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  • Czeiter, EndreDepartment of Neurosurgery, University of Pécs, Pécs, Hungary (author)

Calpain inhibition reduces axolemmal leakage in traumatic axonal injury

  • Article/chapterEnglish2009

Publisher, publication year, extent ...

  • 2009-12-09
  • MDPI,2009
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:oru-113422
  • https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-113422URI
  • https://doi.org/10.3390/molecules14125115DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • This study was supported by the Hungarian Science Founds (OTKA T048724; OTKA PD 72240) and the Békésy Scholarship of the Hungarian Academy of Sciences.
  • Calcium-induced, calpain-mediated proteolysis (CMSP) has recently been implicated to the pathogenesis of diffuse (traumatic) axonal injury (TAI). Some studies suggested that subaxolemmal CMSP may contribute to axolemmal permeability (AP) alterations observed in TAI. Seeking direct evidence for this premise we investigated whether subaxolemmal CMSP may contribute to axolemmal permeability alterations (APA) and pre-injury calpain-inhibition could reduce AP in a rat model of TAI. Horseradish peroxidase (HRP, a tracer that accumulates in axons with APA) was administered one hour prior to injury into the lateral ventricle; 30 min preinjury a single tail vein bolus injection of 30 mg/kg MDL-28170 (a calpain inhibitor) or its vehicle was applied in Wistar rats exposed to impact acceleration brain injury. Histological detection of traumatically injured axonal segments accumulating HRP and statistical analysis revealed that pre-injury administration of the calpain inhibitor MDL-28170 significantly reduced the average length of HRP-labeled axonal segments. The axono-protective effect of pre-injury calpain inhibition recently demonstrated with classical immunohistochemical markers of TAI was further corroborated in this experiment; significant reduction of the length of labeled axons in the drug-treated rats implicate CMSP in the progression of altered AP in TAI. 

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Büki, Andras,1966-Department of Neurosurgery, University of Pécs, Pécs, Hungary(Swepub:oru)asbi (author)
  • Bukovics, PéterDepartment of Neurosurgery, University of Pécs, Pécs, Hungary (author)
  • Farkas, OrsolyaDepartment of Neurosurgery, University of Pécs, Pécs, Hungary (author)
  • Pál, JózsefDepartment of Neurosurgery, University of Pécs, Pécs, Hungary (author)
  • Kövesdi, ErzsébetDepartment of Neurosurgery, University of Pécs, Pécs, Hungary (author)
  • Dóczi, TamásDepartment of Neurosurgery, University of Pécs, Pécs, Hungary (author)
  • Sándor, JánosDepartment of Public Health, Institute of Applied Health Sciences, University of Pécs, Pécs, Hungary (author)
  • Department of Neurosurgery, University of Pécs, Pécs, HungaryDepartment of Public Health, Institute of Applied Health Sciences, University of Pécs, Pécs, Hungary (creator_code:org_t)

Related titles

  • In:Molecules: MDPI14:12, s. 5115-51231431-51571420-3049

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