| Literature DB >> 26455340 |
Tatsuya Fukuta1, Takayuki Ishii2, Tomohiro Asai2, Akihiko Sato2, Takashi Kikuchi2, Kosuke Shimizu2, Tetsuo Minamino3, Naoto Oku4.
Abstract
Since the proportion of patients given thrombolytic therapy with tissue plasminogen activator (t-PA) is very limited because of the narrow therapeutic window, the development of new therapies for ischemic stroke has been desired. We previously reported that liposomes injected intravenously accumulate in the ischemic region of the brain via disruption of the blood-brain barrier that occurs under cerebral ischemia. In the present study, we investigated the efficacy of a liposomal neuroprotective agent in middle cerebral artery occlusion (MCAO) rats to develop ischemic stroke therapy prior to the recovery of cerebral blood flow. For this purpose, PEGylated liposomes encapsulating FK506 (FK506-liposomes) were prepared and injected intravenously into MCAO rats after a 1-h occlusion. This treatment significantly suppressed the expansion of oxidative stress and brain cell damage. In addition, administration of FK506-liposomes before reperfusion significantly ameliorated motor function deficits of the rats caused by ischemia/reperfusion injury. These findings suggest that FK506-liposomes effectively exerted a neuroprotective effect during ischemic conditions, and that combination therapy with a liposomal neuroprotectant plus t-PA could be a promising therapeutic strategy for ischemic stroke.Entities:
Keywords: FK506; Ischemic stroke; Liposomes; Middle cerebral artery occlusion; Neuroprotectants; Thrombolytic therapy
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Year: 2015 PMID: 26455340 DOI: 10.1016/j.ejpb.2015.09.020
Source DB: PubMed Journal: Eur J Pharm Biopharm ISSN: 0939-6411 Impact factor: 5.571