Contaminantes atmosféricos y su incidencia sobre la reproducción en murinos y humanos

Autores/as

  • Yulieth Guerra-Rangel Institución Universitaria Colegio Mayor de Antioquia
  • Viviana Torres-Osorio Universidad CES

DOI:

https://doi.org/10.17533/udea.acbi/v45n118a02

Palabras clave:

embriones, espermatozoides, material particulado , ovocitos

Resumen

La contaminación atmosférica se da por la presencia o combinación de contaminantes físicos, químicos o biológicos en el aire. En los últimos años, el más estudiado es el material particulado (PM), una mezcla variada de partículas sólidas y líquidas, que, además, transporta elevados componentes tóxicos provenientes de la combustión del humo del cigarrillo, con diferentes tamaños microscópicos presentes en la atmósfera, las cuales pueden inhalarse y provocar graves problemas de salud debido a la toxicidad a nivel celular y consecuencias a nivel inflamatorio. Actualmente, la exposición al PM se ha asociado con alteraciones en los procesos reproductivos en mamíferos, afectando la viabilidad de gametos y embriones. El objetivo de esta revisión fue describir los efectos de los contaminantes atmosféricos en el ámbito reproductivo y los posibles mecanismos de acción tanto celulares como moleculares, los cuales son de interés en las ciencias de la salud humana y animal. Los estudios evidencian una relación de causa-efecto entre la exposición a los contaminantes y la calidad de los gametos, generando daños del ADN, modificaciones epigenéticas, aumento de estrés oxidativo y alteraciones morfológicas. Asimismo, se reportan efectos en el periodo prenatal y postnatal, como nacimientos prematuros, neonatos con bajo peso y abortos espontáneos. Los resultados de revisión evidencian que los contaminantes atmosféricos influyen negativamente en el proceso reproductivo de algunos mamíferos, debido a que pueden alterar los mecanismos de regulación oxidativa y regulación en la expresión génica en los gametos, lo que conlleva a toxicidad celular y potenciales alteraciones en la estabilidad genómica.

|Resumen
= 943 veces | PDF (ENGLISH)
= 237 veces| | PDF
= 561 veces| | HTML (ENGLISH)
= 18 veces| | XML (ENGLISH)
= 8 veces| | RESUMEN GRÁFICO
= 75 veces|

Descargas

Los datos de descargas todavía no están disponibles.

Biografía del autor/a

Yulieth Guerra-Rangel, Institución Universitaria Colegio Mayor de Antioquia

Institución Universitaria Colegio Mayor de Antioquia, Facultad Ciencias de la salud. Grupo de Investigación Huellas calidad de vida. Medellín,Antioquia, Colombia.

Viviana Torres-Osorio, Universidad CES

Universidad CES, Facultad de Ciencias y Biotecnología. Grupo de Investigación Biología CES. Medellín, Antioquia, Colombia.

Citas

An, J., Yin, L., Shang, Y., Zhong, Y., Zhang, X., Wu, M., Yu, Z., Sheng, G., Fu, J., & Huang, Y. (2011). The combined effects of BDE47 and BaP on oxidatively generated DNA damage in L02 cells and the possible molecular mechanism. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 721(2), 192-198. https://doi.org/10.1016/j.mrgentox.2011.02.002

Anderson, R. A., McIlwain, L., Coutts, S., Kinnell, H. L., Fowler, P. A., & Childs, A. J. (2014). Activation of the aryl hydrocarbon receptor by a component of cigarette smoke reduces germ cell proliferation in the human fetal ovary. Molecular Human Reproduction, 20(1), 42-48. https://doi.org/10.1093/molehr/gat059

Benavides, F., & Guénet, J. -L. (2001). Modelos murinos de enfermedades humanas. 61, 215-231. http://www.medicinabuenosaires.com/revistas/vol61-01/2/modelosmurinos.htm

Calogero, A. E., La Vignera, S., Condorelli, R. A., Perdichizzi, A., Valenti, D., Asero, P., Carbone, U., Boggia, B., De Rosa, N., Lombardi, G., D’Agata, R., Vicari, L. O., Vicari, E., & De Rosa, M. (2011). Environmental car exhaust pollution damages human sperm chromatin and DNA. Journal of Endocrinological Investigation, 34(6), e139-e143. https://doi.org/10.1007/BF03346722

