Literature DB >> 2735184

Morphological studies on cerebral cortical lesions induced by transient ischemia in Mongolian gerbil--diffuse and peripheral pallor of the neuronal perikarya.

Y Nishikawa1, T Takahashi, A Shimoda.   

Abstract

Unilateral transient cerebral ischemia was produced in Mongolian gerbils by clipping the left common carotid artery for 1 h. About 60% of the gerbils with neurological symptoms had post-ischemic seizures. The majority of those that had seizures died within a few days, and sections of their cerebral cortices contained many dark and shrunken neurons. However, the gerbils that did not have seizures survived without any severe complications. In the cerebral cortex of the latter, the neurons with diffuse or peripheral pallor of the perikarya were seen along with a small number of dark and shrunken neurons. Diffuse pallor occurred within a few hours following ischemia in layers III, V, and VI, and disappeared 1 or 2 days after recirculation. Electron microscopically, these neurons showed dispersion of ribosomes, simple and elongated profiles of rough endoplasmic reticulum (r-ER), clustered vacuoles, and mild to moderate mitochondrial swelling. Occasional net-like tubulomembranous structures, probably derived from r-ER, were observed. On the other hand, peripheral pallor became apparent after 5 days following ischemia, usually involving layer II first and gradually extending to the deeper layers. Concomitantly, the amount of neuropil decreased and the dendrites exhibited tortuosity and irregularity in layer II. Electron microscopically, these neurons showed marked swelling of peripheral perikarya and polyribosomes and organelles were located peripherally to the nuclei. In addition, numerous degenerated axon terminals and distended dendrites were observed around the neurons. These observations indicate that diffuse pallor represents damage directly induced by ischemia and subsequent recirculation, while peripheral pallor is the delayed and remote effect of ischemia, probably due to degeneration of neuronal processes.

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Year:  1989        PMID: 2735184     DOI: 10.1007/bf00687395

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


  32 in total

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Journal:  J Cereb Blood Flow Metab       Date:  1984-06       Impact factor: 6.200

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Authors:  H Kalimo; Y Olsson; L Paljärvi; B Söderfeldt
Journal:  J Cereb Blood Flow Metab       Date:  1982       Impact factor: 6.200

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Journal:  Lab Invest       Date:  1975-12       Impact factor: 5.662

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Authors:  W A Pulsinelli; J B Brierley
Journal:  Stroke       Date:  1979 May-Jun       Impact factor: 7.914

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Journal:  Exp Neurol       Date:  1966-11       Impact factor: 5.330

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Journal:  Acta Neurol Scand       Date:  1984-06       Impact factor: 3.209

9.  Pathogenesis of brain lesions caused by experimental epilepsy. Light- and electron-microscopic changes in the rat cerebral cortex following bicuculline-induced status epilepticus.

Authors:  B Söderfeldt; H Kalimo; Y Olsson; B Siesjö
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

10.  The ultrastructure of "brain death". II. Electron microscopy of feline cortex after complete ischemia.

Authors:  H Kalimo; J H Garcia; Y Kamijyo; J Tanaka; B F Trump
Journal:  Virchows Arch B Cell Pathol       Date:  1977-11-03
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  4 in total

1.  Selective vulnerability in the gerbil hippocampus: morphological changes after 5-min ischemia and long survival times.

Authors:  P Bonnekoh; A Barbier; U Oschlies; K A Hossmann
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

2.  Electron microscopic evidence against apoptosis as the mechanism of neuronal death in global ischemia.

Authors:  F Colbourne; G R Sutherland; R N Auer
Journal:  J Neurosci       Date:  1999-06-01       Impact factor: 6.167

3.  Silver impregnability of ischemia-sensitive neocortical neurons after 15 minutes of cardiac arrest in the dog.

Authors:  I Vanický; M Marsala; J Orendácová; J Marsala
Journal:  Anat Embryol (Berl)       Date:  1992-07

4.  Intraventricular infusion of N-methyl-D-aspartate. 2. Acute neuronal consequences.

Authors:  W D Dietrich; M Halley; O Alonso; M Y Globus; R Busto
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

  4 in total

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