Arii T, Kamiya T, Arii K, Ueda M, Nito C, Katsura K I, Katayama Y
The Second Department of Internal Medicine, Nippon Medical School, Tokyo, Japan.
Neurol Res. 2001 Oct;23(7):755-60. doi: 10.1179/016164101101199135.
Tacrolimus (FK506), an immunosuppressant currently used in clinic, is known to have neuroprotective properties. However, effects in focal ischemia are shown only in a endothelin induced middle cerebral artery (MCA) occlusion model or with filament technique at a relatively high dose. We have previously shown that FK506 had significant protective effects at a low dose of 0.3 mg kg(-1) when administered immediately after ischemia. In this study, we explored the therapeutic time window of FK506 at this low dose, in a transient focal ischemia model using filament technique. Male Sprague-Dawley rats were subjected to 2 h MCA occlusion and subsequent reperfusion. They received FK506 or vehicle (0.3 mg kg(-1)) i.v. at 30, 60 or 120 min after induction of ischemia, and were decapitated 24 h after ischemia. FK506 injected at 30 and 60 min significantly reduced cortical infarction volume (FK506 vs. vehicle; 30 min: 95 +/- 33 mm3 vs. 170 +/- 62 mm3, p < 0.05; 60 min: 93 +/- 45 mm3, vs. 168 +/- 35 mm3, p < 0.05, respectively). FK506 was ineffective when given at 120 min after ischemia. FK506 had no effect on edema formation, nor on the infarct volume in striatum. The therapeutic time window for this low dose of FK506 given i.v. is between 60 and 120 min in this model.
他克莫司(FK506)是目前临床上使用的一种免疫抑制剂,已知具有神经保护特性。然而,其在局灶性缺血中的作用仅在一种内皮素诱导的大脑中动脉(MCA)闭塞模型中或使用线栓法且剂量相对较高时才得以显现。我们之前已经表明,在缺血后立即给予低剂量0.3mg/kg的FK506具有显著的保护作用。在本研究中,我们在使用线栓法的短暂局灶性缺血模型中,探究了该低剂量FK506的治疗时间窗。雄性Sprague-Dawley大鼠经历2小时的MCA闭塞及随后的再灌注。在缺血诱导后30、60或120分钟,它们接受静脉注射FK506或溶剂(0.3mg/kg),并在缺血后24小时断头。在30和60分钟注射FK506显著减小了皮质梗死体积(FK506与溶剂组相比;30分钟:95±33mm³对170±62mm³,p<0.05;60分钟:93±45mm³对168±35mm³,p<0.05)。在缺血后120分钟给予FK506无效。FK506对水肿形成以及纹状体梗死体积均无影响。在该模型中,静脉注射此低剂量FK506的治疗时间窗在60至120分钟之间。