Cargando…

Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure

BACKGROUND: AF-16 is a 16-amino-acid-long peptide derived from the amino-terminal part of the endogenous protein, antisecretory factor (AF). AF-16 in vivo has been shown to regulate dysfunctions in the water and ion transport system under various pathological conditions and also to counteract experi...

Descripción completa

Detalles Bibliográficos
Autores principales: Al-Olama, Mohamed, Lange, Stefan, Lönnroth, Ivar, Gatzinsky, Kliment, Jennische, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281356/
https://www.ncbi.nlm.nih.gov/pubmed/25248325
http://dx.doi.org/10.1007/s00701-014-2221-7
_version_ 1782350981157093376
author Al-Olama, Mohamed
Lange, Stefan
Lönnroth, Ivar
Gatzinsky, Kliment
Jennische, Eva
author_facet Al-Olama, Mohamed
Lange, Stefan
Lönnroth, Ivar
Gatzinsky, Kliment
Jennische, Eva
author_sort Al-Olama, Mohamed
collection PubMed
description BACKGROUND: AF-16 is a 16-amino-acid-long peptide derived from the amino-terminal part of the endogenous protein, antisecretory factor (AF). AF-16 in vivo has been shown to regulate dysfunctions in the water and ion transport system under various pathological conditions and also to counteract experimentally increased tissue pressure. METHODS: Rats were subjected to a cryogenic brain injury in order to increase the intracranial pressure (ICP). The distribution of AF-16 in blood and CSF after intravenous or intranasal administration was determined in injured and control rats. ICP was monitored in freely moving, awake rats, by means of an epidural pressure transducer catheter connected to a wireless device placed subcutaneously on the skull. The continuous ICP registrations were achieved by means of telemetry. RESULTS: Intranasal administration of AF-16 resulted in a significantly higher CSF concentrations of AF-16 in injured than in control rats, 1.3 versus 0.6 ng/ml, whereas no difference between injured and control rats was seen when AF-16 was given intravenously. Rats subjected to cryogenic brain injury developed gradually increasing ICP levels. Intranasal administration of AF-16 suppressed the increased ICP to normal values within 30 min. CONCLUSION: Optimal AF-16 concentrations in CSF are achieved after intranasal administration in rats subjected to a cryogenic brain injury. The ability of AF-16 to suppress an increased ICP was manifested.
format Online
Article
Text
id pubmed-4281356
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Springer Vienna
record_format MEDLINE/PubMed
spelling pubmed-42813562015-01-05 Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure Al-Olama, Mohamed Lange, Stefan Lönnroth, Ivar Gatzinsky, Kliment Jennische, Eva Acta Neurochir (Wien) Experimental Research - Brain Injury BACKGROUND: AF-16 is a 16-amino-acid-long peptide derived from the amino-terminal part of the endogenous protein, antisecretory factor (AF). AF-16 in vivo has been shown to regulate dysfunctions in the water and ion transport system under various pathological conditions and also to counteract experimentally increased tissue pressure. METHODS: Rats were subjected to a cryogenic brain injury in order to increase the intracranial pressure (ICP). The distribution of AF-16 in blood and CSF after intravenous or intranasal administration was determined in injured and control rats. ICP was monitored in freely moving, awake rats, by means of an epidural pressure transducer catheter connected to a wireless device placed subcutaneously on the skull. The continuous ICP registrations were achieved by means of telemetry. RESULTS: Intranasal administration of AF-16 resulted in a significantly higher CSF concentrations of AF-16 in injured than in control rats, 1.3 versus 0.6 ng/ml, whereas no difference between injured and control rats was seen when AF-16 was given intravenously. Rats subjected to cryogenic brain injury developed gradually increasing ICP levels. Intranasal administration of AF-16 suppressed the increased ICP to normal values within 30 min. CONCLUSION: Optimal AF-16 concentrations in CSF are achieved after intranasal administration in rats subjected to a cryogenic brain injury. The ability of AF-16 to suppress an increased ICP was manifested. Springer Vienna 2014-09-24 2015 /pmc/articles/PMC4281356/ /pubmed/25248325 http://dx.doi.org/10.1007/s00701-014-2221-7 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Experimental Research - Brain Injury
Al-Olama, Mohamed
Lange, Stefan
Lönnroth, Ivar
Gatzinsky, Kliment
Jennische, Eva
Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
title Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
title_full Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
title_fullStr Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
title_full_unstemmed Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
title_short Uptake of the antisecretory factor peptide AF-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
title_sort uptake of the antisecretory factor peptide af-16 in rat blood and cerebrospinal fluid and effects on elevated intracranial pressure
topic Experimental Research - Brain Injury
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281356/
https://www.ncbi.nlm.nih.gov/pubmed/25248325
http://dx.doi.org/10.1007/s00701-014-2221-7
work_keys_str_mv AT alolamamohamed uptakeoftheantisecretoryfactorpeptideaf16inratbloodandcerebrospinalfluidandeffectsonelevatedintracranialpressure
AT langestefan uptakeoftheantisecretoryfactorpeptideaf16inratbloodandcerebrospinalfluidandeffectsonelevatedintracranialpressure
AT lonnrothivar uptakeoftheantisecretoryfactorpeptideaf16inratbloodandcerebrospinalfluidandeffectsonelevatedintracranialpressure
AT gatzinskykliment uptakeoftheantisecretoryfactorpeptideaf16inratbloodandcerebrospinalfluidandeffectsonelevatedintracranialpressure
AT jennischeeva uptakeoftheantisecretoryfactorpeptideaf16inratbloodandcerebrospinalfluidandeffectsonelevatedintracranialpressure