Alejandro Ávalos-Rodríguez
Universidad Autónoma Metropolitana
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Alejandro Ávalos-Rodríguez.
Theriogenology | 2003
Israel Alonso-Pozos; Ana María Rosales-Torres; Alejandro Ávalos-Rodríguez; Marcela Vergara-Onofre; Adolfo Rosado-Garcı́a
Changes in granulosa cell lysosomal and mitochondrial functions in relation to follicular size and to the stage of atresia were studied by fluorescent emission spectra and intensity using flow cytometry. Antral follicles were grouped by size in two groups: small, 3-6 mm and large, >6mm in diameter, and classified into three stages of atresia: non-atretic, initially atretic and advanced atretic. Differences in Rhodamine 123 (Rh123) and Acridine Orange (AO) fluorescent intensity indicated that changes in mitochondrial function are the primary mechanism of granulosa cell death in atretic follicles 3-6 mm in diameter, while its role in granulosa cell death in >6 mm atretic follicles seemed to be less important. However, modifications in lysosomal function (shown by a decrease in fluorometric intensity of AO incubated granulosa cells) were mainly associated with cell death in large atretic follicles. Our results support the hypothesis that the pathway of granulosa cell death during follicular atresia depends on the state of energy metabolism or on the production of hypoxic conditions related to follicular size. Changes in mitochondrial membrane potential and production of permeability transition pores were the main changes found in small follicles, while lysosomal function destabilization seemed to be the major cause of granulosa cell death during atresia in large follicles.
Molecular and Cellular Biochemistry | 2006
Clara Ortega-Camarillo; A. M. Guzmán-Grenfell; Rebeca García-Macedo; Ana María Rosales-Torres; Alejandro Ávalos-Rodríguez; Genoveva Durán-Reyes; Rafael Medina-Navarro; Miguel Cruz; Margarita Díaz-Flores; Jesús Kumate
The mechanisms related to hyperglycemia-induced pancreatic β-cell apoptosis are poorly defined. Rat insulin-producing cells (RINm5F) cultured in high glucose concentrations (30 mM) showed increased apoptosis and protein p53 translocation to mitochondria. In addition, hyperglycemia induced both the disruption of mitochondrial membrane potential (Δ < eqid1 > m), and an increase in reactive oxygen species (ROS), as shown by fluorescence changes of JC-1 and dichlorodihydrofluorescein-diacetate (DCDHF-DA), respectively. The increased intracellular ROS by high glucose exposure was blunted by mitochondrial-function and NADPH-oxidase inhibitors. We postulate that the concomitant mobilization of p53 protein to the mitochondria and the subsequent changes on the Δ < eqid2 > m, lead to an important pancreatic β-cell apoptosis mechanism induced by oxidative stress caused by hyperglycemia.
Molecular Reproduction and Development | 2000
Ana María Rosales-Torres; Alejandro Ávalos-Rodríguez; Marcela Vergara-Onofre; Omar Hernández‐Pérez; Luz María Ballesteros; Rebeca García-Macedo; Vianney Ortiz-Navarrete; A. Rosado
The differential quantitative participation of apoptosis and necrosis in ewe antral follicles of two different sizes, separated in four stages of atresia using macroscopic, histologic, and esteroid quantification methods was assessed. Annexin V binding and propidium iodide (PI) uptake was used to detect healthy live cells (Annexin V negative/PI negative), early apoptotic cells (Annexin V+/PI−), and necrotic or late apoptotic cells (PI+). Additionally we used internucleosomal DNA fragmentation as a quantitative estimate of apoptosis. Presence and distribution of lysosomal enzymes in follicular fluid and granulosa cells was used as a measure of necrotic cell death. DNA flow citometry and gel electrophoresis were positively correlated with the progression of atresia, small atretic follicles tend to have higher percentages of internucleosomal cleaved DNA than follicles >6 mm. Annexin/PI binding also indicates that apoptosis and necrosis increase with atresia progression, generally apoptosis outweighs necrosis in small follicles. Acid phosphatase and glucosaminidase in follicular fluid of 3–6 mm follicles showed no significant modifications between healthy and initially atretic follicles, and only a small, but significant increase in activity in advancedly atretic follicles. On the contrary, lysosomal enzyme activity in follicles >6 mm showed positive correlation between atresia stages and the activities of acid phosphatase and glucosaminidase in follicular fluid. A similar size‐differential behavior was found in free or membrane‐bound lysosomal enzyme activity of granulosa cells. Necrosis, but principally apoptosis, were present during all stages of follicular maturation indicating that growth and maturation of ovarian follicles involves a continuous renewal of granulosa cells, regulated by apoptosis. Mechanisms regulating this equilibrium may participate in the final destiny, whether ovulation or atresia of ovarian follicles. Mol. Reprod. Dev. 55:270–281, 2000.
