The development of polymerized pyridoxylated hemoglobin solution as a red cell substitute

Experiments were designed to establish whether the estrogens penetrate the membrane of the red cells or are transported by it. By hemolyzing red cells and reconditioning the ghosts, it was shown that the enzyme, estronase, follows the hemoglobin and therefore indicates that estrone and estradiol penetrate the membrane. Distribution of estradiol between intact red cells or reconditioned ghosts and ghost-free hemolysates of red cells or crystallized hemoglobin solution was proportional to the hemoglobin content when a correction for water solubility was made. Since the ghosts had frac13 the attraction of the intact cell, penetration is required to account for the distribution in the intact cell. Red cell ghost concentrates when prepared under certain conditions were found to have considerable affinity for estradiol, but on the basis of their low concentration per cell could account for only a fraction of the red cell affinity instrumental for estrogen orientation, even if their behavior did not reflect a change in properties during preparation. Ghosts prepared under the mildest conditions failed to demonstrate this affinity for estradiol. Submitted on September 14, 1959

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Acellular hemoglobin solution enters compressed lung capillaries more readily than red blood cells

Journal of Applied Physiology ◽

10.1152/jappl.2000.89.3.1198 ◽

2000 ◽

Vol 89 (3) ◽

pp. 1198-1204 ◽

Cited By ~ 5

Author(s):

Robert L. Conhaim ◽

Lance A. Rodenkirch ◽

Kal E. Watson ◽

Bruce A. Harms

Keyword(s):

Red Blood Cells ◽

Blood Cells ◽

Hemoglobin Concentration ◽

Red Cells ◽

Red Cell ◽

Hemoglobin Solution ◽

Lung Inflation ◽

Hemoglobin Mass ◽

Lung Capillaries ◽

Alveolar Septa

High lung inflation pressures compress alveolar septal capillaries, impede red cell transit, and interfere with oxygenation. However, recently introduced acellular hemoglobin solutions may enter compressed lung capillaries more easily than red blood cells. To test this hypothesis, we perfused isolated rat lungs with fluorescently labeled diaspirin cross-linked hemoglobin (DCLHb; 10%) and/ or autologous red cells (hematocrit, 20). Septal capillaries were compressed by setting lung inflation pressure above vascular pressures (zone 1). Examination by confocal microscopy showed that DCLHb was distributed throughout alveolar septa. Furthermore, this distribution was not affected by adding red blood cells to the perfusate. We estimated the maximum acellular hemoglobin mass within septa to be equivalent to that of 15 red blood cells. By comparison, we found an average of 2.7 ± 4.6 red cells per septum in zone 1. These values increased to 30.4 ± 25.8 and 50.4 ± 22.1 cells per septum in zones 2 and 3, respectively. We conclude that perfusion in zone 1 with a 10% acellular hemoglobin solution may increase the hemoglobin concentration per septum up to fivefold compared with red cell perfusion.

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Gas transfer in isolated lungs perfused with red cell suspension or hemoglobin solution

Respiration Physiology ◽

10.1016/0034-5687(89)90027-3 ◽

1989 ◽

Vol 77 (1) ◽

pp. 31-39 ◽

Cited By ~ 12

Author(s):

Jürg Geiser ◽

Daniel C. Betticher

Keyword(s):

Cell Suspension ◽

Gas Transfer ◽

Red Cell ◽

Hemoglobin Solution ◽

Isolated Lungs

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The orientation of sickle hemoglobin fibers within fascicles

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100104066 ◽

1988 ◽

Vol 46 ◽

pp. 400-401

Author(s):

Christopher A. Miller ◽

Bridget Carragher ◽

William A. McDade ◽

Robert Josephs

Keyword(s):

Sickle Cell ◽

Sickle Cell Anemia ◽

Relative Orientation ◽

Unit Cell ◽

Red Cell ◽

High Ph ◽

Sickle Hemoglobin ◽

Polar Crystal ◽

Helical Configuration

Highly ordered bundles of deoxyhemoglobin S (HbS) fibers, termed fascicles, are intermediates in the high pH crystallization pathway of HbS. These fibers consist of 7 Wishner-Love double strands in a helical configuration. Since each double strand has a polarity, the odd number of double strands in the fiber imparts a net polarity to the structure. HbS crystals have a unit cell containing two double strands, one of each polarity, resulting in a net polarity of zero. Therefore a rearrangement of the double strands must occur to form a non-polar crystal from the polar fibers. To determine the role of fascicles as an intermediate in the crystallization pathway it is important to understand the relative orientation of fibers within fascicles. Furthermore, an understanding of fascicle structure may have implications for the design of potential sickling inhibitors, since it is bundles of fibers which cause the red cell distortion responsible for the vaso-occlusive complications characteristic of sickle cell anemia.

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Erythrophagocytosis in the Liver in Hemolytic Anemias

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100100664 ◽

1968 ◽

Vol 26 ◽

pp. 184-185

Author(s):

O. T. Minick ◽

E. Orfei ◽

F. Volini ◽

G. Kent

Keyword(s):

Acid Phosphatase ◽

Oxidative Damage ◽

Phosphatase Activity ◽

Kupffer Cells ◽

Acid Phosphatase Activity ◽

Common Type ◽

Red Cell ◽

Cell Fragments ◽

Reticulo Endothelial System ◽

Important Site

Hemolytic anemias were produced in rats by administering phenylhydrazine or anti-erythrocytic (rooster) serum, the latter having agglutinin and hemolysin titers exceeding 1:1000.Following administration of phenylhydrazine, the erythrocytes undergo oxidative damage and are removed from the circulation by the cells of the reticulo-endothelial system, predominantly by the spleen. With increasing dosage or if animals are splenectomized, the Kupffer cells become an important site of sequestration and are greatly hypertrophied. Whole red cells are the most common type engulfed; they are broken down in digestive vacuoles, as shown by the presence of acid phosphatase activity (Fig. 1). Heinz body material and membranes persist longer than native hemoglobin. With larger doses of phenylhydrazine, erythrocytes undergo intravascular fragmentation, and the particles phagocytized are now mainly red cell fragments of varying sizes (Fig. 2).

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