Hyperbaric oxygen treatment attenuated the decrease in regional glucose metabolism of rats subjected to focal cerebral ischemia: A high resolution positron emission tomography study

被引:55
作者
Lou, M. [1 ]
Zhang, H.
Wang, J.
Wen, S.-Q.
Tang, Z.-Q.
Chen, Y. Z.
Yan, W.-Q
Ding, M.-P.
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Dept Neurol, Sch Med, Hangzhou 310009, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Dept Nucl Med, Sch Med, Hangzhou 310009, Peoples R China
[3] Zhejiang Calif Int Nanosyst Inst, Hangzhou 310009, Peoples R China
[4] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Hyperbar Oxygen, Hangzhou 310009, Peoples R China
[5] Zhejiang Univ, Sch Med, Dept Neurobiol, Hangzhou 310058, Peoples R China
[6] Zhejiang Univ, Clin Res Ctr, Affiliated Hosp 2, Sch Med, Hangzhou 310009, Peoples R China
基金
中国国家自然科学基金;
关键词
hyperbaric oxygen; brain ischemia; positron emission tomography; glucose utilization;
D O I
10.1016/j.neuroscience.2007.01.046
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cerebral hypoxia may be the main component of cell damage caused by ischemia. Previous studies demonstrated a neuroprotective effect of early hyperbaric oxygen (HBO) treatment in various animal models of focal cerebral ischemia. Neuropathologic study showed that exposure of HBO may prevent cell death in ischemic cortex. In the present study, we aimed to assess cellular function of ischemic rat brain after HBO treatment by means of a high-resolution positron emission tomography scanner (microPET) used specifically for small animal imaging. The male Sprague-Dawley rats were subjected to permanent middle cerebral artery occlusion (MCAO), with the regional cerebral blood flow monitored in vivo by laser Doppler flowmetry. One hour after ischemia, HBO therapy (3 atm absolute, 1 h) was initiated. Local cerebral glucose utilization in the ischemic area was measured before, 1 h and 3 h after ischemia, with 2-[F-18]fluoro-2-deoxy-d-glucose (FDG) as a tracer. Neurological deficits and infarct volumes were assessed at 24 h after ischemia. Our study showed that early HBO therapy significantly reduced infarct volume of brain 24 h after ischemia. Moreover, glucose utilization in the ischemic area underwent a severe decrease during 1-3 h after MCAO, while the early HBO treatment significantly attenuated the decrease in cerebral metabolic rate of glucose in the ischemic core of the cortex compared with controls. We report for the first time the application of microPET to quantify the rates of glucose metabolism in the ischemic core of rats exposed to HBO. Our results suggest that the early exposure of HBO can partially reverse the downward trend for glucose utilization in the ischemic core, which might contribute to the reported beneficial effects of early HBO therapy on permanent cerebral ischemia. (C) 2007 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:555 / 561
页数:7
相关论文
共 34 条
[21]   Hyperbaric oxygen treatment:: the influence on the hippocampal superoxide dismutase and Na+,K+-ATPase activities in global cerebral ischemia-exposed rats [J].
Mrsic-Pelcic, J ;
Pelcic, G ;
Vitezic, D ;
Antoncic, I ;
Filipovic, T ;
Simonic, A ;
Zupan, G .
NEUROCHEMISTRY INTERNATIONAL, 2004, 44 (08) :585-594
[22]   QUANTITATIVE ASSESSMENT OF EARLY BRAIN-DAMAGE IN A RAT MODEL OF FOCAL CEREBRAL-ISCHEMIA [J].
OSBORNE, KA ;
SHIGENO, T ;
BALARSKY, AM ;
FORD, I ;
MCCULLOCH, J ;
TEASDALE, GM ;
GRAHAM, DI .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (04) :402-410
[23]  
Paxinos G, 1998, RAT BRAIN IN STEREOTAXIC COORDINATES, FOURTH ED., pix
[24]   Effects of hyperbaric oxygen on neurologic outcome for cerebral ischemia in rats [J].
Roos, JA ;
Jackson-Friedman, C ;
Lyden, P .
ACADEMIC EMERGENCY MEDICINE, 1998, 5 (01) :18-24
[25]   Demonstration of hyperaccumulation of [18F]2-fluoro-2-deoxy-D-glucose under oxygen deprivation in living brain slices using bioradiography [J].
Sasaki, T ;
Yamaguchi, M ;
Kojima, S .
SYNAPSE, 2005, 55 (04) :252-261
[26]   Neuroprotection by hyperbaric oxygenation after experimental focal cerebral ischemia monitored by MRI [J].
Schäbitz, WR ;
Schade, H ;
Heiland, S ;
Kollmar, R ;
Bardutzky, J ;
Henninger, N ;
Müller, H ;
Carl, U ;
Toyokuni, S ;
Sommer, C ;
Schwab, S .
STROKE, 2004, 35 (05) :1175-1179
[27]   Intravenous brain-derived neurotrophic factor reduces infarct size and counterregulates Bax and Bcl-2 expression after temporary focal cerebral ischemia [J].
Schäbitz, WR ;
Sommer, C ;
Zoder, W ;
Kiessling, M ;
Schwaninger, M ;
Schwab, S .
STROKE, 2000, 31 (09) :2212-2217
[28]   Mitochondrial contributions to tissue damage in stroke [J].
Sims, NR ;
Anderson, MF .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (06) :511-526
[29]   Hyperbaric oxygen reduces infarct volume in rats by increasing oxygen supply to the ischemic periphery [J].
Sunami, K ;
Takeda, Y ;
Hashimoto, M ;
Hirakawa, M .
CRITICAL CARE MEDICINE, 2000, 28 (08) :2831-2836
[30]   MicroPET II: design, development and initial performance of an improved microPET scanner for small-animal imaging [J].
Tai, YC ;
Chatziioannou, AF ;
Yang, YF ;
Silverman, RW ;
Meadors, K ;
Siegel, S ;
Newport, DF ;
Stickel, JR ;
Cherry, SR .
PHYSICS IN MEDICINE AND BIOLOGY, 2003, 48 (11) :1519-1537