Selenium can counteract methylmercury (MeHg) neurotoxicity. However, data about the neuroprotective effects of sodium selenite (Na(2)SeO(3)) on the activity of mitochondrial complexes and creatine kinase (mtCK) are scarce. Therefore, this study investigated the effects of the chronic exposure to Na(2)SeO(3) on brain energy metabolism and oxidative stress parameters in MeHg-poisoned mice. Adult male mice were orally treated with MeHg (40 mg L(-1) in drinking water, ad libitum) during 21 days and simultaneously administrated with daily subcutaneous injections of Na(2)SeO(3) (5 μmol kg(-1)), a potential neuroprotectant. Mitochondrial complexes I to IV and mtCK activities were measured in cerebral cortex mitochondria. The cerebro-cortical tissue was also used to evaluate the antioxidant enzymes glutathione peroxidase (GPx) and glutathione reductase (GR) activities, as well as lipid peroxidation. Metal deposition was followed autometalographically (AMG). Na(2)SeO(3) partially prevented MeHg-induced inhibition of complexes II-III, IV and mtCK activities; however, it was unable to prevent MeHg-induced complex I and II inhibition. MeHg increased lipid peroxidation, GR activity and decreased GPx activity in the cerebral cortex; however, Na(2)SeO(3) did not modify such events. Furthermore, Na(2)SeO(3)per se inhibited complexes I, II-III and IV and mtCK activities and increased GPx and GR activities and lipid peroxidation. These data show that inorganic selenium was ineffective in preventing most of the MeHg-induced brain biochemical alterations. However, the most prominent finding was the selenium-induced reduction of cells labelled for metal deposition. Although, the literature supports the beneficial effects of selenium against mercury toxicity, the toxic effects elicited by Na(2)SeO(3), alone or in combination with mercury, should be considered when this compound is proposed as a potential protective therapy for MeHg poisoning.

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The embryonic development of four species of the family Palaemonidae was studied under laboratory conditions. Adults of Macrobrachium olfersi (Wiegman, 1836), Macrobrachium potiuna (Müller, 1880), Palaemon pandaliformis (Stimpson, 1871) and Palaemonetes argentinus (Nobili, 1901) were collected in Santa Catarina Island, Santa Catarina, Brazil and maintained at 26ºC. The following embryonic characters were analyzed: egg shape, yolk organization and cleavage plane, naupliar and post-naupliar appendages, stomodeum, optical lobes, eyes, telson, embryo curvature and the space occupied by the embryo in the egg. Different rates of development were observed for the four species, with M. potiuna showing the longest time of embryogenesis. The species studied followed the pattern of embryogenesis of centrolecithal eggs, enabling the identification of similar features of the development, and the establishment of eight common embryonic stages.

Interest in organoselenide chemistry and biochemistry has increased in the past three decades, mainly due to their chemical and biological activities. Here, we investigated the protective effect of the organic selenium compound diphenyl diselenide (PhSe)2 (5 μmol/kg), in a mouse model of methylmercury (MeHg)-induced brain toxicity. Our group has previously demonstrated that the oral and repeated administration (21 days) of MeHg (40 mg/L) induced MeHg brain accumulation at toxic concentrations, and a pattern of severe cortical and cerebellar biochemical and behavioral. In order to assess neurotoxicity, the neurochemical parameters, namely, mitochondrial complexes I, II, II-III and IV, glutathione peroxidase (GPx) and glutathione reductase (GR) activities, the content of thiobarbituric acid-reactive substances (TBA-RS), 8-hydroxy-2'-deoxyguanosine (8-OHdG), and brain-derived neurotrophic factor (BDNF), as well as, metal deposition were investigated in mouse cerebral cortex. Cortical neurotoxicity induced by brain MeHg deposition was characterized by the reduction of complexes I, II, and IV activities, reduction of GPx and increased GR activities, increased TBA-RS and 8-OHdG content, and reduced BDNF levels. The daily treatment with (PhSe)2 was able to counteract the inhibitory effect of MeHg on mitochondrial activities, the increased oxidative stress parameters, TBA-RS and 8-OHdG levels, and the reduction of BDNF content. The observed protective (PhSe)2 effect could be linked to its antioxidant properties and/or its ability to reduce MeHg deposition in brain, which was here histochemically corroborated. Altogether, these data indicate that (PhSe)2 could be consider as a neuroprotectant compound to be tested under neurotoxicity.

Methylmercury (MeHg) is an environmental pollutant known to induce neurotoxicity in several animal species, including humans. However, studies focusing the effects of MeHg poisoning in chicks were based on phenomenological approaches and did not delve into the molecular mechanisms. The purpose of this study was to evaluate the postnatal consequences of the in ovo exposure to MeHg on behavioral, morphological and biochemical parameters in chicks. At the fifth embryonic day (E5), Gallus domesticus eggs were submitted to a single injection of 0.1 microg MeHg/0.05 ml saline. After treatment, the eggs returned to the incubator until hatching (E21). From first to fifth postnatal days (PN 1-PN 5), the MeHg-treated chicks showed lower frequency of exploratory movements and a significantly higher frequency of wing and anomalous movements. Cerebellar glutathione (GSH) levels and the activities of the GSH-related enzymes GSH reductase and GSH peroxidase were significantly higher (70, 72, and 80%, respectively) in MeHg exposed chicks in comparison to controls. Mercury impregnation was densest in the granular layer, followed by the Purkinje and molecular layers of treated chicks. A significant reduction of the number of Purkinje cells, as well as a greater distance between these cells were observed in chicks of MeHg group. Our results disclose that the prehatching exposure to MeHg induced motor impairments, which were correlated to histological damage and alterations on the cerebellar GSH system's development from PN 1 to PN 5.

ABSTRACT. Reproductive biology of Macrobrachium o({ersii (Wiegman) (Crustacea, Decapoda, Palaemonidae) collected at Santa Catarina's lsland, Brazil. The aim of this study is to characterize the reproductive features of Macrobrachium olfersii (Wiegman, 1836) from Santa Catarina' s Island. The animaIs were collected in freshwater streams ofthe Ratones Hidrografic Basin (site A I) and at the Peri's Pond (site A2). In the laboratmy, the procedures of sexual differentiation were canied out to c1assify the individuaIs in males, females or ovigerous females, followed by the detennination oftotal weight (g), quelipod relative weight (g) and totallength (mm). The eggs were removed from the ovigerous females and counled. Sexual malurity and fecundity were analyzed based in the dimensions and number of eggs carried by ovigerous females. The water temperature on lhe capture sites varied from 17 to 29°C throughout lhe months of study. A total of 503 individuaIs were captured, wilh 129 individuaIs from site A I and 374 ll'om site A2 . The mean total size and lenglh was 49.65 mm and 3.79 g for lhe males, 38.75 mm and 1.61 g for lhe females and 36.19 mm and 1.08 g for the ovigerous females. At the sites A I and A2, the individual sexual maturity was reached with 27.3 and 21.2 mm of total length, respectively, while populational sexual maturity was estimated for the 45.0 to 50.0 mm c1ass at site AI and for the 30.0 to 35.0 mm class at site A2. The ovigerous females carried an average of 3464 eggs at site A I, and 1440 eggs at site A2. These reproduclive feature s, presented by M olfersii, show the species' plasticity, which can be associated with environmental variations, contributing to ils reproductive success. KEY WORDS. Macrobrachium olf ersii, fecundity, sexual maturity, environmental condilions Na Ilha de Santa Catarina foram registrados representantes da família Palaemonidae (Rafinesque, 1815), identificadas como Macrobrachium acanthurus

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