Cechetto D F, Wilson J X, Smith K E, Wolski D, Silver M D, Hachinski V C
Department of Stroke and Aging, John P. Roberts Research Institute, London, Ont., Canada.
Brain Res. 1989 Nov 20;502(2):296-305. doi: 10.1016/0006-8993(89)90625-2.
Stroke models in larger animals such as the cat, dog and monkey are becoming increasingly more expensive and less readily available. However, the rat is an excellent model for focal cerebral ischemia. Rats are readily available, inexpensive and their neuroanatomy and brain function have been studied extensively. Increases in plasma catecholamines and myocardial damage have been observed in clinical stroke. We examined autonomic and myocardial changes in two rat stroke models. In one model only the middle cerebral artery was occluded (MCAO) while the other model involved occlusion of both the MCA and the common carotid artery (MCAO/CCAO). Arterial blood pressure and heart rate were monitored continuously in 25 male rats (326-430 g) that underwent one of the following procedures: (1) MCAO only; (2) MCAO/CCAO; (3) CCAO only; and (4) sham occlusions (SHAM). Arterial blood samples (0.5 ml) for radioenzymatic assay of norepinephrine (NE) and epinephrine (E) were taken twice before the occlusions and at 90 and 180 min after the occlusions. The animals were perfused at the end of the experiment and the heart removed and examined histologically. Tetrazolium salts were reacted with oxidative enzymes to delineate the region of inadequate perfusion. The mean blood pressure and pulse pressure of the SHAM, MCAO/CCAO and CCAO groups significantly declined from initial values (from an average of 78 to 53 mm Hg) during the course of the experiment. However, the mean blood pressure and pulse pressure of the MCAO rats did not change during the experiment, so that the final mean blood pressure and pulse pressure were significantly higher than in the other 3 groups. The levels of both NE and E increased significantly (NE, 1443 +/- 285.9 to 4095 +/- 929 pg/ml; E, 2402 +/- 623 to 3741 +/- 1166 pg/ml) following occlusion in the MCAO group only while the other 3 groups did not change. Four of 6 hearts in the MCAO group were abnormal, showing evidence of subendocardial hemorrhage, ischemic damage or subendocardial congestion. MCAO also resulted in a consistent region of the brain with inadequate perfusion including the insular cortex. These autonomic and myocardial changes appear to mimic some of the changes seen clinically in stroke patients and provide the first acute stroke model for studying autonomic dysfunction in the rat.
诸如猫、狗和猴子等较大型动物的中风模型正变得越来越昂贵且难以获得。然而,大鼠是局灶性脑缺血的优秀模型。大鼠容易获得、价格低廉,并且它们的神经解剖学和脑功能已得到广泛研究。在临床中风中已观察到血浆儿茶酚胺增加和心肌损伤。我们在两种大鼠中风模型中研究了自主神经和心肌的变化。在一种模型中,仅闭塞大脑中动脉(MCAO),而另一种模型则涉及闭塞大脑中动脉和颈总动脉(MCAO/CCAO)。对25只雄性大鼠(326 - 430克)进行连续动脉血压和心率监测,这些大鼠接受了以下操作之一:(1)仅MCAO;(2)MCAO/CCAO;(3)仅CCAO;(4)假闭塞(SHAM)。在闭塞前以及闭塞后90分钟和180分钟采集动脉血样本(0.5毫升),用于放射性酶法测定去甲肾上腺素(NE)和肾上腺素(E)。在实验结束时对动物进行灌注,取出心脏并进行组织学检查。用四氮唑盐与氧化酶反应以描绘灌注不足的区域。在实验过程中,SHAM、MCAO/CCAO和CCAO组的平均血压和脉压从初始值(平均从78毫米汞柱降至53毫米汞柱)显著下降。然而,MCAO大鼠的平均血压和脉压在实验过程中没有变化,因此最终的平均血压和脉压显著高于其他3组。仅在MCAO组闭塞后,NE和E的水平均显著升高(NE,从1443±285.9皮克/毫升升至4095±929皮克/毫升;E,从2402±623皮克/毫升升至3741±1166皮克/毫升),而其他3组没有变化。MCAO组6颗心脏中有4颗异常,显示有内膜下出血、缺血损伤或内膜下充血的迹象。MCAO还导致大脑中包括岛叶皮质在内的一个一致的灌注不足区域。这些自主神经和心肌变化似乎模拟了中风患者临床所见的一些变化,并为研究大鼠自主神经功能障碍提供了首个急性中风模型。