Canipari, R., De Santis, L., & Cecconi, S. (2020). Female Fertility and Environmental Pollution. International Journal of Environmental Research and Public Health, 17(23), 8802. https://doi.org/10.3390/ijerph17238802

Cardenas, J. (2017). La calidad del aire en Colombia: Un problema de salud pública, un problema de todos. Revista Biosalud, 16(2), 5-6. https://doi.org/10.17151/biosa.2017.16.2.1

Casanello, P., Krause, B. J., Castro-Rodriguez, J. A., & Uauy, R. (2015). Programación fetal de enfermedades crónicas: Conceptos actuales y epigenética. Revista chilena de pediatría, 86(3), 135-137. https://doi.org/10.1016/j.rchipe.2015.06.008

Caserta, D., Bordi, G., Di Segni, N., D’Ambrosio, A., Mallozzi, M., & Moscarini, M. (2013). The influence of cigarette smoking on a population of infertile men and women. Archives of Gynecology and Obstetrics, 287(4), 813-818. https://doi.org/10.1007/s00404-012-2643-5

Chen, Z., Myers, R., Wei, T., Bind, E., Kassim, P., Wang, G., Ji, Y., Hong, X., Caruso, D., Bartell, T., Gong, Y., Strickland, P., Navas-Acien, A., Guallar, E., & Wang, X. (2014). Placental transfer and concentrations of cadmium, mercury, lead, and selenium in mothers, newborns, and young children. Journal of Exposure Science & Environmental Epidemiology, 24(5), 537-544. https://doi.org/10.1038/jes.2014.26

Cheng, Y., Zhang, J., Wu, T., Jiang, X., Jia, H., Qing, S., An, Q., Zhang, Y., & Su, J. (2019). Reproductive toxicity of acute Cd exposure in mouse: Resulting in oocyte defects and decreased female fertility. Toxicology and Applied Pharmacology, 379, 114684. https://doi.org/10.1016/j.taap.2019.114684

Conforti, A., Mascia, M., Cioffi, G., De Angelis, C., Coppola, G., De Rosa, P., Pivonello, R., Alviggi, C., & De Placido, G. (2018). Air pollution and female fertility: A systematic review of literature. Reproductive Biology and Endocrinology, 16(1), 117. https://doi.org/10.1186/s12958-018-0433-z

Córdova, A., Saltijeral, J., Ruiz, G., Xolalpa, V., Cortés, S., Peña, S., Córdova, C., Córdova, M., Méndez, M., Huerta, R., Juárez., & Guerra, J. (2010). Estrés oxidativo en gametos. REDVET. Revista Electrónica de Veterinaria, 11(7), 1-32. Disponible en: https://www.redalyc.org/articulo.oa?id=63614251015

D’Amato, G., Cecchi, L., D’Amato, M., & Liccardi, G. (2010). Urban air pollution and climate change as environmental risk factors of respiratory allergy: An update. Journal of Investigational Allergology and Clinical Immunology, 20(2), 95-102.

Dastoorpoor, M., Idani, E., Goudarzi, G., & Khanjani, N. (2018). Acute effects of air pollution on spontaneous abortion, premature delivery, and stillbirth in Ahvaz, Iran: A time-series study. Environmental Science and Pollution Research, 25(6), 5447-5458. https://doi.org/10.1007/s11356-017-0692-9

Díez, F. B., Tenías, J. M., & Pérez-Hoyos, S. (1999). Efectos de la contaminación atmosférica sobre la salud: Una introducción. Revista Española de Salud Pública, 73, 109-121. https://doi.org/10.1590/S1135-57271999000200002

Elminir, H. K. (2005). Dependence of urban air pollutants on meteorology. Science of The Total Environment, 350(1), 225-237. https://doi.org/10.1016/j.scitotenv.2005.01.043

Esteller, M. (2008). Epigenetics in Cancer. New England Journal of Medicine, 358(11), 1148-1159. https://doi.org/10.1056/NEJMra072067

