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Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats

BACKGROUND: The objective of this study was to develop a simple and inexpensive animal model of induced obstructive hydrocephalus with minimal tissue inflammation, as an alternative to kaolin injection. MATERIALS: Two-hundred and two male Sprague-Dawley rats aged 3 weeks received intracisternal inje...

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Autores principales: Slobodian, Ili, Krassioukov-Enns, Dmitri, Del Bigio, Marc R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2045091/
https://www.ncbi.nlm.nih.gov/pubmed/17894867
http://dx.doi.org/10.1186/1743-8454-4-9
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author Slobodian, Ili
Krassioukov-Enns, Dmitri
Del Bigio, Marc R
author_facet Slobodian, Ili
Krassioukov-Enns, Dmitri
Del Bigio, Marc R
author_sort Slobodian, Ili
collection PubMed
description BACKGROUND: The objective of this study was to develop a simple and inexpensive animal model of induced obstructive hydrocephalus with minimal tissue inflammation, as an alternative to kaolin injection. MATERIALS: Two-hundred and two male Sprague-Dawley rats aged 3 weeks received intracisternal injections of kaolin (25% suspension), Matrigel, type 1 collagen from rat tail, fibrin glue (Tisseel), n-butyl-cyanoacrylate (NBCA), or ethylene vinyl alcohol copolymer (Onyx-18 and Onyx-34). Magnetic resonance imaging was used to assess ventricle size. Animals were euthanized at 2, 5, 10 and 14 days post-injection for histological analysis. RESULTS: Kaolin was associated with 10% mortality and successful induction of hydrocephalus in 97% of survivors (ventricle area proportion 0.168 ± 0.018). Rapidly hardening agents (fibrin glue, NBCA, vinyl polymer) had high mortality rates and low success rates in survivors. Only Matrigel had relatively low mortality (17%) and moderate success rate (20%). An inflammatory response with macrophages and some lymphocytes was associated with kaolin. There was negligible inflammation associated with Matrigel. A severe inflammatory response with giant cell formation was associated with ethylene vinyl alcohol copolymer. CONCLUSION: Kaolin predictably produces moderate to severe hydrocephalus with a mild chronic inflammatory reaction and fibrosis of the leptomeninges. Other synthetic polymers and biopolymers tested are unreliable and cause different types of inflammation.
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spelling pubmed-20450912007-10-30 Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats Slobodian, Ili Krassioukov-Enns, Dmitri Del Bigio, Marc R Cerebrospinal Fluid Res Research BACKGROUND: The objective of this study was to develop a simple and inexpensive animal model of induced obstructive hydrocephalus with minimal tissue inflammation, as an alternative to kaolin injection. MATERIALS: Two-hundred and two male Sprague-Dawley rats aged 3 weeks received intracisternal injections of kaolin (25% suspension), Matrigel, type 1 collagen from rat tail, fibrin glue (Tisseel), n-butyl-cyanoacrylate (NBCA), or ethylene vinyl alcohol copolymer (Onyx-18 and Onyx-34). Magnetic resonance imaging was used to assess ventricle size. Animals were euthanized at 2, 5, 10 and 14 days post-injection for histological analysis. RESULTS: Kaolin was associated with 10% mortality and successful induction of hydrocephalus in 97% of survivors (ventricle area proportion 0.168 ± 0.018). Rapidly hardening agents (fibrin glue, NBCA, vinyl polymer) had high mortality rates and low success rates in survivors. Only Matrigel had relatively low mortality (17%) and moderate success rate (20%). An inflammatory response with macrophages and some lymphocytes was associated with kaolin. There was negligible inflammation associated with Matrigel. A severe inflammatory response with giant cell formation was associated with ethylene vinyl alcohol copolymer. CONCLUSION: Kaolin predictably produces moderate to severe hydrocephalus with a mild chronic inflammatory reaction and fibrosis of the leptomeninges. Other synthetic polymers and biopolymers tested are unreliable and cause different types of inflammation. BioMed Central 2007-09-25 /pmc/articles/PMC2045091/ /pubmed/17894867 http://dx.doi.org/10.1186/1743-8454-4-9 Text en Copyright © 2007 Slobodian et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Slobodian, Ili
Krassioukov-Enns, Dmitri
Del Bigio, Marc R
Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
title Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
title_full Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
title_fullStr Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
title_full_unstemmed Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
title_short Protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
title_sort protein and synthetic polymer injection for induction of obstructive hydrocephalus in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2045091/
https://www.ncbi.nlm.nih.gov/pubmed/17894867
http://dx.doi.org/10.1186/1743-8454-4-9
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