Antonio Luiz Gomes Júnior
International Federation of the Phonographic Industry
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Featured researches published by Antonio Luiz Gomes Júnior.
Oxidative Medicine and Cellular Longevity | 2015
Antonio Luiz Gomes Júnior; Márcia Fernanda Correia Jardim Paz; Laís Iasmin Soares da Silva; Simone da Costa e Silva Carvalho; André Luiz Pinho Sobral; Kátia da Conceição Machado; Paulo Michel Pinheiro Ferreira; Prabodh Satyal; Rivelilson Mendes de Freitas; Ana Amélia de Carvalho Melo Cavalcante
The aim of this study was to evaluate the oxidative parameters of erythrocytes and genotoxicity in leukocytes of patients with breast cancer. Oxidative parameters were detected by spectrophotometry and genotoxic damage by single cell gel electrophoresis. Twenty-eight women with breast cancer were monitored before chemotherapy and after the second and fourth cycles of therapy with cyclophosphamide and doxorubicin. After the fourth cycle, increases (P < 0.05) in the reactive substances to thiobarbituric acid levels, nitrite content, and superoxide dismutase activity and high rates of DNA damage in leukocytes were observed when compared with healthy women group and baseline levels. Similarly, after the second cycle, the same parameters were increased (P < 0.05) when compared with baseline levels. Increase in catalase activity was detected only after the fourth cycle and reduced glutathione levels and glutathione peroxidase activity were decreased in all cycles when compared with healthy women, as well as after the second and fourth chemotherapy cycles compared to baseline (P < 0.05). Patients with breast cancer presented an indicative of oxidative stress before, during, and after chemotherapy, as well as increased genotoxic damage in all stages of treatment, demonstrating the clinical applicability of this investigation.
Frontiers in Genetics | 2018
Márcia Fernanda Correia Jardim Paz; Marcus Vinícius Oliveira Barros de Alencar; Antonio Luiz Gomes Júnior; Keylla da Conceição Machado; Muhammad Torequl Islam; Eunüs S. Ali; Manik Chandra Shill; Md. Iqbal Ahmed; Shaikh Jamal Uddin; Ana Maria Oliveira Ferreira da Mata; Ricardo Melo de Carvalho; Kátia da Conceição Machado; André Luiz Pinho Sobral; Felipe Cavalcanti Carneiro da Silva; João Marcelo de Castro e Souza; Daniel Dias Rufino Arcanjo; Paulo Michel Pinheiro Ferreira; Siddhartha Kumar Mishra; Juliana da Silva; Ana Amélia de Carvalho Melo-Cavalcante
Molecular epidemiological studies have identified several risk factors linking to the genes and external factors in the pathogenesis of breast cancer. In this sense, genetic instability caused by DNA damage and DNA repair inefficiencies are important molecular events for the diagnosis and prognosis of therapies. Therefore, the objective of this study was to analyze correlation between sociocultural, occupational, and lifestyle risk factors with levels of genetic instability in non-neoplastic cells of breast cancer patients. Total 150 individuals were included in the study that included 50 breast cancer patients submitted to chemotherapy (QT), 50 breast cancer patients submitted to radiotherapy (RT), and 50 healthy women without any cancer. Cytogenetic biomarkers for apoptosis and DNA damage were evaluated in samples of buccal epithelial and peripheral blood cells through micronuclei and comet assay tests. Elder age patients (61–80 years) had higher levels of apoptosis (catriolysis by karyolysis) and DNA damage at the diagnosis (baseline damage) with increased cell damage during QT and especially during RT. We also reported the increased frequencies of cytogenetic biomarkers in patients who were exposed to ionizing radiation as well as for alcoholism and smoking. QT and RT induced high levels of fragmentation (karyorrhexis) and nuclear dissolution (karyolysis) and DNA damage. Correlations were observed between age and karyorrhexis at diagnosis; smoking and karyolysis during RT; and radiation and karyolysis during QT. These correlations indicate that risk factors may also influence the genetic instability in non-neoplastic cells caused to the patients during cancer therapies.
Food and Chemical Toxicology | 2017
José Williams Gomes de Oliveira Filho; Muhammad Torequl Islam; Eunüs S. Ali; Shaikh Jamal Uddin; Jose Victor de Oliveira Santos; Marcus Vinícius Oliveira Barros de Alencar; Antonio Luiz Gomes Júnior; Márcia Fernanda Correia Jardim Paz; Maria dos Remédios Mendes de Brito; João Marcelo de Castro e Sousa; Subrata Shaw; Maria das Graças Freire de Medeiros; Sandra Maria Mendes de Moura Dantas; Hercília Maria Lins Rolim; Paulo Michel Pinheiro Ferreira; Mohammad A. Kamal; Magdalena D. Pieczynska; Niranjan Das; Vijai Kumar Gupta; Andrei Mocan; Teresinha de Jesus Aguiar dos Santos Andrade; Brahma N. Singh; Siddhartha Kumar Mishra; Atanas G. Atanasov; Ana Amélia de Carvalho Melo-Cavalcante
Citrinin (CIT) is a mycotoxin which causes contamination in the food and is associated with different toxic effects. A web search on CIT has been conducted covering the timespan since 1946. The accumulated data indicate that CIT is produced by several fungal strains belonging to Penicillium, Aspergillus and Monascus genera, and is usually found together with another nephrotoxic mycotoxin, ochratoxin A. Although, it is evident that CIT exposure can exert toxic effects on the heart, liver, kidney, as well as reproductive system, the mechanism of CIT-induced toxicity remains largely elusive. It is still controversial what are the genotoxic and mutagenic effects of CIT. Until now, its toxic effect has been linked to the CIT-mediated oxidative stress and mitochondrial dysfunction in biological systems. However, the toxicity strongly depends on its concentration, route, frequency and time of exposure, as well as from the used test systems. Besides the toxic effects, CIT is also reported to possess a broad spectrum of bioactivities, including antibacterial, antifungal, and potential anticancer and neuro-protective effects in vitro. This systematic review presents the current state of CIT research with emphasis on its bioactivity profile.
International Archives of Medicine | 2016
Ronald Gerard Silva; Marcus Vinícius Oliveira Barros de Alencar; Jadson Silva Teixeira; Reyca e Silva; Márcia Fernanda Correia Jardim Paz; João Marcelo de Castro e Sousa; Raí Pablo Sousa de Aguiar; Ricardo Melo de Carvalho; Antonio Luiz Gomes Júnior; Ana Maria Oliveira Ferreira da Mata; Jose Victor de Oliveira Santos; Mohammed Torequl Islam; Paulo Michel Pinheiro Ferreira; Ana Amélia de Carvalho Melo-Cavalcante; Jaqueline Nascimento Picada
Occupational exposure to ionizing radiation (IR) can damage DNA. The study evaluated the genotoxic profile and repair indicatives of DNA from peripheral blood lymphocytes of health workers exposed occupationally to IR by adopting comet assay. Biomonitoring was done with ninety individuals; among them 45 were health professionals and the rests were non-professionals. Blood samples were collected after 48 h (2 d; non-exposed) and 168 h (7 d; exposed). The 7 d IR exposed group significantly increased in the rates and frequency of damage, while 2 d unexposed group exhibited more than 20% of DNA repair as compared to the respective control groups. The DNA damage was observed in more significant to the younger workers (18-27 y). However, the hematological abnormalities were not observed, despite of their positive correlation in genotoxic profile. Significant and positive correlations were observed in relation to the used medicaments, low consumption of vegetables as well as the type and place of work. In conclusion, biomarkers involved in comet assay can be applied in biomonitoring of genetic instability, including IR induced phenomena.
Seizure-european Journal of Epilepsy | 2018
Jana Tchekalarova; Keylla da Conceição Machado; Antonio Luiz Gomes Júnior; Ana Amélia de Carvalho Melo Cavalcante; Albena Momchilova; Rumyana Tzoneva
PURPOSE Activation of CB1 receptors, produces anticonvulsant effect accompanied by memory disturbance both in animal seizure tests and in patients with epilepsy. Few reports considered the role of CB2 receptor on seizure susceptibility and cognitive functions. The aim of the present study was to explore the effect of a selective CB2 receptor agonist β-caryophyllene (BCP) in models of seizures and cognition in mice. METHODS Dose-dependent effects of BCP was studied in maximal electroshock seizure (MES) test, subcutaneous pentylenetetrazole (scPTZ) test and Morris water maze test. Phenytoin and diazepam were used as reference drugs in seizure tests. The effect of sub-chronic treatment with BCP for 7 days (50 and 100 mg kg-1) was assessed on status epilepticus (SE) induced by kainic acid (KA) model and oxidative stress through measurement of malondialdehyde (MDA) level in the hippocampus. The acute neurotoxicity was determined by a rotarod test. RESULTS The BCP exerted a protection in the MES test at the lowest dose of 30 mg kg-1 at the 4-h interval tested comparable to that of the referent drug phenytoin. The CB2 agonist was ineffective in the scPTZ test. The BCP displayed no neurotoxicity in the rotarod test. The BCP decreased the seizure scores in the KA-induced SE, which effect correlated with a diminished lipid peroxidation. The CB2 agonist exerted a dose-dependent decrease of latency to cross the target area during the three days of testing in the Morris water maze test. CONCLUSION Our results suggest that the CB2 receptor agonists might be clinically useful as an adjunct treatment against seizure spread and status epilepticus and concomitant oxidative stress, neurotoxicity and cognitive impairments.
