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Mol Med Rep ; 11(4): 3009-14, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25523640

ABSTRACT

Hypothermia is an effective neuroprotective treatment for brain injury caused by intracerebral hemorrhage (ICH). It is reported to reduce brain edema and neuronal cell death. Thrombin, a coagulation protease released from blood clots, is critical in brain edema formation following ICH. Protease activated receptor­1 (PAR­1), matrix metalloproteinase­9 (MMP­9) and aquaporin 4 (AQP4) are edema­associated mediators that have been implicated in ICH pathology. In the present study, thrombin was used to induce brain edema in adult male Sprague­Dawley rats. Differences between a focal mild hypothermic group (33±0.5˚C) and a normothermic group (37˚C) were investigated. Following hypothermia, brain water content and blood­brain barrier (BBB) disruption was assessed at 6, 24 and 48 h and subsequently at 3, 5 and 7 days. At the same time, the mRNA and protein expression of PAR­1, MMP­9 and AQP4 were also determined. It was identified that brain water content and BBB disruption increased at 6 h and reached a maximal level at 24 h in the normothermic group. The mRNA and protein expression levels of PAR­1, MMP­9 and AQP4 started to increase at 24 h and reached a maximal level at 48 h. Focal mild hypothermia tended to significantly reduce brain water content, BBB disruption and PAR­1, MMP­9 and AQP expression at 24 and 48 h. The present data suggest that focal mild hypothermia is an effective treatment for edema formation through moderation of the mRNA and protein expression of PAR­1, MMP­9 and AQP4.


Subject(s)
Aquaporin 4/genetics , Brain Edema/genetics , Gene Expression , Hypothermia, Induced , Matrix Metalloproteinase 9/genetics , Receptor, PAR-1/genetics , Animals , Aquaporin 4/metabolism , Blood-Brain Barrier/metabolism , Brain Edema/chemically induced , Brain Edema/metabolism , Brain Edema/therapy , Disease Models, Animal , Male , Matrix Metalloproteinase 9/metabolism , Permeability , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Receptor, PAR-1/metabolism , Thrombin/adverse effects
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