Cerebral Metabolic Consequences of Hypotensive Challenges in Hemodiluted Pigs With and Without Cardiopulmonary Bypass

We tested the hypothesis that progressive aortic hypotension with bicarotid occlusion produces greater reductions in cerebral blood flow (CBF) and more flow-metabolism mismatching with hemodilution during cardiopulmonary bypass (CPB) than with hemodilution alone. In Yorkshire pigs randomized to hemodilution with CPB (n = 10) or hemodilution without CPB (control; n = 9), the effects of bicarotid ligation and graded hypotension on CBF (microspheres), the electroencephalogram (EEG), and cortical energy metabolites were examined. After bicarotid ligation, systemic flow was reduced for 15-min intervals of 80, 60, and 40 mm Hg aortic pressure, followed by a cortical brain biopsy. At baseline, CBF was lower in CPB (58 +/- 3 mL centered dot 100 g-1 centered dot min-1) than control (90 +/- 3 mL centered dot 100 g-1 centered dot min (-1); P < 0.05) animals, as was cerebral oxygen metabolism (3.1 +/- 0.1 vs 4.2 +/- 0.2 mL centered dot min-1 centered dot 100 g-1; P < 0.05). Although CBF remained 40% lower at each level of hypotension in CPB than control animals (P < 0.05), EEG scores showed no intergroup differences, indicating similar flow-metabolism matching. Brain metabolites were similar between CPB and control groups (adenosine triphosphate, 9.6 +/- 2.4 vs 12.4 +/- 1.9 micro mol/g; adenosine diphosphate, 6.0 +/- 0.7 vs 6.3 +/- 0.4 micro mol/g; adenosine monophosphate, 4.8 +/- 0.9 vs 3.8 +/- 0.8 micro mol/g; creatine phosphate, 8.3 +/- 1.8 vs 7.9 +/- 1.0 micro mol/g; and lactate, 178.4 +/- 20.2 vs 150.8 +/- 13.9 micro mol/g). Thus, despite significantly lower CBF during hypotension with bicarotid occlusion in hemodiluted animals during normothermic CPB, cortical electrical activity and the balance between flow and metabolism did not differ from those in control animals without CPB. (Anesth Analg 1995;81:911-8)

[1]  D. Deyo,et al.  Increasing organ blood flow during cardiopulmonary bypass in pigs: comparison of dopamine and perfusion pressure. , 1995, Critical care medicine.

[2]  D. Prough,et al.  Hyperglycemia during Hypothermic Canine Cardiopulmonary Bypass Increases Cerebral Lactate , 1995, Anesthesiology.

[3]  D. Prough,et al.  Arterial Microsphere Concentrations in Cats Are Not Affected by Changes in Hematocrit , 1994, Stroke.

[4]  D. Prough,et al.  Significance of Gaseous Microemboli in the Cerebral Circulation During Cardiopulmonary Bypass in Dogs , 1993, Circulation.

[5]  W. White,et al.  Pulsatile versus nonpulsatile reperfusion improves cerebral blood flow after cardiac arrest. , 1993, The Annals of thoracic surgery.

[6]  R. Heros,et al.  Mechanism of Cerebral Blood Flow Augmentation by Hemodilution in Rabbits , 1992, Stroke.

[7]  D. Prough,et al.  Regional cerebrovascular responses to progressive hypotension after traumatic brain injury in cats. , 1992, The American journal of physiology.

[8]  J. Weeks,et al.  Cerebral blood flow, blood volume, and brain tissue hematocrit during isovolemic hemodilution with hetastarch in rats. , 1992, The American journal of physiology.

[9]  S. Endo,et al.  Differences in critical cerebral blood flow with age in swine. , 1991, Journal of neurosurgery.

[10]  Jon M. Fukuto,et al.  Shear Stress‐Induced Release of Nitric Oxide From Endothelial Cells Grown on Beads , 1991, Hypertension.

[11]  J. French,et al.  An analysis of factors predisposing to neurological injury in patients undergoing coronary bypass operations. , 1989, The Quarterly journal of medicine.

[12]  A. Gelb,et al.  Nonpulsatile Cardiopulmonary Bypass Decreases Cerebral Metabolic Rate by Functional Cerebral Capillary Closure , 1989 .

[13]  Y. Tu,et al.  Isovolemic hemodilution in experimental focal cerebral ischemia. Part 2: Effects on regional cerebral blood flow and size of infarction. , 1988, Journal of neurosurgery.

[14]  A. Gjedde,et al.  Brain microvascular function during cardiopulmonary bypass. , 1987, The Journal of thoracic and cardiovascular surgery.

[15]  B. Tranmer,et al.  Pulsatile versus nonpulsatile blood flow in the treatment of acute cerebral ischemia. , 1986, Neurosurgery.

[16]  A. Gjedde,et al.  Nonpulsatile cardiopulmonary bypass disrupts the flow-metabolism couple in the brain. , 1985, The Journal of thoracic and cardiovascular surgery.

[17]  K. Shimoji,et al.  The effects of extreme hemodilutions on the autoregulation of cerebral blood flow, electroencephalogram and cerebral metabolic rate of oxygen in the dog. , 1985, Stroke.

[18]  J. Wood,et al.  Rheology of the Cerebral Circulation , 1984, Neurosurgery.

[19]  C. Wolferth,et al.  Effects of pulsatile and non-pulsatile perfusion upon cerebral and conjunctival microcirculation in dogs. , 1971, The American surgeon.

[20]  R B Shepard,et al.  Relation of pulsatile flow to oxygen consumption and other variables during cardiopulmonary bypass. , 1969, The Journal of thoracic and cardiovascular surgery.

[21]  R B Shepard,et al.  Energy equivalent pressure. , 1966, Archives of surgery.

[22]  O. Creech,et al.  Cerebral blood flow, metabolism, and brain volume in extracorporeal circulation. , 1958, The Journal of thoracic surgery.

[23]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[24]  S. Kobayashi,et al.  Effect of haemodilution on experimental cerebral ischaemia. , 1989, Clinical and experimental neurology.

[25]  H. Okino [Pulsatile blood flow]. , 1972, Kokyu to junkan. Respiration & circulation.

[26]  R. Lees The Effects of Extreme Hemodilutions on the Autoregulation of Cerebral Blood Flow , Electroencephalogram and Cerebral Metabolic Rate of Oxygen in the Dog , 2022 .