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RESUMO Extratos etanólicos de Luehea paniculata, Anadenanthera colubrina, Cariniana rubra, Hancornia speciosa, Qualea grandiflora, Kielmeyera coriaceae e Palicourea rigida, coletadas no Cerrado de Mato Grosso foram submetidos à análise fitoquímica preliminar para identificação das principais classes de metabolitos secundários e à quantificação do teor de compostos fenólicos totais, flavonoides e cumarinas. O estudo também descreve a atividade antimicrobiana, antioxidante e a toxicidade preliminar frente a larvas de Artemia salina. Os extratos de C. rubra e Q. grandiflora foram os mais ativos contra as cepas fúngicas de C. neoformans (CIM 3,91 µg/mL), C. krusei(CIM 15,63 µg/mL), C. parapsilosis (CIM 31,25 µg/mL) e C. albicans (CIM 62,5 µg/mL), ambos com os mesmos resultados para estes microrganismos. Em relação às cepas bacterianas a mais sensível foi S. aureus com CIM de 250 µg/mL para todos os extratos testados. Luhea paniculata e Q. grandiflora foram as espécies vegetais mais ativas contra E. coli (CIM 500 e 250 µg/mL, respectivamente) e E. faecalis (CIM 250 e 500 µg/mL, respectivamente). No teste do DPPH, merece destaque as espécies K. coriaceae (Ca) (IC50 = 0,72 ± 0,51 μg /mL), K. coriaceae (Fo) (IC50 = 1,34 ± 0,53 μg /mL), H. speciosa (Fo)(IC50 = 1,03 ± 0,52 μg /mL), Q. grandiflora (Fo) (IC50 = 1,31 ± 0,19 μg /mL) e P. rigida (Fo) (IC50 = 1,39 ± 0,53 μg /mL). Com exceção de L. paniculata(Fo), que apresentou IC50 de 14,40 ± 0,34 μg /mL e teor de flavonoides de 295,5 mg/g, todas as espécies que tiverem significativa atividade no teste do DPPH, também apresentaram teor de flavonoides semelhante ao padrão, ou seja, H. speciosa (Fo) (280,5 mg/g), Q. grandiflora(Fo) (260,5 mg/g), K. coriaceae (Ca) (250,5 mg/g), K. coriaceae (Fo) (235,5 mg/g). Quanto à determinação de fenóis totais e cumarinas os resultados foram inferiores quando comparados aos padrões.

ABSTRACT Ethanol extracts of Luehea paniculata, Anadenanthera colubrina, Cariniana rubra, Hancornia speciosa, Qualea grandiflora, Kielmeyera coriaceae and Palicourea rigida, collected in the Cerrado of Mato Grosso went through preliminary phytochemical analysis in order to identify major classes of secondary metabolites and also to quantify the total content of phenolics, flavonoids and coumarins. The study also describes the antimicrobial and antioxidant activity and the toxicity of the larva of Artemia salina. The C. rubra extracts and the Q. grandiflora were the most active against fungal strains of C. neoformans (MIC 3.91 µg/ml), C. krusei (MIC 15.63 µg/ml), C. parapsilosis(31.25 MIC µg/ml) and C. albicans (MIC 62.5 µg/ml), both with the same results for these organisms. Regarding the bacterial strains, the most sensitive one was the S. aureus with 250 µg/ml MIC for all the tested extracts. The Luhea paniculata and the Q. grandiflora were the most active against E. coli species (MIC 500 and 250 µg/ml, respectively) and E. faecalis (MIC 250 and 500 µg/ml, respectively). In the test of DPPH, K. coriaceae (Ca) (IC50 = 0.72 ± 0.51 µg/mL), K. coriaceae (Fo) (IC50 = 1.34 ± 0.53 µg/mL), H. speciosa (Fo) (IC50= 1.03 ± 0.52 µg/mL), Q. grandiflora (Fo) (IC50 = 1.31 ± 0.19 µg/ml) and P. rigida (Fo) (1.39 ± 0,53 µg/ml) stood out. With the exception of the L. paniculata (Fo), which showed an IC50 of 14.40 ± 0.34 µg/ml and a flavonoid content of 295.5 mg/g, all species that had significant activity in the DPPH test, also showed flavonoid content similar to the standard one, or H. speciosa (Fo) (280.5 mg/g) Q. grandiflora (Fo) (260.5 mg/g), K. coriaceae (Ca) (250.5 mg/g), K. coriaceae (Fo) (235.5 mg/g).

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Zidovudine therapy of AIDS patients has been shown to cause only transient improvements in the numbers of circulating CD4+ cells and the in vitro functional activities of cultured lymphocytes. The present studies were undertaken to determine whether prolonged zidovudine therapy enhanced reactivity in two sensitive assays of T-cell function: the ability of phytohemagglutinin (PHA)-stimulated cells to form T-cell colonies and their capacity to express receptors for the growth factor interleukin-2 (IL-2). Treated patients, studied over periods of 20-60 weeks, showed no improvement in colony formation at any time interval, even in plates supplemented with exogenous IL-2. However, mitogen-stimulated T lymphocytes showed a significant increase in the capacity to express IL-2 receptors (CD25). This enhanced expression resulted primarily from activation of the CD8+ cell subset.

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