Nicotinamide reduces infarction up to two hours after the onset of permanent focal cerebral ischemia in Wistar rats

被引:106
作者
Ayoub, IA
Lee, EJ
Ogilvy, CS
Beal, MF
Maynard, KI
机构
[1] Massachusetts Gen Hosp, Neurophysiol Lab, Neurosurg Serv, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
[3] Cornell Univ, Dept Neurol, Coll Med, New York, NY 10021 USA
关键词
stroke; energy metabolism; poly(ADP-ribose) polymerase; window of opportunity; poly(ADP-ribose) synthetase; therapeutic window;
D O I
10.1016/S0304-3940(98)00881-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ischemia depletes ATP and initiates cascades leading to irreversible tissue injury. Nicotinamide is a precursor of nicotinamide adenine dinucleotide (NAD(+)) which increases neuronal ATP concentration and protects against malonate-induced neurotoxicity, trauma and nitric oxide toxicity. We therefore examined whether nicotinamide could protect against stroke, using a model of permanent middle cerebral artery occlusion (MCA) occlusion in Wistar rats. Nicotinamide reduced neuronal infarction in a dose-specific manner. Furthermore, nicotinamide (500 mg/kg) reduced infarcts when administered up to 2 h after the onset of permanent MCA occlusion. The mechanism of action underlying the neuroprotection observed with nicotinamide remains to be clarified. These results are potentially important since nicotinamide is already used clinically, though not in the treatment of stroke. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 24
页数:4
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