Camino Fierro-Castro

Dr. Camino Fierro-Castro

Molecular Biology, University of Leon, León, Castille-Leon, Spain
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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1 April 2017 in Fish & Shellfish Immunology
Verified
Journal Article
Closed access
JDJessica Douxfils
Jessica Douxfils
CFCamino Fierro-Castro
Camino Fierro-Castro
SMS.N.M. Mandiki
S.N.M. Mandiki
WEWakson Emile
Wakson Emile
LTLluis Tort
Lluis Tort
PKPatrick Kestemont
Patrick Kestemont

1 September 2013 in Fish & Shellfish Immunology
Verified
Journal Article
Closed access
CFCamino Fierro-Castro
Camino Fierro-Castro
LBL. Barrioluengo
L. Barrioluengo
PLP. López-Fierro
P. López-Fierro
BRB.E. Razquin
B.E. Razquin
AVAlberto J. Villena
Alberto J. Villena


1 August 2016 in Aquatic Toxicology
Verified
Journal Article
Closed access
MTMariana Teles
Mariana Teles
CFCamino Fierro-Castro
Camino Fierro-Castro
PNP. Na-Phatthalung
P. Na-Phatthalung
ATAsta Tvarijonaviciute
Asta Tvarijonaviciute
Tito TrindadeTito Trindade
Tito Trindade
Miguel OliveiraMiguel Oliveira
Miguel Oliveira

1 March 2013 in Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology
Verified
Journal Article
Closed access
MTMariana Teles
Mariana Teles
RTR. Tridico
R. Tridico
ACA. Callol
A. Callol
CFCamino Fierro-Castro
Camino Fierro-Castro
Lluis TortLluis Tort
Lluis Tort

27 September 2017 in Frontiers in Immunology
Verified
Journal Article
Open access
RARita Azeredo
Rita Azeredo
MMMarina Machado
Marina Machado
AAAntónio Afonso
António Afonso
CFCamino Fierro-Castro
Camino Fierro-Castro
Felipe E. Reyes-LópezFelipe E. Reyes-López
Felipe E. Reyes-López
Benjamin CostasBenjamin Costas
Benjamin Costas
Methionine and tryptophan appear to be fundamental in specific cellular pathways involved in the immune response mechanisms, including stimulation of T-regulatory cells by tryptophan metabolites or pro-inflammatory effects upon methionine supplementation. Thus, the aim of this study was to evaluate the immunomodulatory effect of these amino acids on the inflammatory and neuroendocrine responses in juveniles of European seabass, Dicentrarchus labrax. To achieve this goal fish were fed for fourteen days methionine and tryptophan-supplemented diets (MET and TRP, respectively, 2× dietary requirement level) or a control diet meeting the amino acids requirement levels (CTRL). Fish were sampled for immune status assessment and the remaining fish were challenged with intraperitoneally-injected inactivated Photobacterium damselae subsp. piscicida and sampled either 4 or 24 h post-injection. Respiratory burst activity, brain monoamines, plasma cortisol and immune-related gene expression showed distinct and sometimes opposite patterns regarding the effects of dietary amino acids. While neuroendocrine intermediates were not affected by any dietary treatment at the end of the feeding trial, both supplemented diets led to increased levels of plasma cortisol after the inflammatory insult while brain monoamine content was higher in TRP-fed fish. Peripheral blood respiratory burst was higher in TRP-fed fish injected with the bacteria inoculum but only compared to those fed MET. However, no changes were detected in total antioxidant capacity. Complement factor 3 was up-regulated in MET-fed fish but methionine seemed to poorly affect other genes expression patterns. In contrast, fish fed MET showed increased immune cells numbers both before and after immune challenge, suggesting a strong enhancing effect of methionine on immune cells proliferation. Differently, tryptophan effects on inflammatory transcripts suggested an inhibitory mode of action. This, together with a high production of brain monoamine and cortisol levels, suggests that tryptophan might mediate regulatory mechanisms of neuroendocrine and immune systems cooperation. Overall, more studies are needed to ascertain the role of methionine and tryptophan in modulating (stimulate or regulate) fish immune and neuroendocrine responses.