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Biomedical subjects

L Iwanowski

Publications and source records attributed to L Iwanowski.

At least 37 records · Page 2Linked to original sources

Ultrastructural cytochemical studies of cerebral microvasculature in scrapie infected mice.

Alkaline phosphatase, 5'-nucleotidase nucleoside diphosphatase and thiamine pyrophosphatase activities were studied by cytochemical method applied to electron microscopy of brain microvasculature in normal and scrapie infected mice. In control mice, the major location of all phosphatases studied was the luminal plasma membrane of the endothelial cells. In scrapie infected mice, changes in activity and distribution of the above mentioned phosphatases manifested themselves in the appearance of the reaction product on the abluminal side of the vessel wall. Our data presents evidence that following scrapie infection, these enzymes change their specific localization along the endothelial cell membranes. These enzymatic changes may serve as useful indicators of some alterations in the mammalian blood-brain barrier following infection by scrapie agent in the mouse.

Alkaline Phosphatase↗

New ultrastructural evidence for a protein transport system in endothelial cells of gerbil brains.

Pathways for transfer of horseradish peroxidase (HRP) across the cerebral microvasculature were studied in Mongolian gerbils after inducing either unilateral carotid-artery ligation or intracarotid air embolism. Electron microscopy on samples from both ipsilateral and contralateral brain hemispheres showed the reaction product (HRP) in the endothelial cytoplasm of capillaries and arteriols in all animals; in the basal lamina, HRP was seen only after long (3--4 h) ischemic periods. HRP was seen within both spherical and tubular structures, with the latter appearing in obliquely or longitudinally sectioned blood vessels. These endothelial channel-like structures are part of a tubulovesicular network which seemingly exists in the normal endothelium of the gerbil brain. The tubules serve as pathways for proteins into the brain; protein transfer becomes enhanced following circulatory injuries such as ischemia.

Animals↗

[Amyotrophic lateral sclerosis].

The literature on amyotrophic lateral sclerosis from the years 1995/96 is reviewed including the topics of the World Congress of Neurology in Buenos Aires in September 1997. The problems of a) changed criteria of diagnosis and course of SLA after the time of the first definitions by classical neurological authors, b) the concepts concerning the aetiology and mechanisms of the disease, c) the present studies on drugs and their tentative clinical applications are discussed.

Amyotrophic Lateral Sclerosis↗

[Case of multiple sclerosis with Devic's syndrome and secondary cerebellar signs].

The authors describe a 43-year-old woman treated for multiple sclerosis during 11 years in whom at the end of her life tetraplegia, bulbar syndrome and cerebellar syndrome developed. Postmortem examination of the brain disclosed changes compatible with the diagnosis of multiple sclerosis, diffuse sclerosis and neuromyelitis optica. The variability of the demyelinating process is discussed. In this case this variability was responsible for successive appearance of various nosological entities depending on the "balance of power" between the factors damaging myelin and the resistance of the organism.

Adult↗