Hemoglobin and oxygen: different affinities in two species of rodents (Mus musculus and Pitymys duodecimcostatus)

Five different hemoglobins have been demonstrated by polyacrylamide-gel disk electrophoresis in the species Mus musculus. Oxygen affinities of hemoglobin (P50) from Mus musculus and Pitymys duodecimcostatus hemolysates were determined at pH 7.4 and 37 degrees C. Values obtained for delta log P50/delta pH in hemolysates from both species point out a more pronounced Bohr effect in Pitymys duodecimcostatus.     

Achiasmatic sex chromosomes in Pitymys duodecimcostatus: mechanisms of association and segregation

The meiotic behavior of the sex chromosomes of Pitymys duodecimcostatus was studied by electron microscopy of whole-mount synaptonemal complex preparations. The results established that the sex chromosomes of this species are achiasmatic and remain unassociated throughout meiotic prophase I in most spermatocytes. In other cells, nonspecific association of the X and Y occurred by means of filamentous bridges. Pitymys duodecimcostatus represents an additional example of a mammalian species lacking a homologous pairing segment in its sex chromosomes and extends current knowledge about this controversial subject. In this regard, we suggest that sex-chromosome association is a characteristic that probably followed different evolutionary paths in different mammals, leading to loss of the homologous segment in some species and its conservation in others. It is also suggested that in P. duodecimcostatus, and probably in many other species as well, three mechanisms may act in concert to permit joining of the X and Y chromosomes during meiotic prophase, and, consequently, to ensure proper segregation during anaphase I: (1) joining of the sex-chromosome axes at their ends to the nuclear membrane, (2) formation of fibrillar structures to hold the sex chromosomes together, and (3) cohesiveness due to sex-vesicle formation.     

The synaptic sequence in hydroxyurea-treated spermatocytes of Pitymys duodecimcostatus (Rodentia, Microtidae)

A number of Pitymys duodecimcostatus males from a natural population were treated with hydroxyurea, which produces a gap in the spermatogenic line, to study the synaptic sequence of meiotic prophase. The use of substaging criteria, based on the morphological characteristics of the meiotic cells themselves, gave rise to a classification scheme consistent with the chronological sequence revealed by hydroxyurea treatment, which supports the usefulness of these independent criteria. The characteristics of meiotic prophase in P. duodecimcostatus are also described and discussed.     

Circulating plasma proteins in experimental acute hemorrhage and transfusion of blood components

In the experiments of dogs reactive changes of proteins in circulation in acute blood loss were studied. With the aim of prevention of homeostasis disorders caused by deficit of plasma proteins, blood protein components should be included into transfusion means.     

Ovulation and fertilization in the vole, Pitymys subterraneus

The females of Pitymys subterraneus bred in laboratory conditions have an irregular sexual cycle and induced ovulation. The first freshly ovulated eggs, surrounded by dense cumulus cells, appear in oviducts 10 h after copulation. Administering exogenous gonadotropins: pregnant mare's serum (PMS), human chorionic gonadotropin (hCG) or luteinizing hormone releasing hormone (LHRH), also induces ovulation in mature females of Pitymys subterraneus. In these experimental conditions females ovulate a similar number of eggs as after copulation. Dual stimulation (PMS and hCG plus copulation) does not result in the ovulation of a large number of normal ova, however, it does cause a release of degenerated oocytes.     

Hemoglobin can nitrate itself and other proteins.

Incubation of human hemoglobin with nitrite and hydrogen peroxide was found to induce autonitration and nitration of another protein (bovine serum albumin), as demonstrated by detection of nitrotyrosine residues in Western blots of separated membrane proteins. Inhibition of nitration by conversion of hemoglobin into the cyanmet form demonstrates that nitration is due to the pseudoperoxidase activity of hemoglobin. Incubation of whole erythrocytes with nitrite and hydrogen peroxide induces nitration of erythrocyte membrane proteins, much stronger when cellular catalase was inhibited with azide. These results suggest that hemoglobin and other hemoproteins may contribute to the tyrosine nitration in vivo.     

Oxidized proteins in Alzheimer's plasma

The levels of oxidatively modified proteins were examined in blood from Alzheimer's disease (AD) patients, non-AD controls, and AD relatives. Oxidative modification was measured by reacting the protein carbonyls with 2,4-dinitrophenyl hydrazine (DNPH). The total oxidized proteins were determined by HPLC, while specific protein oxidation was assessed from Western blots of electrophoretic gels using antibody to the DNP derivatives. Statistically significant elevations (P < 0.05) of total oxidized proteins were observed in both AD subjects and AD relatives when compared with non-AD controls. Moreover, a protein band (e.g., MW = 78-kDa) was uniquely oxidized in the plasma of AD subjects. Furthermore, this protein from AD subjects was more susceptible to in vitro oxidation. These data suggest that such oxidized proteins may be useful as biomarkers for the detection and evaluation of AD.     

Age-related differences in plasma proteins: how plasma proteins change from neonates to adults

The incidence of major diseases such as cardiovascular disease, thrombosis and cancer increases with age and is the major cause of mortality world-wide, with neonates and children somehow protected from such diseases of ageing. We hypothesized that there are major developmental differences in plasma proteins and that these contribute to age-related changes in the incidence of major diseases. We evaluated the human plasma proteome in healthy neonates, children and adults using the 2D-DIGE approach. We demonstrate significant changes in number and abundance of up to 100 protein spots that have marked differences in during the transition of the plasma proteome from neonate and child through to adult. These proteins are known to be involved in numerous physiological processes such as iron transport and homeostasis, immune response, haemostasis and apoptosis, amongst others. Importantly, we determined that the proteins that are differentially expressed with age are not the same proteins that are differentially expressed with gender and that the degree of phosphorylation of plasma proteins also changes with age. Given the multi-functionality of these proteins in human physiology, understanding the differences in the plasma proteome in neonates and children compared to adults will make a major contribution to our understanding of developmental biology in humans.     

Distribution of pyridoxal-5-phosphate between proteins and low molecular weight components of plasma: effect of acetaldehyde

It is found that approximately 65-70% of pyridoxal-P at physiological concentrations is bound to plasma proteins; 15% of its amount is bound to amino acids and peptides as a result of the Schiff base formation. Over 85% of pyridoxal-P associated with plasma proteins is bound to serum albumin. Inorganic phosphate and NaCl decrease the affinity of pyridoxal-P for albumin or other proteins. Acetaldehyde interacts with the alpha-amino group of the aspartic acid residue of the N-end of the polypeptide chain of the albumin molecule and with two epsilon-amino groups of the lysine residues having anomalously low value of pKa and deprotonated at physiological values of pH of the medium. Acetaldehyde competes with pyridoxal-P for the first (of the highest affinity) binding site of the coenzyme on serum albumin. Acetaldehyde is not bound at the second site of high affinity for pyridoxal-P on serum albumin.