Intermittent Exposure to Aflatoxin B1 Did Not Affect Neurobehavioral Parameters and Biochemical Markers of Oxidative Stress.

Aflatoxin B1 (AFB1) is the most common toxic mycotoxin that contaminates food. The treatment of its intoxication and the management of contaminations are a constant subject of health agendas worldwide. However, such efforts are not always enough to avoid population intoxication. Our objective was to investigate whether intermittent exposure to AFB1 would cause any impairment in biochemical and behavioral parameters, intending to simulate an irregular consumption. Male Wistar rats received four AFB1 administrations (250 µg/kg) by intragastric route separated by a 96-h interval. Toxicity was evaluated using behavioral tests (open field, object recognition, nest construction, marble burying, and splash test), biochemical markers of oxidative stress (cerebral cortex, hippocampus, liver, and kidneys), and plasma parameters of hepatic and renal functions. The intermittent exposure caused no modification in body weight gain as well as in organ weight. Both control and AFB1 groups presented similar profiles of behavior to all tests performed. Furthermore, AFB1 administrations alter neither antioxidant defenses nor markers of oxidation in all assayed tissues and in the plasma markers of hepatic and renal functions. Therefore, AFB1 intermittent administration did not cause its common damage from exposure to this toxicant, which must be avoided, and additional studies are required.

Repeated co-exposure to aflatoxin B1 and aspartame disrupts the central nervous system homeostasis: Behavioral, biochemical, and molecular insights.

Several studies demonstrated the toxicity of aspartame (ASP) and aflatoxin B1 (AFB1 ) in preclinical models. Although the majority of these reports assessed the toxic effects of each substance separately, their concomitant exposure and hazardous consequences are scarce. Importantly, the deleterious effects at the central nervous system caused by ASP and AFB1 co-exposure are rarely addressed. We evaluated if concomitant exposure to AFB1 and ASP would cause behavioral impairment and alteration in oxidative status of the brain in male rats. Animals received once a day for 14 days AFB1 (250 µg/kg, intragastric gavage [i.g.]), ASP (75 mg/kg, i.g.), or both substances (association). On day 14, they were subjected to behavioral evaluation, and biochemical and molecular parameters of oxidative status were measured in the cerebral cortex and hippocampus. In the open field test, AFB1 and combination treatments modified the motor, exploratory, and grooming behavior. In the splash test, all treatments caused a reduction in grooming time compared to the control group. An increase in thiobarbituric acid-reactive substances content induced by AFB1 and combination treatments was observed. The antioxidant defenses (vitamin C, nonprotein sulfhydryl, and ferric reducing antioxidant power) were impaired in all groups compared to control. Regarding molecular evaluation, mitochondrial superoxide dismutase-2 immunoreactivity decreased after AFB1 or ASP exposition in the hippocampus. Thus, co-exposure to ASP and AFB1 was potentially more toxic because it aggravated behavioral impairments and oxidative status disbalance in comparison to the groups that received only ASP or AFB1 . Therefore, our data suggest that those substances caused a disruption in brain homeostasis.

Hepatic susceptibility to oxidative damage after repeated concomitant exposure to aspartame and aflatoxin B1 in rats.

The potential interactions among food additives/contaminants and the consequences to biological systems is a topic that is rarely addressed in scientific literature. Thus, the current study investigated if the combined administration of ASP and AFB1 would impair hepatic and renal oxidative status. Male Wistar rats received during 14 days once a day ASP (75 mg/Kg) and/or AFB1 (250 µg/Kg) through intragastric route. At the end of experimental protocol, samples of liver and kidneys were collected for assessing biochemical markers of oxidative status. In the hepatic tissue, the treatment with a single substance (ASP or AFB1) caused an increase in TBARS levels, and a reduction in non-enzymatic antioxidant defenses (Vit C and NPSH levels and FRAP test). In the kidneys, TBARS levels were increased only in the group that received ASP + AFB1. The association reduced NPSH content, while the treatment with AFB1 reduced the FRAP levels. GST and CAT activities were increased in all treatments. Overall, ASP and AFB1 association presented higher toxic effects to the tissues. To the best of our knowledge, this is the first study demonstrating that the associated use of both ASP and AFB1 induces more extensive injuries in comparison to the effects caused by each one alone. Therefore, these data demonstrated that concomitant exposure to ASP and AFB1 potentiated their oxidative damage in hepatic tissue, suggesting that this organ is particularly sensitive to the toxic action induced by these substances.

