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Characterization of the effects of a polyunsaturated fatty acid (PUFA) on mitochondrial bioenergetics of chronologically aged yeast
Authors:Roxana Aguilar-Toral  Maricela Fernández-Quintero  Omar Ortiz-Avila  Lucio Hernández de la Paz  Elizabeth Calderón-Cortés  Alain Raimundo Rodríguez-Orozco  Alfredo Saavedra-Molina  Marissa Calderón-Torres  Christian Cortés-Rojo
Affiliation:1. Instituto de Investigaciones Químico-Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Edificio B-3, Avenida Fco. J. Mújica S/N, Morelia, Mich, 58030, México
2. Facultad de Enfermería, Universidad Michoacana de San Nicolás de Hidalgo, Avenida Ventura Puente No. 115 Col. Centro, Morelia, Mich, 58000, México
3. Facultad de Ciencias Médicas y Biológicas “Dr. Ignacio Chávez”, Universidad Michoacana de San Nicolás de Hidalgo, Avenida Rafael Carrillo y Dr. González Herrejón S/N, Col. Cuauhtémoc, Morelia, Mich, 58020, México
4. Unidad de Biomedicina, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Avenida de los Barrios No. 1, Los Reyes-Iztacala, Tlalnepantla, Estado de México, 54090, México
Abstract:Increased membrane unsaturation has been associated with shorter longevity due to higher sensitivity to lipid peroxidation (LP) leading to enhanced mitochondrial dysfunction and ROS overproduction. However, the role of LP during aging has been put in doubt along with the participation of electron leak at the electron transport chain (ETC) in ROS generation in aged organisms. Thus, to test these hypothesis and gain further information about how minimizing LP preserves ETC function during aging, we studied the effects of α-linolenic acid (C18:3) on in situ mitochondrial ETC function, ROS production and viability of chronologically aged cells of S. cerevisiae, whose membranes are intrinsically resistant to LP due to the lack of PUFA. Increased sensitivity to LP was observed in cells cultured with C18:3 at 6 days of aging. This was associated with higher viability loss, dissipated membrane potential, impaired respiration and increased ROS generation, being these effects more evident at 28 days. However, at this point, lower sensitivity to LP was observed without changes in the membrane content of C18:3, suggesting the activation of a mechanism counteracting LP. The cells without C18:3 display better viability and mitochondrial functionality with lower ROS generation even at 28 days of aging and this was attributed to full preservation of complex III activity. These results indicate that the presence of PUFA in membranes enhances ETC dysfunction and electron leak and suggest that complex III is crucial to preserve membrane potential and to maintain a low rate of ROS production during aging.
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