Reducing hemorrhagic complication by dabigatran via neurovascular protection after recanalization with tissue plasminogen activator in ischemic stroke of rat. Issue 1 (4th November 2013)
- Record Type:
- Journal Article
- Title:
- Reducing hemorrhagic complication by dabigatran via neurovascular protection after recanalization with tissue plasminogen activator in ischemic stroke of rat. Issue 1 (4th November 2013)
- Main Title:
- Reducing hemorrhagic complication by dabigatran via neurovascular protection after recanalization with tissue plasminogen activator in ischemic stroke of rat
- Authors:
- Kono, Syoichiro
Deguchi, Kentaro
Omote, Yoshio
Yunoki, Taijun
Yamashita, Toru
Kurata, Tomoko
Ikeda, Yoshio
Abe, Koji - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>This study assesses the risks and benefits of tissue plasminogen activator (tPA) treatment under oral anticoagulation with dabigatran compared with warfarin or vehicle control in transient middle cerebral artery occlusion (tMCAO). After pretreatment with warfarin (0.2 mg/kg/day), dabigatran (20 mg/kg/day), or vehicle (0.5% carboxymethyl cellulose sodium salt) for 7 days, tMCAO was induced for 120 min, followed by reperfusion and tPA (10 mg/kg/10 ml). Clinical parameters, including cerebral infarction volume, hemorrhagic volume, and blood coagulation, were examined. At 24 hr after reperfusion, markers for the neurovascular unit at the peri‐ischemic lesion were immunohistochemically examined in brain sections, and MMP‐9 activity was measured by zymography. Paraparesis and intracerebral hemorrhage volume were significantly improved in the dabigatran‐pretreated group compared with the warfarin‐pretreated group. A marked dissociation between astrocyte foot processes and the basal lamina or pericyte was observed in the warfarin‐pretreated group, which was greatly improved in the dabigatran‐pretreated group. Furthermore, a remarkable activation of MMP‐9 in the ipsilateral warfarin‐pretreated rat brain was greatly reduced in dabigatran‐pretreated rats. The present study reveals that the mechanism of intracerebral hemorrhage with warfarin‐pretreatment plus tPA in ischemic stroke rats is the<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>This study assesses the risks and benefits of tissue plasminogen activator (tPA) treatment under oral anticoagulation with dabigatran compared with warfarin or vehicle control in transient middle cerebral artery occlusion (tMCAO). After pretreatment with warfarin (0.2 mg/kg/day), dabigatran (20 mg/kg/day), or vehicle (0.5% carboxymethyl cellulose sodium salt) for 7 days, tMCAO was induced for 120 min, followed by reperfusion and tPA (10 mg/kg/10 ml). Clinical parameters, including cerebral infarction volume, hemorrhagic volume, and blood coagulation, were examined. At 24 hr after reperfusion, markers for the neurovascular unit at the peri‐ischemic lesion were immunohistochemically examined in brain sections, and MMP‐9 activity was measured by zymography. Paraparesis and intracerebral hemorrhage volume were significantly improved in the dabigatran‐pretreated group compared with the warfarin‐pretreated group. A marked dissociation between astrocyte foot processes and the basal lamina or pericyte was observed in the warfarin‐pretreated group, which was greatly improved in the dabigatran‐pretreated group. Furthermore, a remarkable activation of MMP‐9 in the ipsilateral warfarin‐pretreated rat brain was greatly reduced in dabigatran‐pretreated rats. The present study reveals that the mechanism of intracerebral hemorrhage with warfarin‐pretreatment plus tPA in ischemic stroke rats is the dissociation of the neurovascular unit, including the pericyte. Neurovascular protection by dabigatran, which was first shown in this study, could partially explain the reduction in hemorrhagic complication by dabigatran reported from clinical study. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Journal of neuroscience research. Volume 92:Issue 1(2014:Jan.)
- Journal:
- Journal of neuroscience research
- Issue:
- Volume 92:Issue 1(2014:Jan.)
- Issue Display:
- Volume 92, Issue 1 (2014)
- Year:
- 2014
- Volume:
- 92
- Issue:
- 1
- Issue Sort Value:
- 2014-0092-0001-0000
- Page Start:
- 46
- Page End:
- 53
- Publication Date:
- 2013-11-04
- Subjects:
- Neurobiology -- Periodicals
612 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4547 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/109668564 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jnr.23302 ↗
- Languages:
- English
- ISSNs:
- 0360-4012
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5022.090000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3251.xml