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Astrocyte and microglia cells play an important role in the central nervous system (CNS). They react to various external aggressions by becoming reactive and releasing neurotrophic and/or neurotoxic factors. Rutin is a flavonoid found in many plants and has been shown to have some biological activities, but its direct effects on cells of the CNS have not been well studied. To investigate its potential effects on CNS glial cells, we used both astrocyte primary cultures and astrocyte/microglia mixed primary cell cultures derived from newborn rat cortical brain. The cultures were treated for 24 h with rutin (50 or 100 micromol/L) or vehicle (0.5% dimethyl sulfoxide). Mitochondrial function on glial cells was not evidenced by the MTT test. However, an increased lactate dehydrogenase activity was detected in the culture medium of both culture systems when treated with 100 micromol/L rutin, suggesting loss of cell membrane integrity. Astrocytes exposed to 50 micromol/L rutin became reactive as revealed by glial fibrillary acidic protein (GFAP) overexpression and showed a star-like phenotype revealed by Rosenfeld's staining. The number of activated microglia expressing OX-42 increased in the presence of rutin. A significant increase of nitric oxide (NO) was observed only in mixed cultures exposed to 100 micromol/L rutin. Enhanced TNFalpha release was observed in astrocyte primary cultures treated with 100 micromol/L rutin and in mixed primary cultures treated with 50 and 100 micromol/L, suggesting different sensitivity of both activated cell types. These results demonstrated that rutin affects astrocytes and microglial cells in culture and has the capacity to induce NO and TNFalpha production in these cells. Hence, the impact of these effects on neurons in vitro and in vivo needs to be studied.

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Environmental factors are constantly changing in the intertidal region. Consequently, the various benthic organisms that densely colonize this ocean area had to adapt to these constant changes. Reproductive strategy might be considered one of these adaptations. However, knowledge about this aspect of the biology of marine invertebrates is still contentious for some groups, especially with regard to sponges (Porifera). Here, we investigated the effects of different environmental factors on the timing and effort of sexual and asexual reproduction in Cinachyrella apion and Tethya maza, two oviparous demosponges in Salvador, Bahia, Brazil. We analyzed the influence of humidity, atmospheric temperature, seawater temperature, photoperiod, rainfall, height of low tides, and chlorophyll-a concentration on the density and size of oocytes and buds of these sponges. Both species reproduced aperiodically.Cinachyrella apion had a maximum 2.8 ± 4.04 oocytes/mm 2 and 0.73 ± 0.15 buds/ mm 2 , whereas T. maza had a maximum 6.0 ± 12.21 oocytes/mm 2 and 0.31 ± 0.13 buds/mm 2 . The density of oocytes in C. apion was positively influenced by chlorophyll-a concentration, whereas that of T. maza was negatively modulated by relative humidity. We did not observe any relationship between the environmental factors and bud density in C. apion, but bud density variation in T. maza was positively related to chlorophyll-a concentration and to seawater temperature. It seems that individuals of both species alternated between the production of sexual and asexual propagules, suggesting a trade-off between reproductive modes. Therefore, asexual and sexual reproduction seems to impact population growth and reproduction of both species, likely contributing to the recruitment of new sponges. In tropical intertidal regions, multiple environmental factors seem to contribute more to determining the quantity of sexual and asexual reproductive elements rather than the species' reproductive period.

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