Hyperbaric oxygen therapy for treatment of postischemic stroke in adult rats

被引:73
作者
Chang, CF
Niu, KC
Hoffer, BJ
Wang, Y
Borlongan, CV [1 ]
机构
[1] NIDA, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[2] Natl Def Med Ctr, Grad Inst Med Sci, Taipei, Taiwan
[3] Chi Mei Hosp, Tainan, Taiwan
关键词
cerebral ischemia; reperfusion; hyperoxygenation; hyperbaric pressure; plasma pH; arterial pressure; motor asymmetry;
D O I
10.1006/exnr.2000.7506
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The efficacy of hyperbaric oxygen (HBO) therapy for treatment of stroke remains to be validated in the laboratory. We report here that adult rats subjected to occlusion of the middle cerebral artery and subsequently exposed to HBO (3 atm, 2 x 90 min at a 24-h intervals; animals terminated shortly after the second treatment) or hyperbaric pressure (HBP; 3 atm, 2 x 90 min at a 24-h interval; animals terminated shortly after the second treatment) immediately after the ischemia or after a 60-min delay generally displayed recovery from motor deficits at 2.5 and 24 h of reperfusion, as well as a reduction in cerebral infarction at 24 h of reperfusion compared to ischemic animals subjected to normal atmospheric pressure. While both HBO and HBP treatments promoted beneficial effects, HBO produced more consistent protection than HBP. Treatment with HBO immediately or 60 min after reperfusion equally produced significant attenuations of cerebral infarction and motor deficits. In contrast, protective effects of HBP treatment against ischemia were noted only when administered immediately after ischemia, which resulted in a significantly reduced infarction volume, but only produced a trend toward decreased behavioral deficits. The present results demonstrate that HBO and, to some extent, HBP reduced ischemic brain damage and behavioral dysfunctions.
引用
收藏
页码:298 / 306
页数:9
相关论文
共 55 条
[1]   Neuroprotective strategies for basal ganglia degeneration: Parkinson's and Huntington's diseases [J].
Alexi, T ;
Borlongan, CV ;
Faull, RLM ;
Williams, CE ;
Clark, RG ;
Gluckman, PD ;
Hughes, PE .
PROGRESS IN NEUROBIOLOGY, 2000, 60 (05) :409-470
[2]   An alternative method for the quantitation of neuronal damage after experimental middle cerebral artery occlusion in rats: Analysis of behavioral deficit [J].
Aronowski, J ;
Samways, E ;
Strong, R ;
Rhoades, HM ;
Grotta, JC .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (04) :705-713
[3]  
BEAL MF, 1992, J NEUROL SCI, V108, P80
[4]   RAT MIDDLE CEREBRAL-ARTERY OCCLUSION - EVALUATION OF THE MODEL AND DEVELOPMENT OF A NEUROLOGIC EXAMINATION [J].
BEDERSON, JB ;
PITTS, LH ;
TSUJI, M ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, H .
STROKE, 1986, 17 (03) :472-476
[5]   STRIATAL DOPAMINE-MEDIATED MOTOR BEHAVIOR IS ALTERED FOLLOWING OCCLUSION OF THE MIDDLE CEREBRAL-ARTERY [J].
BORLONGAN, CV ;
MARTINEZ, R ;
SHYTLE, RD ;
FREEMAN, TB ;
CAHILL, DW ;
SANBERG, PR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1995, 52 (01) :225-229
[6]   Viability and survival of hNT neurons determine degree of functional recovery in grafted ischemic rats [J].
Borlongan, CV ;
Saporta, S ;
Poulos, SG ;
Othberg, A ;
Sanberg, PR .
NEUROREPORT, 1998, 9 (12) :2837-2842
[7]   Transplantation of cryopreserved human embryonal carcinoma-derived neurons (NT2N cells) promotes functional recovery in ischemic rats [J].
Borlongan, CV ;
Tajima, Y ;
Trojanowski, JQ ;
Lee, VMY ;
Sanberg, PR .
EXPERIMENTAL NEUROLOGY, 1998, 149 (02) :310-321
[8]   Early assessment of motor dysfunctions aids in successful occlusion of the middle cerebral artery [J].
Borlongan, CV ;
Hida, H ;
Nishino, H .
NEUROREPORT, 1998, 9 (16) :3615-3621
[9]   Glial cell survival is enhanced during melatonin-induced neuroprotection against cerebral ischemia [J].
Borlongan, CV ;
Yamaoto, M ;
Takei, N ;
Kumazaki, M ;
Ungsuparkorn, C ;
Hida, H ;
Sanberg, PR ;
Nishino, H .
FASEB JOURNAL, 2000, 14 (10) :1307-1317
[10]   LOCOMOTOR AND PASSIVE-AVOIDANCE DEFICITS FOLLOWING OCCLUSION OF THE MIDDLE CEREBRAL-ARTERY [J].
BORLONGAN, CV ;
CAHILL, DW ;
SANBERG, PR .
PHYSIOLOGY & BEHAVIOR, 1995, 58 (05) :909-917