Regional Cerebral Blood Flow during and after 2 Hours of Middle Cerebral Artery Occlusion in the Rat

In this study we explored if the secondary bioenergetic failure, which occurs a few hours after recirculation, following transient middle cerebral artery occlusion (MCAO) in rats, is caused by a compromised reflow. We induced 2 hours of MCAO and measured CBF at the end of the ischemia, as well as 15 minutes, 1, 2, and 4 hours after the start of recirculation, using autoradiographic or tissue sampling 14C-iodoantipyrine techniques. After 2 hours of MCAO, the autoradiographically measured CBF in the ischemic core areas was reduced to 3 to 5% of contralateral values. The reduction in CBF was less in neighboring, penumbral areas. After recirculation, flow already normalized in core tissues after 15 minutes, and remained close to normal for the 4 hours recirculation period studied. However, in penumbral tissues, recovery CBF values were usually below normal. The results show that tissues that are heavily compromised by the 2-hour period of ischemia and are destined to incur infarction, show a “relative hyperemia” during recirculation. In fact, some areas of the previously densely ischemic tissue showed overt hyperperfusion. This finding raises the question whether the relative or absolute hyperemia reflects events that are pathogenetically important. Because drugs that clearly ameliorate the final damage incurred fail to alter the relative hyperperfusion of previously ischemic tissues, it is concluded that vascular events in the reperfusion period do not play a major role in causing the final damage.

[1]  Yoji Yoshida,et al.  Experimental studies of ischemic brain edema , 1986 .

[2]  W. Pulsinelli,et al.  Temporal thresholds for neocortical infarction in rats subjected to reversible focal cerebral ischemia. , 1991, Stroke.

[3]  B. Siesjö,et al.  Recirculation in the Rat Brain following Incomplete Ischemia , 1983, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[4]  H. Kontos George E. Brown memorial lecture. Oxygen radicals in cerebral vascular injury. , 1985, Circulation research.

[5]  G. Schmid-Schönbein,et al.  Polymorphonuclear Leukocytes Occlude Capillaries Following Middle Cerebral Artery Occlusion and Reperfusion in Baboons , 1991, Stroke.

[6]  J. Garcìa,et al.  Influx of leukocytes and platelets in an evolving brain infarct (Wistar rat). , 1994, The American journal of pathology.

[7]  T. Hougen,et al.  Insulin effects on monovalent cation transport and Na-K-ATPase activity. , 1978, The American journal of physiology.

[8]  U. Dirnagl Cerebral ischemia: the microcirculation as trigger and target. , 1993, Progress in brain research.

[9]  M. Moskowitz,et al.  Oxygen radicals in cerebral ischemia. , 1992, The American journal of physiology.

[10]  B. Siesjö,et al.  Local Cerebral Blood Flow in the Recovery Period following Complete Cerebral Ischemia in the Rat , 1983, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[11]  Y. Shiga,et al.  Role of cell adhesion molecules in brain injury after transient middle cerebral artery occlusion in the rat , 1994, Brain Research.

[12]  K. Hossmann Glutamate‐Mediated Injury in Focal Cerebral Ischemia: The Excitotoxin Hypothesis Revised , 1994, Brain pathology.

[13]  W. Pulsinelli,et al.  Antagonism of the NMDA and non-NMDA receptors in global versus focal brain ischemia. , 1993, Progress in brain research.

[14]  M Chopp,et al.  Anti-intercellular adhesion molecule-1 antibody reduces ischemic cell damage after transient but not permanent middle cerebral artery occlusion in the Wistar rat. , 1995, Stroke.

[15]  L. Sokoloff,et al.  Measurement of local cerebral blood flow with iodo [14C] antipyrine. , 1978, The American journal of physiology.

[16]  D. Graham,et al.  Recirculation model following MCA occlusion in rats. Cerebral blood flow, cerebrovascular permeability, and brain edema. , 1985, Journal of neurosurgery.

[17]  M. Ingvar,et al.  Effect of Indomethacin on Local Cerebral Blood Flow in Awake, Minimally Restrained Rats , 1981, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[18]  H. Kontos Oxygen Radicals in Cerebral Vascular Injury , 1985 .

[19]  A. Buchan,et al.  A New Model of Temporary Focal Neocortical Ischemia in the Rat , 1992, Stroke.

[20]  B. Siesjö,et al.  N-tert-butyl-alpha-phenylnitrone improves recovery of brain energy state in rats following transient focal ischemia. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[21]  W. Paschen,et al.  Threshold relationship between cerebral blood flow, glucose utilization, and energy metabolites during development of stroke in gerbils , 1992, Experimental Neurology.

[22]  L. Pitts,et al.  Rat middle cerebral artery occlusion: evaluation of the model and development of a neurologic examination. , 1986, Stroke.

[23]  G. Mies,et al.  Ischemic Thresholds of Cerebral Protein Synthesis and Energy State following Middle Cerebral Artery Occlusion in Rat , 1991, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[24]  Delayed treatment with alpha-phenyl-N-tert-butyl nitrone (PBN) attenuates secondary mitochondrial dysfunction after transient focal cerebral ischemia in the rat. , 1996, Neurobiology of disease.

[25]  B. Siesjö,et al.  Penumbral Tissues Salvaged by Reperfusion Following Middle Cerebral Artery Occlusion in Rats , 1992, Stroke.

[26]  A. Hakim The Cerebral Ischemic Penumbra , 1987, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[27]  Á. Almeida,et al.  Effect of Reperfusion Following Cerebral Ischaemia on the Activity of the Mitochondrial Respiratory Chain in the Gerbil Brain , 1995, Journal of neurochemistry.

[28]  N. Sims,et al.  The Calcium Content of Mitochondria from Brain Subregions Following Short‐Term Forebrain Ischemia and Recirculation in the Rat , 1994, Journal of neurochemistry.

[29]  M. Ingvar,et al.  Influence of Nitrous Oxide on Local Cerebral Blood Flow in Awake, Minimally Restrained Rats , 1981, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[30]  B. Siesjö,et al.  Thresholds in cerebral ischemia - the ischemic penumbra. , 1981, Stroke.

[31]  D. Graham,et al.  Focal cerebral ischemia in the rat: Topography of hemodynamic and histopathological changes , 1984, Annals of neurology.

[32]  S. Kuroda,et al.  Delayed Treatment with α-Phenyl-N-tert-butyl Nitrone (PBN) Attenuates Secondary Mitochondrial Dysfunction after Transient Focal Cerebral Ischemia in the Rat , 1996, Neurobiology of Disease.

[33]  Fred Plum,et al.  Temporal profile of neuronal damage in a model of transient forebrain ischemia , 1982, Annals of neurology.

[34]  F. Barone,et al.  Cytokines, inflammation, and brain injury: role of tumor necrosis factor-alpha. , 1994, Cerebrovascular and brain metabolism reviews.

[35]  B. Siesjö,et al.  Mechanisms of secondary brain damage in global and focal ischemia: a speculative synthesis. , 1995, Journal of neurotrauma.

[36]  W. Pulsinelli,et al.  Pathophysiology of acute ischaemic stroke , 1992, The Lancet.

[37]  J. Michenfelder,et al.  Incomplete versus complete cerebral ischemia: Improved outcome with a minimal blood flow , 1979, Annals of neurology.

[38]  G. D. del Zoppo Microvascular changes during cerebral ischemia and reperfusion. , 1994, Cerebrovascular and brain metabolism reviews.

[39]  S. Kuroda,et al.  Secondary bioenergetic failure after transient focal ischaemia is due to mitochondrial injury. , 1996, Acta physiologica Scandinavica.

[40]  B. Siesjö Pathophysiology and treatment of focal cerebral ischemia. Part II: Mechanisms of damage and treatment. , 1992, Journal of neurosurgery.

[41]  B. Siesjö,et al.  Delayed treatment with the spin trap alpha-phenyl-N-tert-butyl nitrone (PBN) reduces infarct size following transient middle cerebral artery occlusion in rats. , 1994, Acta physiologica Scandinavica.

[42]  R. Morawetz,et al.  Differential regional vulnerability in transient focal cerebral ischemia. , 1982, Stroke.

[43]  B. Siesjö,et al.  Mechanisms of secondary brain injury. , 1996, European journal of anaesthesiology.

[44]  Maj-Lis Smith,et al.  Hyperthermia complicates middle cerebral artery occlusion induced by an intraluminal filament , 1994, Brain Research.

[45]  W D Heiss,et al.  Experimental Evidence of Ischemic Thresholds and Functional Recovery , 1992, Stroke.

[46]  R. Rosenthal,et al.  Postischemic inhibition of cerebral cortex pyruvate dehydrogenase. , 1994, Free radical biology & medicine.

[47]  Kiyoshi Takagi,et al.  Local hemodynamic changes during transient middle cerebral artery occlusion and recirculation in the rat: a [14C]iodoantipyrine autoradiographic study , 1995, Brain Research.

[48]  W. Pulsinelli,et al.  The CBF Threshold and Dynamics for Focal Cerebral Infarction in Spontaneously Hypertensive Rats , 1992, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[49]  R. Crowell,et al.  Selective Necrosis and Total Necrosis in Focal Cerebral ischemia. Neuropathologic Observations on Experimental Middle Cerebral Artery Occlusion in the Macaque Monkey , 1984, Journal of neuropathology and experimental neurology.

[50]  K. Kogure,et al.  Correlation between cerebral blood flow and histologic changes in a new rat model of middle cerebral artery occlusion. , 1989, Stroke.

[51]  J. Hallenbeck,et al.  Inflammatory reactions at the blood-endothelial interface in acute stroke. , 1996, Advances in neurology.

[52]  B. Siesjö,et al.  Cerebral blood flow in ischemia caused by carotid artery ligation in the rat. , 1973, Acta physiologica Scandinavica.

[53]  M. Chopp,et al.  Postischemic Administration of an Anti‐Mac‐1 Antibody Reduces Ischemic Cell Damage After Transient Middle Cerebral Artery Occlusion in Rats , 1994, Stroke.