Estrada, A., Gallo, M., & Nuñez, E. (2016). Contaminación ambiental, su influencia en el ser humano, en especial: El sistema reproductor femenino. Revista Universidad y Sociedad, 8(3), 80-86. http://scielo.sld.cu/scielo.php?script=sci_abstract&pid=S2218-36202016000300010&lng=es&nrm=iso&tlng=en

Ewa, B., & Danuta, M. (2017). Polycyclic aromatic hydrocarbons and PAH-related DNA adducts. Journal of Applied Genetics, 58(3), 321-330. https://doi.org/10.1007/s13353-016-0380-3

Filomeni, G., Piccirillo, S., Graziani, I., Cardaci, S., Da Costa Ferreira, A. M., Rotilio, G., & Ciriolo, M. R. (2009). The isatin-Schiff base copper(II) complex Cu(isaepy) 2 acts as delocalized lipophilic cation, yields widespread mitochondrial oxidative damage and induces AMP-activated protein kinase-dependent apoptosis. Carcinogenesis, 30(7), 1115-1124. https://doi.org/10.1093/carcin/bgp105

Fowler, P. A., Childs, A. J., Courant, F., MacKenzie, A., Rhind, S. M., Antignac, J.-P., Le Bizec, B., Filis, P., Evans, F., Flannigan, S., Maheshwari, A., Bhattacharya, S., Monteiro, A., Anderson, R. A., & O’Shaughnessy, P. J. (2014). In utero exposure to cigarette smoke dysregulates human fetal ovarian developmental signalling. Human Reproduction, 29(7), 1471-1489. https://doi.org/10.1093/humrep/deu117

Garza, A., Chávez, H., Vega, R., & Soto, E. (2005). Mecanismos celulares y moleculares de la neurotoxicidad por plomo. Salud Mental, 28(2), 48-58. https://www.medigraphic.com/pdfs/salmen/sam-2005/sam052e.pdf

Godwin, H. A. (2001). The biological chemistry of lead. Current Opinion in Chemical Biology, 5(2), 223-227. https://doi.org/10.1016/S1367-5931(00)00194-0

Goeden, N., Velasquez, J., Arnold, K. A., Chan, Y., Lund, B. T., Anderson, G. M., & Bonnin, A. (2016). Maternal Inflammation Disrupts Fetal Neurodevelopment via Increased Placental Output of Serotonin to the Fetal Brain. Journal of Neuroscience, 36(22), 6041-6049. https://doi.org/10.1523/JNEUROSCI.2534-15.2016

Gonzales, H., & Gonzales, H. M. (2017). Las espermatogonias de mamíferos. Biotempo, 14(2), 233-243. https://doi.org/10.31381/biotempo.v14i2.1359

Guo, J., Zhang, L., Li, C., Qin, Y., Liu, W., Li, J., & Huang, G. (2020). Benzo[b]fluoranthene Impairs Mouse Oocyte Maturation via Inducing the Apoptosis. Frontiers in Pharmacology, 11, 1226. https://doi.org/10.3389/fphar.2020.01226

Guo, Y., Cao, Z., Jiao, X., Bai, D., Zhang, Y., Hua, J., Liu, W., & Teng, X. (2021). Pre-pregnancy exposure to fine particulate matter (PM2.5) increases reactive oxygen species production in oocytes and decrease litter size and weight in mice. Environmental Pollution, 268, 115858. https://doi.org/10.1016/j.envpol.2020.115858

Hammoud, A., Carrell, D. T., Gibson, M., Sanderson, M., Parker-Jones, K., & Peterson, C. M. (2010). Decreased sperm motility is associated with air pollution in Salt Lake City. Fertility and Sterility, 93(6), 1875-1879. https://doi.org/10.1016/j.fertnstert.2008.12.089

Han, X., Zhou, N., Cui, Z., Ma, M., Li, L., Cai, M., Li, Y., Lin, H., Li, Y., Ao, L., Liu, J., & Cao, J. (2011). Association between Urinary Polycyclic Aromatic Hydrocarbon Metabolites and Sperm DNA Damage: A Population Study in Chongqing, China. Environmental Health Perspectives, 119(5), 652-657. https://doi.org/10.1289/ehp.1002340

