[Construction of a nuclear medicine data collecting and processing system by coupling 2 microcomputers].
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to T Rösner.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Isolated rabbit hearts were perfused aerobically (45 min) and hypoxically (105 min), using a modified Langendorff technique. The mean functional diameter of capillaries (MFDC) was calculated from the perfusion rate per minute and the inflow resistance by the model of Hagen-Poiseuille. The MFDC expresses the mean lumen of all capillaries of the heart, regardless of the different behaviour of the capillaries in the different regions of the myocardium. The MFDC decreased very rapidly after the onset of a hypoxia from 3.5 +/- 0.3 micron to about 70% of the initial diameter within 5-10 min (p less than 0.01) and then in a slower range within the following 70 min to about 44% of the initial diameter. The release of lactate dehydrogenase (LDH) from the hypoxic myocardium was detectable after 45 min of hypoxia and rose drastically after 60 min of hypoxia in our model. The decrease of the MFDC as well as the release of LDH from the hypoxic myocardium can be diminished by application of O-(beta-hydroxyethyl)-rutoside or 10 mM mannitol to the hypoxic perfusion medium. Both substances have antioxidant activities. It is discussed that the injury of the microvasculature is an early process during hypoxia, which can potentiate the hypoxic changes of the myocardial cells by additional diminution of the supply with oxygen and substrates. The protecting activities of substances with antioxidant actions to hypoxic myocardium were supported.
Explore the source record for details and available documents.
A simple approach to evaluate logical pharmacophores on the base of topological features is described. It is based on considerations of the relative frequencies of structural features within different classes of activity. Shannon's entropy is used in the case of more than two classes. To obtain a pharmacophore a stepwise interactive procedure is performed. The algorithm is applied to fungicidal carboxamides and beta-adrenergic phenethylamine agonists and antagonists. In both cases meaningful pharmacophores could be obtained.
A method is proposed which yields an approximate solution of the Free-Wilson model very rapidly without using a computer. Although the resulting group contributions are numerically somewhat different from the exact Free-Wilson solution they correctly reflect the relative order of the substituents with respect to their effect on biological activity within each position as well as the relative importance of different positions. Thus, the approximate results can well be used to select the most promising candidates for further synthesis and testing.