2012
DOI: 10.1016/j.jneuroim.2012.03.019
|View full text |Cite
|
Sign up to set email alerts
|

Increased expression of Toll-like receptors 2 and 4 is associated with poor outcome in intracerebral hemorrhage

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
35
0

Year Published

2013
2013
2019
2019

Publication Types

Select...
7
3

Relationship

0
10

Authors

Journals

citations
Cited by 56 publications
(36 citation statements)
references
References 17 publications
1
35
0
Order By: Relevance
“…In fact, our recent findings have evidenced that TLR4 acts as a neuroprotection agent against neuroinflammatory processes, myelin dysfunctions, and even neurodegeneration (Alfonso-Loeches et al, 2010. Moreover, increased TLR2 and TLR4 expressions have been associated with deprived functional outcome and greater residual volume in the inflammatory response from patients with intracerebral haemorrhage (Rodriguez-Yanez et al, 2012).…”
Section: Discussionmentioning
confidence: 95%
“…In fact, our recent findings have evidenced that TLR4 acts as a neuroprotection agent against neuroinflammatory processes, myelin dysfunctions, and even neurodegeneration (Alfonso-Loeches et al, 2010. Moreover, increased TLR2 and TLR4 expressions have been associated with deprived functional outcome and greater residual volume in the inflammatory response from patients with intracerebral haemorrhage (Rodriguez-Yanez et al, 2012).…”
Section: Discussionmentioning
confidence: 95%
“…Proposed mechanisms include damage to the blood-brain barrier, binding to chemoattractant proteins in cerebral vessels that promotes neuronal death and cell injury, 12 and contribution to cerebral edema. 13 …”
Section: Discussionmentioning
confidence: 99%
“…Treatment with the TLR4 inhibitor ethyl (6R)-6-[N-(2-chloro-4-fluorophenyl) sulfamoyl]-cyclohex-1-ene-1-carboxylate (TAK-242) or genetic deletion of TLR4 in mice decreases inflammation-mediated brain damage and improves neurologic function after ICH [71, 7780]. Recent clinical studies also have shown that increased expression of TLR4 is associated with poorer functional outcome and greater residual volume in ICH patients [81]. Compared with wild-type (WT) mice, TLR4 knockout ( −/− ) mice exhibited less water content and fewer neurologic deficits [71].…”
Section: Microgliamentioning
confidence: 99%