Hanna, C., Bloom, M., Robinson, W., Kim, D., Parsons, P., vom Saal, F., Taylor, J., Steuerwald, A., & Fujimoto, V. (2012). DNA methylation changes in whole blood is associated with exposure to the environmental contaminants, mercury, lead, cadmium and bisphenol A, in women undergoing ovarian stimulation for IVF. Human Reproduction, 27(5), 1401-1410. https://doi.org/10.1093/humrep/des038

Hoque, S., Umehara, T., Kawai, T., & Shimada, M. (2021). Adverse effect of superoxide-induced mitochondrial damage in granulosa cells on follicular development in mouse ovaries. Free Radical Biology and Medicine, 163, 344-355. https://doi.org/10.1016/j.freeradbiomed.2020.12.434

Huang, J., Li, T., Ding, C. -H., Brosens, J., Zhou, C. -Q., Wang, H. -H., & Xu, Y. -W. (2012). Insufficient histone-3 lysine-9 deacetylation in human oocytes matured in vitro is associated with aberrant meiosis. Fertility and Sterility, 97(1), 178-184.e3. https://doi.org/10.1016/j.fertnstert.2011.10.023

Ji, G., Yan, L., Wu, S., Liu, J., Wang, L., Zhang, S., Shi, L., & Gu, A. (2013). Bulky DNA adducts in human sperm associated with semen parameters and sperm DNA fragmentation in infertile men: A cross-sectional study. Environmental Health, 12(1), 82. https://doi.org/10.1186/1476-069X-12-82

Jiang, X., Xing, X., Zhang, Y., Zhang, C., Wu, Y., Chen, Y., Meng, R., Jia, H., Cheng, Y., Zhang, Y., & Su, J. (2021). Lead exposure activates the Nrf2/Keap1 pathway, aggravates oxidative stress, and induces reproductive damage in female mice. Ecotoxicology and Environmental Safety, 207, 111231. https://doi.org/10.1016/j.ecoenv.2020.111231

Jurewicz, J., Radwan, M., Sobala, W., Brzeźnicki, S., Ligocka, D., Radwan, P., Bochenek, M., & Hanke, W. (2013). Association between a biomarker of exposure to polycyclic aromatic hydrocarbons and semen quality. International Journal of Occupational Medicine and Environmental Health, 26(5), 790-801. https://doi.org/10.2478/s13382-013-0152-9

Jurewicz, J., Radwan, M., Sobala, W., Polańska, K., Radwan, P., Jakubowski, L., Ulańska, A., & Hanke, W. (2015). The relationship between exposure to air pollution and sperm disomy: Air Pollution and Sperm Aneuploidy. Environmental and Molecular Mutagenesis, 56(1), 50-59. https://doi.org/10.1002/em.21883

Kilic, S., Yuksel, B., Lortlar, N., Sertyel, S., Aksu, T., & Batioglu, S. (2012). Environmental tobacco smoke exposure during intrauterine period promotes granulosa cell apoptosis: A prospective, randomized study. The Journal of Maternal-Fetal & Neonatal Medicine, 25(10), 1904-1908. https://doi.org/10.3109/14767058.2012.678440

Lafuente, A. (2013). The hypothalamic–pituitary–gonadal axis is target of cadmium toxicity. An update of recent studies and potential therapeutic approaches. Food and Chemical Toxicology, 59, 395-404. https://doi.org/10.1016/j.fct.2013.06.024

Legro, R., Sauer, M., Mottla, G., Richter, K., Li, X., Dodson, W., & Liao, D. (2010). Effect of air quality on assisted human reproduction. Human Reproduction, 25(5), 1317-1324. https://doi.org/10.1093/humrep/deq021

Ling, X., Zhang, G., Sun, L., Wang, Z., Zou, P., Gao, J., Peng, K., Chen, Q., Yang, H., Zhou, N., Cui, Z., Zhou, Z., Liu, J., Cao, J., & Ao, L. (2017). Polycyclic aromatic hydrocarbons exposure decreased sperm mitochondrial DNA copy number: A cross-sectional study (MARHCS) in Chongqing, China. Environmental Pollution, 220, 680-687. https://doi.org/10.1016/j.envpol.2016.10.026

