The effect of selective neuronal nitric oxide synthase inhibitor on apoptosis of neurons after hypoxic-ischemic brain damage in neonatal rats

被引:0
|
作者
Yao, Y [1 ]
Yu, HM [1 ]
Li, JC [1 ]
Yu, ZS [1 ]
机构
[1] Zhejiang Univ, Coll Med, Affiliated Hosp 2, Hangzhou 310009, Peoples R China
来源
IEEE-EMBS ASIA PACIFIC CONFERENCE ON BIOMEDICAL ENGINEERING - PROCEEDINGS, PTS 1 & 2 | 2000年
关键词
apoptosis; nitric oxide; hypoxic-ischemic; 7-nitroindazole (7-NI);
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Apoptosis which is one of the main patterns of neuronal death plays an important role in the delayed brain damage after hypoxic-ischemic brain damage (HIBD). We have studied the effect of 7-nitroindazole (7-NI)-selective neuronal NOS (nNOS) inhibitor on apoptosis of neurons after HIBD. The HIBD model was produced in the 7-day postnatal SD rats which were subjected to permanent unilateral carotid artery ligation followed by an hypoxic (8% oxygen) insult of 2 hours. 7-Ni and PBS were administered after HIBD respectively. Neuronal apoptosis was examined using HE-staining, TUNEL staining and electron microscopy 24 hours later. Morphological characteristic changes of apoptosis in different stages were revealed. The number of neuronal apoptosis in hippocampus and cortex in the 7-NI group at 24h after HIBD was significantly lower than that in the PBS group (p<0.005). This study demonstrated that apoptosis play important role in the delayed neuronal death after HIBD, and first proved it is selective NOS inhibitors (7-NI) that shows its anti-apoptosis effect on HIBD.
引用
收藏
页码:595 / 596
页数:2
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