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Biomedical subjects

N O Solum

Publications and source records attributed to N O Solum.

At least 91 records · Page 5Linked to original sources
PubMed1978

A syndrome of factor VII deficiency and abnormal platelet release reaction.

A 15-year-old girl with severe factor VII deficiency and chronic arthropathy showed an excessively prolonged bleeding time. Further studies demonstrated low platelet adhesiveness and abnormal platelet aggregation with ADP, collagen and epinephrine. Release of 14C-serotonin was deficient after aggregation with ADP and epinephrine, but was normal with thrombin. Transfusion of plasma or prothrombin complex concentrate resulted in a partial or complete correction of the bleeding time, respectively, but had no effect on in vitro platelet function tests. Both parents and the only sister had factor VII activities of 42%-72% and factor VII antigen levels of 45%-66% of normal and may thus be heterozygotes with respect to factor VII deficiency. All three had normal bleeding times in spite of abnormal in vitro platelet functions. The observations are interpreted to mean that in this family with factor VII deficiency and abnormal platelet release reaction the platelet abnormality as such was not sufficiently severe to prolong the bleeding time unless the factor VII activity was also very low.

Adenosine Diphosphate↗
PubMed1978

Studies on cold insoluble globulin. I Concentrations in citrated plasma in rheumatic disorders.

Cold insoluble globulin (CIG) is a normal glycoprotein of human serum and plasma. The physiological significance of this protein is unknown, but is shows a temperature-dependent relation to fibrinogen and fibrin. It is possible that it represents a substrate for activated fibrin-stabilising factor in the polymerisation of fibrin. CIG is found on the surface of fibroblasts. In the present study CIG was estimated in citrated plasma in 115 patients with rheumatic diseases. Increased amounts were found in patients with systemic lupus erythematosus, secondary amyloidosis in classical and definite rheumatoid arthritis, and in male patients with juvenile rheumatoid arthritis.

Adolescent↗
PubMed1976

Studies on subcellular fractions of human platelets by the lactoperoxidase-iodination technique.

Lactoperoxidase-catalyzed 125I iodination and sodium dodecyl sulphate-polyacrylamide gel electrophoresis have been performed on whole, washed platelets as well as on isolated platelet membranes and granules. Electrophoresis of the whole platelets demonstrated two major radioactive peaks, corresponding to glycopolypeptides of estimated molecular weights of 120 000 and 100 000. A small, but consistent amount of radioactivity was also associated with a 147 000 dalton glycopolypeptide. The membranes showed the same pattern of radioactivity as the whole platelets, whereas only negligible amounts of labeled material was found in the soluble and granule fractions. Practically all the polypeptides were labeled in membranes iodinated after their isolation. A glycopolypeptide of 147 000 molecular weight was observed also in the soluble and the granule fractions, but no radioactivity was associated with these substances. In unreduced form, the granule glycopolypeptide penetrated only slightly into the polyacrylamide gel. Thrombin induced the relase of this granule-located substance from whole platelets, as observed by gel electrophoresis of the supernatant after release reaction (secretion). The granule glycoproteins were only partly exposed on the granule membrane since about 50% of the acid-hydrolyzable sialic acid could be liberated by neuraminidase treatment of isolated granules. In whole, iodinated granules the bulk of the radioactivity was associated with a polypeptide of estimated molecular weight 46 000 (possibly actin). This polypeptide was not seen in the supernatant after removal of the thrombin-degranulated platelets by centrifugation, which indicates that the granule membrane is retained with the platelets during the secretion process.

Blood Platelets↗
PubMed1975

Adenine nucleotide metabolism during the aggregation of human platelets by bovine factor VIII.

Human platelets, prelabelled with [3H]-adenine in vitro, were aggregated biphasically by bovine fibrinogen/factor VIII, and the amounts and specific radioactivity of ADP and ATP as well as the radioactivity of ATP, ADP, AMP, IMP and hypoxanthine + inosine were determined intracellularly and extracellularly. During the second phase of aggregation, ATP and ADP were released (50% of total) with a specific radioactivity 15-20 times lower than that of the ATP and ADP retained in the cells. The specific radioactivity of the ATP and ADP in the cells increased during release. Radioactive ATP was converted to radioactive hypoxanthine during release. These findings correlated well with those obtained with collagen, and indicate that bovine factor VIII induces the platelet release reaction whereby the storage (non-metabolic) pool of ATP and ADP is released while the metabolic pool is retained.

Adenine Nucleotides↗