Astrocyte lesions in cerebral cortex and cerebellum of dogs with congenital ortosystemic shunting.


Journal

Journal of veterinary science
ISSN: 1976-555X
Titre abrégé: J Vet Sci
Pays: Korea (South)
ID NLM: 100964185

Informations de publication

Date de publication:
May 2020
Historique:
received: 05 11 2019
revised: 18 03 2020
accepted: 23 03 2020
entrez: 2 6 2020
pubmed: 2 6 2020
medline: 21 10 2020
Statut: ppublish

Résumé

Congenital portosystemic shunt (cPSS) is one of the most common congenital disorders diagnosed in dogs. Hepatic encephalopathy (HE) is a frequent complication in dogs with a cPSS and is a major cause of morbidity and mortality. Despite HE been a major cause of morbidity in dogs with a cPSS, little is known about the cellular changes that occur in the central nervous system of dogs with a cPSS. The objective of this study was to characterise the histological changes in the cerebral cortex and cerebellum of dogs with cPSS with particular emphasis on astrocyte morphology. Eight dogs with a confirmed cPSS were included in the study. Six dogs had substantial numbers of Alzheimer type II astrocytes and all cases had increased immunoreactivity for glial fibrillary acidic protein in the cerebral cortex, even if there were minimal other morphological changes. This study demonstrates that dogs with a cPSS have marked cellular changes in the cerebral cortex and cerebellum. The cellular changes that occur in the cerebral cortex and cerebellum of dogs with spontaneously arising HE are similar to changes which occur in humans with HE, further validating dogs with a cPSS as a good model for human HE.

Sections du résumé

BACKGROUND BACKGROUND
Congenital portosystemic shunt (cPSS) is one of the most common congenital disorders diagnosed in dogs. Hepatic encephalopathy (HE) is a frequent complication in dogs with a cPSS and is a major cause of morbidity and mortality. Despite HE been a major cause of morbidity in dogs with a cPSS, little is known about the cellular changes that occur in the central nervous system of dogs with a cPSS.
OBJECTIVES OBJECTIVE
The objective of this study was to characterise the histological changes in the cerebral cortex and cerebellum of dogs with cPSS with particular emphasis on astrocyte morphology.
METHODS METHODS
Eight dogs with a confirmed cPSS were included in the study.
RESULTS RESULTS
Six dogs had substantial numbers of Alzheimer type II astrocytes and all cases had increased immunoreactivity for glial fibrillary acidic protein in the cerebral cortex, even if there were minimal other morphological changes.
CONCLUSIONS CONCLUSIONS
This study demonstrates that dogs with a cPSS have marked cellular changes in the cerebral cortex and cerebellum. The cellular changes that occur in the cerebral cortex and cerebellum of dogs with spontaneously arising HE are similar to changes which occur in humans with HE, further validating dogs with a cPSS as a good model for human HE.

Identifiants

pubmed: 32476318
pii: 21.e44
doi: 10.4142/jvs.2020.21.e44
pmc: PMC7263922
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e44

Informations de copyright

© 2020 The Korean Society of Veterinary Science.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

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Auteurs

Alun Williams (A)

Department of Veterinary Medicine, University of Cambridge, Cambridge, CB3 0ES, United Kingdom.

Adam Gow (A)

Royal (Dick) School of Veterinary Studies and The Roslin Institute, The University of Edinburgh, Edinburgh, EH25 9RG, United Kingdom.

Scott Kilpatrick (S)

Royal (Dick) School of Veterinary Studies and The Roslin Institute, The University of Edinburgh, Edinburgh, EH25 9RG, United Kingdom.

Mickey Tivers (M)

Bristol Veterinary School, University of Bristol, Bristol, BS40 5DU, United Kingdom.

Vicky Lipscomb (V)

Department of Clinical Sciences and Services, Royal Veterinary College, London, AL97TA, United Kingdom.

Ken Smith (K)

Department of Pathobiology and Population Sciences, Royal Veterinary College, London, AL97TA, United Kingdom.

Michael Oliver Day (MO)

Bristol Veterinary School, University of Bristol, Bristol, BS40 5DU, United Kingdom.

Nick Jeffery (N)

Department of Small Animal Clinical Studies, Texas A&M University, College Station, TX 77843-4474, USA.

Richard John Mellanby (RJ)

Royal (Dick) School of Veterinary Studies and The Roslin Institute, The University of Edinburgh, Edinburgh, EH25 9RG, United Kingdom. Richard.Mellanby@ed.ac.uk.

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Classifications MeSH