Oxidative Medicine and Cellular Longevity | 2018
Márcia Fernanda Correia Jardim Paz; André Luiz Pinho Sobral; Jaqueline Nascimento Picada; Ivana Grivicich; Antonio Luiz Gomes Júnior; Ana Maria Oliveira Ferreira da Mata; Marcus Vinícius Oliveira Barros de Alencar; Rodrigo Mendes de Carvalho; Kátia da Conceição Machado; Muhammad Torequl Islam; Ana Amélia de Carvalho Melo Cavalcante; Juliana da Silva
This study aimed to evaluate DNA damage in patients with breast cancer before treatment (background) and after chemotherapy (QT) and radiotherapy (RT) treatment using the Comet assay in peripheral blood and the micronucleus test in buccal cells. We also evaluated repair of DNA damage after the end of RT, as well as the response of patients cells before treatment with an oxidizing agent (H2O2; challenge assay). Fifty women with a mammographic diagnosis negative for cancer (control group) and 100 women with a diagnosis of breast cancer (followed up during the treatment) were involved in this study. The significant DNA damage was observed by increasing in the index and frequency of damage along with the increasing of the frequency of micronuclei in peripheral blood and cells of the buccal mucosa, respectively. Despite the variability of the responses of breast cancer patients, the individuals presented lesions on the DNA, detected by the Comet assay and micronucleus Test, from the diagnosis until the end of the oncological treatment and were more susceptible to oxidative stress. We can conclude that the damages were due to clastogenic and/or aneugenic effects related to the neoplasia itself and that they increased, especially after RT.
Journal of Experimental Agriculture International | 2018
Antonio Luiz Gomes Júnior; Jackson Silva; Moisés Tiodoso da Silva; J. Teixeira; Artur Pv Carvalho; Kleyton Danilo da Silva Costa; Jorge Luiz Xavier Lins Cunha
This plant was cultivated long ago. However, the proper management of Biquinho pepper in relation to the production of the seedlings is unknown, being this a fundamentally important stage of the productive system. In which the quality of the seedling will directly influence the final performance of the plants, nutritional quality of the fruits, and in the time for seedling production. Thus, the present research had the objective of evaluating the effect of alternative substrates and trays for the production of Biquinho pepper seedlings. Five substrates and two types of trays were evaluated. Substrates were S1: Bioplant® commercial substrate (control); S2: earthworm humus; S3: soil; S4: 50% soil + 50% earthworm humus and S5: 75% soil + 25% earthworm humus, and tray types B1: with 98 cells, and B2: with 200 cells, in a completely randomized design, in the 5 x 2 factorial scheme, with four replications. For MSPA and MSSR it can be observed that substrates S1, S2, S4 and S5 had the best results, this was due to the accumulation of photoassimilates. Note that for both characteristics B1 provided the highest values, generating the greatest development of seedlings, S2, S4 and S5 substrates, combined with the B1 type of tray in the production of Biquinho pepper seedlings (Capsicum Chinense) are recommended.
Iubmb Life | 2018
Antonio Luiz Gomes Júnior; Jana Tchekalarova; Keylla da Conceição Machado; Arkellau Kenned Silva Moura; Márcia Fernanda Correia Jardim Paz; Ana Maria Oliveira Ferreira da Mata; Tiago Rocha Nogueira; Muhammad Torequl Islam; Maria Alexsandra de Sousa Rios; Antônia Maria das Graças Lopes Citó; Shaikh Jamal Uddin; Jamil A. Shilpi; Asish K. Das; Luciano da Silva Lopes; Ana Amélia de Carvalho Melo-Cavalcante
Antianxiety drugs currently in use are associated with a number of serious side effects. Present study was designed to evaluate the efficacy of anacardic acids (AAs) isolated from cashew nut (Anacardium occidentale L.) shell liquid (CNSL) to treat anxiety as well as its role in oxidative stress in mice model. Anxiolytic effect of AA was evaluated using rota‐rod and a set of behavioral tests in male Swiss albino mice at the doses of 10, 25, and 50 mg/kg. Flumazenil was used to evaluate the possible involvement of GABAergic system in the mechanism of action of AA. The effect of AA on oxidative stress in mice was evaluated by determining the concentration of malondialdehyde (MDA), reduced glutathione, and catalase (CAT) activity. The detection of DNA damage of the treated animals was performed using alkaline comet test in the hippocampus and frontal cortex of the animals. The results demonstrated that AA did not produce myorelaxant and sedative effects, nor did it cause a decrease in locomotor activity. The anxiolytic effect of AA was well‐evident in all tests, especially at higher dose levels (25 and 50 mg/mg). Flumazenil reversed the anxiolytic effect of AA at all doses. In addition, AA reduced oxidative stress by decreasing the concentration of MDA and increasing the levels of reduced glutathione (GSH) and CAT activity. Statistical analysis by Pearsons correlation indicated a positive correlation between anxiolytic effect of AA to its antioxidant and lipid peroxidation inhibitory activity. Furthermore, increased CAT activity and GSH concentrations in the hippocampus and frontal cortex of mice was also complementary to the reduced genotoxic damage observed in the study. In comet assay, AA did not increase in DNA damage. In conclusion, the results supported that AA possesses GABAA receptor mediated anxiolytic activity with the lack of myorelaxation and genotoxicity.
