Lourdes Rodríguez-Fragoso

Lourdes Rodríguez-Fragoso

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Lourdes Rodríguez-Fragoso

Univ Autonoma Del Estado de Morelos

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

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

Representative Publications

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1 February 2008 in Toxicology and Applied Pharmacology
Verified
Journal Article
Closed access
LRLourdes Rodriguez-Fragoso
Lourdes Rodriguez-Fragoso
JRJorge Reyes-Esparza
Jorge Reyes-Esparza
SBScott W. Burchiel
Scott W. Burchiel
DHDea Herrera-Ruiz
Dea Herrera-Ruiz
ETEliseo Torres
Eliseo Torres

5 May 2011 in Journal of Food Science
Verified
Journal Article
Closed access
PDF file
LRLourdes Rodríguez‐Fragoso
Lourdes Rodríguez‐Fragoso
JMJosé Luis Martínez‐Arismendi
José Luis Martínez‐Arismendi
DODanae Orozco‐Bustos
Danae Orozco‐Bustos
JRJorge Reyes‐Esparza
Jorge Reyes‐Esparza
ETEliseo Torres
Eliseo Torres
SBScott W. Burchiel
Scott W. Burchiel

1 October 2006 in Annals of Hepatology
Verified
Journal Article
Open access
JPJorge Luis Poo
Jorge Luis Poo
JGJulieta Góngora
Julieta Góngora
FSFrancisco Sánchez-Ávila
Francisco Sánchez-Ávila
SASergio Aguilar-Castillo
Sergio Aguilar-Castillo
GGGuillermo García-Ramos
Guillermo García-Ramos
MUMisael Uribe
Misael Uribe
Despite steady progress in therapeutics of liver disease, portal systemic encephalopathy remains to be a great challenge for clinicians because of the heterogeneity of neuropsychiatric symptoms, multiple risk factors and complexity on achieving a sustained response. We aimed to evaluate the efficacy of L-Ornithin, L-Aspartate versus lactulose in Mexican patients with hyperammonemic hepatic encephalopathy. A total of 20 patients were randomly allocated to receive either lactulose(n = 10) or L-ornithine - L-aspartate (n = 10) for 2 weeks. At baseline, patients of both groups were comparable in age (64 +/- 7 versus 60 +/- 6) and degree of hepatic failure according to the Child-Pugh scale (9.2 +/- 1.3 versus 9.2 +/- 1.1). A significant decrease in ammonia levels was observed both in the lactulose group (120.4 +/- 8.1 versus 91.4 +/- 10, p < 0.05) and in the LOLA group (141.6 +/- 9.1 versus 96.9 +/- 9.3, p < 0.05). Moreover, in patients who received LOLA a significant improvement was observed in mental status (1.0 +/- 0.14 versus 0.4 +/- 0.16, p < 0.05), Number Connection Test (184 +/- 43 versus 88 +/- 7, p < 0.05), asterixis (14.6 +/- 2.8 versus 6.7 +/- 1.5, p < 0.05), as well as EEG findings (6.8 +/- 0.6 versus 8.1 +/- 0.2 cycles per second, p < 0.05). Compliance with study medications was similar between the lactulose group (94%) and the LOLA group (100%). No serious adverse events were reported in the two groups; however, in the lactulose group an increase in the number of weekly defecations was reported, as well as a higher incidence of abdominal pain or flatulence. Finally, both patient groups reported an improvement in the Visual Analogue Scale for EuroQol index (51.1 +/- 24.1 versus 61.5 +/- 15.8, p < 0.05, in the lactulose group; 56.5 +/- 24.5 versus 70 +/- 19.4, p < 0.05, in the LOLA group). In conclusion, oral administration of lactulose or L-ornithine - L-aspartate to Mexican patients with cirrhosis and hyperammonemic encephalopathy significantly reduced serum ammonia levels in study groups and additionally improved mental status parameters, number connection test, asterixis scores, and EEG activity in the group receiving L-ornithine-L-aspartate.

30 June 2022 in Membranes
Verified
Journal Article
Open access
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THTammy Haro-Reyes
Tammy Haro-Reyes
LDLucero Díaz-Peralta
Lucero Díaz-Peralta
AGArturo Galván-Hernández
Arturo Galván-Hernández
ARAnahi Rodríguez-López
Anahi Rodríguez-López
LRLourdes Rodríguez-Fragoso
Lourdes Rodríguez-Fragoso
IOIván Ortega-Blake
Iván Ortega-Blake
This review examined a collection of studies regarding the molecular properties of some polyene antibiotic molecules as well as their properties in solution and in particular environmental conditions. We also looked into the proposed mechanism of action of polyenes, where membrane properties play a crucial role. Given the interest in polyene antibiotics as therapeutic agents, we looked into alternative ways of reducing their collateral toxicity, including semi-synthesis of derivatives and new formulations. We follow with studies on the role of membrane structure and, finally, recent developments regarding the most important clinical applications of these compounds.

1 March 2012 in Toxicology Letters
Verified
Journal Article
Closed access
Angel León-BuitimeaAngel León-Buitimea
Angel León-Buitimea
LRLourdes Rodríguez-Fragoso
Lourdes Rodríguez-Fragoso
FLFredine T. Lauer
Fredine T. Lauer
HBHarmony Bowles
Harmony Bowles
TTTodd A. Thompson
Todd A. Thompson
SBScott W. Burchiel
Scott W. Burchiel

1 May 2007 in Journal of Pharmacy and Pharmacology
Verified
Journal Article
Closed access
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CRCésar Ruiz-Marcial
César Ruiz-Marcial
RRRicardo Reyes-Chilpa
Ricardo Reyes-Chilpa
EEElizabeth Estrada
Elizabeth Estrada
JRJorge Reyes-Esparza
Jorge Reyes-Esparza
GFGermán Garrido Fariña
Germán Garrido Fariña
LRLourdes Rodríguez-Fragoso
Lourdes Rodríguez-Fragoso
Among the eight Calophyllum species found on the American continent, Calophyllum brasiliense is the most widely distributed. Chemical analysis of this species has shown the presence of xanthones with cancer chemopreventive properties and antifungal activity. Recently, three new coumarins with antineoplastic properties have been found. In this study, we have evaluated the biological effects of the antiproliferative activity of coumarins isolated from C. brasiliense on the survival, cell cycle and apoptosis of cells in-vitro and their antitumour effects in mice. The cytological study showed that coumarins from C. brasiliense reduce the survival of BMK cells (baby mouse kidney cells) by inducing apoptosis and, to a lesser degree, necrosis. The cell cycle was arrested in S-phase and the division of BMK cells was inhibited. Coumarins had caused a reduction of experimental tumours in 83% of animals by the end of the treatment. Therefore, coumarins have the potential to be used alone or in combination with other antineoplastic drugs, and they might increase the effectiveness of other treatments for cancer.