David Calderón-Guzmán
National Autonomous University of Mexico
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Featured researches published by David Calderón-Guzmán.
Archives of Medical Research | 2002
M.Gerardo Barragán-Mejı́a; Luis Castilla-Serna; David Calderón-Guzmán; J.Luis Hernández-Islas; Norma Angélica Labra-Ruíz; R.Antonio Rodrı́guez-Pérez; Daniel Santamaría del Ángel
BACKGROUND Ozone is an environmental pollutant that has widely documented deleterious effects on exposed organisms. In Mexico City, this pollutant frequently reaches concentrations that surpass safe health limits. In addition, it has been reported that the prevalence of malnutrition remains high in our childhood population. This experiment was carried out to determine whether malnutrition is a factor contributing to an increase in the risk of damage associated with ozone exposure. METHODS Using an experimental animal model, 21-day-old rats fed normally or with induced malnutrition were subchronically exposed to 0.5 ppm of ozone or fresh air, respectively, for 30 days. At the end of this period and using HPLC, serotonin concentrations were measured in four areas of the brain: cortex, hemispheres, cerebellum, and medulla oblongata. RESULTS Malnourished animals had a significant weight deficit beginning at 28 days with respect to well-fed animals. Among the well-fed animals, this phenomenon is seen at 35 days in exposed and non-exposed animals. In the four regions of the brain, malnourished animals show low serotonin concentrations with respect to well-nourished animals. In the cerebellum, there was an interaction between the nutritional factor and ozone exposure, while in the medulla oblongata both factors acted independently. CONCLUSIONS Our results suggest a multiplicative effect from the nutritional factor and ozone exposure in the changes observed concerning serotonergic metabolism.
Human & Experimental Toxicology | 2009
David Calderón-Guzmán; Norma Osnaya-Brizuela; Raquel García-Álvarez; Ernestina Hernández-García; Hugo Juárez-Olguín
The objective of the study is to determine the damage by oxidative stress induced by morphine in brain of rats fed with a protein-deficient diet. Twenty-eight malnourished male Wistar rats, 30 days old, were used in the study. The animals were divided into four groups of 7 rats per group. Group I received NaCl and the groups II; III and IV intraperitoneally received 3, 6 and 12 mg/kg of morphine sulphate, respectively, in a single dose. Animals were sacrificed and the levels of glutathione (GSH), dopamine, tryptophan and 5-hydroxyindole-3-acetic acid (5-HIAA) as well as, Na+/K+ ATPase and total ATPase activity in the brain were measured. Tryptophan levels and Na+/K + ATPase activity showed non-significant changes in the experimental group. Levels of 5-HIAA decreased significantly (p = .03) in animals that received 12 mg/kg of morphine and in animals that received 3 mg/kg, levels of GSH and dopamine were found to have a significant decrease (p < .05), but a significant increase in the group that received 12 mg/kg of morphine (p < .05). Total ATPase activity increased significantly in the groups that received 3 mg/kg (p = .015) and 6 mg/kg (p = .0001) of morphine. The results show that malnutrition induces changes in cellular regulation and biochemical responses to oxidative stress caused by morphine sulphate.
Biomedicine & Pharmacotherapy | 2016
Daniel Santamaría del Ángel; Norma Angélica Labra-Ruíz; Mercedes Edna García-Cruz; David Calderón-Guzmán; Armando Valenzuela-Peraza; Hugo Juárez-Olguín
UNLABELLED The aim of this work was to compare the effects of catechin (CAT), epicatechin (EPI) and N-ω-l-nitroarginine (L-NARG) on different endpoints of oxidative stress induced by quinolinic acid (QUIN) in a simple tissue preparation, rat striatal slices - with particular emphasis in the glutathione system - in order to provide revealing information on the antioxidant efficacy of these agents in an excitotoxic model. METHODS Rat striatal slices were incubated for 1h in the presence of 100 μM QUIN and/or 85 μM CAT or EPI, or 100 μM L-NARG. Lipid peroxidation (LP) and the levels of reduced and oxidized glutathione (GSH and GSSG) were determined. RESULTS The three agents tested completely blocked the QUIN-induced lipid peroxidation and recovered the QUIN-induced altered GSH/GSSG balance. No statistical differences were detected among the protective effects exerted by these antioxidants, suggesting similar efficacy and common antioxidant mechanisms. The antioxidant properties exhibited by these molecules on the excitotoxic model tested herein support an active role of glutathione and prompt their use as therapeutic tools in models of neurodegenerative disorders.
Journal of The Saudi Pharmaceutical Society | 2016
David Calderón-Guzmán; Hugo Juárez-Olguín; Ernestina Hernández-García; Alejandro Medina-Andrade; Belen Juarez Tapia
Background: The knowledge about the pattern of prescription and consumption of solid oral drugs dispensed as unitary doses (UD) in Mexico is sparing. Purpose: The aim of this study was to describe the pattern of prescription and consumption of solid oral drugs dispensed as unitary doses (UD) in a third level private hospital of Mexico. A retrospective study of a 60-month period (from 2007 to 2011) was carried out to know the pattern of drugs dispensed as UD in a third level hospital. Results: Among the principal drugs consumed were analgesic, antihypertensive, antibiotic, anti-inflammatory, antiepileptic, and diuretics. The dispensation of drugs per year was as follows: 181 drugs with 85,167 UD in 2007; 199 with 90,519 UD in 2008; 193 with 101,479 UD in 2009; 195 with 100,798 UD in 2010; and 198 with 103,913 UD in 2011. Conclusion: The findings confirmed that prescription and consumption of unitary doses in the hospitalization service increased, and revealed the extensive use of analgesics as the principal prescribed drug in this kind of hospital.
Archives of Medical Research | 2004
David Calderón-Guzmán; José Luis Hernández-Islas; Ivonne Espitia-Vázquez; Gerardo Barragán-Mejía; Ernestina Hernández-García; Daniel Santamaría del Ángel; Hugo Juárez-Olguín
Neurochemical Research | 2005
David Calderón-Guzmán; Ivonne Espitia-Vázquez; Alejandra López-Domínguez; Ernestina Hernández-García; Bernardino Huerta-Gertrudis; Elvia Coballase-Urritia; Hugo Juárez-Olguín; Beatriz García-Fernández
Regulatory Toxicology and Pharmacology | 2005
David Calderón-Guzmán; José Luis Hernández-Islas; Ivonne R. Espítia Vázquez; Gerardo Barragán-Mejía; Ernestina Hernández-García; Daniel Santamaría del Ángel; Hugo Juárez-Olguín
Proceedings of the Western Pharmacology Society | 2008
David Calderón-Guzmán; Norma Osnaya-Brizuela; Raquel García-Álvarez; Ernestina Hernández García; Adrián Guillé Pérez; Hugo Juárez Olguín
Acta Pediátrica de México | 2009
David Calderón-Guzmán; Ángeles Guevara; Ernestina Hernández-García; Arturo Juárez-Jacobo; Lourdes Segura; Gerardo Barragán; Hugo Juárez-Olguín
Acta Pediátrica de México | 2011
David Calderón-Guzmán; Ernestina Hernández-García; Gerardo Barragán-Mejía; Liliana Carmona-Aparicio