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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Increase of prothrombin-mRNA after global cerebral ischemia in rats, with constant expression of protease nexin-1 and protease-activated receptors.
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Increase of prothrombin-mRNA after global cerebral ischemia in rats, with constant expression of protease nexin-1 and protease-activated receptors.

机译:大鼠全脑缺血后凝血酶原-mRNA的增加,蛋白酶nexin-1和蛋白酶激活受体的恒定表达。

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摘要

Prothrombin, protease-activated receptors (PARs) and the specific thrombin inhibitor protease nexin-1 (PN-1) are expressed in the brain. Recent studies have shown that the serine protease thrombin, depending on its concentration, plays an important role in neuronal degeneration or protection after cerebral ischemia. However, it is still uncertain whether a change in prothrombin or alterations in the expression of specific PAR-subtypes or PN-1 are associated with postischemic thrombin effects. Using semi-quantitative reverse transcription-polymerase chain reaction analysis, we show that prothrombin was up-regulated in the hippocampal formation 24 h after transient global ischemia in rats (two-vessel occlusion with hypotension), whereas the expression of PN-1 and the expression of PAR-subtypes 1-3 did not change significantly. Thus, control of the balance between the expression of prothrombin and PN-1 may reflect an important mechanism that underlies postischemic thrombin effects.
机译:凝血酶原,蛋白酶激活受体(PARs)和特定的凝血酶抑制剂蛋白酶nexin-1(PN-1)在大脑中表达。最近的研究表明,丝氨酸蛋白酶凝血酶根据其浓度在脑缺血后神经元变性或保护中起重要作用。但是,尚不确定凝血酶原的改变或特定PAR亚型或PN-1表达的改变是否与缺血后凝血酶的作用有关。使用半定量逆转录-聚合酶链反应分析,我们显示,大鼠短暂性整体缺血(低血压的两支血管闭塞)后24小时,凝血酶原在海马结构中上调,而PN-1和PAR亚型1-3的表达没有明显改变。因此,控制凝血酶原和PN-1表达之间的平衡可能反映了缺血后凝血酶作用基础的重要机制。

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