López, G., Gómez, P., & Duaso, A. (2016). Hidrocarburos aromáticos policíclicos (HAPs) (I): Toxicidad, exposición de la población y alimentos implicados. Revista Complutense de Ciencias Veterinarias, 10(1), 1-15. https://doi.org/10.5209/rev_RCCV.2016.v10.n1.51869

Macedo, A. (2012). La producción de especies reactivas de oxígeno (EROs) en las mitocondrias de Saccharomyces cerevisiae. TIP. Revista especializada en ciencias químico-biológicas, 15(2), 97-103. http://www.scielo.org.mx/scielo.php?script=sci_abstract&pid=S1405-888X2012000200003&lng=es&nrm=iso&tlng=es

Martínez, E., Sánchez, M., & Hafidi E. (2005). Participación de la mitocondria en el desarrollo de estrés oxidativo en la obesidad. Bioquimia, 30(3), 82-89. https://www.redalyc.org/articulo.oa?id=57630304

Mathur, P., & D’Cruz, S. (2011). The effect of environmental contaminants on testicular function. Asian Journal of Andrology, 13(4), 585-591. https://doi.org/10.1038/aja.2011.40

Mendiola, J., Moreno, J. M., Roca, M., Vergara-Juárez, N., Martínez-García, M. J., García-Sánchez, A., Elvira-Rendueles, B., Moreno-Grau, S., López-Espín, J. J., Ten, J., Bernabeu, R., & Torres-Cantero, A. M. (2011). Relationships between heavy metal concentrations in three different body fluids and male reproductive parameters: A pilot study. Environmental Health, 10(1), 6. https://doi.org/10.1186/1476-069X-10-6

Nandi, P., Banerjee, S., Basu, S., Das, M., Dasgupta, P., & Varghese, A. (2011). A preliminary study on heavy metals (Lead, Cadmium and Arsenic) in follicular fluid and its effect on oocyte, embryo quality and outcome of IVF treatment. Fertility and Sterility, 96(3), 155. https://doi.org/10.1016/j.fertnstert.2011.07.609

Nicolich, A., Lafuente R., López G., Peiró, A., & Brassesco M. (2013). Análisis del estrés oxidativo en el eyaculado mediante la determinación del anión superóxido. Revista Asebir, 18(1), 15-19. https://revista.asebir.com/assets/AF_revista_jun2013_comp.pdf

Organización de las Naciones Unidas, ONU. (2019, octubre 24). Se avecina otra crisis que puede extinguirnos: La contaminación con sustancias tóxicas. Noticias ONU. https://news.un.org/es/story/2019/10/1464381

Organización Mundial de la Salud, OMS. (2019, mayo 31). Día mundial sin tabaco 2019- Tabaco y salud pulmonar. https://www.who.int/es/news-room/events/detail/2019/05/31/default-calendar/world-no-tobacco-day

Paixão, L., Gaspar, R., Gonzalez, G., Santos, A., Santana, A., Santos, R., Spritzer, P., & Nascimento, C. (2012). Cigarette smoke impairs granulosa cell proliferation and oocyte growth after exposure cessation in young Swiss mice: An experimental study. Journal of Ovarian Research, 5(1), 25. https://doi.org/10.1186/1757-2215-5-25

Pedersen, M., Giorgis, L., Bernard, C., Aguilera, I., Andersen, A., Ballester, F., Beelen, R., Chatzi, L., Cirach, M., Danileviciute, A., Dedele, A., Eijsden, M. van, Estarlich, M., Fernández, A., Fernández, M., Forastiere, F., Gehring, U., Grazuleviciene, R., Gruzieva, O., & Slama, R. (2013). Ambient air pollution and low birthweight: A European cohort study (ESCAPE). The Lancet. Respiratory Medicine, 1(9), 695-704. https://doi.org/10.1016/S2213-2600(13)70192-9

Pintó, X. (2000). La homocisteína como factor de riesgo cardiovascular. Medicina Integral, 36(5), 179-185. https://www.elsevier.es/es-revista-medicina-integral-63-articulo-la-homocisteina-como-factor-riesgo-10022224

PND. (2019). Plan Nacional de Desarrollo 2018-2022 «Pacto por Colombia, pacto por la equidad». https://www.dnp.gov.co:443/DNPN/Paginas/Plan-Nacional-de-Desarrollo.aspx

