The impact of chronic exposure to air pollution over oxidative stress parameters and brain histology.

Air pollution (AP) triggers neuroinflammation and lipoperoxidation involved in physiopathology of several neurodegenerative diseases. Our study aims to investigate the effect of chronic exposure to ambient AP in oxidative stress (OS) parameters and number of neurons and microglial cells of the cortex and striatum. Seventy-two male Wistar rats were distributed in four groups of exposure: control group (FA), exposed throughout life to filtered air; group PA-FA, pre-natal exposed to polluted air until weaning and then to filtered air; group FA-PA, pre-natal exposed to filtered air until weaning and then to polluted air; and group PA, exposed throughout life to polluted air. After 150 days of exposure, the rats were euthanized for biochemical and histological determinations. The malondialdehyde concentration in the cortex and striatum was significantly higher in the PA group. The activity of superoxide dismutase was significantly decreased in the cortex of all groups exposed to AP while activity of catalase was not modified in the cortex or striatum. The total glutathione concentration was lower in the cortex and higher in the striatum of the FA-PA group. The number of neurons or microglia in the striatum did not differ between FA and PA. On the other hand, neurons and microglia cell numbers were significantly higher in the cortex of the FA-PA group. Our findings suggest that the striatum and cortex have dissimilar thresholds to react to AP exposure and different adaptable responses to chronically AP-induced OS. At least for the cortex, changing to a non-polluted ambient early in life was able to avoid and/or reverse the OS, although some alterations in enzymatic antioxidant system may be permanent. As a result, it is important to clarify the effects of AP in the cortical organization and function because of limited capacity of brain tissue to deal with threatening environments.

Estudo dos resultados das análises de monitoramento dos produtos contendo hipoclorito de sódio em ambiente hospitalar na região da 1ª e18ª Coordenadorias Regionais de Saúde (CRS) no ano de 2011-2012 / Study of the results of monitoring analyses of products containing sodium hypochlorite in hospital environment in the region of the 1st and 18th Regional Health Coordinators (RHC) in 2011-2012

O objetivo deste trabalho foi a verificação da qualidade do hipoclorito de sódio em solução aquosa em relação às concentrações dessa substância fabricados no Brasil e diluídos em ambiente hospitalar para o uso nos processos de limpeza. (AU)

Direct contact with particulate matter increases oxidative stress in different brain structures.

INTRODUCTION: Several experimental and epidemiological studies have demonstrated the neurological adverse effects caused by exposure to air pollution, specifically in relation to pollutant particulate matter (PM). The objective of this study was to investigate the direct effect of PM in increased concentrations in different brain regions, as well as the mechanisms involving its neurotoxicity, by evaluating oxidative stress parameters in vitro. METHODS: Olfactory bulb, cerebral cortex, striatum, hippocampus and cerebellum of rats were homogenized and incubated with PM < 2.5 µm of diameter (PM2.5) at concentrations of 3, 5 and 10 µg/mg of tissue. The oxidative damage caused by lipid peroxidation of these structures was determined by testing the thiobarbituric acid reactive species (TBA-RS). In addition, we measured the activity of antioxidant enzyme catalase (CAT) and superoxide dismutase (SOD). RESULTS: All PM concentrations were able to damage the cerebellum and hippocampus, strongly enhancing the lipid peroxidation in both structures. PM incubation also decreased the CAT activity of the hippocampus, cerebellum, striatum and olfactory bulb, though it did not generate higher levels of lipid peroxidation in either of the last two structures. PM incubation did not alter any measurement of the cerebral cortex. CONCLUSION: The cerebellum and hippocampus seem to be more susceptible than other brain structures to in vitro direct PM exposure assay and the oxidative stress pathway catalyzes the neurotoxic effect of PM exposure, as evidenced by high consumption of CAT and high levels of TBA-RS. Thus, PM direct exposure seems to activate toxic neurological effects.

Hippocampus lipid peroxidation induced by residual oil fly ash intranasal instillation versus habituation to the open field.