Fumonisin B1 facilitates seizures induced by pentylenetetrazol in mice.

Fumonisin B1 (FB1) is a Fusarium spp. mycotoxin which constitutes a major public health issue because of its worldwide distribution and diversity of toxic effects.While the liver and kidney are considered the major target organs of FB1 toxicity in several species, evidence indicates that FB1 may be toxic to the brain. To further investigate the effects of FB1 on the central nervous system the present study aimed to test the hypothesis that acute FB1 exposure causes brain hyperexcitability and the potential underlying mechanisms. For these purposes, adult male C57BL/6 mice were injected with FB1 (8 mg/kg, i.p.) or its vehicle and 30 min thereafter received with a low dose of the classical convulsant pentylenetetrazol (PTZ, 30 mg/kg, i.p.) or its vehicle. After behavioral evaluation the cerebral cortex and the hippocampus were collected for analysis of Na(+),K(+)-ATPase activity, mitochondrial membrane potential (ΔΨm) and mitochondrial complex I and II activities. We found that FB1 reduced the latency for PTZ-induced myoclonic jerks and increased the number of these events. After exposure to FB1 total and α1 Na(+),K(+)-ATPase activities increased in cerebral cortex, whereas the same enzyme activities decreased in the hippocampus. Although no changes in mitochondrial complex I and II activities were found, acute exposure to FB1 increased ΔΨm in the cerebral cortex. Altogether, present results indicate that FB1 causes brain hyperexcitability in vivo, and that mitochondrial dysfunction may represent a potential underlying mechanism.

Bifenilos policlorados em arroz e feijão do estado do Rio Grande do Sul / Polychlorinated biphenyls in rice and beans from Rio Grande do Sul state, Brazil

Os bifenilos policlorados (PCBs) estão entre os poluentes mais tóxicos presentes no meio ambiente, apresentando os alimentos como principal fonte de exposição humana. Com base nisso, este trabalho teve como objetivo determinar os sete PCBs indicadores de contaminação ambiental em 22 amostras de arroz e 18 de feijão do estado do Rio Grande do Sul, Brasil. Além disso, objetivou-se calcular a ingestão diária estimada de resíduos, a partir da contaminação existente no arroz e feijão, assim como determinar o teor de gordura das amostras para correlacioná-lo com os níveis de PCBs. A extração e purificação dos compostos foram realizadas pelo método QuEChERS, seguido de identificação e quantificação por CG-EM. Os PCBs 153 e 101 apresentaram as maiores concentrações médias nas amostras de arroz e feijão, respectivamente. Considerando o somatório dos PCBs, este foi de 4,39ng g-1 para o arroz e de 4,17ng g-1 para o feijão. Quanto à ingestão diária estimada, esta foi de 7,82ng kg-1 e de 3,14ng kg-1 de peso corporal por dia, para o arroz e o feijão, respectivamente. Em relação ao percentual de gordura, o arroz e o feijão apresentaram teores de gordura de 0,32% e de 1,1%, respectivamente. No entanto, a correlação com os níveis de PCBs não foi significativa. Os resultados demonstram que o estado do RS apresenta fontes importantes de contaminação desses resíduos químicos persistentes.

Polychlorinated biphenyls (PCBs) are among the most toxic pollutants in the environment showing foods as the main source of human exposure. Based on this, this study aimed to determine 7 PCBs indicators of environmental contamination in 22 samples of rice and 18 samples of beans in Rio Grande do Sul state, Brazil. Furthermore, this study aimed to calculate the waste estimated daily intake, starting from the existing contamination in rice and beans, as well as wanted to determine the samples fat content to correlate with levels of PCBs. The extraction and purification of the compounds were performed via QuEChERS method followed by identification and quantification by GC-MS. PCBs 153 and 101 showed the highest mean concentration in the samples of rice and bean, respectively. Considering the sum of PCBs in the samples, this was 4.39ng g-1 for the rice and 4.17ng g-1 for the beans. In estimated daily intake, this was 7.82ng kg-1 and 3.14ng kg-1 of body weight per day, for the rice and beans, respectively. Regarding the percentage of fat the rice and beans samples had fat contents of 0.32% and 1.1%, respectively. However, the correlation with the PCBs levels was not significant. The results demonstrate that the State of RS has important sources of these persistent chemical waste contaminations.