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轻度低温对犬脑缺血诱导的内皮素-1释放的影响。

Effect of mild hypothermia on ischemia-induced release of endothelin-1 in dog brain.

作者信息

Takasu A, Yagi K, Okada Y

机构信息

Department of Traumatology and Critical Care Medicine, National Defense Medical College, Saitama, Japan.

出版信息

Resuscitation. 1996 Feb;31(1):59-64. doi: 10.1016/0300-9572(95)00907-8.

Abstract

Endothelin-1 (ET-1) plays an important role in the physiologic or pathophysiologic regulation of cerebral circulation. To evaluate the effect of mild hypothermia on the cerebral concentration of ET-1 and on the cerebral metabolism of oxygen after complete global cerebral ischemia, we occluded the ascending aorta and caval veins of 9 dogs for 15 min. A fiberoptic catheter was inserted into the sagittal sinus to monitor venous oxygen saturation (S(SO)2) continuously. Blood samples were collected 30 min before and 30 min, 1 h, 2 h, 4 h and 6 h after the ischemic insult. Concentrations of ET-1 were assayed in the blood of the sagittal sinus and abdominal aorta. Before, during and after the aortic occlusion, we compared findings in a normothermic control Group 1 (pulmonary artery temperature 38.5 degrees C) (n = 4) with those in the mildly hypothermic Group 2 (pulmonary artery temperature 34.0 degrees C) (n = 5) by surface cooling induced before and maintained during and after ischemia for 6 h. Following ischemia, the plasma concentration difference of ET-1 (sagittal sinus--arterial) was significantly decreased in Group 2 (P < 0.05). Differences in S(SO)2 between the two groups were not statistically significant. Mild hypothermia reduced the ET-1 release in the cerebral circulation but did not improve cerebral oxygen metabolism after complete cerebral ischemia. Findings indicated that the decrease in ET-1 induced by mild hypothermia contributes to the improvement of the cerebral microcirculation after ischemia.

摘要

内皮素 -1(ET -1)在脑循环的生理或病理生理调节中起重要作用。为了评估轻度低温对全脑完全缺血后ET -1脑浓度及脑氧代谢的影响,我们阻断了9只犬的升主动脉和腔静脉15分钟。将光纤导管插入矢状窦以连续监测静脉血氧饱和度(S(SO)2)。在缺血性损伤前30分钟以及损伤后30分钟、1小时、2小时、4小时和6小时采集血样。测定矢状窦和腹主动脉血中ET -1的浓度。在主动脉阻断前、阻断期间和阻断后,我们通过在缺血前诱导并在缺血期间及缺血后6小时维持体表降温,将常温对照组1(肺动脉温度38.5℃)(n = 4)的结果与轻度低温组2(肺动脉温度34.0℃)(n = 5)的结果进行比较。缺血后,第2组ET -1的血浆浓度差(矢状窦 - 动脉)显著降低(P < 0.05)。两组间S(SO)2的差异无统计学意义。轻度低温可减少全脑缺血后脑循环中ET -1的释放,但并未改善脑氧代谢。研究结果表明,轻度低温诱导的ET -1降低有助于改善缺血后脑微循环。

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