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亲免素介导FK506在局灶性脑缺血中的神经保护作用。

Immunophilins mediate the neuroprotective effects of FK506 in focal cerebral ischaemia.

作者信息

Sharkey J, Butcher S P

机构信息

Fujisawa Institute of Neuroscience, Department of Pharmacology, University of Edinburgh, UK.

出版信息

Nature. 1994 Sep 22;371(6495):336-9. doi: 10.1038/371336a0.

Abstract

The immunosuppressive action of the drug FK506 involves inhibition of calcineurin in T-lymphocytes by a complex of FK506 and an FK506 binding protein, FKBP12, a member of the immunophilin protein family. The functional role of brain immunophilins is, however, unclear. We show here that FK506 is a powerful neuroprotective agent in an in vivo model of focal cerebral ischaemia when administered up to 60 min post-occlusion. The minimum effective neuroprotective dose is comparable with the immunosuppressant dose in humans, suggesting that FK506 may have clinical potential for the treatment of stroke. Although the related immunosuppressants rapamycin and cyclosporin failed to reduce brain damage, the finding that rapamycin pretreatment blocked the effect of FK506 confirms a role for immunophilins in the neuroprotective mechanism.

摘要

药物FK506的免疫抑制作用涉及FK506与一种FK506结合蛋白FKBP12(免疫亲和素蛋白家族的一员)形成的复合物对T淋巴细胞中钙调神经磷酸酶的抑制。然而,脑免疫亲和素的功能作用尚不清楚。我们在此表明,在局灶性脑缺血的体内模型中,在闭塞后60分钟内给药时,FK506是一种强大的神经保护剂。最小有效神经保护剂量与人类免疫抑制剂剂量相当,这表明FK506可能具有治疗中风的临床潜力。尽管相关免疫抑制剂雷帕霉素和环孢素未能减轻脑损伤,但雷帕霉素预处理可阻断FK506的作用这一发现证实了免疫亲和素在神经保护机制中的作用。

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