedge Formation in Lhx2 Mutant Mice.

Authors:  Gregory A Chinn; Karla E Hirokawa; Tony M Chuang; Cecilia Urbina; Fenil Patel; Jeanette Fong; Nobuo Funatsu; Edwin S Monuki
Journal:  Cereb Cortex       Date:  2014-04-29       Impact factor: 5.357

4.  Partial agenesis of the corpus callosum in spina bifida meningomyelocele and potential compensatory mechanisms.

Authors:  H Julia Hannay; Maureen Dennis; Larry Kramer; Susan Blaser; Jack M Fletcher
Journal:  J Clin Exp Neuropsychol       Date:  2008-12-03       Impact factor: 2.475

5.  Long-distance aberrant heterotopic connectivity in a mouse strain with a high incidence of callosal anomalies.

Authors:  Diego Szczupak; Cirong Liu; Cecil C C Yen; Sang-Ho Choi; Fernanda Meireles; Caroline Victorino; Linda Richards; Roberto Lent; Afonso C Silva; Fernanda Tovar-Moll
Journal:  Neuroimage       Date:  2020-04-23       Impact factor: 6.556

6.  Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis.

Authors:  Diane T Stephenson; Sharon M O'Neill; Sapna Narayan; Aadhya Tiwari; Elizabeth Arnold; Harry D Samaroo; Fu Du; Robert H Ring; Brian Campbell; Mathew Pletcher; Vidita A Vaidya; Daniel Morton
Journal:  Mol Autism       Date:  2011-05-16       Impact factor: 7.509

  6 in total

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