Literature DB >> 35919976

Effect of cilia-induced surface velocity on cerebrospinal fluid exchange in the lateral ventricles.

Haruki Yoshida1, Shunichi Ishida1, Taiki Yamamoto2, Takayuki Ishikawa2, Yuichi Nagata2, Kazuhito Takeuchi2, Hironori Ueno3, Yohsuke Imai1.   

Abstract

Ciliary motility disorders are known to cause hydrocephalus. The instantaneous velocity of cerebrospinal fluid (CSF) flow is dominated by artery pulsation, and it remains unclear why ciliary dysfunction results in hydrocephalus. In this study, we investigated the effects of cilia-induced surface velocity on CSF flow using computational fluid dynamics. A geometric model of the human ventricles was constructed using medical imaging data. The CSF produced by the choroid plexus and cilia-induced surface velocity were given as the velocity boundary conditions at the ventricular walls. We developed healthy and reduced cilia motility models based on experimental data of cilia-induced velocity in healthy wild-type and Dpcd-knockout mice. The results indicate that there is almost no difference in intraventricular pressure between healthy and reduced cilia motility models. Additionally, it was found that newly produced CSF from the choroid plexus did not spread to the anterior and inferior horns of the lateral ventricles in the reduced cilia motility model. These findings suggest that a ciliary motility disorder could delay CSF exchange in the anterior and inferior horns of the lateral ventricles.

Entities:  

Keywords:  cerebrospinal fluid; computational fluid dynamics; hydrocephalus; lattice Boltzmann method

Mesh:

Year:  2022        PMID: 35919976      PMCID: PMC9346361          DOI: 10.1098/rsif.2022.0321

Source DB:  PubMed          Journal:  J R Soc Interface        ISSN: 1742-5662            Impact factor:   4.293


  40 in total

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Journal:  Development       Date:  2005-12       Impact factor: 6.868

7.  Loss of Dishevelleds disrupts planar polarity in ependymal motile cilia and results in hydrocephalus.

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Authors:  Jeffrey J Iliff; Minghuan Wang; Yonghong Liao; Benjamin A Plogg; Weiguo Peng; Georg A Gundersen; Helene Benveniste; G Edward Vates; Rashid Deane; Steven A Goldman; Erlend A Nagelhus; Maiken Nedergaard
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9.  Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.

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10.  Integration of the subarachnoid space and lymphatics: is it time to embrace a new concept of cerebrospinal fluid absorption?

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