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The Cerebral Surfactant System and Its Alteration in Hydrocephalic Conditions.
Schob, Stefan; Lobsien, Donald; Friedrich, Benjamin; Bernhard, Matthias K; Gebauer, Corinna; Dieckow, Julia; Gawlitza, Matthias; Pirlich, Mandy; Saur, Dorothee; Bräuer, Lars; Bechmann, Ingo; Hoffmann, Karl-Titus; Mahr, Cynthia V; Nestler, Ulf; Preuß, Matthias.
Afiliação
  • Schob S; Department of Neuroradiology, University Leipzig, Germany.
  • Lobsien D; Department of Neuroradiology, University Leipzig, Germany.
  • Friedrich B; Department of Diagnostic and Interventional Radiology, University Leipzig, Germany.
  • Bernhard MK; Division of Neuropediatrics, University Leipzig, Germany.
  • Gebauer C; Department of Neonatology, University Leipzig, Germany.
  • Dieckow J; Department of Ophthalmology, University Leipzig, Germany.
  • Gawlitza M; Department of Neuroradiology, University Leipzig, Germany.
  • Pirlich M; Department of Neurology, University Leipzig, Germany.
  • Saur D; Department of Neurology, University Leipzig, Germany.
  • Bräuer L; Institute of Anatomy, University of Erlangen-Nuremberg, Germany.
  • Bechmann I; Institute of Anatomy, University Leipzig, Germany.
  • Hoffmann KT; Department of Neuroradiology, University Leipzig, Germany.
  • Mahr CV; Department of Neurosurgery, University Leipzig, Germany.
  • Nestler U; Department of Neurosurgery, University Leipzig, Germany.
  • Preuß M; Department of Neurosurgery, University Leipzig, Germany.
PLoS One ; 11(9): e0160680, 2016.
Article em En | MEDLINE | ID: mdl-27656877
ABSTRACT

INTRODUCTION:

Pulmonary Surfactant reduces surface tension in the terminal airways thus facilitating breathing and contributes to host's innate immunity. Surfactant Proteins (SP) A, B, C and D were recently identified as inherent proteins of the CNS. Aim of the study was to investigate cerebrospinal fluid (CSF) SP levels in hydrocephalus patients compared to normal subjects. PATIENTS AND

METHODS:

CSF SP A-D levels were quantified using commercially available ELISA kits in 126 patients (0-84 years, mean 39 years). 60 patients without CNS pathologies served as a control group. Hydrocephalus patients were separated in aqueductal stenosis (AQS, n = 24), acute hydrocephalus without aqueductal stenosis (acute HC w/o AQS, n = 16) and idiopathic normal pressure hydrocephalus (NPH, n = 20). Furthermore, six patients with pseudotumor cerebri were investigated.

RESULTS:

SP A-D are present under physiological conditions in human CSF. SP-A is elevated in diseases accompanied by ventricular enlargement (AQS, acute HC w/o AQS) in a significant manner (0.67, 1.21 vs 0.38 ng/ml in control, p<0.001). SP-C is also elevated in hydrocephalic conditions (AQS, acute HC w/o AQS; 0.87, 1.71 vs. 0.48 ng/ml in controls, p<0.001) and in Pseudotumor cerebri (1.26 vs. 0.48 ng/ml in controls, p<0.01). SP-B and SP-D did not show significant alterations.

CONCLUSION:

The present study confirms the presence of SPs in human CSF. There are significant changes of SP-A and SP-C levels in diseases affecting brain water circulation and elevation of intracranial pressure. Cause of the alterations, underlying regulatory mechanisms, as well as diagnostic and therapeutic consequences of cerebral SP's requires further thorough investigations.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha