Jorge Alberto Perez-Leon

Dr. Jorge Alberto Perez-Leon

Universidad Autonoma de Ciudad Juarez
+1
orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

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

Representative Publications

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23 August 2006 in European Journal of Neuroscience
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Journal Article
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JPJorge Alberto Perez-Leon
Jorge Alberto Perez-Leon
EWErin J. Warren
Erin J. Warren
CACharles N. Allen
Charles N. Allen
DRDavid W. Robinson
David W. Robinson
RBR Lane Brown
R Lane Brown

13 November 2007 in European Journal of Neuroscience
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Journal Article
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CMCatherine W. Morgans
Catherine W. Morgans
WLWeiwei Liu
Weiwei Liu
TWTheodore G Wensel
Theodore G Wensel
RBR. Lane Brown
R. Lane Brown
JPJorge Alberto Perez-Leon
Jorge Alberto Perez-Leon
RDRobert M. Duvoisin
Robert M. Duvoisin

1 January 2016 in Oxidative Medicine and Cellular Longevity
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Journal Article
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GBGuillermo Barraza-Garza
Guillermo Barraza-Garza
HCHiram Castillo-Michel
Hiram Castillo-Michel
LRLaura A. De la Rosa
Laura A. De la Rosa
AMAlejandro Martinez-Martinez
Alejandro Martinez-Martinez
JPJorge Alberto Perez-Leon
Jorge Alberto Perez-Leon
Emilio Alvarez-ParrillaEmilio Alvarez-Parrilla
Emilio Alvarez-Parrilla
The protective effect of different polyphenols, catechin (Cat), quercetin (Qc) (flavonoids), gallic acid (GA), caffeic acid (CfA), chlorogenic acid (ChA) (phenolic acids), and capsaicin (Cap), against H2O2‐induced oxidative stress was evaluated in rat enterocytes using Attenuated Total Reflectance‐Fourier Transform Infrared (ATR‐FTIR) Spectroscopy and Fourier Transform Infrared Microspectroscopy (FTIRM), and results were compared to standard lipid peroxidation techniques: conjugated dienes (CD) and Thiobarbituric Acid Reactive Substances (TBARS). Analysis of ATR‐FTIR and FTIRM spectral data allowed the simultaneous evaluation of the effects of H2O2and polyphenols on lipid and protein oxidation. All polyphenols showed a protective effect against H2O2‐induced oxidative stress in enterocytes, when administered before or after H2O2. Cat and capsaicin showed the highest protective effect, while phenolic acids had weaker effects and Qc presented a mild prooxidative effect (IR spectral profile of biomolecules between control and H2O2‐treated cells) according to FTIR analyses. These results demonstrated the viability to use infrared spectroscopy to evaluate the oxidant and antioxidant effect of molecules in cell systems assays.

Isaac Chávez-GuevaraIsaac Chávez-Guevara
Isaac Chávez-Guevara
RURené Urquidez-Romero
René Urquidez-Romero
JPJorge Alberto Perez-Leon
Jorge Alberto Perez-Leon
EREverardo Gonzalez Rodriguez
Everardo Gonzalez Rodriguez
VMVerónica Moreno-Brito
Verónica Moreno-Brito
ARArnulfo Ramos-Jiménez
Arnulfo Ramos-Jiménez
Exercise training performed at the maximal fat oxidation intensity (FMT) stands out as a potential treatment of overweight and obesity. This work is a meta-analysis of randomized clinical trials of studies about the effect of FMT on fat mass and maximal oxygen consumption using PubMed, SCOPUS, EBSCOhost, and ScienceDirect as databases. Two independent reviewers selected 11 trials from 356 publications identified by the following keywords: fatmax, lipoxmax, maximal fat oxidation, peak of fat oxidation, physical training, physical exercise, body fat (BF), fat mass, overweight, and obesity. The risk of bias was assessed following the Cochrane Guidelines. The pooled mean difference was computed for each outcome with the random-effects model and the inverse-variance method. The meta-analysis was performed with the RevMan software v 5.3, and the heterogeneity across studies by the I2. The statistical significance was accepted at p < 0.05. Results showed that the FMT reduced body weight (MD = −4.30 kg, p < 0.01, I2 = 0%), fat mass (MD = −4.03 kg, p < 0.01, I2 = 0%), and waist circumference (MD = −3.34 cm, p < 0.01). Fat-free mass remains unchanged (MD = 0.08 kg, p = 0.85), but maximal oxygen consumption increased (MD = 2.96 mL∙kg−1∙min−1, p < 0.01, I2 = 0%). We conclude that FMT at short and medium-term (eight to twenty weeks) reduces body weight and BF, increasing cardiovascular fitness in low physical fitness people with obesity.

20 March 2013 in Neurochemical Research
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Journal Article
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JPJorge Alberto Perez-Leon
Jorge Alberto Perez-Leon
IOIxchel Osorio-Paz
Ixchel Osorio-Paz
LFLiliana Francois
Liliana Francois
RSRocio Salceda
Rocio Salceda

Isaac Chávez-GuevaraIsaac Chávez-Guevara
Isaac Chávez-Guevara
RHRosa Patricia Hernández-Torres
Rosa Patricia Hernández-Torres
MTMarina Trejo-Trejo
Marina Trejo-Trejo
EREverardo Gonzalez Rodriguez
Everardo Gonzalez Rodriguez
VMVerónica Moreno-Brito
Verónica Moreno-Brito
ARArnulfo Ramos-Jiménez
Arnulfo Ramos-Jiménez
Obesity is thought to be associated with a reduced capacity to increase fat oxidation in response to physical exercise; however, scientific evidence supporting this paradigm remains scarce. This study aimed to determine the interrelationship of different submaximal exercise metabolic flexibility (Metflex) markers and define its association with body fatness on subjects with obesity. Twenty-one male subjects with obesity performed a graded-intensity exercise protocol (Test 1) during which cardiorespiratory fitness (CRF), maximal fat oxidation (MFO) and its corresponding exercise intensity (FATmax) were recorded. A week afterward, each subject performed a 60-min walk (treadmill) at FATmax (Test 2), and the resulting fat oxidation area under the curve (TFO) and maximum respiratory exchange ratio (RERpeak) were recorded. Blood lactate (LAb) levels was measured during both exercise protocols. Linear regression analysis was used to study the interrelationship of exercise Metflex markers. Pearson’s correlation was used to evaluate all possible linear relationships between Metflex and anthropometric measurement, controlling for CRF). The MFO explained 38% and 46% of RERpeak and TFO’s associated variance (p < 0.01) while TFO and RERpeak were inversely related (R2 = 0.54, p < 0.01). Body fatness positively correlated with MFO (r = 0.64, p < 0.01) and TFO (r = 0.63, p < 0.01) but inversely related with RERpeak (r = −0.67, p < 0.01). This study shows that MFO and RERpeak are valid indicators of TFO during steady-state exercise at FATmax. The fat oxidation capacity is directly associated with body fatness in males with obesity.