Polak, G., Wertel, I., Barczyński, B., Kwaśniewski, W., Bednarek, W., & Kotarski, J. (2013). Increased levels of oxidative stress markers in the peritoneal fluid of women with endometriosis. European Journal of Obstetrics & Gynecology and Reproductive Biology, 168(2), 187-190. https://doi.org/10.1016/j.ejogrb.2012.12.043

Radwan, M., Dziewirska, E., Radwan, P., Jakubowski, L., Hanke, W., & Jurewicz, J. (2018). Contaminación del aire y proporción sexual de espermatozoides humanos. American Journal of Men’s Health, 12(4), 907-912. https://doi.org/10.1177/1557988317752608

Ramirez, R., Esparza, H., Varela, A., Astorga, A., & Roman, A. (2009). Characterization of Inhalable Particulate Matter in Ambient Air by Scanning Electron Microscopy and Energy-Dispersive X-ray Analysis. Microscopy and Microanalysis, 15, 1320. https://doi.org/10.1017/S1431927609097335

Rebelo, F., & Caldas, E. (2016). Arsenic, lead, mercury and cadmium: Toxicity, levels in breast milk and the risks for breastfed infants. Environmental Research, 151, 671-688. https://doi.org/10.1016/j.envres.2016.08.027

Rogers, J. M. (2019). Smoking and pregnancy: Epigenetics and developmental origins of the metabolic syndrome. Birth defects research, 111(17), 1259-1269. https://doi.org/10.1002/bdr2.1550

Romero, R., Friel, A., Velez, D., Kusanovic, J., Hassan, S., Mazaki, S., Vaisbuch, E., Kim, C., Erez, O., Chaiworapongsa, T., Pearce, B., Bartlett, J., Salisbury, B., Anant, M., Vovis, G., Lee, M., Gomez, R., Behnke, E., Oyarzun, E., & Menon, R. (2010). A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM). American Journal of Obstetrics and Gynecology, 203(4), 361.e1-361.e30. https://doi.org/10.1016/j.ajog.2010.05.026

Scirè, A., Cianfruglia, L., Minnelli, C., Bartolini, D., Torquato, P., Principato, G., Galli, F., & Armeni, T. (2019). Glutathione compartmentalization and its role in glutathionylation and other regulatory processes of cellular pathways. BioFactors, 45(2), 152-168. https://doi.org/10.1002/biof.1476

Shomper, M., Lappa, C., & FitzHarris, G. (2014). Kinetochore microtubule establishment is defective in oocytes from aged mice. Cell Cycle (Georgetown, Tex.), 13(7), 1171-1179. https://doi.org/10.4161/cc.28046

Sierra, M., Guzmán, A., Olivares, I., Torres, Y., & Hicks, J. (2004). Participación de las especies reactivas del oxígeno en las enfermedades pulmonares. Revista del Instituto Nacional de Enfermedades Respiratorias, 17(2), 135-148. http://www.scielo.org.mx/scielo.php?script=sci_abstract&pid=S0187-75852004000200010&lng=es&nrm=iso&tlng=es

Simmons, R. (2005). Developmental origins of adult metabolic disease: Concepts and controversies. Trends in Endocrinology and Metabolism: TEM, 16(8), 390-394. https://doi.org/10.1016/j.tem.2005.08.004

Sobinoff, A., Beckett, E., Jarnicki, A., Sutherland, J., McCluskey, A., Hansbro, P., & McLaughlin, E. (2013). Scrambled and fried: Cigarette smoke exposure causes antral follicle destruction and oocyte dysfunction through oxidative stress. Toxicology and Applied Pharmacology, 271(2), 156-167. https://doi.org/10.1016/j.taap.2013.05.009

Suarez, L., Ramadhani, T., Felkner, M., Canfield, M., Brender, J., Romitti, P., & Sun, L. (2011). Maternal Smoking, Passive Tobacco Smoke, and Neural Tube Defects. Birth defects research. Part A, Clinical and molecular teratology, 91(1), 29-33. https://doi.org/10.1002/bdra.20743

