Tales Lyra Oliveira

Dr. Tales Lyra Oliveira

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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

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

Representative Publications

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23 February 2016 in Scientific Reports
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TOTales Lyra Oliveira
Tales Lyra Oliveira
NCNávylla Candeia-Medeiros
Návylla Candeia-Medeiros
PCPolliane M. Cavalcante-Araújo
Polliane M. Cavalcante-Araújo
IMIgor Santana Melo
Igor Santana Melo
EFElaine Fávaro-Pípi
Elaine Fávaro-Pípi
RSRobinson Sabino-Silva
Robinson Sabino-Silva
High glucose concentration in the airway surface liquid (ASL) is an important feature of diabetes that predisposes to respiratory infections. We investigated the role of alveolar epithelial SGLT1 activity on ASL glucose concentration and bacterial proliferation. Non-diabetic and diabetic rats were intranasally treated with saline, isoproterenol (to increase SGLT1 activity) or phlorizin (to decrease SGLT1 activity); 2 hours later, glucose concentration and bacterial proliferation (methicillin-resistant Sthaphylococcus aureus, MRSA and Pseudomonas aeruginosa, P. aeruginosa) were analyzed in bronchoalveolar lavage (BAL); and alveolar SGLT1 was analyzed by immunohistochemistry. BAL glucose concentration and bacterial proliferation increased in diabetic animals: isoproterenol stimulated SGLT1 migration to luminal membrane, and reduced (50%) the BAL glucose concentration; whereas phlorizin increased the BAL glucose concentration (100%). These regulations were accompanied by parallel changes of in vitro MRSA and P. aeruginosa proliferation in BAL (r = 0.9651 and r = 0.9613, respectively, Pearson correlation). The same regulations were observed in in vivo P. aeruginosa proliferation. In summary, the results indicate a relationship among SGLT1 activity, ASL glucose concentration and pulmonary bacterial proliferation. Besides, the study highlights that, in situations of pulmonary infection risk, such as in diabetic subjects, increased SGLT1 activity may prevent bacterial proliferation whereas decreased SGLT1 activity can exacerbate it.

1 November 2019 in Travel Medicine and Infectious Disease
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Lysien Ivania ZambranoLysien Ivania Zambrano
Lysien Ivania Zambrano
EREdith Rodriguez
Edith Rodriguez
IEIván Alfonso Espinoza-Salvado
Iván Alfonso Espinoza-Salvado
IFItzel Carolina Fuentes-Barahona
Itzel Carolina Fuentes-Barahona
TOTales Lyra Oliveira
Tales Lyra Oliveira
Alfonso J. Rodriguez-MoralesAlfonso J. Rodriguez-Morales
Alfonso J. Rodriguez-Morales
After serious epidemics of chikungunya (CHIKV) and Zika (ZIKV) in the Americas, dengue (DENV) have reemerged in most countries. We analyzed the incidence, incidence rates, and evolution of DENV cases in Honduras from 2015 to 2018 and the ongoing 2019 epidemic. Using epidemiological weeks (EW) surveillance data on the DENV in Honduras, we estimated incidence rates (cases/100,000 population), and developed maps at national, departmental, and municipal levels. From January 1, 2016 to July 21, 2019, a total of 109,557 cases of DENV were reported, 28,603 in 2019, with an incidence rate of 312.32 cases/100,000 population this year; 0.13% laboratory-confirmed. The highest peak was reached on the EW 28°, 2019 (5299 cases; 57.89 cases/100,000 population). The department with the highest number of cases and incidence rate was Cortes (8404 cases, 479.68 cases/100,000 population in 2019). The pattern and evolution of DENV epidemic in 2019 in Honduras has been similar to that which occurred for in 2015. As previously reported, this epidemic involved the north and central areas of the country predominantly, reaching municipality incidences there >1000 cases/100,000 population (or 1%). Studies using geographical information systems linked with clinical disease characteristics are necessary to obtain accurate epidemiological data for public health systems. Such information is also useful for assessment of risk for travelers who visit specific areas in a destination country.

