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Thrombolysis with rhPro-UK 3 to 6 hours after embolic stroke in rat.
- Source :
- Neurological Research; Nov2019, Vol. 41 Issue 11, p1034-1042, 9p
- Publication Year :
- 2019
-
Abstract
- Objectives: To investigate the thrombolysis with recombinant human prourokinase (rhPro-UK) on thromboembolic stroke in rats at different therapeutic time windows (TTW). Methods: Rats were subjected to embolic middle cerebral artery occlusion. RhPro-UK and positive control drugs rt-PA,UK were administered 3 h, 4.5 h, 6 h after inducing thromboem-bolic stroke. Neurological deficit scoring (NDS) was evaluated at 6 h and 24 h after the treatment. The lesion volume in cerebral hemispheres was measured by MRI scanning machine after 6 h of thrombolysis, and the infarct volume was measured by TTC stain, together with hemorrhagic volume quantified by a spectrophotometric assay after 24 h of thrombolysis. Results: RhPro-UK 10, 20 × 10<superscript>4</superscript> U/kg significantly improved the NDS after cerebral thromboembolism in rats at 3 h, 4.5 h TTW, and at the 6 h TTW, the NDS was improved by 28.0% (P = 0.0690) and 29.2% (P = 0.0927) at 6 h and 24 h after rhPro-UK 20 ×10<superscript>4</superscript> U/kg administration, respectively. RhPro-UK 10, 20 × 10<superscript>4</superscript> U/kg significantly reduced the brain lesions measured by MRI at 3 h and 4.5 h TTW. RhPro-UK 10, 20 × 10<superscript>4</superscript> U/kg significantly reduced the cerebral infarction measured by TTC at 3 h, 4.5 h TTW. There was no increase in cerebral hemorrhage compared with untreated group after rhPro-UK administration. Conclusions: RhPro-UK had an obvious therapeutic effect on ischemic stroke caused by thrombosis, and could be started within 4.5 h TTW with less side effects of cerebral hemorrhage than that of UK. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 01616412
- Volume :
- 41
- Issue :
- 11
- Database :
- Supplemental Index
- Journal :
- Neurological Research
- Publication Type :
- Academic Journal
- Accession number :
- 139136323
- Full Text :
- https://doi.org/10.1080/01616412.2019.1672388