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免疫抑制剂FK506可改善大鼠脑缺血损伤。

The immunosuppressant FK506 ameliorates ischaemic damage in the rat brain.

作者信息

Drake M, Friberg H, Boris-Möller F, Sakata K, Wieloch T

机构信息

Laboratory for Experimental Brain Research, University of Lund, Lund University Hospital, Sweden.

出版信息

Acta Physiol Scand. 1996 Oct;158(2):155-9. doi: 10.1046/j.1365-201X.1996.535298000.x.

Abstract

The effect of the immunosuppressant FK506 on ischaemic neuronal damage was studied in a rat model of transient cerebral ischemia induced by occlusion of both common carotid arteries in combination with hypotension for 10 min. Neuronal damage was assessed morphologically after 4 days of recovery. Treatment with FK506, given at a dose of 2 mg kg-1 by intraperitoneal injections 30 min prior to ischemia and once daily during recovery, decreased neuronal damage by 52% in the hippocampal CA1 region and by 48% in the temporal cortex. The protection was not due to diminished body temperature or a marked reduction of ischaemia-induced synaptic overflow of glutamate. We propose that FK506 decreases neuronal damage either by inhibiting calcineurin-mediated events or by preserving mitochondrial function.

摘要

在双侧颈总动脉闭塞联合低血压10分钟诱导的短暂性脑缺血大鼠模型中,研究了免疫抑制剂FK506对缺血性神经元损伤的影响。恢复4天后,通过形态学评估神经元损伤情况。在缺血前30分钟腹腔注射剂量为2 mg kg-1的FK506,并在恢复期间每天注射一次,结果显示海马CA1区的神经元损伤减少了52%,颞叶皮质的神经元损伤减少了48%。这种保护作用并非由于体温降低或缺血诱导的谷氨酸突触溢出显著减少所致。我们认为,FK506可能通过抑制钙调神经磷酸酶介导的事件或通过维持线粒体功能来减少神经元损伤。

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