Robson Cavalcante Veras

Dr. Robson Cavalcante Veras

Federal University of Paraíba, João Pessoa, Paraíba, Brazil
orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

View All Publications
1 December 2015 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
Klinger RodriguesKlinger Rodrigues
Klinger Rodrigues
CDCínthia Nóbrega de Sousa Dias
Cínthia Nóbrega de Sousa Dias
PNPatrícia Lima Do Nascimento Néris
Patrícia Lima Do Nascimento Néris
JRJuliana da Câmara Rocha
Juliana da Câmara Rocha
Marcus ScottiMarcus Scotti
Marcus Scotti
MOMárcia Rosa de Oliveira
Márcia Rosa de Oliveira

1 July 2009 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
OAOluwatosin Adekunle Adaramoye
Oluwatosin Adekunle Adaramoye
RARaline M. Anjos
Raline M. Anjos
MAMônica M. Almeida
Mônica M. Almeida
RVRobson Cavalcante Veras
Robson Cavalcante Veras
DSDarìzy F. Silvia
Darìzy F. Silvia
IMIsac Almeida de Medeiros
Isac Almeida de Medeiros

12 August 2018 in Immunology
Verified
Journal Article
Closed access
PDF file
CDCinthia Nóbrega de Sousa Dias
Cinthia Nóbrega de Sousa Dias
BGBruna Macêdo Gois
Bruna Macêdo Gois
VLViviane Silva Lima
Viviane Silva Lima
IGIsabel Cristina Guerra‐Gomes
Isabel Cristina Guerra‐Gomes
JAJosélio Maria Galvão Araújo
Josélio Maria Galvão Araújo
Tatjana Souza Lima KeesenTatjana Souza Lima Keesen
Tatjana Souza Lima Keesen

30 January 2020 in Nutrients
Verified
Journal Article
Open access
PDF file
JLJéssica Vanessa De Carvalho Lisboa
Jéssica Vanessa De Carvalho Lisboa
MRMarina Ramalho Ribeiro
Marina Ramalho Ribeiro
Rafaella Cristhine Pordeus LunaRafaella Cristhine Pordeus Luna
Rafaella Cristhine Pordeus Luna
RLRaquel Ataide Lima
Raquel Ataide Lima
RNRayner Anderson Ferreira Do Nascimento
Rayner Anderson Ferreira Do Nascimento
MCMaria José De Carvalho Costa
Maria José De Carvalho Costa
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism associated with body fat accumulation could possibly trigger an inflammatory process by elevating homocysteine levels and increasing cytokine production, causing several diseases. This study aimed to evaluate the effects of food intervention, and not folate supplements, on the levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) in overweight and obese women with the MTHFR C677T polymorphism. A randomized, double-blind eight-week clinical trial of 48 overweight and obese women was conducted. Participants were randomly assigned into two groups. They received 300 g of vegetables daily for eight weeks containing different doses of folate: 95 µg/day for Group 1 and 191 µg/day for Group 2. MTHFR C677T polymorphism genotyping was assessed by digestion with HinfI enzyme and on 12% polyacrylamide gels. Anthropometric measurements, 24-h dietary recall, and biochemical analysis (blood folic acid, vitamin B12, homocysteine (Hcy), TNF-α, IL-1β, and IL-6) were determined at the beginning and end of the study. Group 2 had a significant increase in folate intake (p < 0.001) and plasma folic acid (p < 0.05) for individuals with the cytosine–cytosine (CC), cytosine–thymine (CT), and thymine–thymine (TT) genotypes. However, only individuals with the TT genotype presented reduced levels of Hcy, TNF-α, IL-6, and IL-1β (p < 0.001). Group 1 showed significant differences in folate consumption (p < 0.001) and folic acid levels (p < 0.05) for individuals with the CT and TT genotypes. Food intervention with folate from vegetables increased folic acid levels and reduced interleukins, TNF-α, and Hcy levels, mainly for individuals with the TT genotype.

8 August 2011 in Basic & Clinical Pharmacology & Toxicology
Verified
Journal Article
Closed access
PDF file
DSDarízy Flávia Silva
Darízy Flávia Silva
IAIslania G. A. Araújo
Islania G. A. Araújo
JAJosé G. F. Albuquerque
José G. F. Albuquerque
DPDayanne L. Porto
Dayanne L. Porto
KDKaty L. G. Dias
Katy L. G. Dias
IMIsac Almeida de Medeiros
Isac Almeida de Medeiros

10 August 2012 in Molecules
Verified
Journal Article
Open access
PDF file
JPJoão Carlos Lima Rodrigues Pita
João Carlos Lima Rodrigues Pita
AXAline Lira Xavier
Aline Lira Xavier
TSTatyanna Kelvia Gomes de Sousa
Tatyanna Kelvia Gomes de Sousa
VMVivianne Mendes Mangueira
Vivianne Mendes Mangueira
JTJosean Tavares
Josean Tavares
MBMarianna Castello Branco
Marianna Castello Branco
Trachylobane-360 (ent-7α-acetoxytrachyloban-18-oic acid) was isolated from Xylopia langsdorffiana. Studies have shown that it has weak cytotoxic activity against tumor and non-tumor cells. This study investigated the in vitro and in vivo antitumor effects of trachylobane-360, as well as its cytotoxicity in mouse erythrocytes. In order to evaluate the in vivo toxicological aspects related to trachylobane-360 administration, hematological, biochemical and histopathological analyses of the treated animals were performed. The compound exhibited a concentration-dependent effect in inducing hemolysis with HC50 of 273.6 µM, and a moderate in vitro concentration-dependent inhibitory effect on the proliferation of sarcoma 180 cells with IC50 values of 150.8 µM and 150.4 µM, evaluated by the trypan blue exclusion test and MTT reduction assay, respectively. The in vivo inhibition rates of sarcoma 180 tumor development were 45.60, 71.99 and 80.06% at doses of 12.5 and 25 mg/kg of trachylobane-360 and 25 mg/kg of 5-FU, respectively. Biochemical parameters were not altered. Leukopenia was observed after 5-FU treatment, but this effect was not seen with trachylobane-360 treatment. The histopathological analysis of liver and kidney showed that both organs were mildly affected by trachylobane-360 treatment. Trachylobane-360 showed no immunosuppressive effect. In conclusion, these data reinforce the anticancer potential of this natural diterpene.