Neuroprotective effect of 4-amino-1,8-napthalimide, a poly(ADP ribose) polymerase inhibitor in middle cerebral artery occlusion-induced focal cerebral ischemia in rat

被引:39
作者
Kabra, DG [1 ]
Thiyagarajan, M [1 ]
Kaul, CL [1 ]
Sharma, SS [1 ]
机构
[1] NIPER, Dept Pharmacol & Toxicol, Punjab 160062, India
关键词
stroke; middle cerebral artery occlusion; poly(ADP-ribose) polymerase inhibitor; cerebral infarction; NAD; apoptosis; TUNEL;
D O I
10.1016/j.brainresbull.2003.11.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present study, neuroprotective effect of 4-amino-1,8-napthalimide (4-ANI), a poly(ADP-ribose) polymerase (PARP) inhibitor was investigated in middle cerebral artery occlusion (MCAo)-induced focal ischemia. Sprague-Dawley rats were subjected to 2 h of middle cerebral artery occlusion followed by 22 h of reperfusion. After 22 h of reperfusion rats were evaluated for cerebral infarction, neurological deficits, brain NAD levels, and in situ terminal deoxynucleotidyl transferase mediated dUTP-biotin nick end labeling (TUNEL). Focal ischemia produced significant infarct volume (201 +/- 14 mm(3)), neurological scores (2 +/- 0.5) and 28 +/- 4.5% brain NAD depletion. Ischemia was associated with increased in TUNEL positive cells in brain sections indicating DNA fragmentation. 4-ANI treatment (1 and 3 mg/kg, i.p.) significantly decreased infarct volume to 35 +/- 7% and 70 +/- 6%, respectively. Neurological functions were also significantly improved at these doses. 4-ANI (3 mg/kg) completely reversed brain NAD depletion and significantly reduced the increase in the number of TUNEL positive cells. Nevertheless, 4-ANI treatment did not alter cerebral blood flow and blood pressure. Our study suggests 4-ANI is a potent neuroprotective agent in focal cerebral ischemia and its neuroprotective effects may be attributed to reduction of NAD depletion and DNA fragmentation. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:425 / 433
页数:9
相关论文
共 44 条
[1]   Nicotinamide reduces infarction up to two hours after the onset of permanent focal cerebral ischemia in Wistar rats [J].
Ayoub, IA ;
Lee, EJ ;
Ogilvy, CS ;
Beal, MF ;
Maynard, KI .
NEUROSCIENCE LETTERS, 1999, 259 (01) :21-24
[2]   SYMPOSIUM - CELLULAR-RESPONSE TO DNA DAMAGE - THE ROLE OF POLY(ADP-RIBOSE) - POLY(ADP-RIBOSE) IN THE CELLULAR-RESPONSE TO DNA DAMAGE [J].
BERGER, NA .
RADIATION RESEARCH, 1985, 101 (01) :4-15
[3]   Effects of inhibitors of the activity of poly (ADP-ribose) synthetase on the liver injury caused by ischaemia-reperfusion: a comparison with radical scavengers [J].
Bowes, J ;
Thiemermann, C .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 124 (06) :1254-1260
[4]   POLY(ADENOSINE DIPHOSPHATE RIBOSE) POLYMERASE IN PHYSARUM-POLYCEPHALUM [J].
BRIGHTWELL, MD ;
LEECH, CE ;
OFARRELL, MK ;
WHISH, WJD ;
SHALL, S .
BIOCHEMICAL JOURNAL, 1975, 147 (01) :119-129
[5]   Nicotinamide and ketamine reduce infarct volume and DNA fragmentation in rats after brain ischemia and reperfusion [J].
Chang, ML ;
Yang, J ;
Kem, S ;
Klaidman, L ;
Sugawara, T ;
Chan, PH ;
Adams, JD .
NEUROSCIENCE LETTERS, 2002, 322 (03) :137-140
[6]   Poly(ADP-ribose) polymerase inhibition prevents both apoptotic-like delayed neuronal death and necrosis after H2O2 injury [J].
Cole, KK ;
Perez-Polo, JR .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (01) :19-29
[7]   DIFFERENT BASAL NAD LEVELS DETERMINE OPPOSITE EFFECTS OF POLY(ADP-RIBOSYL)POLYMERASE INHIBITORS ON H2O2-INDUCED APOPTOSIS [J].
COPPOLA, S ;
NOSSERI, C ;
MARESCA, V ;
GHIBELLI, L .
EXPERIMENTAL CELL RESEARCH, 1995, 221 (02) :462-469
[8]   Implication of poly(ADP-ribose) polymerase (PARP) in neurodegeneration and brain energy metabolism -: decreases in mouse brain NAD+ and ATP caused by MPTP are prevented by the PARP inhibitor benzamide [J].
Cosi, C ;
Marien, M .
NEUROPROTECTIVE AGENTS: FOURTH INTERNATIONAL CONFERENCE, 1999, 890 :227-239
[9]   Functional association of poly(ADP-ribose) polymerase with DNA polymerase α-primase complex:: A link between DNA strand break detection and DNA replication [J].
Dantzer, F ;
Nasheuer, HP ;
Vonesch, JL ;
de Murcia, G ;
Menissier-De Murcia, J .
NUCLEIC ACIDS RESEARCH, 1998, 26 (08) :1891-1898
[10]   Poly(ADP-ribose) polymerase gene disruption renders mice resistant to cerebral ischemia [J].
Eliasson, MJL ;
Sampei, K ;
Mandir, AS ;
Hurn, PD ;
Traystman, RJ ;
Bao, J ;
Pieper, A ;
Wang, ZQ ;
Dawson, TM ;
Snyder, SH ;
Dawson, VL .
NATURE MEDICINE, 1997, 3 (10) :1089-1095