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

被引:38
作者
Farkas, O
Tamás, A
Zsombok, A
Reglödi, D
Pál, J
Büki, A
Lengvári, I
Povlishock, JT
Dóczi, T
机构
[1] Univ Pecs, Hungarian Acad Sci, Neurohumoral Regulat Res Grp, Dept Anat,Med Fac, H-7624 Pecs, Hungary
[2] Univ Pecs, Fac Med, Dept Cent Lab Anim Res, H-7624 Pecs, Hungary
[3] Univ Pecs, Fac Med, Dept Neurosurg, H-7624 Pecs, Hungary
[4] Virginia Commonwealth Univ, Dept Anat & Neurobiol, Richmond, VA USA
基金
美国国家卫生研究院; 匈牙利科学研究基金会;
关键词
neuroprotection; traumatic brain injury; beta-amyloid precursor protein; corticospinal tract; traumatic axonal injury;
D O I
10.1016/j.regpep.2004.05.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 mug PACAP significantly reduced the density of damaged, beta-amyloid precursor protein-immunoreactive axons in the corticospinal tract. (C) 2004 Elsevier B.V All rights reserved.
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页码:69 / 75
页数:7
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