Epidemiological studies have demonstrated the adverse effects of particulate matter (PM) inhalation on the respiratory and cardiovascular systems. It has been reported that air pollution may affect the central nervous system and decrease cognitive function. In rats, residual oil fly ash (ROFA) instillation causes decreased motor activity and increased lipid peroxidation in the striatum and the cerebellum. Our objective was to determine whether chronic instillation of particles induces changes in learning and memory in rats and whether oxidants in the hippocampus may contribute to these adverse effects. Forty-five-day-old male Wistar rats were exposed to ROFA by intranasal instillation and were treated with N-acetylcysteine (NAC) at 150 mg/kg i.p. for 30 days. Control groups were exposed to ROFA, NAC, or neither. On days 1, 8, and 30 of the protocol, rats were submitted to the open field test to evaluate habituation. After the last open field session, the rats were killed by decapitation. The hippocampus was used to determine lipid peroxidation (LP) by the thiobarbituric acid-reactive substances test. ROFA instillation induced an increase in LP in the hippocampus compared to all treatment groups (p = .012). NAC treatment blocked these changes. All of the treatment groups presented a decrease in the frequency of peripheral walking (p = .001), rearing (p = .001), and exploration (p = .001) over time. Our study demonstrates that exposure to particles for 30 days and/or NAC treatment do not modify habituation to an open field, a simple form of learning and memory in rats, and that oxidative damage induced by ROFA does not modulate these processes.

Estudo das alterações no desenvolvimento, no comportamento e na bioquímica cerebral de ratos machos adultos expostos à poluição atmosférica ambiental durante a fase intra-uterina e o período de lactação / Study of the alterations in the development, behavior and cerebral biochemistry of male rats exposed to the environmental atmospheric pollution in the intra-uterine phase

Estudos experimentais feitos em nosso laboratório comprovaram que a inalação de material particulado proveniente da queima de combustíveis fósseis utilizados em siderurgia pelos ratos adultos diminuiu a atividade motora dos animais no campo aberto. Além disso, provamos que os ratos habituaram ao ambiente desse teste, o que significa que a inalação desse tipo de material não provocou variação em termos de aprendizado simples. Uma das causas da alteração no comportamento em relação à motricidade seria o estresse oxidativo causado pelo material particulado no estriado e cerebelo desses animais. Entretanto, em nossa cidade não existem estudos que demonstrem a estreita associação entre inalação de poluentes, estresse oxidativo e alterações comportamentais. Baseados nos nossos trabalhos anteriores e na literatura, nosso objetivo foi investigar se a poluição atmosférica a nível ambiental durante as fases pré e pós-natal alteraria a memória discriminativa de curta-duração e a memória espacial. Além disso, avaliamos o papel do estresse oxidativo como o mecanismo propulsor dessas mudanças de comportamento. Para tal, ratas prenhas foram expostas ao ar filtrado e ao ar não filtrado durante os 21 dias de gestação. Ao final do período de amamentação, os machos foram separados e subdividos em 4 grupos experimentais (n=24): 1) Filtrado: nasceu e viveu em ambiente cujo ar era filtrado, 2) NFF: nasceu em ambiente cujo ar era não filtrado e viveu a partir do 21o dia do pós-natal no ambiente com ar filtrado, 3) FNF: nasceu sob ar filtrado e viveu a partir do 21o dia do pós-natal sob ar não filtrado, 4)NF: nasceu e viveu em ambiente cujo ar era não filtrado. Os animais ficaram expostos a poluição por 150 dias. Os animais foram divididos em 3 lotes: lote 1: n=6 animais por grupo; após anestesia profunda, os animais foram perfundidos com soro fisiológico seguido de paraformaldeído 4%, o encéfalo foi retirado e dissecado em córtex, hipocampo e estriado para análises...

Experimental studies done at our laboratory demonstrated that the inhalation of residual oil fly ash by the adult rats decreased motor activity of the animals in the open-field test. Additionaly, we showed that rats which inhalated residual oil fly ash preserved its habituation capacity. In this study, oxidative stress in striatum and cerebellum might be the cause of motor activity alterations. However, there were any studies about air pollution and behavioral alterations in Porto Alegre. Based on our previous works and in the literature, our objective was to investigate if the exposure to air pollution during intrauterine and lactation periods would damage the short term discriminative and spatial memories and if the mechanisms would be dependent of oxidants. For such, female pregnant rats were exposed to the filtered air and to the non filtered air during the 21 days of gestation. At the end of the breast-feeding period, the males were separate and divided in 4 experimental groups (n =24): 1) Filtered (F): - pre and post-natal exposure until adulthood in filtered air; 2) non filtered/filtered air (NFF): pre-natal period in non-filtered air until PND21 and post-natal in filtered air until adulthood; 3) filtered air/non-filtered air (FNF): pre-natal period in filtered air until PND 21 and post-natal period in non-filtered air until adulthood; 4) non filtered air (NF): pre and post-natal periods in non-filtered air.The animals were exposed the pollution for 150 days. The animals were divided in 3 lots: lot 1: n=6 animals per group; after anesthesia, the animals were perfused with saline solution following by paraformaldehyde 4%, the brain was removed and dissected in cortex, hippocampus and striatum for histological analyses by stereological techniques; lot 2: n=12 rats per group; submitted to behavioral tests; one day after the tests, those animals were euthanized by decapitation, the brain was removed and dissected in the same way mentioned previously...

