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Topoisomerase inhibitors are agents with anticancer activity. 7"-O-Methyl-agathisflavone (I) and amentoflavone (II) are biflavonoids and were isolated from the Brazilian plants Ouratea hexasperma and O. semiserrata, respectively. These biflavonoids and the acetyl derivative of II (IIa) are inhibitors of human DNA topoisomerases I at 200 microM, as demonstrated by the relaxation assay of supercoiled DNA, and only agathisflavone (I) at 200 microM also inhibited DNA topoisomerases II-alpha, as observed by decatenation and relaxation assays. The biflavonoids showed concentration-dependent growth inhibitory activities on Ehrlich carcinoma cells in 45-h culture, assayed by a tetrazolium method, with IC50 = 24 +/- 1.4 microM for I, 26 +/- 1.1 microM for II and 10 +/- 0.7 microM for IIa. These biflavonoids were assayed against human K562 leukemia cells in 45-h culture, but only I showed 42% growth inhibitory activity at 90 microM. Our results suggest that biflavonoids are targets for DNA topoisomerases and their cytotoxicity is dependent on tumor cell type.

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Topoisomerase inhibitors are agents with anticancer activity. 7"-O-Methyl-agathisflavone (I) and amentoflavone (II) are biflavonoids and were isolated from the Brazilian plants Ouratea hexasperma and O. semiserrata, respectively. These biflavonoids and the acetyl derivative of II (IIa) are inhibitors of human DNA topoisomerases I at 200 æM, as demonstrated by the relaxation assay of supercoiled DNA, and only agathisflavone (I) at 200 æM also inhibited DNA topoisomerases II-alpha, as observed by decatenation and relaxation assays. The biflavonoids showed concentration-dependent growth inhibitory activities on Ehrlich carcinoma cells in 45-h culture, assayed by a tetrazolium method, with IC50 = 24 ± 1.4 æM for I, 26 ± 1.1 æM for II and 10 ± 0.7 æM for IIa. These biflavonoids were assayed against human K562 leukemia cells in 45-h culture, but only I showed 42 percent growth inhibitory activity at 90 æM. Our results suggest that biflavonoids are targets for DNA topoisomerases and their cytotoxicity is dependent on tumor cell type

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Bajo condiciones experimentales se estudia el curso de la infección primaria y la respuesta a las reinfecciones por Trypanosoma rangeli en ratones albinos y Didelphis marsupialis. Durante el curso de la infección primaria en ratones, se observa una parasitemia relativamente baja y de corta duración. Los mismos muestran durante la primera reinfección una parasitemia escasa de cuatro días de duración, siendo resistentes a las sucesivas reinfecciones con T. rangeli. Los ejemplares de D. marsupialis exhiben una parasitemia de más larga duración, pero con un nivel de parásitos sanguícolas mucho menor que el detectado en el modelo ratón, siendo la respuesta a las reinfecciones similar a la observada en ratones. Se detectan anticuerpos hemaglutinantes en los sueros inmunes de ratones y Didelphis marsupialis, sometidos a la reinfección por T. rangeli. Se especula sobre la posible acción sinérgica de una respuesta inmune en el sitio de deposición en contra de las formas metacíclicas de T. rangeli y la acción de anticuerpos circulantes en contra de las formas sanguícolas, para explicar la resistencia de ambos modelos a las reinfecciones por T. rangeli

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Under experimental conditions, the course of the infection and the response to the reinfection by Trypanosoma rangeli in mice and Didelphis marsupialis, are studied. During the initial infection the mice show a relatively low parasitaemia and a short patent period. A scanty parasitaemia level of four days length, was observed following the first reinfection, being the mice resistant to new reinfections by T. rangeli. In opossums a lower parasitaemia and a longer patent period than that detected in mice, were observed during the initial infection. The response to reinfections in this mammal, was similar to that observed in mice. After reinfection with T. rangeli, haemagglutinant antibodies in immune-sera of both mice and opossums, were detected. The possible immune-response at the site of deposition against the metacyclic-forms of T. rangeli, and the action of circulating antibodies against the blood forms of the parasite, are speculated to explain the resistance of mice and opossums to the reinfection by T. rangeli.

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Thermal neutron activation analysis and instrumental gamma-ray spectrometry were used to analyze the elemental constituents in the head hair from sedentary Indian populations in the Venezuelan Amazonas region. Concentration values for 30 elements were determined quantitatively, and the presence of 7 others was detected qualitatively. The remoteness of the area and the primitive ecological conditions of the local population prevents the exposure of their biological systems to industrial and agricultural contamination, either external or metabolic. These conditions are reflected in a marked decrease of the concentration ranges of the trace elements, and a significant reduction or even the total absence of some components. The results demonstrate that closed groups of individuals exposed to similar dietary and environmental conditions exhibit closely similar trace element patterns in their hair and, consequently, in other biological tissue. This fact severely limits the use of trace element patterns in hair for forensic comparisons. The results also indicate that a large part of the constituents found in hair is probably deposited externally from ambient contamination and that any metabolic deposition occurs much more uniformly and probably in lower concentrations. Tables of analytical results in parts per million are presented, together with representative gamma-ray spectra of the hair. Comparison with earlier data in the literature is also shown.

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Resting human muscle blood flow (MBF) was determined simultaneously in the usual intramuscular injection sites to resolve whether variance in MBF could account for differences in drug absorption. Three pairs of muscles (gluteus maximus, vastus lateralis, and deltoid) were studied in each of 20 adult subjects. Use of dual, matched linear rate meters allowed two muscles to be studied simultaneously, with the order of injection random within an incomplete block design. MBF was calculated from the 133xenon washout rate using a single exponential that the computer found to best fit the data. Deltoid MBF (11.6 ml/100 gm/min plus or minus 0.5) was significantly (p smaller than 0.05) greater than gluteus MBF (9.6 plus or minus 0.5), with vastus or between right and left sides for each muscle. These data indicate that there are consistent differencies in resting MBF among specific muscle groups of sufficient magnitude (19%) to affect the rate of absorption and peak serum levels following intramuscular administration of drugs.

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