Literature DB >> 12854754

Poly(adenosine diphosphate-ribose) polymerase expression in human traumatic brain injury.

Beng Ti Ang1, Elgin Yap, Joyce Lim, Wan Loo Tan, Puay Yong Ng, Ivan Ng, Tseng Tsai Yeo.   

Abstract

OBJECT: This study was designed to elucidate the pattern of expression of poly(adenosine diphosphate-ribose) polymerase (PARP) in human pericontusional brain tissue and to correlate these findings with commonly used clinical parameters.
METHODS: The expression of PARP was ascertained using immunohistochemical studies in eight specimens of human pericontusional brain tissue obtained when the patients underwent craniotomy for mass effect. The following demographic and clinical parameters were also analyzed for each patient: age, sex, postresuscitation Glasgow Coma Scale score (GCS), computerized tomography findings, intracranial pressure (ICP) recordings during the first 24 hours postsurgery, and the time interval from injury to surgery. The authors observed that PARP was present in neurons of pericontusional tissue and that it conformed to two patterns of subcellular localization; it was found either in the nucleus exclusively or in both nuclear and cytoplasmic compartments. They showed that a preponderance of cytoplasmic staining in neurons was significantly correlated with a short time interval from trauma to surgery (< or = 4 hours). There was no correlation, however, between the subcellular distribution of PARP and clinical parameters such as admission GCS score and ICP readings obtained intra- and postoperatively.
CONCLUSIONS: As in earlier studies in which it has been suggested that caspase-cleaved PARP translocates to the cytoplasm during apoptosis, the authors' results indicate that apoptosis may predominate in the initial time frame after head injury. This information may well influence the timing of administration of antiapoptotic neuronal salvage agents for adjunctive therapy of head injury in the future.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12854754     DOI: 10.3171/jns.2003.99.1.0125

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  11 in total

1.  Incretin Mimetics as Rational Candidates for the Treatment of Traumatic Brain Injury.

Authors:  Elliot J Glotfelty; Thomas Delgado; Luis B Tovar-Y-Romo; Yu Luo; Barry Hoffer; Lars Olson; Tobias Karlsson; Mark P Mattson; Brandon Harvey; David Tweedie; Yazhou Li; Nigel H Greig
Journal:  ACS Pharmacol Transl Sci       Date:  2019-02-11

2.  Brain energy depletion in a rodent model of diffuse traumatic brain injury is not prevented with administration of sodium lactate.

Authors:  Ruth Prieto; Barbara Tavazzi; Keisuke Taya; Laura Barrios; Angela M Amorini; Valentina Di Pietro; José M Pascual; Anthony Marmarou; Christina R Marmarou
Journal:  Brain Res       Date:  2011-06-12       Impact factor: 3.252

3.  Traumatic Brain Injury-Induced Neuronal Apoptosis is Reduced Through Modulation of PI3K and Autophagy Pathways in Mouse by FTY720.

Authors:  Li Zhang; Ke Ding; Handong Wang; Yong Wu; Jianguo Xu
Journal:  Cell Mol Neurobiol       Date:  2015-06-23       Impact factor: 5.046

4.  Neuronal and glial apoptosis in human traumatic brain injury.

Authors:  J Dressler; U Hanisch; E Kuhlisch; K D Geiger
Journal:  Int J Legal Med       Date:  2006-11-15       Impact factor: 2.686

Review 5.  Role of the peroxynitrite-poly(ADP-ribose) polymerase pathway in human disease.

Authors:  Pal Pacher; Csaba Szabo
Journal:  Am J Pathol       Date:  2008-06-05       Impact factor: 4.307

Review 6.  Drug targets for traumatic brain injury from poly(ADP-ribose)polymerase pathway modulation.

Authors:  Valerie C Besson
Journal:  Br J Pharmacol       Date:  2009-04-09       Impact factor: 8.739

Review 7.  Bench-to-bedside review: Apoptosis/programmed cell death triggered by traumatic brain injury.

Authors:  Xiaopeng Zhang; Yaming Chen; Larry W Jenkins; Patrick M Kochanek; Robert S B Clark
Journal:  Crit Care       Date:  2004-09-03       Impact factor: 9.097

Review 8.  The role of excitotoxic programmed necrosis in acute brain injury.

Authors:  Denson G Fujikawa
Journal:  Comput Struct Biotechnol J       Date:  2015-03-28       Impact factor: 7.271

9.  Behavior, protein, and dendritic changes after model traumatic brain injury and treatment with nanocoffee particles.

Authors:  Whitney A Ratliff; Jessica N Saykally; Ronald F Mervis; Xiaoyang Lin; Chuanhai Cao; Bruce A Citron
Journal:  BMC Neurosci       Date:  2019-08-22       Impact factor: 3.288

10.  Endoplasmic reticulum stress-induced apoptosis in the penumbra aggravates secondary damage in rats with traumatic brain injury.

Authors:  Guo-Zhu Sun; Fen-Fei Gao; Zong-Mao Zhao; Hai Sun; Wei Xu; Li-Wei Wu; Yong-Chang He
Journal:  Neural Regen Res       Date:  2016-08       Impact factor: 5.135

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.