EXPERIMENTAL THERAPIES TO IMPROVE DELIVERY OF OXYGEN AND SUBSTRATE IN ACUTE STROKE

被引:9
作者
PACZYNSKI, RP [1 ]
DIRINGER, MN [1 ]
HSU, CY [1 ]
机构
[1] WASHINGTON UNIV, MED CTR, DEPT NEUROL, CTR STUDY NERVOUS SYST INJURY, ST LOUIS, MO 63110 USA
关键词
D O I
10.1097/00019052-199502000-00003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The results of large-scale clinical trials of hemodilution therapy and vasodilators for acute stroke have been disappointing. However, interventions involving the manipulation of whole blood viscosity, blood oxygen-carrying capacity, cardiac output, and the resistance properties of cerebral vessels are viable therapeutic modalities currently being investigated. The central aim of all of these therapies is the timely improvement of perfusion and substrate delivery to ischemic brain regions. Better understanding of cerebrovascular flow regulation and the physiology of microvessels may give rise to more effective therapies. In the past, overemphasis on hematocrit reduction and cerebral vasodilators has obscured the potential risks of reducing blood oxygen content and vascular resistance during acute stroke and the importance of optimizing oxygen delivery by other means, in particular by cardiac output augmentation and manipulation of plasma properties. A broader approach to therapeutic strategies for acute stroke includes not only increasing cerebral blood flow, but also interventions that will create favorable changes in the humoral microenvironment and promote overall substrate delivery to the brain.
引用
收藏
页码:6 / 14
页数:9
相关论文
共 78 条
[31]   TREATMENT OF ISCHEMIC DEFICITS FROM VASOSPASM WITH INTRAVASCULAR VOLUME EXPANSION AND INDUCED ARTERIAL-HYPERTENSION [J].
KASSELL, NF ;
PEERLESS, SJ ;
DURWARD, QJ ;
BECK, DW ;
DRAKE, CG ;
ADAMS, HP .
NEUROSURGERY, 1982, 11 (03) :337-343
[32]  
KEIPERT PE, 1994, ADV EXP MED BIOL, V317, P197
[33]  
KEIPERT PE, 1992, ADV EXP MED BIOL, V317, P465
[34]   MODIFICATION OF FOCAL CEREBRAL-ISCHEMIA BY CARDIAC-OUTPUT AUGMENTATION [J].
KELLER, TS ;
MCGILLICUDDY, JE ;
LABOND, VA ;
KINDT, GW .
JOURNAL OF SURGICAL RESEARCH, 1985, 39 (05) :420-432
[35]   EFFECTS OF HEMATOCRIT ON BRAIN METABOLISM IN EXPERIMENTALLY INDUCED CEREBRAL-ISCHEMIA IN SPONTANEOUSLY HYPERTENSIVE RATS (SHR) [J].
KIYOHARA, Y ;
FUJISHIMA, M ;
ISHITSUKA, T ;
TAMAKI, K ;
SADOSHIMA, S ;
OMAE, T .
STROKE, 1985, 16 (05) :835-840
[36]   FRUCTOSE-1,6-BISPHOSPHATE REDUCES INFARCT VOLUME AFTER REVERSIBLE MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS [J].
KULUZ, JW ;
GREGORY, GA ;
HAN, YX ;
DIETRICH, WD ;
SCHLEIEN, CL .
STROKE, 1993, 24 (10) :1576-1583
[37]   BLOOD-BRAIN-BARRIER DISRUPTION AND EXACERBATION OF ISCHEMIC BRAIN EDEMA AFTER RESTORATION OF BLOOD-FLOW IN EXPERIMENTAL FOCAL CEREBRAL-ISCHEMIA [J].
KUROIWA, T ;
SHIBUTANI, M ;
OKEDA, R .
ACTA NEUROPATHOLOGICA, 1988, 76 (01) :62-70
[38]  
KUSCHINSKY W, 1992, CEREBROVAS BRAIN MET, V4, P261
[39]   EFFECTS OF HEMATOCRIT VARIATIONS ON CEREBRAL BLOOD-FLOW AND OXYGEN-TRANSPORT IN ISCHEMIC CEREBROVASCULAR-DISEASE [J].
KUSUNOKI, M ;
KIMURA, K ;
NAKAMURA, M ;
ISAKA, Y ;
YONEDA, S ;
ABE, H .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1981, 1 (04) :413-417
[40]   POLYETHYLENE GLYCOL-CONJUGATED SUPEROXIDE-DISMUTASE AND CATALASE REDUCE ISCHEMIC BRAIN INJURY [J].
LIU, TH ;
BECKMAN, JS ;
FREEMAN, BA ;
HOGAN, EL ;
HSU, CY .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (02) :H589-H593