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Biomedical subjects

B A Murray

Publications and source records attributed to B A Murray.

39 records · Page 3Linked to original sources

Na/K- and Mg-ATPase activity in the placenta and in maternal and cord erythrocytes of pre-eclamptic patients.

Abnormal sodium balance is known to be associated with pre-eclampsia, but no investigations have been conducted concerning the enzyme which regulates active sodium transport at the cellular level. In this study, the enzyme responsible for active sodium transport--Na/K-ATPase and a nonspecific ATPase Mg-ATPase--were assayed in the placenta and in maternal and fetal (cord) erythrocytes of pregnant women with and without pre-eclampsia. Placental ATPase activity was unaffected by pre-eclampsia. However, in infants of pre-eclamptic mothers, fetal erythrocytes were found to have significantly less activity (42 per cent) of both enzymes than fetal erythrocytes from infants of normal mothers. In pre-eclamptic mothers, erythrocyte Mg-atpase activity was significantly less (41 per cent) than normal and Na/K-ATPase activity was slightly decreased (16 per cent). These results indicate that disruption of active sodium transport in fetal erythrocytes is associated with pre-eclampsia and are not inconsistent with the hypothesis of a circulating "toxin."

Adenosine Triphosphatases↗

Postembedding ultrastructural in situ hybridization on ultrathin cryosections and LR white resin sections.

A method was developed for nonisotopic postembedding in situ hybridization (ISH) on ultrathin sections of frozen and of LR White resin-embedded material at the electron microscopic level. The method was successfully applied to detect Epstein-Barr virus (EBV) DNA in the P3HR1 human Burkitt's lymphoma cell line. Each of the steps in the procedure had to be optimized for successful ISH on the frozen and LR White sections. The most important conditions are described. Predigestion with proteinase K was only necessary with the resin sections. Sections were treated with sodium hydroxide to denature target DNA and were hybridized with a biotinylated probe. The probe was best detected with a primary antibody to biotin followed by a gold-conjugated secondary antibody. EBV DNA was detected in the nucleus and/or cytoplasm in 10% to 20% of P3HR1 cells. A similar percentage of cells in thin L-sectioned material prepared by routine methods showed virus particles at different stages of maturation.

Acrylic Resins↗