Assessment of magnesium influence on fatty acid content in isolated rat hepatocytes subjected to incubation.

Magnesium salts are components of many dietary supplements used in treatment or prevention of magnesium deficiency. Hypomagnesemia usually results from an improper lifestyle, including unbalanced diet. Isolated hepatocytes of animals or humans are the preferred model used to study the in vitro effects of exogenous factors on cellular metabolic changes. The aim of this study was to evaluate the content of saturated, monounsaturated and polyunsaturated fatty acids and their esters in isolated rat hepatocytes influenced by different magnesium concentrations. The isolated rat hepatocytes were used as the test material. Hepatocytes were prepared in culture medium (Hepatocyte Medium) + MgCl(2) solution to concentrations of 2 mM/dm(3) MgCl(2), 4 mM/dm(3) MgCl(2). After incubation with different concentrations of magnesium ions, changes in the content of fatty acids and their esters were found for the whole hepatocytes and hepatocyte membranes. Despite changes in the fatty acid content in the whole hepatocytes and their membranes, there were no changes in the coefficient of degree of saturation of fatty acids when different concentrations of MgCl2 were used.

Monitoring of radioactive contamination in Polish surface waters in 2012-2013.

The 90Sr and 137Cs contamination in Polish surface waters has been monitoring since 1994. Surface water samples from six lakes and the Vistula and Oder Rivers were collected in spring and autumn 2012 and 2013. The mean 90Sr and 137Cs concentrations were 3.92 ± 0.40 and 4.49 ± 2.00 mBq L-1, respectively. Correlations were identified between the radionuclide concentrations and meteorological conditions and the original fallout distribution from the Chernobyl disaster. The annual average radionuclide concentrations were not significantly different from the concentrations found between 1994 and 2011. The 137Cs and 90Sr concentrations have been decreasing only slowly.

[Prader-Willi syndrome in 22-year-old man--case study]. / Przypadek zespolu Pradera-Williego u 22-letniego mezczyzny.

Prader-Willi syndrome is a rare genetic disorder with characteristic neonatal hypotonia, followed by obesity, low height, hypogonadism and mental retardation. In this paper a case of 22-year-old man suffering from Prader-Willi syndrome is described.