Chemico-Biological Interactions | 2018
Keylla da Conceição Machado; George Layson da Silva Oliveira; Muhammad Torequl Islam; Antonia Amanda Cardoso de Almeida; Antonio Luiz Gomes Júnior; Kátia da Conceição Machado; Damião Pergentino de Sousa; Ana Amélia de Carvalho Melo-Cavalcante; Rivelilson Mendes de Freitas
This study aimed to evaluate the anxiolytic-like effect and the possible neuronal mechanism of action of isopentyl ferulate (IF). For this purpose, we used the marble burying test in Swiss albino mice. The biomarkers involved in oxidative stress were measured in the hippocampus homogenate of the test animals. In addition, the toxicity and antioxidant capacities were tested in Artemia salina and rat erythrocytes, respectively. The results suggest that, an acute administration of the IF at doses of 25, 50, 75 and 150 mg/kg (intraperitoneal, i.p.) significantly (p < 0.05) reduced the marble burying behavior of the animals as compared to the vehicle group, which demonstrates a calming effect of this chemical. It was observed that, the pre-treatment with flumazenil (2.5 mg/kg, i.p.), an antagonist of the gamma-amino butyrinc acid (GABAA) receptor, significantly reversed the marble burying behavioral activity in the animals treated with the IF 150 mg/kg dose. Moreover, the reduction in nitrite content and lipid peroxidation levels, while an increased in the reduced glutathione (GSH), glutathione peroxidase (GPx), superoxide dismutase (SOD) and catalase (CAT) activities were also observed their hippocampus. Although, IF (2.36-14.16 mM) did not show toxicity in A. salina but exhibited a prominent antioxidant capacity in hydrogen peroxide-induced oxidative damage in rat erythrocytes. In conclusion, IF exhibited an anxiety-like effect in mice along with a potent antioxidant capacity, and we suppose it may have neuroprotective effects possibly via GABAergic transmission pathway.
Biomedicine & Pharmacotherapy | 2018
Antonio Luiz Gomes Júnior; Jana Tchekalarova; Milena Atanasova; Keylla da Conceição Machado; Maria Alexsandra de Sousa Rios; Márcia Fernanda Correia Jardim Paz; Mihnea-Alexandru Găman; Amelia Maria Găman; Santosh Yele; Manik Chandra Shill; Ishaq N. Khan; Md. Amirul Islam; Eunüs S. Ali; Siddhartha Kumar Mishra; Muhammad Torequl Islam; Mohammad S. Mubarak; Luciano da Silva Lopes; Ana Amélia de Carvalho Melo-Cavalcante
Epilepsy is a neurological disease affecting people of all ages worldwide. Side effects of antiepileptic drugs and their association with oxidative stress stimulate the search for new drugs, which would be more affordable with fewer adverse effects. Accordingly, the aim of the present work is to evaluate the anticonvulsant effect of anacardic acid (AA), a natural compound extracted from cashew liquid (Anacardium occidentalis), in murine models, as well as its antioxidant actions in Saccharomyces cerevisiae. AA (>90% purity) was tested, in vivo, in male Swiss mice (25-30 g) with four convulsive models, (1) pentylenetetrazole, (2) pilocarpine, (3) electroshock, and (4) kainic acid, at doses of 25, 50, and 100 mg/kg, body weight (B.W.) Additionally, the effective dose, toxic dose, and protective index studies were also performed. Results revealed that AA exhibits anticonvulsive effects in models 1, 3, and 4, with a mean effective dose (ED50) of 39.64 (model 1) >100 mg/kg, B.W. (model 2), and 38.36 (model 3); furthermore, AA displays a protection index of 1.49 (model 1), <0.6 (model 2, and 1.54 (model 3). In addition, AA showed antioxidant activities in S. cerevisiae mutated for superoxide dismutases (SOD). In conclusion, these results show that AA exhibits significant anticonvulsant and antioxidant activities and may be used as a promising natural product for the treatment of epilepsy.
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Ana Amélia de Carvalho Melo-Cavalcante
Universidade Federal do Rio Grande do Sul
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Centro Federal de Educação Tecnológica de Minas Gerais
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