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Sökning: WFRF:(FINK R) > (2020-2024) > Early Blood–Brain B...

Early Blood–Brain Barrier Impairment as a Pathological Hallmark in a Novel Model of Closed-Head Concussive Brain Injury (CBI) in Mice

Blaschke, Stefan J. (författare)
University Hospital of Cologne,Jülich Research Centre
Rautenberg, Nora (författare)
Jülich Research Centre,University Hospital of Cologne
Endepols, Heike (författare)
University Hospital of Cologne,Jülich Research Centre
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Jendro, Aileen (författare)
University Hospital of Cologne
Konrad, Jens (författare)
Jülich Research Centre
Vlachakis, Susan (författare)
University Hospital of Cologne
Wiedermann, Dirk (författare)
Schroeter, Michael (författare)
Jülich Research Centre,University Hospital of Cologne
Hoffmann, Bernd (författare)
Jülich Research Centre
Merkel, Rudolf (författare)
Jülich Research Centre
Marklund, Niklas (författare)
Lund University,Lunds universitet,Neurokirurgi,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,LUBIN Lab- Lunds laboratorium för neurokirurgisk hjärnskadeforskning,Forskargrupper vid Lunds universitet,Neurosurgery,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine,LUBIN Lab- Lund Brain Injury laboratory for Neurosurgical research,Lund University Research Groups
Fink, Gereon R. (författare)
Jülich Research Centre,University Hospital of Cologne
Rueger, Maria A. (författare)
Jülich Research Centre,University Hospital of Cologne
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 (creator_code:org_t)
2024
2024
Engelska.
Ingår i: International Journal of Molecular Sciences. - 1661-6596. ; 25:9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Concussion, caused by a rotational acceleration/deceleration injury mild enough to avoid structural brain damage, is insufficiently captured in recent preclinical models, hampering the relation of pathophysiological findings on the cellular level to functional and behavioral deficits. We here describe a novel model of unrestrained, single vs. repetitive concussive brain injury (CBI) in male C56Bl/6j mice. Longitudinal behavioral assessments were conducted for up to seven days afterward, alongside the evaluation of structural cerebral integrity by in vivo magnetic resonance imaging (MRI, 9.4 T), and validated ex vivo by histology. Blood–brain barrier (BBB) integrity was analyzed by means of fluorescent dextran- as well as immunoglobulin G (IgG) extravasation, and neuroinflammatory processes were characterized both in vivo by positron emission tomography (PET) using [18F]DPA-714 and ex vivo using immunohistochemistry. While a single CBI resulted in a defined, subacute neuropsychiatric phenotype, longitudinal cognitive testing revealed a marked decrease in spatial cognition, most pronounced in mice subjected to CBI at high frequency (every 48 h). Functional deficits were correlated to a parallel disruption of the BBB, (R2 = 0.29, p < 0.01), even detectable by a significant increase in hippocampal uptake of [18F]DPA-714, which was not due to activation of microglia, as confirmed immunohistochemically. Featuring a mild but widespread disruption of the BBB without evidence of macroscopic damage, this model induces a characteristic neuro-psychiatric phenotype that correlates to the degree of BBB disruption. Based on these findings, the BBB may function as both a biomarker of CBI severity and as a potential treatment target to improve recovery from concussion.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

blood–brain barrier
mice
mild traumatic brain injury
neuroinflammation
PET
repetitive concussion

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