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AE0047对猫大脑中动脉闭塞后脑缺血和脑水肿的影响。

Effects of AE0047 on cerebral ischaemia and oedema after middle cerebral artery occlusion in cats.

作者信息

Shinyama H, Hayashi K, Kawamura T, Nakamura N, Kagitani Y

机构信息

Pharmacology Laboratories, Green Cross Corporation, Osaka, Japan.

出版信息

Clin Exp Pharmacol Physiol. 1997 Nov;24(11):824-30. doi: 10.1111/j.1440-1681.1997.tb02698.x.

Abstract
  1. AE0047 is a new dihydropyridine calcium antagonist with protective effects against cerebral ischaemia and the occurrence of stroke in several animal models. 2. In the present study we investigated whether AE0047 would improve the reduced cerebral blood flow (CBF) and oedema formation in cats subjected to middle cerebral artery (MCA) occlusion and compared it for efficacy with other dihydropyridine calcium antagonists with different moieties, such as nilvadipine and nicardipine. 3. Middle cerebral artery occlusion reduced local CBF (ICBF), as measured by the hydrogen clearance method, while dry weight measurement showed that water content in the cortical tissues surrounding each ICBF measurement electrode had increased after 4 h ischaemia. 4. Both AE0047 (10 micrograms/kg) and nilvadipine (30 micrograms/kg), given intravenously 20 min after MCA occlusion, produced an approximate 10% hypotensive response and significantly increased ICBF in severely and moderately ischaemic regions, grouped according to the initial reduced flow values. However, nicardipine (5 micrograms/kg bolus followed by infusion of 3 micrograms/kg per min for 60 min) failed to mitigate the reduction in ICBF despite an increase in the ICBF of the contralateral cortex. In addition, AE0047 tended to prevent an increase in cortical water content in severely ischaemic regions, whereas water content in both nilvadipine- and nicardipine-treated groups tended to increase. 5. These results suggest that dihydropyridine calcium antagonists act differently on cerebral ischaemia and oedema formation in a manner dependent on their side-chain structures and that AE0047 effectively attenuates ischaemic brain damage without aggravating oedema.
摘要
  1. AE0047是一种新型二氢吡啶类钙拮抗剂,在多种动物模型中对脑缺血和中风的发生具有保护作用。2. 在本研究中,我们调查了AE0047是否能改善大脑中动脉(MCA)闭塞猫的脑血流量(CBF)降低和水肿形成情况,并将其与其他具有不同基团的二氢吡啶类钙拮抗剂(如尼伐地平、尼卡地平)的疗效进行比较。3. 大脑中动脉闭塞会降低局部脑血流量(ICBF),采用氢清除法测量,而干重测量显示,缺血4小时后,每个ICBF测量电极周围皮质组织的含水量增加。4. MCA闭塞20分钟后静脉注射AE0047(10微克/千克)和尼伐地平(30微克/千克),根据初始血流降低值分组,在严重和中度缺血区域均产生了约10%的降压反应,并显著增加了ICBF。然而,尼卡地平(5微克/千克静脉推注,随后以3微克/千克/分钟的速度输注60分钟)尽管对侧皮质的ICBF增加,但未能减轻ICBF的降低。此外,AE0047倾向于防止严重缺血区域皮质含水量增加,而尼伐地平和尼卡地平治疗组的含水量均有增加趋势。5. 这些结果表明,二氢吡啶类钙拮抗剂对脑缺血和水肿形成的作用方式不同,取决于其侧链结构,且AE0047能有效减轻缺血性脑损伤而不加重水肿。

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