Literature DB >> 2432749

Extensive intraneuronal spread of horseradish peroxidase from a focus of vasogenic edema into remote areas of central nervous system. Observations on mouse central nervous system subjected to cortical cold injury.

C Tengvar.   

Abstract

A study was made of the uptake of horseradish peroxidase (HRP) into neurons from a cryogenic cortical lesion in the mouse brain associated with vasogenic edema, following intravenous administration of the tracer. Particular emphasis was placed on the axonal spread of HRP from the primary lesion to other areas of the central nervous system. The distribution of HRP was studied by light microscopy, using highly sensitive histochemical methods, 3-144 h after the onset of the injury. Extravasated HRP was taken up into nerve cell bodies in and around the primary lesion, forming different patterns of labelling: (1) granular, (2) diffuse, and (3) a combination of granular and diffuse staining. Granularity is considered to be the result of HRP accumulation in lysosomes occurring in undamaged or slightly damaged nerve cells, whereas the diffuse, non-granular pattern presumably occurs in severely damaged neurons. Nerve cell bodies containing HRP reaction product were also found in the contralateral cortex, ipsilateral thalamus, substantia nigra, amygdala and ventral tegmental area, presumably a consequence of retrograde axonal transport of the tracer from the primary injury. HRP-containing axons were present in the corpus callosum and in the pyramidal tract of the injured hemisphere all the way down to the cervical spinal cord. Labelling of axonal terminals and preterminal axons in the ipsilateral thalamus, entopeduncular nucleus, subthalamic nucleus, substantia nigra and pons indicated anterograde transport of HRP to these regions. Thus very extensive intraneuronal spread of a macromolecular edema component takes place from a primary focal brain lesion to areas located far away from but neuroanatomically connected to this injured region. The brain thus seems to be affected by focal vasogenic edema in many more ways than are recognized at present.

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Year:  1986        PMID: 2432749     DOI: 10.1007/bf00688038

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  32 in total

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Journal:  J Histochem Cytochem       Date:  1966-04       Impact factor: 2.479

6.  Uptake of macromolecules into neurons from a focal vasogenic cerebral edema and subsequent axonal spread to other brain regions. A preliminary study in the mouse with horseradish peroxidase as a tracer.

Authors:  C Tengvar; Y Olsson
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

7.  Chronological sequences and blood-brain barrier permeability changes in local injury as assessed by nuclear magnetic resonance (NMR) images from sliced rat brain.

Authors:  R Asato; H Handa; T Hashi; J Hatta; M Komoike; T Yazaki
Journal:  Stroke       Date:  1983 Mar-Apr       Impact factor: 7.914

8.  An improved Percoll density gradient for measurements of experimental brain edema. Addition of sucrose to an isotonic gradient in an attempt to balance osmotic conditions during density determinations.

Authors:  C Tengvar; D Hultström; Y Olsson
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

9.  Dynamics of cerebral edema. The role of an intact vascular bed in the production and propagation of vasogenic brain edema.

Authors:  B Aarabi; D M Long
Journal:  J Neurosurg       Date:  1979-12       Impact factor: 5.115

10.  Evaluation of the dye-protein tracers in pathophysiology of the blood-brain barrier.

Authors:  M Wolman; I Klatzo; E Chui; F Wilmes; K Nishimoto; K Fujiwara; M Spatz
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

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  6 in total

1.  Uptake of plasma proteins into damaged neurons. An experimental study on cryogenic lesions in rats.

Authors:  E M Løberg; A Torvik
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

2.  Effects of the noradrenaline neurotoxin N-2-chloroethyl-N-ethyl-2-bromo-benzylamine hydrochloride (DSP4) on the blood-brain barrier. An experimental study in the mouse using protein tracer and density determination techniques.

Authors:  C Tengvar; C A Pettersson; A K Mohammed; Y Olsson
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

3.  An immunocytochemical study of protein clearance in brain infusion edema.

Authors:  K Ohata; A Marmarou; J T Povlishock
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

4.  Cerebrovascular permeability and brain edema after cortical photochemical infarcts in the rat.

Authors:  H Laursen; A J Hansen; M Sheardown
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

Review 5.  Observations on exsudation of fibronectin, fibrinogen and albumin in the brain after carotid infusion of hyperosmolar solutions. An immunohistochemical study in the rat indicating longlasting changes in the brain microenvironment and multifocal nerve cell injuries.

Authors:  T S Salahuddin; H Kalimo; B B Johansson; Y Olsson
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

6.  The relationship between plasma protein extravasation and remote tissue changes after experimental brain infarction.

Authors:  C Nordborg; T E Sokrab; B B Johansson
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

  6 in total

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