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高血压与脑水肿:大鼠急性和慢性高血压的实验研究

Hypertension and brain oedema: an experimental study on acute and chronic hypertension in the rat.

作者信息

Johansson B B, Linder L E

出版信息

J Neurol Neurosurg Psychiatry. 1981 May;44(5):402-6. doi: 10.1136/jnnp.44.5.402.

Abstract

To determine under what circumstances hypertension is associated with brain oedema, the specific gravity of the brain was measured in acutely hypertensive, renal hypertensive and spontaneously hypertensive rats. Maximum mean arterial pressure (MAP) in acute hypertension induced by intravenous amphetamine or bicuculline was 171 +/- 5 and 181 +/- 5 mmHg respectively. In spite of pronounced extravasation of Evans blue-albumin, there was no decrease in specific gravity except in the diencephalon in rats given bicuculline (p less than 0.05). Cortical and cerebellar samples from renal hypertensive rats (MAP 174 +/- 14 mmHg) were lighter than corresponding regions in normotensive rats (p less than 0.001) although the brains showed little or no macroscopic extravasation of Evans blue-albumin. Neither macroscopic protein leakage nor increase in water content was observed in brains from spontaneously hypertensive rats (MAP 210 +/- 5 mmHg). It is concluded that renal hypertension is more likely to lead to brain oedema than spontaneous genetic hypertension or acute hypertension.

摘要

为了确定高血压在何种情况下与脑水肿相关,我们测定了急性高血压大鼠、肾性高血压大鼠和自发性高血压大鼠大脑的比重。静脉注射苯丙胺或荷包牡丹碱诱发的急性高血压中,平均动脉压(MAP)最大值分别为171±5和181±5 mmHg。尽管伊文思蓝 - 白蛋白有明显外渗,但除了给予荷包牡丹碱的大鼠间脑比重降低外(p<0.05),其他部位比重并无下降。肾性高血压大鼠(MAP 174±14 mmHg)的皮质和小脑样本比正常血压大鼠相应区域的样本轻(p<0.001),尽管大脑几乎没有或没有伊文思蓝 - 白蛋白的宏观外渗。自发性高血压大鼠(MAP 210±5 mmHg)的大脑既未观察到宏观蛋白质渗漏,也未观察到含水量增加。结论是,与自发性遗传性高血压或急性高血压相比,肾性高血压更易导致脑水肿。

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引用本文的文献

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The blood brain barrier in renal hypertensive rats.肾性高血压大鼠的血脑屏障
Clin Exp Hypertens (1978). 1980;2(6):983-93. doi: 10.3109/10641968009037156.
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Adv Exp Med Biol. 1980;131:211-26. doi: 10.1007/978-1-4684-3752-2_17.
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Arch Neurol. 1966 Jun;14(6):631-43. doi: 10.1001/archneur.1966.00470120063010.
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J Appl Physiol. 1971 Feb;30(2):268-71. doi: 10.1152/jappl.1971.30.2.268.
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Arch Neurol. 1970 Jul;23(1):18-22. doi: 10.1001/archneur.1970.00480250022004.
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