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Erythrocyte,normal

It is concluded that under equihbrium conditions Upids do not easily undergo transbilayer movement in liposomes or membranes [149-151]. On the other hand, phospholipids and cholesterol have been shown to undergo transmembrane movement in erythrocytes under non-equilibrium conditions or following membrane perturbation such as ghost formation or phospholipase treatment [152-154]. More recently Lange and co-workers have made studies of the rate of transmembrane movement of cholesterol in the membranes of human erythrocytes. Normally, cholesterol in intact erythrocytes is not accessible to cholesterol oxidase [155]. [Pg.163]

Red blood cells (erythrocytes). Normally they are disc-shaped, but with a single amino acid defect in two of the protein chains, they adopt the pointed sickle shape. Sickle cell anemia is an inherited (genetic) disease caused by a flaw in DNA. [Pg.380]

Er rophilic y-globulin predominantly IgG and a minor amount of IgM (see liamunoglobulins) which coats the surface of erythrocyte membrane, and is necessary for the integrity and normal survival of the erythrocyte. Normal plasma contains about 3,000 mg E.y-g. per liter, and about 250 mg of bound E. /-g is present in 1 liter of packed er hrocytes. After splenectomy, production of E.y-g is markedly decreased, and the half life of the er3rthrocyte is decreased by up to 50 %. During the 4-8 month period after splenectomy, E.y-g. levels gradually return to normal, as does the half-life of the erythrocytes. [Pg.202]

O Rourke et al. 1990 England healthy controls (w = 14) nonfasting erythrocytes normal (73 131 ng/mL) ... [Pg.267]

Bailey et al. 1994 England adolescents (w = 54) fasting erythrocytes normal 216.5 21.0 nmol/L ... [Pg.267]

Herve France healthy controls fasting erythrocytes normal 4.0 2.0 nmol <2 nmol/L 176.0 28.0 nmol/L... [Pg.269]

Tallaksen et al. Norway healthy controls fasting erythrocytes normal (13.2-35.3 nmol/L) (2.1 13.9 nmol/L) (229.3 35.2 nmol/L)... [Pg.269]

Mancinelli et al. Italy healthy controls fasting erythrocytes normal 89.6 22.7 nmol/L 4.4 6.6 nmol/L 222.2 56.3 nmol/L... [Pg.269]

Lynch et al. 1997 England healthy controls (n = 45) nonfasting erythrocytes normal 174.0 34.0 nmol/L... [Pg.270]

The membrane-bound HG-PRT and A-PRT activities could also be demonstrated in the intact erythrocytes. Normal red cells were incubated with C-hypoxanthine, C-guanine and C-Adenine, respectively in the presence or absence of PRPP in the incubation medium. [Pg.224]

Deficiency. Macrocytic anemia, megaloblastic anemia, and neurological symptoms characterize vitamin B 2 deficiency. Alterations in hematopoiesis occur because of the high requirement for vitamin B 2 for normal DNA repHcation necessary to sustain the rapid turnover of the erythrocytes. Abnormal DNA repHcation secondary to vitamin B 2 deficiency produces a defect in the nuclear maturational process of committed hematopoietic stem cells. As a result, the erythrocytes are either morphologically abnormal or die during development. [Pg.112]

Obsessive-compulsive disorders Erythrocytes from patients with obsessive-compulsive disorder have significantly higher calpain activities than normal controls which could not be attributed to differences in memory function46... [Pg.313]

Neurological effects related to cholinesterase depression occurred in seven children acutely exposed to methyl parathion by inhalation as well as orally and dermally (Dean et al. 1984). The children were admitted to a local hospital with signs and symptoms of lethargy, increased salivation, increased respiratory secretions, and miosis. Two of the children were in respiratory arrest. Two children died within several days of each other. All of the children had depressed plasma and erythrocyte cholinesterase levels (Table 3-2). These effects are similar to those occurring in methyl parathion intoxication by other routes (see Sections 3.2.2.4 and 3.2.3.4). Three adults exposed in the same incident had normal plasma (apart from one female) and red blood cell cholinesterase, and urinary levels of 4-nitrophenol (0.46-12.7 ppm) as high as some of the ill children. [Pg.45]

Plasma also contains numerous other enzymes that perform no known physiologic function in blood. These apparently nonfunctional plasma enzymes arise from the routine normal destruction of erythrocytes, leukocytes, and other cells. Tissue damage or necrosis resulting from injury or disease is generally accompanied by increases in the levels of several nonfunctional plasma enzymes. Table 7-2 lists several enzymes used in diagnostic enzymology. [Pg.57]

This is true of skeletal muscle, particularly the white fibers, where the rate of work output—and therefore the need for ATP formation—may exceed the rate at which oxygen can be taken up and utilized. Glycolysis in erythrocytes, even under aerobic conditions, always terminates in lactate, because the subsequent reactions of pymvate are mitochondrial, and erythrocytes lack mitochondria. Other tissues that normally derive much of their energy from glycolysis and produce lactate include brain, gastrointestinal tract, renal medulla, retina, and skin. The liver, kidneys, and heart usually take up... [Pg.139]

Routine hematological Investigation showed a hemoglobin concentration of 15.6 g/100 ml, a packed red cell volume of 45%, normal erythrocyte morphology, and no Indication of excessive hemolysis. The same abnormal hemoglobin was found In one son. [Pg.37]

Many microorganisms minimize the effects of the host s defence system against them by mimicking the antigenic stmcture of the host tissne. The eventual immunological response of the host to infection then leads to the autoimmune destmction of itself. Thus, infections with Mycoplasma pneumoniae can lead to production of antibody against normal Group 0 erythrocytes with concomitant haemolytic anaemia. [Pg.86]

The 4 g of iron in the human body is normally com-partmented into its functional locations in the haem- and non-haem-containing, and iron-binding proteins and enzymes (Fig. 3.5). The majority (65%) of the iron is in the divalent state in haemoglobin and myoglobin, which are involved in the transport and storage of oxygen in erythrocytes and myocytes, respectively. The remainder is distributed between storage sites, predominantly in the... [Pg.45]


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