Reproduction | 2009
Clara Ortega-Camarillo; Alicia González-González; Marcela Vergara-Onofre; Everardo González-Padilla; Alejandro Ávalos-Rodríguez; Margarita Gutiérrez-Rodríguez; Lourdes Arriaga-Pizano; Miguel A. Cruz; Luis Arturo Baiza-Gutman; Margarita Díaz-Flores
Apoptosis of granulosa cells during follicular atresia is preceded by oxidative stress, partly due to a drop in the antioxidant glutathione (GSH). Under oxidative stress, GSH regeneration is dependent on the adequate supply of NADPH by glucose-6-phosphate dehydrogenase (G6PD). In this study, we analyzed the changes of G6PD, GSH, and oxidative stress of granulosa cells and follicular liquid and its association with apoptosis during atresia of small (4-6 mm) and large (>6 mm) sheep antral follicles. G6PD activity was found to be higher in granulosa cells of healthy small rather than large follicles, with similar GSH concentration in both cases. During atresia, increased apoptosis and protein oxidation, as well as a drop in GSH levels, were observed in follicles of both sizes. Furthermore, the activity of G6PD decreased in atretic small follicles, but not in large ones. GSH decreased and protein oxidation increased in follicular fluid. This was dependent on the degree of atresia, whereas the changes in G6PD activity were based on the type of follicle. The higher G6PD activity in the small follicles could be related to granulosa cell proliferation, follicular growth, and a lower sensitivity to oxidative stress when compared with large follicles. The results also indicate that GSH concentration in atretic follicles depends on other factors in addition to G6PD, such as de novo synthesis or activity of other NADPH-producing enzymes. Finally, lower G6PD activity in large follicles indicating a higher susceptibility to oxidative stress associated to apoptosis progression in follicle atresia.
Archives of Andrology | 2004
Alejandro Ávalos-Rodríguez; A. R. Ortíz-Muñíz; Clara Ortega-Camarillo; Marcela Vergara-Onofre; A. Rosado-García; Ana María Rosales-Torres
This study was conducted to evaluate phosphatidylserine translocation in head plasma membrane of Percoll-gradient purified of rabbit cauda epididymal sperm during capacitation and acrosome reaction (AR) using Annexin-V. Propidium iodide was used as control to reject dead or dying cells. The presence and distribution of Annexin-V binding sites were analyzed using flow fluorocytometry and confocal microscopy. After 6 h of incubation of sperm in capacitation medium, the number of cells positively stained with Annexin-V showed a small but significant increment. The Annexin-V binding sites produced during capacitation were found mainly in the post-acrosomal region of the sperm head plasma membrane. After AR induction with progesterone, the localization of phosphatidylserine was changed and the Annexin-V binding sites were found almost only in the acrosomal region, but with higher number of binding sites in the equatorial area. On the contrary, after AR induction with A23187, phosphatidylserine translocation, although predominant over the acrosomal region, was also observed in the post-acrosomal region. Plasma membrane destabilization during capacitation and AR may be important for sperm-oocyte fusion.
International Journal of Morphology | 2013
Juan José Pérez-Rivero; Emilio Rendón-Franco; Mario Pérez-Martínez; Alejandro Ávalos-Rodríguez; Rafael Ávila-Flores
La mayoria de los murcielagos neotropicales se reproducen de manera estacional. El objetivo de este estudio fue determinar los cambios morfometricos en el parenquima testicular del murcielago Tadarida brasiliensis que habita en un area urbana del sur de la Ciudad de Mexico durante las estaciones de verano, otono e invierno. Se obtuvieron fragmentos de tejido testicular para su estudio histologico. Se midio el diametro de los tubulos seminiferos y el espacio interstisial y se identificaron y contaron distintos tipos celulares. En las muestras de junio se encontro un menor diametro de los tubulos seminiferos y un mayor espacio intersticial entre los tubulos; tambien hubo un menor numero de celulas del epitelio germinal y no hubo presencia de espermatides. En las muestras de tejido obtenidas en el mes de septiembre y febrero se observo un incremento significativo en el diametro del tubulo, grosor del epitelio germinal y numero de celulas del epitelio germinal cuando fueron comparadas con las muestras de junio (p 0.05). Solo en las muestras de febrero hubo presencia de espermatides. En conjunto, nuestros resultados sugieren la existencia de variaciones estacionales en la actividad reproductiva de T. brasiliensis, bajo las condiciones en que se realizo el estudio.
Molecular and Cellular Biochemistry | 2015
R. Barzalobre-Gerónimo; Luis Antonio Flores-López; Luis Arturo Baiza-Gutman; Miguel Cruz; Rebeca García-Macedo; Alejandro Ávalos-Rodríguez; A. Contreras-Ramos; Margarita Díaz-Flores; Clara Ortega-Camarillo
In the original article the authors appear with full first names and the last name only with initials. This is not correct. Everything else in the paper remains correct.
Molecular Biology Reports | 2013
Luis Antonio Flores-López; Margarita Díaz-Flores; Rebeca García-Macedo; Alejandro Ávalos-Rodríguez; Marcela Vergara-Onofre; Miguel Cruz; Alejandra Contreras-Ramos; Mina Königsberg; Clara Ortega-Camarillo
Immunoendocrinology | 2015
Clara Ortega-Camarillo; Luis Antonio Flores-López; Alejandro Ávalos-Rodríguez
Gaceta Medica De Mexico | 2001
Clara Ortega-Camarillo; Margarita Díaz-Flores; Alejandro Ávalos-Rodríguez; Marcela Vergara-Onofre; Ana María Rosales-Torres