Maria Pardo

Dr. Maria Pardo

Grupo Obesidómica, Instituto de Investigación Sanitaria de Santiago, Santiago de Compostela, Galicia, Spain
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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11 April 2013 in PLOS ONE
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Journal Article
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ARArturo Roca-Rivada
Arturo Roca-Rivada
CCCecilia Castelao
Cecilia Castelao
LSLucía L. Senin
Lucía L. Senin
MLMaría O. Landrove
María O. Landrove
JBJavier Baltar
Javier Baltar
Maria PardoMaria Pardo
Maria Pardo
Exercise provides clear beneficial effects for the prevention of numerous diseases. However, many of the molecular events responsible for the curative and protective role of exercise remain elusive. The recent discovery of FNDC5/irisin protein that is liberated by muscle tissue in response to exercise might be an important finding with regard to this unsolved mechanism. The most striking aspect of this myokine is its alleged capacity to drive brown-fat development of white fat and thermogenesis. However, the nature and secretion form of this new protein is controversial. The present study reveals that rat skeletal muscle secretes a 25 kDa form of FNDC5, while the 12 kDa/irisin theoretical peptide was not detected. More importantly, this study is the first to reveal that white adipose tissue (WAT) also secretes FNDC5; hence, it may also behave as an adipokine. Our data using rat adipose tissue explants secretomes proves that visceral adipose tissue (VAT), and especially subcutaneous adipose tissue (SAT), express and secrete FNDC5. We also show that short-term periods of endurance exercise training induced FNDC5 secretion by SAT and VAT. Moreover, we observed that WAT significantly reduced FNDC5 secretion in fasting animals. Interestingly, WAT of obese animals over-secreted this hormone, which might suggest a type of resistance. Because 72% of circulating FNDC5/irisin was previously attributed to muscle secretion, our findings suggest a muscle-adipose tissue crosstalk through a regulatory feedback mechanism.

28 May 2013 in PLOS ONE
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MQMaría Isabel Queipo-Ortuño
María Isabel Queipo-Ortuño
LSLuisa María Seoane
Luisa María Seoane
Mora MurriMora Murri
Mora Murri
Maria PardoMaria Pardo
Maria Pardo
JGJuan Miguel Gomez-Zumaquero
Juan Miguel Gomez-Zumaquero
FTFrancisco J Tinahones
Francisco J Tinahones
Background Several evidences indicate that gut microbiota is involved in the control of host energy metabolism. Objective To evaluate the differences in the composition of gut microbiota in rat models under different nutritional status and physical activity and to identify their associations with serum leptin and ghrelin levels. Methods In a case control study, forty male rats were randomly assigned to one of these four experimental groups: ABA group with food restriction and free access to exercise; control ABA group with food restriction and no access to exercise; exercise group with free access to exercise and feed ad libitum and ad libitum group without access to exercise and feed ad libitum. The fecal bacteria composition was investigated by PCR-denaturing gradient gel electrophoresis and real-time qPCR. Results In restricted eaters, we have found a significant increase in the number of Proteobacteria, Bacteroides, Clostridium, Enterococcus, Prevotella and M. smithii and a significant decrease in the quantities of Actinobacteria, Firmicutes, Bacteroidetes, B. coccoides-E. rectale group, Lactobacillus and Bifidobacterium with respect to unrestricted eaters. Moreover, a significant increase in the number of Lactobacillus, Bifidobacterium and B. coccoides–E. rectale group was observed in exercise group with respect to the rest of groups. We also found a significant positive correlation between the quantity of Bifidobacterium and Lactobacillus and serum leptin levels, and a significant and negative correlation among the number of Clostridium, Bacteroides and Prevotella and serum leptin levels in all experimental groups. Furthermore, serum ghrelin levels were negatively correlated with the quantity of Bifidobacterium, Lactobacillus and B. coccoides–Eubacterium rectale group and positively correlated with the number of Bacteroides and Prevotella . Conclusions Nutritional status and physical activity alter gut microbiota composition affecting the diversity and similarity. This study highlights the associations between gut microbiota and appetite-regulating hormones that may be important in terms of satiety and host metabolism.

