Protective effect of prostaglandin I2 analogs on ischemic delayed neuronal damage in gerbils

被引:23
作者
Cui, YL
Kataoka, Y
Satoh, T
Yamagata, A
Shirakawa, N
Watanabe, Y
Suzuki, M
Yanase, H
Kataoka, K
Watanabe, Y
机构
[1] Osaka Biosci Inst, Dept Neurosci, Suita, Osaka 5650874, Japan
[2] Gifu Univ, Fac Engn, Dept Biomol Sci, Gifu 5011193, Japan
[3] Ehime Univ, Sch Med, Dept Physiol, Shigenobu, Ehime 7910204, Japan
[4] Osaka City Univ, Sch Med, Dept Physiol, Abeno Ku, Osaka 5458585, Japan
基金
日本学术振兴会;
关键词
D O I
10.1006/bbrc.1999.1671
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We found a novel subtype of prostaglandin (PG) I-2 receptor (IP2) expressed in the central nervous system. Recently we have demonstrated that (15R)-16-m-tolyl-17,18,19,20-tetranorisocarbacyclin (15R-TIC) and 15-deoxy-16-m-tolyl-17,18,19,20-tetranorisocarbacyclin (15-deoxy-TIC), IP2-specific ligands, significantly prevented high (50%) oxygen-induced apoptotic neuronal death in cultured hippocampal neurons, We report here a potent neuroprotective effect of such analogs on delayed neuronal death of hippocampal CA1 neurons following transient ischemia for 3 min in gerbils, (15S)-16-m-tolyl-17,18,19,20-tetranorisocarbacyclin (15S-TIC), which nonselectively acts both on the PGI(2) receptor expressed in the peripheral tissue (IP1) and on IP2, also showed a neuroprotective effect on such an ischemic model at higher doses than those for 15R-TIC and 15-deoxy-TIC. These PGI(2) analogs did not affect brain temperature, indicating that the agents showed the neuroprotective effect not by a hypothermic effect, but rather by the direct action on neurons, (C) 1999 Academic Press.
引用
收藏
页码:301 / 304
页数:4
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