Literature DB >> 9219868

New therapeutic possibility of blocking cytokine-induced neutrophil chemoattractant on transient ischemic brain damage in rats.

Y Yamasaki1, Y Matsuo, J Zagorski, N Matsuura, H Onodera, Y Itoyama, K Kogure.   

Abstract

Earlier we indicated that neutrophilic invasion into cerebral parenchyma is an important step in rat cerebral ischemia-reperfusion injury and the production of chemotactic factors, cytokine-induced neutrophil chemoattractant (CINC) precede the neutrophilic invasion. The aim of the present study was to evaluate the role of CINC production and the therapeutic possibility of blocking CINC activity in the transient ischemic brain damage in rats. Focal transient ischemia was produced by intraluminal occlusion of the right middle cerebral artery for 60 min. An enzyme immunoassay was used to measure the brain concentration of CINC and myeloperoxidase activity in ischemic areas was measured as a marker of neutrophilic accumulation. An immunohistochemical staining technique was used to detect the immunopositive cells for anti-CINC antibody. Further, application of anti-CINC antibody or anti-neutrophil antibody to rats was used to evaluate the role of CINC production. In ischemic areas, CINC production was detected and peaked 12 h after reperfusion, which followed 60 min of ischemia. Intraperitoneal injection of anti-neutrophil antibody 24 h before and immediately after reperfusion significantly reduced the brain water content and partially reduced the CINC production in ischemic areas. Further, immunohistochemical staining showed that anti-CINC antibody was found on the endothelial surface of venules and on parts of neutrophils that had invaded the ischemic area 6 to 24 h after reperfusion. Also, treatment with anti-CINC antibody reduced ischemic edema formation 24 h after reperfusion and the size of infarction areas 7 days after reperfusion. It thus appears that CINC, mainly produced by endothelium activated by factors released from neutrophils, plays an important role in ischemic brain damage. Furthermore, the blocking of CINC activity with antibody suggests an immuno-therapeutic approach to the treatment of stroke patients.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9219868     DOI: 10.1016/s0006-8993(97)00251-5

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  27 in total

1.  Blood-brain barrier pathophysiology in traumatic brain injury.

Authors:  Adam Chodobski; Brian J Zink; Joanna Szmydynger-Chodobska
Journal:  Transl Stroke Res       Date:  2011-12       Impact factor: 6.829

2.  Vasopressin amplifies the production of proinflammatory mediators in traumatic brain injury.

Authors:  Joanna Szmydynger-Chodobska; Leora M Fox; Kirsten M Lynch; Brian J Zink; Adam Chodobski
Journal:  J Neurotrauma       Date:  2010-08       Impact factor: 5.269

Review 3.  Role of chemokines in ischemic neuronal stress.

Authors:  Masabumi Minami; Masamichi Satoh
Journal:  Neuromolecular Med       Date:  2005       Impact factor: 3.843

Review 4.  Mechanisms of ischemic brain damage.

Authors:  Kristian P Doyle; Roger P Simon; Mary P Stenzel-Poore
Journal:  Neuropharmacology       Date:  2008-01-25       Impact factor: 5.250

5.  Shiga toxin 1-induced inflammatory response in lipopolysaccharide-sensitized astrocytes is mediated by endogenous tumor necrosis factor alpha.

Authors:  Verónica I Landoni; Marcelo de Campos-Nebel; Pablo Schierloh; Cecilia Calatayud; Gabriela C Fernandez; M Victoria Ramos; Bárbara Rearte; Marina S Palermo; Martín A Isturiz
Journal:  Infect Immun       Date:  2009-12-14       Impact factor: 3.441

6.  Soluble epoxide hydrolase: regulation by estrogen and role in the inflammatory response to cerebral ischemia.

Authors:  Ines P Koerner; Wenri Zhang; Jian Cheng; Susan Parker; Patricia D Hurn; Nabil J Alkayed
Journal:  Front Biosci       Date:  2008-01-01

7.  Tenoxicam exerts a neuroprotective action after cerebral ischemia in rats.

Authors:  Rita I M Galvão; João P L Diógenes; Graziela C L Maia; Emídio A S Filho; Silvânia M M Vasconcelos; Dalgimar B de Menezes; Geanne M A Cunha; Glauce S B Viana
Journal:  Neurochem Res       Date:  2005-01       Impact factor: 3.996

8.  Activated polymorphonuclear cells promote injury and excitability of dorsal root ganglia neurons.

Authors:  S K Shaw; S A Owolabi; J Bagley; N Morin; E Cheng; B W LeBlanc; M Kim; P Harty; S G Waxman; C Y Saab
Journal:  Exp Neurol       Date:  2007-12-04       Impact factor: 5.330

9.  Interleukin 1beta and interleukin 6 relationship with paediatric head trauma severity and outcome.

Authors:  Antonio Chiaretti; Orazio Genovese; Luigi Aloe; Alessia Antonelli; Marco Piastra; Giancarlo Polidori; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2004-09-29       Impact factor: 1.475

10.  Inflammatory profile of awake function-controlled craniotomy and craniotomy under general anesthesia.

Authors:  Markus Klimek; Jaap W Hol; Stephan Wens; Claudia Heijmans-Antonissen; Sjoerd Niehof; Arnaud J Vincent; Jan Klein; Freek J Zijlstra
Journal:  Mediators Inflamm       Date:  2009-06-08       Impact factor: 4.711

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.