29 August 2008 in Glycobiology
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UHUmi M Abd Hamid
Umi M Abd Hamid
LRLouise Royle
Louise Royle
RSRadka Saldova
Radka Saldova
CRCatherine M Radcliffe
Catherine M Radcliffe
DHDavid J Harvey
David J Harvey
PRPauline M Rudd
Pauline M Rudd
Aberrant glycosylation on glycoproteins that are either presented on the surface or secreted by cancer cells is a potential source of disease biomarkers and provides insights into disease pathogenesis. N-Glycans of the total serum glycoproteins from advanced breast cancer patients and healthy individuals were sequenced by HPLC with fluorescence detection coupled with exoglycosidase digestions and mass spectrometry. We observed a significant increase in a trisialylated triantennary glycan containing α1,3-linked fucose which forms part of the sialyl Lewis x epitope. Following digestion of the total glycan pool with a combination of sialidase and β-galactosidase, we segregated and quantified a digestion product, a monogalactosylated triantennary structure containing α1,3-linked fucose. We compared breast cancer patients and controls and detected a 2-fold increase in this glycan marker in patients. In 10 patients monitored longitudinally, we showed a positive correlation between this glycan marker and disease progression and also demonstrated its potential as a better indicator of metastasis compared to the currently used biomarkers, CA 15-3 and carcinoembryonic antigen (CEA). A pilot glycoproteomic study of advanced breast cancer serum highlighted acute-phase proteins α1-acid glycoprotein, α1-antichymotrypsin, and haptoglobin β-chain as contributors to the increase in the glycan marker which, when quantified from each of these proteins, marked the onset of metastasis in advance of the CA 15-3 marker. These preliminary findings suggest that specific glycans and glycoforms of proteins may be candidates for improved markers in the monitoring of breast cancer progression.

1 January 2014 in International Journal of Endocrinology
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Maria PardoMaria Pardo
Maria Pardo
Ana B. CrujeirasAna B. Crujeiras
Ana B. Crujeiras
MAMaría Amil
María Amil
Zaida AgüeraZaida Agüera
Zaida Agüera
Susana Jiménez-MurciaSusana Jiménez-Murcia
Susana Jiménez-Murcia
FCFelipe F. Casanueva
Felipe F. Casanueva
FNDC5/irisin has been recently postulated as beneficial in the treatment of obesity and diabetes because it is induced in muscle by exercise, increasing energy expenditure. However, recent reports have shown that WAT also secretes irisin and that circulating irisin is elevated in obese subjects. The aim of this study was to evaluate irisin levels in conditions of extreme BMI and its correlation with basal metabolism and daily activity. The study involved 145 female patients, including 96 with extreme BMIs (30 anorexic (AN) and 66 obese (OB)) and 49 healthy normal weight (NW). The plasma irisin levels were significantly elevated in the OB patients compared with the AN and NW patients. Irisin also correlated positively with body weight, BMI, and fat mass. The OB patients exhibited the highest REE and higher daily physical activity compared with the AN patients but lower activity compared with the NW patients. The irisin levels were inversely correlated with daily physical activity and directly correlated with REE. Fat mass contributed to most of the variability of the irisin plasma levels independently of the other studied parameters.Conclusion. Irisin levels are influenced by energy expenditure independently of daily physical activity but fat mass is the main contributing factor.

5 December 2013 in American Journal of Human Biology
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Ana B. CrujeirasAna B. Crujeiras
Ana B. Crujeiras
Maria PardoMaria Pardo
Maria Pardo
RARoca‐Rivada Arturo
Roca‐Rivada Arturo
Santiago Navas-CarreteroSantiago Navas-Carretero
Santiago Navas-Carretero
MZM. Angeles Zulet
M. Angeles Zulet
FCFelipe F Casanueva
Felipe F Casanueva

1 April 2014 in Metabolism
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Journal Article
Closed access
Ana B. CrujeirasAna B. Crujeiras
Ana B. Crujeiras
MZM. Angeles Zulet
M. Angeles Zulet
PLPatricia Lopez-Legarrea
Patricia Lopez-Legarrea
RIRocio De La Iglesia
Rocio De La Iglesia
Maria PardoMaria Pardo
Maria Pardo
FCFelipe F. Casanueva
Felipe F. Casanueva