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Postinjury administration of pituitary adenylate cyclase activating polypeptide (PACAP) attenuates traumatically induced axonal injury in rats

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; Department of Central Laboratory of Animal Research, University of Pécs, Medical Faculty, Pécs, Hungary
Farkas, Orsolya (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary
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Reglödi, Dóra (författare)
Department of Anatomy, University of Pécs, Medical Faculty, Pécs, Hungary
Pál, József (författare)
Department of Neurosurgery, Universit of Pécs, Medical Faculty, Pécs, Hungary; Clinical Neuroscience Research Group of the Hungarian Academy of Sciences, Department of Neurosurgery, University of Pécs, 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)
Department of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, Virginia, USA
Dóczi, Tamás (författare)
Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary; Clinical Neuroscience Research Group of the Hungarian Academy of Sciences, Department of Neurosurgery, University of Pécs, Medical Faculty, Pécs, Hungary
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 (creator_code:org_t)
Mary Ann Liebert, 2006
2006
Engelska.
Ingår i: Journal of Neurotrauma. - : Mary Ann Liebert. - 0897-7151 .- 1557-9042. ; 23:5, s. 686-695
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Pituitary adenylate cyclase activating polypeptide (PACAP) has several different actions in the nervous system. Numerous studies have shown its neuroprotective effects both in vitro and in vivo. Previously, it has been demonstrated that PACAP reduces brain damage in rat models of global and focal cerebral ischemia. Based on the protective effects of PACAP in cerebral ischemia and the presence of common pathogenic mechanisms in cerebral ischemia and traumatic brain injury (TBI), the aim of the present study was to investigate the possible protective effect of PACAP administered 30 min or 1 h postinjury in a rat model of diffuse axonal injury. Adult Wistar male rats were subjected to impact acceleration, and PACAP was administered intracerebroventricularly 30 min (n = 4), and 1 h after the injury (n = 5). Control animals received the same volume of vehicle at both time-points (n = 5). Two hours after the injury, brains were processed for immunohistochemical localization of damaged axonal profiles displaying either beta-amyloid precursor protein (beta-APP) or RMO-14 immunoreactivity, both considered markers of specific features of traumatic axonal injury. Our results show that treatment with PACAP (100 microg) 30 min or 1 h after the induction of TBI resulted in a significant reduction of the density of beta-APP-immunopositive axon profiles in the corticospinal tract (CSpT). There was no significant difference between the density of beta-APP-immunopositive axons in the medial longitudinal fascicle (MLF). PACAP treatment did not result in significantly different number of RMO-14-immunopositive axonal profiles in either brain areas 2 hours post-injury compared to normal animals. While the results of this study highlighted the complexity of the pathogenesis and manifestation of diffuse axonal injury, they also indicate that PACAP should be considered a potential therapeutic agent in TBI. 

Ämnesord

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

Nyckelord

B-amyloid precursor protein
corticospinal tract
neuroprotection
PACAP
traumatic braininjury

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