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[早期恢复过程中的缺血性神经元损伤。高血糖和正常血糖状态下损伤演变的形态学研究]

[Ischemic neuronal damage in early recovery. A morphological study on evolution of damage in hyperglycemia and normoglycemia].

作者信息

Usuda K, Inamura K, Katayama Y, Terashi A

机构信息

Second Department of Internal Medicine, Nippon Medical School, Japan.

出版信息

Nihon Ika Daigaku Zasshi. 1996 Dec;63(6):460-72. doi: 10.1272/jnms1923.63.460.

Abstract

The evolution of neuronal damage in various regions during ischemia and in early recovery was investigated morphologically using hyperglycemic and normoglycemic Wistar rats. Hyperglycemia (20-35 mu mol/ml plasma) was achieved with the infusion of glucose (i.v.) prior to ischemia. Forebrain ischemia (10 minutes) was induced by bilateral common carotid artery occlusion and hypotension. Normoglycemic rats were fasted prior to ishcemia. Ischemic changes of neurons were quantified by a five-point scale in the caudoputamen (CPu), globus pallidus (GP), hippocampus CA 1 (CA 1), parietal cortex (Par), and substantia nigra reticulata (SNR) during ishcemia and for 90 minutes after recirculation. In the hyperglycemic group, (1), CPu, CA 1 and Par; severely damaged neurons were seen at 60-90 minutes after recirculation. (2) GP; there was little neuronal damage. (3) SNR; immediately after recirculation damaged neurons were observed, and more damage was observed at 90 minutes post recirculation. In the normoglycemic group, no prominent neuronal damage was observed in any region. Hyperglycemia exacerbated ischemic neuronal damage after reperfusion. The evolution of neuronal damage was similar in the CPu and Par regions, but was different in the GP and SNR regions.

摘要

利用高血糖和正常血糖的Wistar大鼠,从形态学角度研究了缺血期间及早期恢复过程中不同区域神经元损伤的演变情况。在缺血前通过静脉输注葡萄糖使血糖升高(血浆葡萄糖浓度为20 - 35 μmol/ml)。通过双侧颈总动脉闭塞和低血压诱导前脑缺血(10分钟)。正常血糖大鼠在缺血前禁食。在缺血期间以及再灌注后90分钟内,采用五点量表对尾壳核(CPu)、苍白球(GP)、海马CA1区(CA1)、顶叶皮质(Par)和黑质网状部(SNR)的神经元缺血变化进行量化。在高血糖组中,(1)尾壳核、CA1区和顶叶皮质;再灌注后60 - 90分钟可见严重受损的神经元。(2)苍白球;几乎没有神经元损伤。(3)黑质网状部;再灌注后立即观察到受损神经元,再灌注后90分钟观察到更多损伤。在正常血糖组中,任何区域均未观察到明显的神经元损伤。高血糖加剧了再灌注后缺血性神经元损伤。尾壳核和顶叶皮质区域的神经元损伤演变相似,但苍白球和黑质网状部区域不同。

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