27 research outputs found
Dexamethasone-dependent modulation of human lymphoblastoid B cell line through sphingosine production
The relationship between dexamethasone-dependent changes in intracellular sphingosine levels, energy and phospholipid metabolism have been investigated by P-31-NMR spectroscopy and high-performance liquid chromatography. The cellular functions have been evaluated by cellular growth and immunoglobulin M secretion (IgM). Significant increases in intracellular phosphorylcholine (PCho), extracellular choline (Cho), and endogenous sphingosine levels were observed only at 30 min incubation with dexamethasone. These results confirmed a sphingosine-dependent hydrolysis of choline-linked phospholipids (Miccheli, A., Ricciolini, R., Piccolella, E., Delfini, M. and Conti, F. (1991) Biochim. Biophys. Acta 1093, 29-35). Furthermore, no significant variations were evidenced at hours 1, 2, 6 and 18 of incubation. Dexamethasone causes an inhibition of cellular growth and IgM secretion as well as the sphingosine treatment. The results suggest that the effect of dexamethasone may be mediated by endogenous sphingosine production in Epstein-Barr virus transformed B lymphocytes
Trypanosoma lewisi: study of the activity of lonidamine in vitro and in vivo in rats
A 0.35 mM concn. of lonidamine produced a 60% inhibition of the replication of T. lewisi in culture. Administered to Fischer rats infected with T. lewisi, lonidamine provoked a 30% decrease in the no. of parasites in the blood on the 5th day of infection. Electron microscopy studies (showing damage to the mitochondrial membrane) and the analyses of phosphorylated metabolites by 31P-NMR spectroscopy (decrease of nucleotide triphosphate and nucleotide dephosphate levels) suggested the presumed interference of lonidamine in the energy metab. of trypanosomes. The presence of 2-amino-3-phosphonopropionic acid and 2-aminoethylphosphonic acid phosphonates in T. lewisi trypomastigotes were also revealed by means of 31P-NMR
Modulation of the free sphingosine levels in Epstein Barr virus transformed human B lymphocites by phorbol dibutyrate
The amounts of free sphingosine in Epstein Barr virus transformed B lymphocytes (EBV-B) treated with sphingosine and phorbol-12,13-dibutyrate (PD) has been quantified by high performance liquid chromatography (HPLC). PD treatment did not affect intracellular sphingosine level, while it seems to lessen the removal of this long chain base in sphingosine-treated EBV-B cells. The previous results relative to sphingosine-dependent changes in choline-metabolite levels have to be interpreted on the basis of these results
P-31 and H-1 studies of ethanolamine-linked phosphoglycerides metabolism in human T Lymphocites
Abstract: Aqueous and organic extracts of peripheral human T Iymphocytes and of T lymphoblastoid cell lines have been examinated by P-31 and H-1 NMR spectroscopy in order to study the metabolism of ethanolamine (Etn) linked phosphoglycerides. The results show that the Etn concentration in the culture medium determines the composition of Etn-containing metabolites and phospholipids. The effect of phorbol esters, stimulating the synthesis and the breakdown of choline-containing phospholipids has been also studied. A phorbol 12-myristate 13-acetate (PMA) dependent membrane phosphatidylethanolamine hydrolysis, presumably mediated by protein kinase C activity, has been demonstrated
Trypanosoma lewisi in liquid culture: findings and comparisons with different types of media. Culture medium for Trypanosoma lewisi.
The culture technique used proved to be more simple and economical than the different culture methods described in literature. This process permits the in vitro growth of parasites for a period long enough (10 days) to determine the possible activity of drugs. On the 10th day the cultures are infectious
Biochemical and biophysical effects of dexamethasone on human lymphoblastoid cell lines, studied by phosphorus-31 and proton NMR spectroscopy and fluorimetry
Recently, it was reported that, in several cell lines, dexamethasone, a synthetic glucocorticoid, modulates the sphingolipid metab. and the intracellular sphingosine levels. It was suggested that its effects could be mediated by the prodn. of sphingosine from membrane sphingomyelin. The present study examd. the effect of dexamethasone on Epstein-Barr virus transformed B lymphocytes on lipid compn. and metab. In particular sphingosine levels by 31P and 1H NMR spectroscopy, high performance liq. chromatog. and dexamethasone effects on membrane structure by fluorimetry were investigated. Furthermore, dexamethasone effects on cellular proliferation and IgM secretion were evaluated
Cerebral metabolic compartmentation as revealed by <sup>13</sup>C NMR analysis of [1-<sup>13</sup>C]glucose metabolism
Dexamethasone-dependent modulation of cholesterol levels in human lymphoblastoid B cell line through sphingosine production
The effect of dexamethasone on lipid composition of Epstein-Barr virus transformed human B lymphocytes have been investigated by 31P- and 1H-NMR spectroscopy and compared to the effects due to exogenous sphingosine treatment. Furthermore, the effects of dexamethasone and sphingosine on membrane structure was evaluated by fluorimetry. No significant changes were evidenced in phospholipid composition and in the ratio of unsaturated to total fatty-acid chains. A significant increase in total cholesterol levels was evident at 30 min incubation with dexamethasone or sphingosine; a parallel increase in DPH polarization at 30 min was also demonstrated. TMA-DPH intensity measurements suggest a slowing of vesicular intracellular traffic due to the treatment. The results suggest a dexamethasone- and sphingosine-dependent inhibition of intracellular cholesterol transport
