Teses em Neurociências e Biologia Celular (Doutorado) - PPGNBC/ICB

URI Permanente para esta coleçãohttps://repositorio.ufpa.br/handle/2011/2390

O Doutorado Acadêmico pertence ao Programa de Pós-Graduação em Neurociências e Biologia Celular (PPGNBC) do Instituto de Ciências Biológicas (ICB) da Universidade Federal do Pará (UFPA).

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Acesso aberto (Open Access)
Acidente vascular encefálico isquêmico na exposição crônica ao etanol: estudo pré-clínico da comorbidade e da resposta a minociclina
(Universidade Federal do Pará, 2015-02-27) FONTES JÚNIOR, Enéas de Andrade; MAIA, Cristiane do Socorro Ferraz; http://lattes.cnpq.br/4835820645258101; CRESPO LÓPEZ, Maria Elena; http://lattes.cnpq.br/9900144256348265
Stroke is the second largest cause of death in the world and the leading in Brazil, with 87% of strokes due to ischemic processes. Chronic ethanol consumption, usually beginning in adolescence, is recognized as an independent risk factor for increased morbidity and mortality by stroke. Although cases combining the two diseases are relatively common, there is no data in animals or clinical models demonstrating the quality or mechanisms of interaction between the two morbidities, nor its impact on therapeutic intervention. Considering the recent studies proposing minocycline as a new therapeutic tool for the treatment of stroke, this study aimed to investigate the interaction between the Chronic Alcoholic Intoxication (CAI) started in adolescence and the stroke in motor cortex of adult rats, and the effects of treatment with minocycline on this interaction, using behavioral, cellular and molecular parameters. Female Wistar rats (35 days-old) were chronically exposed to ethanol (6.5 g/kg/day, 22.5% w/v) or water for 55 days. One day after the end of the CAI focal ischemia was induced in motor cortex with the endothelin-1 (ET-1), followed by seven-day treatment with minocycline or saline. After this period, the animals were assayed with open field and rota rod tests. Immediately, animals were sacrificed and cortex was dissected for evaluation of nitrite and lipid peroxidation levels. In all groups, some animals were perfused and the motor cortex subjected to histological analysis to assess the damage, and immunohistochemical labeling to neuronal death (anti-NeuN), microglial/macrophage (anti-ED1) and astrocytes (anti-GFAP) activation. The ethanol intoxication from puberty to adulthood potentiated the damage caused by stroke, causing major losses in capacity to start and running movements as well as the strength and motor coordination compared to ischemic animals pretreated with water. These manifestations were accompanied by increased neuronal loss, reduced ED-1+ and GFAP+ cells and higher levels of nitrite and lipid peroxidation. Treatment with minocycline was effective in preventing/reverse motor deficits and tissue damage induced by focal ischemia, also inhibiting the increase in oxidative stress markers. The CAI either alone with succeeded by focal ischemia, harmed the outcome of treatment with minocycline. Our results indicate that heavy alcohol intoxication during adolescence exacerbates the motor deficit and tissue damage in animals subjected to focal ischemia. This process appears to be associated with microglia/astroglial activation, but mainly with oxidative stress. It also shows that the previous history of CAI started adolescence interferes significantly in the treatment of cerebral ischemia with minocycline.
Acesso aberto (Open Access)
Análise de parâmetros de exposição mercurial, suscetibilidade genética e intoxicação em populações ribeirinhas do Tapajós e Tucuruí
(Universidade Federal do Pará, 2016-08-30) ARRIFANO, Gabriela de Paula Fonseca; CRESPO LÓPEZ, Maria Elena; http://lattes.cnpq.br/9900144256348265
Mercury is a heavy metal responsible for intoxications worldwide. Most toxic form is methylmercury that has affinity for the central nervous system, with recognized neurotoxicity. Some regions of the Amazon are well characterized by mercury exposure in humans, as the region of the Tapajos, due to local mining activity, for example. However, others, such as Tucuruí, remain virtually unstudied, with only one study in humans to date. In the Amazon, there is a large number of studies showing mercury exposure, however, intoxication and susceptibility studies are far less numerous in the Amazonian populations, and even today, there is no study analyzing simultaneously the three factors. The objective of this study was to determine the exposure (mercury content in the body by using mercury levels in hair samples), the individual susceptibility (genetic predisposition of each individual to suffer a damage because the exposure, using the genotyping of apolipoprotein E) and the intoxication (quantifying the extent of the damage already caused by using biomarkers such as S100B and NSE) in Amazonian riverside populations. Three hundred eighty-eight individuals, selected after inclusion and exclusion criteria were studied. The genotype of apolipoprotein E more frequent was ɛ3/ɛ3, followed by ɛ3/ɛ4. Allelic frequencies were 0.043: 0.784: 0.173 to ε2: ɛ3: ɛ4, respectively. The median level of total mercury in hair was 4.2 μg/g (1.9- 10.2). A significant proportion of participants (24.8%) had mercury levels above 10 μg/g, as recommended by the WHO limit, and 12.8% of participants showed a total content of mercury greater or equal to 20 μg/g. Interestingly, Tucuruí levels were much higher than levels in the Tapajós (area recognized by the presence of mining gold activity). We identified 29% of patients with ApoE4 (considered at risk) and 8 maximum risk individuals (carriers of ApoE4 and mercury content above the limit of 10 μg/g). Moreover, there was a significant difference in mRNA levels of S100B protein between groups exposed to high and low levels of mercury. For the first time, markers of the three spheres of influence in human toxicology (exposure, susceptibility and poisoning) were studied. Our data already support the use of these markers to monitoring the Amazonian populations. This knowledge will assist the development of prevention strategies and making government decisions facing the problem of the impact of the mercury in the Amazon.
Acesso aberto (Open Access)
Exposição à concentração subletal de metilmercúrio: genotoxicidade e alterações na proliferação celular
(Universidade Federal do Pará, 2015-04-01) MALAQUIAS, Allan Costa; CRESPO LÓPEZ, Maria Elena; http://lattes.cnpq.br/9900144256348265
Mercury is a metal that stands out from the rest for present liquid under normal temperature and pressure. This xenobiotic is the largest source of pollution in many parts of the world and has been characterized toxic to the central nervous system (CNS). After dumping in liquid form directly into soil and riverbed, this heavy metal complex with various organic elements or it is converted to methylmercury (MeHg) by aquatic microbiota. The MeHg can move up the food chain, an event known as biomagnification, which directly affects human life. Thereby, the Amazon stands out for having all the components necessary for the maintenance of biogeochemical cycle of mercury as well as populations chronically exposed with this heavy metal. And this metal is considered a public health problem. It is well known that this xenobiotic after acute exposure to high doses promotes disorders related to the emergence of degenerative processes in the CNS, however, the effects at low concentrations are not yet fully described. Despite this cell type play an important role in the mercury intoxication process, the role of this metal on glial cells is not well known, especially on the genome and cell proliferation. Thus, this study aimed to evaluate the effect of exposure to this xenobiotic at low concentration on DNA and cell proliferation in C6 glial lineage cells. The biochemical (mitochondrial activity - measured by MTT assay -) and morphofunctional evaluations (membrane integrity - measured by the assay with dyes and AA BE -) confirmed the absence of cell death after exposure to heavy metals in a concentration of 3 μM for 24 hours. Even without causing cell death processes, the treatment with sublethal concentration of MeHg that was able to significantly increase the levels of markers of genotoxicity (DNA fragmentation, micronuclei, nuclear nucleoplasmic bridges and nuclear bud). At the same time, it was possible to observe a change in the cell cycle by increasing the mitotic index and a change in the cell cycle profile with increased cell population in S and G2 / M phases, suggesting an arrest cell cycle arrest. This change in cell cycle caused by MeHg exposure was followed by number of viable cells and cell confluence decrease, 24 hours after the withdrawal of MeHg of culture medium. The C6 cell line culture in addition showed an increase on doubling time parameter. This study demonstrates for the first time exposure to methylmercury low and sublethal concentration can promote genotoxic events and disturbances in cell proliferation in glial cell origin.
Acesso aberto (Open Access)
Novas ferramentas terapêuticas contra a convulsão e o comportamento tipo depressivo: ensaios pré-clínicos com açaí clarificado
(Universidade Federal do Pará, 2016-09-28) MONTEIRO, José Rogério Souza; CRESPO LÓPEZ, Maria Elena; http://lattes.cnpq.br/9900144256348265
Açai (Euterpe oleracea Mart.) Is a typical northern palm of Brazil, rich in phenolics and anthocyanins, substances with high antioxidant activity, anti-inflammatory and proven beneficial health effects. Oxidative stress and inflammation are involved in the generation and propagation of seizures, main clinical feature of epilepsy, and in the pathogenesis of depression. In this work we investigated the potential neuroprotective effect, anticonvulsant and antidepressant commercial samples of clarified açaí (CA). Only four doses of CA were enough to increase latencies for myoclonic and tonic-clonic seizures and to reduce the total duration of tonic-clonic seizures induced Pentylenetetrazole (PTZ). Eletrocorticográfics changes induced by PTZ were prevented significantly by CA. In the depressive-like behavior model induced by lipopolysaccharide (LPS), CA decreased immobility time and increased significantly the sucrose consumption of animals, indicating that the CA has preventive activity on the appearance of behaviors which are characteristic of clinical depression. Both the PTZ model as LPS CA exhibited potent preventive activity against the oxidative stress. CA prevented lipid peroxidation and elevated nitrite levels in the cerebral cortex, hippocampus, striatum and prefrontal cortex. These results demonstrate for the first time that acai is a fruit that exerts potent protective activity against the development of seizures, the depressive-like behavior and oxidative stress, which is an additional protection for individuals who consume this fruit.
Acesso aberto (Open Access)
Toxicidade in vitro e in vivo do ortobenzamol, análogo do paracetamol
(Universidade Federal do Pará, 2014-01-23) QUEIROZ, Luana Melo Diogo de; CRESPO LÓPEZ, Maria Elena; http://lattes.cnpq.br/9900144256348265
Paracetamol (PAR) is the non-prescription medicine most used worldwide. However, high doses of PAR produce hepatic and/or renal toxicity. In order to minimize the toxicity of PAR and get better analgesic and anti-inflammatory activity, a previous study conducted by modifying the chemical structure of PAR through molecular modeling, gave rise to ortobenzamol (OBZ) – analog of PAR. Thus, the OBZ was synthesized and evaluated in models of nociception and inflammation in animals. The study showed central analgesic activity of OBZ, with superior potency when compared to PAR. In addition, tests showed a significant inhibition in the inflammatory process. However, to the OBZ be able to be considered as an important new therapeutic option for the treatment of pain and/or inflammation is necessary to determine its toxicity. Given that, this study aimed to evaluate the toxicity in vitro and in vivo OBZ and compare it with the PAR. For this purpose, in vitro neurotoxicity was evaluated in primary cultures of cortical neurons through cell viability assays, determination of the levels of total and reduced glutathione, as well as the possible neuroprotective capacity against oxidative stress. In vivo studies were performed in mice, initiated by determining the median effective dose (ED50) of PAR in order to compare it with the OBZ at toxicity models studied. It was determined the liver and brain oxidative stress by analyzing the levels of lipid peroxidation and nitrites. The possible hepatic and renal dysfunction was determined by analyzing plasma enzymes aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma glutamyl transferase (GGT) levels and creatinine in the blood. We evaluated changes in clinical parameters through the CBC, WBC and platelet parameters and was held to determine the acute toxicity. The results of this study showed that in the tested doses, ortobenzamol is safer than paracetamol. The ortobenzamol displayed absence of neurotoxicity, less hepatotoxic and hematotoxic potential, absence of nephrotoxicity and also was rated as a xenobiotic with low toxicity after evaluation of acute toxicity. Therefore, the ortobenzamol can be considered as a safer alternative to the treatment of pain and inflammation when compared to paracetamol.
Acesso aberto (Open Access)
Triagem de cinco espécies de plantas medicinais usadas na Amazônia através da análise de secreção de histamina
(Universidade Federal do Pará, 2013-12-20) OLIVEIRA, Déborah Mara Costa de; CRESPO LÓPEZ, Maria Elena; http://lattes.cnpq.br/9900144256348265
The World Health Organization recommends the study and use of regional medicinal plants as a source of resources to reduce the costs of public health programs and increase the number of beneficiaries, especially in underdeveloped and developing countries. In the Amazon, the practice of herbal medicine is now an integral part of traditional culture, but on many occasions there is a profound lack of scientific knowledge about the effect of these plants. Therefore it is essential to study the scientific basis or not the indication of these plants for treating or preventing diseases. In this context, allergic diseases are the second leading complication that significantly affects the quality of life. In allergies, mast cells are key effector cells participating through the release of several pro- inflammatory mediators, including histamine. The stabilization of mast cells and thus inhibiting histamine release would be a key factor in the prevention and / or control of allergies. Thus the aim of this study was to evaluate the antiallergic potential of 5 or adapted species from the Amazon Connarus perrottetii var.angustifolius (Radlk) (barbatimão do pará), Fridericia chica (Bonpl.) LG Lohmann (pariri), Luehea speciosa Willd (açoita cavalo), Morinda citrifolia Linn (noni ) and Mansoa alliacea (Lam.) AH Gentry (cipó de alho) through the analysis of histamine secretion. Phytochemical screening of the ethanolic crude extracts to 70 % of each plant (fruit, leaves and / or bark) was performed and evaluated the release of histamine from peritoneal mast cells of rat incubated in vitro with different concentrations of the extracts and / or secretory agents (compound 48 /80 and A23187 ionophore). The present study demonstrates for the first time the inhibitory action of these five medicinal plants on the release of histamine. Among these 5 plants, the extract that showed a more potent effect was peeling Connarus perrottetii var. angustifolius ( Radlk ). Further study of this extract showed a low acute toxicity and lack of genotoxicity, which would support its use as a medicinal plant. The aqueous hexane and ethyl acetate fractions of this extract also showed potent inhibitory effect on histamine release induced. The phytochemical analysis by thin layer chromatography revealed the presence of tannins, catechins and flavonoids that could be responsible for these potent effects Through our results, new scientific bases are formed to elucidate the ethnopharmacological information on herbs traditionally used in the Amazon region. Thus, the possibility of investigating alternative therapies with these extracts against allergic affections or conditions in which the secretion of mast cells is relevant, may especially favor the low-income populations and living in areas with limited access to health centers, as often occurs in the Amazon, but otherwise has direct access to medicinal plants.

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