19 September 2019 in PLOS ONE
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LCLéia Cardoso-Sousa
Léia Cardoso-Sousa
EAEmilia Maria Gomes Aguiar
Emilia Maria Gomes Aguiar
DCDouglas Carvalho Caixeta
Douglas Carvalho Caixeta
DVDanielle Diniz Vilela
Danielle Diniz Vilela
DCDanilo Pereira da Costa
Danilo Pereira da Costa
RSRobinson Sabino-Silva
Robinson Sabino-Silva
Respiratory infection can be exacerbated by the high glucose concentration in the airway surface liquid (ASL). We investigated the effects of salbutamol and phlorizin on the pulmonary function, oxidative stress levels and SGLT1 activity in lung, pulmonary histopathological damages and survival rates of rats with sepsis. Sepsis was induced by cecal ligation and puncture surgery (CLP). Twenty-four hours after surgery, CLP rats were intranasally treated with saline, salbutamol or phlorizin. After 2 hours, animals were anesthetized and sacrificed. Sepsis promoted atelectasis and bronchial inflammation, and led to increased expression of SGLT1 on cytoplasm of pneumocytes. Salbutamol treatment reduced bronchial inflammation and promoted hyperinsuflation in CLP rats. The interferon-ɤ and Interleucin-1β concentrations in bronchoalveolar lavage (BAL) were closely related to the bronchial inflammation regulation. Salbutamol stimulated SGLT1 in plasma membrane; whereas, phlorizin promoted the increase of SGLT1 in cytoplasm. Phlorizin reduced catalase activity and induced a significant decrease in the survival rate of CLP rats. Taken together, sepsis promoted atelectasis and lung inflammation, which can be associated with SGLT1 inhibition. The loss of function of SGLT1 by phlorizin are related to the augmented disease severity, increased atelectasis, bronchial inflammation and a significant reduction of survival rate of CLP rats. Alternatively salbutamol reduced BAL inflammatory cytokines, bronchial inflammation, atelectasis, and airway damage in sepsis. These data suggest that this selective β2-adrenergic agonist may protect lung of septic acute effects.

1 December 2017 in Autonomic Neuroscience
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GLGisele S. Lincevicius
Gisele S. Lincevicius
CSCaroline G. Shimoura
Caroline G. Shimoura
ENErika E. Nishi
Erika E. Nishi
TOTales Lyra Oliveira
Tales Lyra Oliveira
JCJuliana G. Cespedes
Juliana G. Cespedes
RCRuy R. De Campos
Ruy R. De Campos

4 January 2019 in Acta Scientiarum. Technology
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TOTales Lyra Oliveira
Tales Lyra Oliveira
FGFábio José Generoso
Fábio José Generoso
TSTaciano Oliveira Da Silva
Taciano Oliveira Da Silva
GSGiovani Levi Sant'ANna
Giovani Levi Sant'ANna
CSCláudio Henrique de Carvalho Silva
Cláudio Henrique de Carvalho Silva
HPHeraldo Nunes Pitanga
Heraldo Nunes Pitanga
Geomechanical properties of mixtures of iron ore tailings improved with Portland cement

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CSCaroline Gusson Shimoura
Caroline Gusson Shimoura
TOTales Lyra Oliveira
Tales Lyra Oliveira
GLGisele Silverio Lincevicius
Gisele Silverio Lincevicius
RCRenato Crajoinas
Renato Crajoinas
EOElizabeth B. Oliveira-Sales
Elizabeth B. Oliveira-Sales
RCRuy R. De Campos
Ruy R. De Campos
The Goldblatt model of hypertension (2K-1C) in rats is characterized by renal sympathetic nerve activity (rSNA). We investigated the effects of unilateral renal denervation of the clipped kidney (DNX) on sodium transporters of the unclipped kidneys and the cardiovascular, autonomic, and renal functions in 2K-1C and control (CTR) rats. The mean arterial pressure (MAP) and rSNA were evaluated in experimental groups. Kidney function and NHE3, NCC, ENaCβ, and ENaCγ protein expressions were assessed. The glomerular filtration rate (GRF) and renal plasma flow were not changed by DNX, but the urinary (CTR: 0.0042 ± 0.001; 2K-1C: 0.014 ± 0.003; DNX: 0.005 ± 0.0013 mL/min/g renal tissue) and filtration fractions (CTR: 0.29 ± 0.02; 2K-1C: 0.51 ± 0.06; DNX: 0.28 ± 0.04 mL/min/g renal tissue) were normalized. The Na+/H+ exchanger (NHE3) was reduced in 2K-1C, and DNX normalized NHE3 (CTR: 100 ± 6; 2K-1C: 44 ± 14, DNX: 84 ± 13%). Conversely, the Na+/Cl− cotransporter (NCC) was increased in 2K-1C and was reduced by DNX (CTR: 94 ± 6; 2K-1C: 144 ± 8; DNX: 60 ± 15%). In conclusion, DNX in Goldblatt rats reduced blood pressure and proteinuria independently of GRF with a distinct regulation of NHE3 and NCC in unclipped kidneys.