Fukuta Tatsuya, Ishii Takayuki, Asai Tomohiro, Sato Akihiko, Kikuchi Takashi, Shimizu Kosuke, Minamino Tetsuo, Oku Naoto
Department of Medical Biochemistry, University of Shizuoka Graduate School of Pharmaceutical Sciences, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan; Japan Society for the Promotion of Science (JSPS), 8 Ichiban-cho, Chiyoda-ku, Tokyo 102-8472, Japan.
Department of Medical Biochemistry, University of Shizuoka Graduate School of Pharmaceutical Sciences, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Eur J Pharm Biopharm. 2015 Nov;97(Pt A):1-7. doi: 10.1016/j.ejpb.2015.09.020. Epub 2015 Oct 9.
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.
由于组织型纤溶酶原激活剂(t-PA)溶栓治疗的患者比例因治疗窗狭窄而非常有限,因此人们一直期望开发新的缺血性中风治疗方法。我们之前报道过,静脉注射的脂质体通过脑缺血时发生的血脑屏障破坏而积聚在脑缺血区域。在本研究中,我们研究了脂质体神经保护剂在大脑中动脉闭塞(MCAO)大鼠中的疗效,以便在脑血流恢复之前开发缺血性中风治疗方法。为此,制备了包裹FK506的聚乙二醇化脂质体(FK506-脂质体),并在闭塞1小时后静脉注射到MCAO大鼠体内。这种治疗显著抑制了氧化应激的扩展和脑细胞损伤。此外,在再灌注前给予FK506-脂质体可显著改善缺血/再灌注损伤引起的大鼠运动功能缺陷。这些发现表明,FK506-脂质体在缺血条件下有效地发挥了神经保护作用,并且脂质体神经保护剂与t-PA的联合治疗可能是缺血性中风的一种有前景的治疗策略。