首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Core and penumbral nitric oxide synthase activity during cerebral ischemia and reperfusion.
【24h】

Core and penumbral nitric oxide synthase activity during cerebral ischemia and reperfusion.

机译:脑缺血和再灌注过程中核心和半影一氧化氮合酶活性。

获取原文
获取原文并翻译 | 示例
       

摘要

BACKGROUND AND PURPOSE: The present studies examined the hypothesis that the distribution of cerebral injury after a focal ischemic insult is associated with the regional distribution of nitric oxide synthase (NOS) activity. METHODS: Based on previous studies that certain anatomically well-defined areas are prone to become either core or penumbra after middle cerebral artery occlusion (MCAO), we measured NOS activity in these areas from the right and left hemispheres in a spontaneously hypertensive rat filament model. Four groups were studied: (1) controls (immediate decapitation); (2) 1.5 hours of MCAO with no reperfusion (R0); (3) 1.5 hours of MCAO with 0.5 hour of reperfusion (R0.5); and (4) 1.5 hours of MCAO with 24 hours of reperfusion (R24). Three groups of corresponding isoflurane sham controls were also included: 1.5 (S1.5) or 2 (S2.0) hours of anesthesia and 1.5 hours of anesthesia+24 hours of observation (S24). RESULTS: Control core NOS activity for combined right and left hemispheres was 129% greater than penumbral NOS activity (P<0.05). Combined core NOS activity was also greater (P<0.05) in the three sham groups: 208%, 122%, and 161%, respectively. In the three MCAO groups, ischemic and nonischemic core NOS remained higher than penumbral regions (P<0.05). However, NOS activity was lower in the ischemic than in the nonischemic core in all three groups: R0 (29% lower), R0.5 (48%), and R24 (86%) (P<0.05). Addition of cofactors (10 micromol/L tetrahydrobiopterin, 3 micromol/L flavin adenine dinucleotide, and 3 micromol/L flavin mononucleotide) increased NOS activity in all groups and lessened the decrease in ischemic core and penumbral NOS. CONCLUSIONS: Greater NOS activity in core regions could explain in part the increased vulnerability of that region to ischemia and could theoretically contribute to the progression of the infarct over time. The data also suggest that NOS activity during ischemia and reperfusion could be influenced by the availability of cofactors.
机译:背景与目的:本研究检验了以下假设:局灶性缺血性损伤后脑损伤的分布与一氧化氮合酶(NOS)活性的区域分布有关。方法:基于先前的研究,某些大脑中动脉闭塞(MCAO)后在解剖学上明确定义的区域易于变成核心或半影,我们在自发性高血压大鼠细丝模型中从左右半球测量了这些区域中的NOS活性。研究了四组:(1)对照(立即斩首); (2)1.5小时MCAO,无再灌注(R0); (3)1.5小时的MCAO和0.5小时的再灌注(R0.5); (4)1.5个小时的MCAO和24个小时的再灌注(R24)。还包括三组相应的异氟醚假手术对照组:麻醉1.5(S1.5)或2(S2.0)小时,麻醉1.5小时+ 24小时观察(S24)。结果:左右半球组合的对照核心NOS活性比半影NOS活性高129%(P <0.05)。三个假手术组的组合核心NOS活性也更高(P <0.05):分别为208%,122%和161%。在三个MCAO组中,缺血性和非缺血性核心NOS仍高于半影区(P <0.05)。但是,在所有三个组中,缺血性NOS活性均低于非缺血性核心:R0(降低29%),R0.5(48%)和R24(86%)(P <0.05)。加入辅因子(10 micromol / L四氢生物蝶呤,3 micromol / L黄素腺嘌呤二核苷酸和3 micromol / L黄素单核苷酸)增加了所有组的NOS活性,并减少了缺血核心和半影NOS的降低。结论:核心区域NOS活性的增加可以部分解释该区域对局部缺血的脆弱性增加,并且理论上可以随着时间的推移促进梗塞的发展。数据还表明,缺血和再灌注过程中的NOS活性可能会受到辅助因子可用性的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号