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预处理肾上腺髓质素可抑制磁共振成像检测到的大鼠短暂性局灶性脑缺血引起的脑水肿。

Pre-treatment of adrenomedullin suppresses cerebral edema caused by transient focal cerebral ischemia in rats detected by magnetic resonance imaging.

机构信息

Institute for Innovation, Ajinomoto Co., Inc., Kawasaki-ku, Kawasaki, Japan.

出版信息

Brain Res Bull. 2011 Jan 15;84(1):69-74. doi: 10.1016/j.brainresbull.2010.11.005. Epub 2010 Nov 11.

DOI:10.1016/j.brainresbull.2010.11.005
PMID:21074599
Abstract

Recent studies suggest the protective effects of adrenomedullin (AM) on ischemic brain damage. The present study was aimed at investigating the effects of AM and its receptor antagonist, AM₂₂₋₅₂, on ischemia-induced cerebral edema and brain swelling in rats using magnetic resonance imaging. Rats were subjected to 60 min of middle cerebral artery occlusion (MCAO) followed by reperfusion. Intravenous injection of AM (1.0 μg/kg), AM₂₂₋₅₂ (1.0 μg/kg), or saline was made before MCAO. Effects of AM injection just after reperfusion were also investigated. One day after ischemia, increases in T₂-weighted signals in the brain were clearly observed. Total edema volume, as well as brain swelling, was greatly and significantly reduced by pre-treatment of AM (reduced by 53%). Extent of brain swelling was significantly correlated with the volume of cerebral edema. The protective effect of AM against edema was more clearly observed in the cerebral cortex (reduced by 63%) than the striatum (reduced by 31%). Increased T₂ relaxation time in the cortex was recovered partially by pre-treatment of AM. Post-treatment of AM had no effects. Pre-treatment of AM₂₂₋₅₂ tended to exacerbate the edema. In another line of experiment, cocktail administration of AM with melatonin, a pineal product having neuroprotective potential as a free radical scavenger, failed to enhance the protective effects of AM alone. The present study clearly suggests the prophylactic effects of AM against cerebral edema, especially the cortical edema, in a rat stroke model.

摘要

最近的研究表明,肾上腺髓质素(adrenomedullin,AM)对缺血性脑损伤具有保护作用。本研究旨在利用磁共振成像技术,研究 AM 及其受体拮抗剂 AM₂₂₋₅₂对大鼠缺血性脑水肿和脑肿胀的影响。大鼠接受 60 分钟大脑中动脉闭塞(MCAO)后再灌注。在 MCAO 前静脉注射 AM(1.0 μg/kg)、AM₂₂₋₅₂(1.0 μg/kg)或生理盐水。还研究了 AM 在再灌注后立即注射的效果。缺血后 1 天,大脑 T₂ 加权信号明显增加。AM 的预处理大大显著减少了总水肿体积和脑肿胀(减少 53%)。脑肿胀程度与脑水肿体积显著相关。AM 对水肿的保护作用在皮质(减少 63%)比纹状体(减少 31%)更为明显。皮质中 T₂ 弛豫时间的增加部分通过 AM 的预处理得到恢复。AM 的后期治疗没有效果。AM₂₂₋₅₂的预处理有加重水肿的趋势。在另一项实验中,AM 与褪黑素联合给药,褪黑素作为一种具有神经保护作用的自由基清除剂,是松果腺的产物,未能增强 AM 单独的保护作用。本研究清楚地表明,AM 对大鼠中风模型的脑水肿,特别是皮质水肿具有预防作用。

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