João Henrique Costa-Silva

Dr. João Henrique Costa-Silva

orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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1 March 2008 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
JCJoão Henrique Costa-Silva
João Henrique Costa-Silva
CLC.R. Lima
C.R. Lima
ESErick J.R. Silva
Erick J.R. Silva
AAA.V. Araújo
A.V. Araújo
MFM.C.C.A. Fraga
M.C.C.A. Fraga
AWAlmir Gonçalves Wanderley
Almir Gonçalves Wanderley

5 August 2015 in PLOS ONE
Verified
Journal Article
Open access
PDF file
GCGermana Freire Rocha Caldas
Germana Freire Rocha Caldas
AOAlisson Rodrigo Da Silva Oliveira
Alisson Rodrigo Da Silva Oliveira
AAAlice Valença Araújo
Alice Valença Araújo
SLSimone Sette Lopes Lafayette
Simone Sette Lopes Lafayette
GAGiwellington Silva Albuquerque
Giwellington Silva Albuquerque
AWAlmir Gonçalves Wanderley
Almir Gonçalves Wanderley
Recently, our research group identified and reported 1,8-cineole (CIN), a monoterpene that naturally occur in many aromatic plants, as one of the major constituent of the essential oil from leaves of Hyptis martiusii (EOHM), as well as characterized the gastroprotective action of this oil. The aim of this study was to investigate the mechanisms of action involved in the antiulcer and healing activity of CIN, in order to confirm its correlation with the gastroprotective effect of EOHM. Wistar rats were exposed to different protocols (acute ulceration, gastrointestinal motility and antisecretory activity). In addition, were determinated the involvement of nitric oxide and sulphydryl groups; the levels of gastric mucus, lipid peroxidation, sulphydryl groups and myeloperoxidase activity. The healing ability was evaluated by acetic acid-induced chronic ulcer and histological and immunohistochemical analysis (PCNA, Ki-67 and BrdU). The treatment with CIN inhibited ethanol-, ethanol/HCl- and indomethacin-induced gastric lesions. The highest doses of CIN inhibited gastric emptying, but did not affect intestinal transit. CIN (100 mg/kg) reduced the volume of basal but not stimulated acid secretion. CIN increased levels of mucus (89.3%), prevented depletion of –SH groups (62.6%) and reduced the level of lipid peroxidation (55.3%) and myeloperoxidase activity (59.4%) in the gastric mucosa. In chronic ulcer model, CIN reduced in 43.1% the gastric area lesion, promoted significant regeneration and restoration of the levels of mucus in glandular cells as confirmed by histological analysis; and promoted increase in cell proliferation as evidenced by reactivity for PCNA, Ki-67 and BrdU. This findings demonstrate the role of 1,8-cineole as an important ulcer healing agent and indicate the involvement of antioxidant and cytoprotective mechanisms in the gastroprotective effect of compound. This study also provides evidence that 1,8-cineole is related to the gastroprotective effect of the essential oil of Hyptis martiusii.

1 June 2011 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
MSMirtes G.B. Silva
Mirtes G.B. Silva
TATiciana P. Aragão
Ticiana P. Aragão
CVCarlos F.B. Vasconcelos
Carlos F.B. Vasconcelos
PFPablo A. Ferreira
Pablo A. Ferreira
BABruno A. Andrade
Bruno A. Andrade
SLSimone S.L. Lafayette
Simone S.L. Lafayette

1 May 2012 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
CLC.R. Lima
C.R. Lima
CVC.F.B. Vasconcelos
C.F.B. Vasconcelos
JCJoão Henrique Costa-Silva
João Henrique Costa-Silva
CMC.A. Maranhão
C.A. Maranhão
JCJ. Costa
J. Costa
AWAlmir Gonçalves Wanderley
Almir Gonçalves Wanderley

6 October 2016 in Frontiers in Physiology
Verified
Journal Article
Open access
PDF file
JAJosé Luiz de Brito Alves
José Luiz de Brito Alves
VSVanessa P. de Sousa
Vanessa P. de Sousa
MNMarinaldo P. Cavalcanti Neto
Marinaldo P. Cavalcanti Neto
MMMarciane Magnani
Marciane Magnani
VBValdir Braga
Valdir Braga
Luciano PirolaLuciano Pirola
Luciano Pirola
Arterial hypertension (AH) is one of the most prevalent risk factors for cardiovascular diseases (CD) and is the main cause of deaths worldwide. Current research establish that dietary polyphenols may help to lower blood pressure (BP), thus contributing to the reduction of cardiovascular complications. In addition, the health benefits of probiotics on BP have also attracted increased attention, as probiotics administration modulates the microbiota, which, by interacting with ingested polyphenols, controls their bioavalability. The aim of the present mini-review is to summarize and clarify the effects of dietary polyphenols and probiotics administration on BP using combined evidence from clinical and experimental studies, as well as to discuss the current debate in the literature about the usefulness of this nutritional approach to manage BP. Clinical trials and experimental studies have demonstrated that consuming dietary polyphenols or probiotics in adequate amounts may improve BP, ranging from modest to greater effects. However, the mechanisms linking probiotic intake and reduced BP levels need to be further elucidated as a definitive consensus on the link between intake of polyphenols or probiotics and improvement of AH has not been reached yet.

2 April 2014 in The Journal of Physiology
Verified
Journal Article
Closed access
PDF file
DMDavi J. A. Moraes
Davi J. A. Moraes
LBLeni G. H. Bonagamba
Leni G. H. Bonagamba
KCKauê M. Costa
Kauê M. Costa
JCJoão Henrique Costa-Silva
João Henrique Costa-Silva
DZDaniel B. Zoccal
Daniel B. Zoccal
BMBenedito H. Machado
Benedito H. Machado