Literature DB >> 452852

Quantitative estimate of pinocytosis in experimental acute hypertension.

S Nag, D M Robertson, H B Dinsdale.   

Abstract

Cerebral cortical arterioles in focal neocortical areas develop increased permeability to plasma proteins and protein tracers in experimental hypertensive encephalopathy. The mechanism underlying this increased permeability has been the subject of several studies. In our previous studies of angiotensin-induced acute hypertension, pinocytosis appeared to be the principal mechanism for the increased blood-brain barrier (BBB) permeability observed. In the present study pinocytotic activity was assessed quantitatively to determine whether enhanced pinocytosis was confined to the permeable arteriolar segments of hypertensive animals. In addition, the effect of horseradish peroxidase (HRP) itself on the pinocytotic activity of normal cerebral cortical arteriolar endothelium was determined. In 12 rats following administration of HRP, hypertension was induced by an infusion of angiotensin. The animals were perfusion-fixed 90 s after the onset of the infusion. Control animals received saline only or HRP only. The area of arteriolar endothelium in cross section was determined by a planimeter from overlapping electron micrographs taken at a constant magnification around the circumference of the vessel wall. Results indicate a significant (P less than 0.001) increase in the number of pinocytotic vesicles in the permeable arteriolar segments of hypertensive animals as compared with nonpermeable arteriolar segments of the same animals and comparable segments of normotensive rats. In addition, eight times as many vesicles appear to be transporting tracer in the permeable arteriolar segments of hypertensive animals as compared to the nonpermeable segments of the same animals and normotensive animals. HRP alone did not affect the pinocytotic index, there being no difference (P greater than 0.05) in the number of vesicles in normotensive animals receiving saline only and those receiving HRP only. Our previous observation that disruption of endothelial cells or their tight junctions did not occur was confirmed.

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Year:  1979        PMID: 452852     DOI: 10.1007/bf00684811

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


  28 in total

1.  Evidence against cerebral vasospasm during acutely induced hypertension.

Authors:  J K Farrar; J V Jones; D I Graham; S Strandgaard; E T MacKenzie
Journal:  Brain Res       Date:  1976-03-05       Impact factor: 3.252

2.  Cerebral blood flow in acute hypertension.

Authors:  H B Dinsdale; D M Robertson; R A Haas
Journal:  Arch Neurol       Date:  1974-08

3.  Resistance of Wistar-Furth rats to the mast cell-damaging effect of horseradish peroxidase.

Authors:  R S Cotran; M J Karnovsky; A Goth
Journal:  J Histochem Cytochem       Date:  1968-05       Impact factor: 2.479

4.  Effects of increased blood pressure on cerebral vessels in mice.

Authors:  W I Rosenblum; H Donnenfeld; F Aleu
Journal:  Arch Neurol       Date:  1966-06

5.  The innervation of the cerebral arteries in the rat: an electron microscope study.

Authors:  D D Samarasinghe
Journal:  J Anat       Date:  1965-10       Impact factor: 2.610

6.  The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique.

Authors:  R C Graham; M J Karnovsky
Journal:  J Histochem Cytochem       Date:  1966-04       Impact factor: 2.479

7.  Arterial hypotension induced by horseradish peroxidase in various rat strains.

Authors:  W Deimann; R Taugner; H D Fahimi
Journal:  J Histochem Cytochem       Date:  1976-12       Impact factor: 2.479

8.  Increased permeability of cerebral vessels to horseradish peroxidase induced by ischemia in Mongolian Gerbils.

Authors:  E Westergaard; G Go; I Klatzo; M Spatz
Journal:  Acta Neuropathol       Date:  1976-08-16       Impact factor: 17.088

9.  The cellular pathology of experimental hypertension. 7. Structure and permeability of the mesenteric vasculature in angiotensin-induced hypertension.

Authors:  J Wiener; F Giacomelli
Journal:  Am J Pathol       Date:  1973-08       Impact factor: 4.307

10.  Increased vesicular transfer of horseradish peroxidase across cerebral endothelium, evoked by acute hypertension.

Authors:  E Westergaard; B van Deurs; H E Brondsted
Journal:  Acta Neuropathol       Date:  1977-02-28       Impact factor: 17.088

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  26 in total

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Review 2.  Pathophysiology of the blood-brain barrier.

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4.  Localisation of calcium-activated adenosine-triphosphatase (Ca2+-ATPase) in intracerebral arterioles in acute hypertension.

Authors:  S Nag
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

5.  Ionic lanthanum passage across cerebral endothelium exposed to hyperosmotic arabinose.

Authors:  K Dorovini-Zis; M Sato; G Goping; S Rapoport; M Brightman
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

6.  The effect of ovariectomy and estrogen on penetrating brain arterioles and blood-brain barrier permeability.

Authors:  Marilyn J Cipolla; Julie A Godfrey; Marchien J Wiegman
Journal:  Microcirculation       Date:  2009-11       Impact factor: 2.628

7.  Effect of an anion transport inhibitor on blood-brain barrier lesions during acute hypertension. Possible prevention of transendothelial vesicular transport.

Authors:  J E Hardebo; B B Johansson
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

8.  Intracerebral arteriolar permeability to lanthanum.

Authors:  S Nag; D M Robertson; H B Dinsdale
Journal:  Am J Pathol       Date:  1982-06       Impact factor: 4.307

9.  Cerebral changes in chronic hypertension: combined permeability and immunohistochemical studies.

Authors:  S Nag
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

10.  Intraventricular infusion of N-methyl-D-aspartate. 1. Acute blood-brain barrier consequences.

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

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