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Effects of pituitary adenylate cyclase activating polypeptide in a rat model of traumatic brain injury

Farkas, Orsolya (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary
Tamás, Andrea (författare)
Department of Anatomy, University of Pécs, Medical Faculty, Pécs, Hungary
Zsombok, Andrea (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary; Dept. of Ctrl. Lab. of Anim. Res., University of Pécs, Medical Faculty, Hungary
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Reglődi, Dóra (författare)
Department of Anatomy, University of Pécs, Medical Faculty, Pécs, Hungary
Pál, József (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary
Büki, Andras, 1966- (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary
Lengvári, István (författare)
Department of Anatomy, University of Pécs, Medical Faculty, Pécs, Hungary
Povlishock, John T. (författare)
Dept. of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, United States
Dóczi, Tamás (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary
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 (creator_code:org_t)
Elsevier, 2004
2004
Engelska.
Ingår i: Regulatory Peptides. - : Elsevier. - 0167-0115 .- 1873-1686. ; 123:1-3, s. 69-75
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Pituitary adenylate cyclase activating polypeptide (PACAP) is a widely distributed neuropeptide that has numerous different actions. Recent studies have shown that PACAP exerts neuroprotective effects not only in vitro but also in vivo, in animal models of global and focal cerebral ischemia, Parkinson's disease and axonal injuries. Traumatic brain injury has an increasing mortality and morbidity and it evokes diffuse axonal injury which further contributes to its damaging effects. The aim of the present study was to examine the possible neuroprotective effect of PACAP in a rat model of diffuse axonal injury induced by impact acceleration. Axonal damage was assessed by immunohistochemistry using an antiserum against beta-amyloid precursor protein, a marker of altered axoplasmic transport considered as key feature in axonal injury. In these experiments, we have established the dose response curves for PACAP administration in traumatic axonal injury, demonstrating that a single post-injury intracerebroventricular injection of 100 microg PACAP significantly reduced the density of damaged, beta-amyloid precursor protein-immunoreactive axons in the corticospinal tract. 

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

Neuroprotection
traumatic brain injury
beta-amyloid precursor protein
corticospinal tract
traumatic axonal injury

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