Neuroprotection against CA1 injury with metalloporphyrins

被引:48
作者
Panizzon, KL
Dwyer, BE
Nishimura, RN
Wallis, RA
机构
[1] VET AFFAIRS MED CTR 111 N1,NEURONAL INJURY LAB,SEPULVEDA,CA 91343
[2] VET AFFAIRS MED CTR 111 N1,IN VITRO REMYELINAT LAB,SEPULVEDA,CA 91343
[3] UNIV CALIF LOS ANGELES,SCH MED,BRAIN RES INST,LOS ANGELES,CA 90024
[4] UNIV CALIF LOS ANGELES,SCH MED,DEPT NEUROL,LOS ANGELES,CA 90024
[5] VET AFFAIRS MED CTR,MOLEC NEUROBIOL LAB,WHITE RIVER JCT,VT 05009
[6] DARTMOUTH COLL SCH MED,DIV NEUROL,DEPT MED,HANOVER,NH 03755
关键词
cerebral ischemia; hypoxia; traumatic brain injury; heme oxygenase; metalloporphyrins; LTP; oxidative stress; slice;
D O I
10.1097/00001756-199601310-00067
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE hippocampal slice was used to examine neuroprotection with metalloporphyrins, a class of drug which inhibits heme oxygenase and which has been found to be effective in the treatment of neonatal hyperbilirubinemia. Tin-protoporphyrin given during hypoxia significantly improved recovery of CA1 antidromic PS to a mean of 82 +/- 2% of initial amplitude, while unmedicated slices regained only 6 +/- 3% of initial amplitude. Tin-protoporphyrin also protected against fluid percussion injury with an EC(50) Of 10 mu M when given after trauma. This protection extended to induction of long-term potentiation. Tin-mesoporphyrin and zinc-protoporphyrin protected against trauma with EC(50)'s of 4 and 32 mu M. Treatment with Sn-PP also protected against exposure to hydrogen peroxide, but not NMDA, AMPA, glycine or nitric oxide. These findings indicate that metalloporphyrins protect against CA1 neuronal injury through direct neural effects.
引用
收藏
页码:662 / 666
页数:5
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