João Batista Júnior

Prof. João Batista Júnior

Independent Reseacher
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 October 2013 in Molecules
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RBRosivaldo Borges
Rosivaldo Borges
João Batista JúniorJoão Batista Júnior
João Batista Júnior
RVRommel Bezerra Viana
Rommel Bezerra Viana
ABAna C. Baetas
Ana C. Baetas
EOEdnilsom Orestes
Ednilsom Orestes
ASAlberico Da Silva
Alberico Da Silva
An antioxidant mechanism of tetrahydrocannabinol (THC) and cannabidiol (CBD) were compared with a simplified model of α-tocopherol, butylhydroxytoluene and hydroxytoluene in order to understand the antioxidant nature of THC and CBD molecules using DFT. The following electronic properties were evaluated: frontier orbitals nature, ionization potential, O-H bond dissociation energy (BDEOH), stabilization energy, and spin density distribution. An important factor that shows an influence in the antioxidant property of THC is the electron abstraction at the phenol position. Our data indicate that the decrease of the HOMO values and the highest ionization potential values are related to phenol, ether, and alkyl moieties. On the other hand, BDEOH in molecules with the cyclohexenyl group at ortho position of phenol are formed from lower energies than the molecules with an ether group at the meta position. In the light of our results, the properties calculated here predict that THC has a sightly higher antioxidant potential than CBD.

1 March 2010 in Mycoses
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João Batista JúniorJoão Batista Júnior
João Batista Júnior
ZRZoilo Rodrigues
Zoilo Rodrigues
GFGeisa Ferreira Fernandes
Geisa Ferreira Fernandes
AVAdriana Pardini Vicentini
Adriana Pardini Vicentini
CFCor Jesus Fernandes Fontes
Cor Jesus Fernandes Fontes
RHRosane Hahn
Rosane Hahn

22 January 2014 in PLOS ONE
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TSTaysa Ribeiro Schalcher
Taysa Ribeiro Schalcher
RBRosivaldo S Borges
Rosivaldo S Borges
MCMichael D. Coleman
Michael D. Coleman
João Batista JúniorJoão Batista Júnior
João Batista Júnior
CSClaudio Guedes Salgado
Claudio Guedes Salgado
MMMarta Monteiro
Marta Monteiro
This study aims to assess the oxidative stress in leprosy patients under multidrug therapy (MDT; dapsone, clofazimine and rifampicin), evaluating the nitric oxide (NO) concentration, catalase (CAT) and superoxide dismutase (SOD) activities, glutathione (GSH) levels, total antioxidant capacity, lipid peroxidation, and methemoglobin formation. For this, we analyzed 23 leprosy patients and 20 healthy individuals from the Amazon region, Brazil, aged between 20 and 45 years. Blood sampling enabled the evaluation of leprosy patients prior to starting multidrug therapy (called MDT 0) and until the third month of multidrug therapy (MDT 3). With regard to dapsone (DDS) plasma levels, we showed that there was no statistical difference in drug plasma levels between multibacillary (0.518±0.029 µg/mL) and paucibacillary (0.662±0.123 µg/mL) patients. The methemoglobin levels and numbers of Heinz bodies were significantly enhanced after the third MDT-supervised dose, but this treatment did not significantly change the lipid peroxidation and NO levels in these leprosy patients. In addition, CAT activity was significantly reduced in MDT-treated leprosy patients, while GSH content was increased in these patients. However, SOD and Trolox equivalent antioxidant capacity levels were similar in patients with and without treatment. These data suggest that MDT can reduce the activity of some antioxidant enzyme and influence ROS accumulation, which may induce hematological changes, such as methemoglobinemia in patients with leprosy. We also explored some redox mechanisms associated with DDS and its main oxidative metabolite DDS-NHOH and we explored the possible binding of DDS to the active site of CYP2C19 with the aid of molecular modeling software.

23 February 2016 in Medicinal Chemistry Research
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RBRosivaldo Borges
Rosivaldo Borges
JVJoyce K. L. Vale
Joyce K. L. Vale
GPGlaécia A. N. Pereira
Glaécia A. N. Pereira
AVAndrex A. S. Veiga
Andrex A. S. Veiga
João Batista JúniorJoão Batista Júnior
João Batista Júnior
ASAlberico Da Silva
Alberico Da Silva

1 February 2010 in Memórias do Instituto Oswaldo Cruz
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João Batista JúniorJoão Batista Júnior
João Batista Júnior
RBRodrigo Berzaghi
Rodrigo Berzaghi
AAAdelita Duanra Medeiros Do Monte Arnaud
Adelita Duanra Medeiros Do Monte Arnaud
CFCor Jesus Fernandes Fontes
Cor Jesus Fernandes Fontes
ZCZoilo Pires de Camargo
Zoilo Pires de Camargo
RHRosane Hahn
Rosane Hahn
This study is the first report on genetic differences between isolates of Paracoccidioides brasiliensis from a single patient. We describe a simultaneous infection with genetically distinct isolates of P. brasiliensis in a patient with chronic paracoccidioidomycosis. The clinical isolates were obtained from lesions in different anatomical sites and were characterised by random amplified polymorphic DNA (RAPD) analysis. The RAPD technique can be helpful for distinguishing between clinical isolates. Different random primers were used to characterise these clinical isolates. The RAPD patterns allowed for differentiation between isolates and the construction of a phenetic tree, which showed more than 28% genetic variability in this fungal species, opening new possibilities for clinical studies of P. brasiliensis. Based on these results and preliminary clinical findings, we suggest that different genotypes of P. brasiliensis might infect the same patient, inducing the active form of the disease.

28 March 2015 in Environmental and Molecular Mutagenesis
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RLRenato M.R. de Lucca
Renato M.R. de Lucca
João Batista JúniorJoão Batista Júnior
João Batista Júnior
CFCor J. Fernandes Fontes
Cor J. Fernandes Fontes
MBMarcelo de Oliveira Bahia
Marcelo de Oliveira Bahia
CBCarmen L. Bassi‐Branco
Carmen L. Bassi‐Branco