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Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus

BACKGROUND: Popular circulation theory of hydrocephalus assumes that the brain is impermeable to cerebrospinal fluid (CSF), and is therefore incapable of absorbing the CSF accumulating within the ventricles. However, the brain parenchyma is permeable to water due to the presence of specific ion chan...

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Autores principales: Krishnamurthy, Satish, Li, Jie, Schultz, Lonni, McAllister, James P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801660/
https://www.ncbi.nlm.nih.gov/pubmed/20003330
http://dx.doi.org/10.1186/1743-8454-6-16
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author Krishnamurthy, Satish
Li, Jie
Schultz, Lonni
McAllister, James P
author_facet Krishnamurthy, Satish
Li, Jie
Schultz, Lonni
McAllister, James P
author_sort Krishnamurthy, Satish
collection PubMed
description BACKGROUND: Popular circulation theory of hydrocephalus assumes that the brain is impermeable to cerebrospinal fluid (CSF), and is therefore incapable of absorbing the CSF accumulating within the ventricles. However, the brain parenchyma is permeable to water due to the presence of specific ion channels as well as aquaporin channels. Thus, the movement of water into and out of the ventricles may be determined by the osmotic load of the CSF. If osmotic load determines the aqueous content of CSF in this manner, it is reasonable to hypothesize that hydrocephalus may be precipitated by pathologies and/or insults that produce sustained elevations of osmotic content within the ventricles. METHODS: We investigated this hypothesis by manipulating the osmotic content of CSF and assaying the development of hydrocephalus in the rat brain. This was achieved by continuously infusing artificial CSF (negative control; group I), fibroblast growth factor (FGF2) solution (positive control; group II) and hyperosmotic dextran solutions (10 KD and 40 KD as experimental solutions: groups III and IV) for 12 days at 0.5 μL/h. The osmolality of the fluid infused was 307, 664, 337 and 328 mOsm/L in Groups I, II, III and IV, respectively. Magnetic resonance imaging (MRI) was used to evaluate the ventricular volumes. Analysis of variance (ANOVA) with pairwise group comparisons was done to assess the differences in ventricular volumes among the four groups. RESULTS: Group I had no hydrocephalus. Group II, group III and group IV animals exhibited significant enlargement of the ventricles (hydrocephalus) compared to group I. There was no statistically significant difference in the size of the ventricles between groups II, III and IV. None of the animals with hydrocephalus had obstruction of the aqueduct or other parts of CSF pathways on MRI. CONCLUSION: Infusing hyperosmolar solutions of dextran, or FGF into the ventricles chronically, resulted in ventricular enlargement. These solutions increase the osmotic load in the ventricles. Water influx (through the choroid plexus CSF secretion and/or through the brain) into the ventricles to normalize this osmotic gradient results in hydrocephalus. We need to revise the popular theory of how fluid accumulates in the ventricles at least in some forms of hydrocephalus.
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spelling pubmed-28016602010-01-05 Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus Krishnamurthy, Satish Li, Jie Schultz, Lonni McAllister, James P Cerebrospinal Fluid Res Research BACKGROUND: Popular circulation theory of hydrocephalus assumes that the brain is impermeable to cerebrospinal fluid (CSF), and is therefore incapable of absorbing the CSF accumulating within the ventricles. However, the brain parenchyma is permeable to water due to the presence of specific ion channels as well as aquaporin channels. Thus, the movement of water into and out of the ventricles may be determined by the osmotic load of the CSF. If osmotic load determines the aqueous content of CSF in this manner, it is reasonable to hypothesize that hydrocephalus may be precipitated by pathologies and/or insults that produce sustained elevations of osmotic content within the ventricles. METHODS: We investigated this hypothesis by manipulating the osmotic content of CSF and assaying the development of hydrocephalus in the rat brain. This was achieved by continuously infusing artificial CSF (negative control; group I), fibroblast growth factor (FGF2) solution (positive control; group II) and hyperosmotic dextran solutions (10 KD and 40 KD as experimental solutions: groups III and IV) for 12 days at 0.5 μL/h. The osmolality of the fluid infused was 307, 664, 337 and 328 mOsm/L in Groups I, II, III and IV, respectively. Magnetic resonance imaging (MRI) was used to evaluate the ventricular volumes. Analysis of variance (ANOVA) with pairwise group comparisons was done to assess the differences in ventricular volumes among the four groups. RESULTS: Group I had no hydrocephalus. Group II, group III and group IV animals exhibited significant enlargement of the ventricles (hydrocephalus) compared to group I. There was no statistically significant difference in the size of the ventricles between groups II, III and IV. None of the animals with hydrocephalus had obstruction of the aqueduct or other parts of CSF pathways on MRI. CONCLUSION: Infusing hyperosmolar solutions of dextran, or FGF into the ventricles chronically, resulted in ventricular enlargement. These solutions increase the osmotic load in the ventricles. Water influx (through the choroid plexus CSF secretion and/or through the brain) into the ventricles to normalize this osmotic gradient results in hydrocephalus. We need to revise the popular theory of how fluid accumulates in the ventricles at least in some forms of hydrocephalus. BioMed Central 2009-12-11 /pmc/articles/PMC2801660/ /pubmed/20003330 http://dx.doi.org/10.1186/1743-8454-6-16 Text en Copyright ©2009 Krishnamurthy 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
Krishnamurthy, Satish
Li, Jie
Schultz, Lonni
McAllister, James P
Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
title Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
title_full Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
title_fullStr Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
title_full_unstemmed Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
title_short Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
title_sort intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2801660/
https://www.ncbi.nlm.nih.gov/pubmed/20003330
http://dx.doi.org/10.1186/1743-8454-6-16
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