Effect of pre- and postnatal exposure to urban air pollution on myocardial lipid peroxidation levels in adult mice.

Exposure to air pollution can elicit cardiovascular health effects. Children and unborn fetuses appear to be particularly vulnerable. However, the mechanisms involved in cardiovascular damage are poorly understood. It has been suggested that the oxidative stress generated by air pollution exposure triggers tissue injury. To investigate whether prenatal exposure can enhance oxidative stress in myocardium of adult animals, mice were placed in a clean chamber (CC, filtered urban air) and in a polluted chamber (PC, São Paulo city) during the gestational period and/or for 3 mo after birth, according to 4 protocols: control group-prenatal and postnatal life in CC; prenatal group-prenatal in PC and postnatal life in CC; postnatal group-prenatal in CC and postnatal life in PC; and pre-post group-prenatal and postnatal life in PC. As an indicator of oxidative stress, levels of lipid peroxidation in hearts were measured by malondialdehyde (MDA) quantification and by quantification of the myocardial immunoreactivity for 15-F2t-isoprostane. Ultrastructural studies were performed to detect cellular alterations related to oxidative stress. Concentration of MDA was significantly increased in postnatal (2.45 +/- 0.84 nmol/mg) and pre-post groups (3.84 +/- 1.39 nmol/mg) compared to the control group (0.31 +/- 0.10 nmol/mg) (p < .01). MDA values in the pre-post group were significantly increased compared to the prenatal group (0.71 +/- 0.15 nmol/mg) (p = .017). Myocardial isoprostane area fraction in the pre-post group was increased compared to other groups (p < or = .01). Results show that ambient levels of air pollution elicit cardiac oxidative stress in adult mice, and that gestational exposure may enhance this effect.

Chronic nasal instillation of residual-oil fly ash (ROFA) induces brain lipid peroxidation and behavioral changes in rats.

Several epidemiological studies have linked particulate matter exposure to numerous adverse health effects on the respiratory, cardiovascular, and reproductive systems (Braga et al., 1999; Zanobetti et al., 2000; Anderson et al., 2001; Farhat et al., 2005). More recently, ambient levels of black carbon were associated to impaired cognitive function in children (Suglia et al., 2008), suggesting that the central nervous system (CNS) may be a target of air pollutants. The present study was conducted to (a) determine whether chronic residual oil fly ash (ROFA) exposure promotes behavioral changes and lipid peroxidation in rat brain areas, and (b) determine whether N-acetylcysteine (NAC), a general antioxidant, prevents these effects. Forty-five-day-old male Wistar rats were exposed or not to ROFA by intranasal instillation and were treated or not with NAC (150 mg/kg) ip for 30 days. One day later, rats were submitted to the open field test to evaluate the motor/exploratory activities and emotionality followed by decapitation. Striatum and cerebellum were dissected to determine lipid peroxidation by the accumulation of thiobarbituric acid-reactive substances (TBARS). ROFA instillation induced an increase in lipid peroxidation level in striatum (p = .033) and cerebellum (p = .030), as compared with the control group. NAC treatment blocked these changes. ROFA promoted a decrease in the frequency of peripheral walking (p = .006) and a decrease in exploration (p = .001), which were not blocked by N-acetylcysteine. The present study provides evidence that toxic particles, administered by the respiratory route, induce oxidative stress in structures of the central nervous system, as well as behavioral alterations. The administration of NAC reduces lipid peroxidation at the striatum and cerebellum levels, but does not influence behavioral disturbances.