Stroke, Vol 25, 2253-2257, Copyright © 1994 by American Heart Association
MP Bowes, KE Burhop and JA Zivin
BACKGROUND AND PURPOSE: Hemodilution using modified hemoglobin solutions
may reduce ischemic central nervous system injury. Purified diaspirin
cross-linked hemoglobin (DCLHb) is a cell-free hemoglobin that is
intramolecularly cross-linked between the two alpha subunits, resulting in
enhanced oxygen offloading to tissues and increased half- life. In the
present experiments, we evaluated the ability of DCLHb to reduce
neurological damage in two rabbit stroke models. METHODS: In a reversible
spinal cord ischemia model, ischemia of the caudal lumbar spinal cord was
produced by temporary occlusion of the abdominal aorta. In an irreversible
model of cerebral ischemia, plastic microspheres (50 microns) were injected
into the internal carotid artery and lodged in the cerebral
microvasculature. DCLHb was administered 5 minutes after initiation of
ischemia as either a 10-mL/kg infusion, 10-mL/kg exchange transfusion, or a
20-mL/kg infusion. Control animals received human serum albumin that was
oncotically matched to the DCLHb. RESULTS: In the spinal cord model, DCLHb
significantly increased the duration of ischemia required to produce
permanent paralysis from 27.33 +/- 8.71 minutes (mean +/- SD) in controls
to 42.59 +/- 10.10 minutes in the 10- mL/kg exchange transfusion group and
to 40.82 +/- 18.16 minutes in the 20-mL/kg infusion condition (P < .05).
DCLHb did not significantly reduce neurological damage in the microsphere
embolization model. CONCLUSIONS: These data suggest that cross-linked
hemoglobin reduces neurological damage after reversible central nervous
system ischemia and that this is not attributable to hemodilution or
hypervolemia only.
ARTICLES
Diaspirin cross-linked hemoglobin improves neurological outcome following reversible but not irreversible CNS ischemia in rabbits
Department of Neurosciences, School of Medicine, University of California San Diego, La Jolla 92093-0624.
This article has been cited by other articles:
![]() |
A. T. Kawaguchi, D. Fukumoto, M. Haida, Y. Ogata, M. Yamano, and H. Tsukada Liposome-Encapsulated Hemoglobin Reduces the Size of Cerebral Infarction in the Rat: Evaluation With Photochemically Induced Thrombosis of the Middle Cerebral Artery Stroke, May 1, 2007; 38(5): 1626 - 1632. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Davis and D. Barer Neuroprotection in acute ischaemic stroke. II: Clinical potential Vascular Medicine, August 1, 1999; 4(3): 149 - 163. [Abstract] [PDF] |
||||
![]() |
R. Saxena, A. D. Wijnhoud, H. Carton, W. Hacke, M. Kaste, R. J. Przybelski, K. N. Stern, and P. J. Koudstaal Controlled Safety Study of a Hemoglobin-Based Oxygen Carrier, DCLHb, in Acute Ischemic Stroke Stroke, May 1, 1999; 30(5): 993 - 996. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. P. Grocott, R. D. Bart, H. Sheng, Y. Miura, R. Steffen, R. D. Pearlstein, D. S. Warner, and E. P. Wei Effects of a Synthetic Allosteric Modifier of Hemoglobin Oxygen Affinity on Outcome From Global Cerebral Ischemia in the Rat • Editorial Comment Stroke, August 1, 1998; 29(8): 1650 - 1655. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Aronowski, R. Strong, J.C. Grotta, and H. A. Kontos Combined Neuroprotection and Reperfusion Therapy for Stroke: Effect of Lubeluzole and Diaspirin Cross-Linked Hemoglobin in Experimental Focal Ischemia Stroke, September 1, 1996; 27(9): 1571 - 1577. [Abstract] [Full Text] |
||||
![]() |
A. Rebel, J. A. Ulatowski, K. Joung, E. Bucci, R. J. Traystman, and R. C. Koehler Regional cerebral blood flow in cats with cross-linked hemoglobin transfusion during focal cerebral ischemia Am J Physiol Heart Circ Physiol, March 1, 2002; 282(3): H832 - H841. [Abstract] [Full Text] [PDF] |
||||
|
Stroke Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1994 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |