Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.

Niemann-Pick A (NPA) disease is a lysosomal storage disorder (LSD) caused by a deficiency in acid sphingomyelinase (ASM) activity. Previously, we reported that biochemical and functional abnormalities observed in ASM knockout (ASMKO) mice could be partially alleviated by intracerebroventricular (ICV...

Full description

Bibliographic Details
Main Authors: Christopher M Treleaven, Thomas Tamsett, Jonathan A Fidler, Tatyana V Taksir, Seng H Cheng, Lamya S Shihabuddin, James C Dodge
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3026829?pdf=render
id doaj-09ab8261b89c4aec8546dd9f80f7989d
record_format Article
spelling doaj-09ab8261b89c4aec8546dd9f80f7989d2020-11-25T00:07:12ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0161e1631310.1371/journal.pone.0016313Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.Christopher M TreleavenThomas TamsettJonathan A FidlerTatyana V TaksirSeng H ChengLamya S ShihabuddinJames C DodgeNiemann-Pick A (NPA) disease is a lysosomal storage disorder (LSD) caused by a deficiency in acid sphingomyelinase (ASM) activity. Previously, we reported that biochemical and functional abnormalities observed in ASM knockout (ASMKO) mice could be partially alleviated by intracerebroventricular (ICV) infusion of hASM. We now show that this route of delivery also results in widespread enzyme distribution throughout the rat brain and spinal cord. However, enzyme diffusion into CNS parenchyma did not occur in a linear dose-dependent fashion. Moreover, although the levels of hASM detected in the rat CNS were determined to be within the range shown to be therapeutic in ASMKO mice, the absolute amounts represented less than 1% of the total dose administered. Finally, our results also showed that similar levels of enzyme distribution are achieved across rodent species when the dose is normalized to CNS weight as opposed to whole body weight. Collectively, these data suggest that the efficacy observed following ICV delivery of hASM in ASMKO mice could be scaled to CNS of the rat.http://europepmc.org/articles/PMC3026829?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Christopher M Treleaven
Thomas Tamsett
Jonathan A Fidler
Tatyana V Taksir
Seng H Cheng
Lamya S Shihabuddin
James C Dodge
spellingShingle Christopher M Treleaven
Thomas Tamsett
Jonathan A Fidler
Tatyana V Taksir
Seng H Cheng
Lamya S Shihabuddin
James C Dodge
Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.
PLoS ONE
author_facet Christopher M Treleaven
Thomas Tamsett
Jonathan A Fidler
Tatyana V Taksir
Seng H Cheng
Lamya S Shihabuddin
James C Dodge
author_sort Christopher M Treleaven
title Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.
title_short Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.
title_full Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.
title_fullStr Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.
title_full_unstemmed Comparative analysis of acid sphingomyelinase distribution in the CNS of rats and mice following intracerebroventricular delivery.
title_sort comparative analysis of acid sphingomyelinase distribution in the cns of rats and mice following intracerebroventricular delivery.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Niemann-Pick A (NPA) disease is a lysosomal storage disorder (LSD) caused by a deficiency in acid sphingomyelinase (ASM) activity. Previously, we reported that biochemical and functional abnormalities observed in ASM knockout (ASMKO) mice could be partially alleviated by intracerebroventricular (ICV) infusion of hASM. We now show that this route of delivery also results in widespread enzyme distribution throughout the rat brain and spinal cord. However, enzyme diffusion into CNS parenchyma did not occur in a linear dose-dependent fashion. Moreover, although the levels of hASM detected in the rat CNS were determined to be within the range shown to be therapeutic in ASMKO mice, the absolute amounts represented less than 1% of the total dose administered. Finally, our results also showed that similar levels of enzyme distribution are achieved across rodent species when the dose is normalized to CNS weight as opposed to whole body weight. Collectively, these data suggest that the efficacy observed following ICV delivery of hASM in ASMKO mice could be scaled to CNS of the rat.
url http://europepmc.org/articles/PMC3026829?pdf=render
work_keys_str_mv AT christophermtreleaven comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
AT thomastamsett comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
AT jonathanafidler comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
AT tatyanavtaksir comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
AT senghcheng comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
AT lamyasshihabuddin comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
AT jamescdodge comparativeanalysisofacidsphingomyelinasedistributioninthecnsofratsandmicefollowingintracerebroventriculardelivery
_version_ 1725419497221783552