Tempest, H., Homa, S., Dalakiouridou, M., Christopikou, D., Wright, D., Zhai, X., & Griffin, D. (2004). The association between male infertility and sperm disomy: Evidence for variation in disomy levels among individuals and a correlation between particular semen parameters and disomy of specific chromosome pairs. Reproductive Biology and Endocrinology, 2(1), 82. https://doi.org/10.1186/1477-7827-2-82

US EPA, O. (2016, abril 19). Particulate Matter (PM) Basics [Overviews and Factsheets]. https://www.epa.gov/pm-pollution/particulate-matter-pm-basics

Vázquez, G., Rubio, J., & Espinosa, J. (2016). Mecanismos de acción del receptor de hidrocarburos de arilos en el metabolismo del benzo[a]pireno y el desarrollo de tumores. TIP. Revista Especializada en Ciencias Químico-Biológicas, 19(1), 54-67. https://doi.org/10.1016/j.recqb.2016.02.006

Vicenta, C., Pavesi, A., Feldman, R., & Bouvet, B. (2015). Importancia de la evaluación del estrés oxidativo en el semen humano. Archivos de Medicina Interna, 37(1), 7-14. http://www.scielo.edu.uy/scielo.php?script=sci_abstract&pid=S1688-423X2015000100002&lng=es&nrm=iso&tlng=es

Vrontikis, A., Chang, P., Kovacs, P., & Lindheim, S. (2010). Antral follice counts (AFC) predict ovarian response and pregnancy outcomes in oocyte donation cycles. Journal of Assisted Reproduction and Genetics, 27(7), 383-389. https://doi.org/10.1007/s10815-010-9421-8

Wang, B., & Xu, A. (2019). Aryl hydrocarbon receptor pathway participates in myocardial ischemia reperfusion injury by regulating mitochondrial apoptosis. Medical Hypotheses, 123, 2-5. https://doi.org/10.1016/j.mehy.2018.12.004

Wei, Y., Zhang, J., Li, Z., Gow, A., Chung, K. F., Hu, M., Sun, Z., Zeng, L., Zhu, T., Jia, G., Li, X., Duarte, M., & Tang, X. (2016). Chronic exposure to air pollution particles increases the risk of obesity and metabolic syndrome: Findings from a natural experiment in Beijing. The FASEB Journal, 30(6), 2115-2122. https://doi.org/10.1096/fj.201500142

Wijesekara, G., Fernando, D., Wijerathna, S., & Bandara, N. (2015). Environmental and occupational exposures as a cause of male infertility: A caveat. Ceylon Medical Journal, 60(2), 52. https://doi.org/10.4038/cmj.v60i2.7090

Wu, G., Brown, J., Zamora, M., Miller, A., Satterfield, M., Meininger, C., Steinhauser, C., Johnson, G., Burghardt, R., Bazer, F., Li, Y., Johnson, N., Molina, M., & Zhang, R. (2019). Adverse organogenesis and predisposed long-term metabolic syndrome from prenatal exposure to fine particulate matter. Proceedings of the National Academy of Sciences, 116(24), 11590-11595. https://doi.org/10.1073/pnas.1902925116

Wu, S., Zhang, Y., Wu, X., Hao, G., Ren, H., Qiu, J., Zhang, Y., Bi, X., Yang, A., Bai, L., & Tan, J. (2021). Association between exposure to ambient air pollutants and the outcomes of in vitro fertilization treatment: A multicenter retrospective study. Environment International, 153, 106544. https://doi.org/10.1016/j.envint.2021.106544

Yang, P., Wang, Y. -X., Sun, L., Chen, Y. -J., Liu, C., Huang, L. -L., Lu, W. -Q., & Zeng, Q. (2017). Urinary metabolites of polycyclic aromatic hydrocarbons, sperm DNA damage and spermatozoa apoptosis. Journal of Hazardous Materials, 329, 241-248. https://doi.org/10.1016/j.jhazmat.2017.01.053

Yin, C., Cai, H., Yang, D., Jian, Y., Zhang, J., Li, Z., & Wang, D. (2021). Cigarette smoke induced neural tube defects by down‐regulating noggin expression. Birth Defects Research, 113(1), 5-13. https://doi.org/10.1002/bdr2.1804

Yorifuji, T., Kashima, S., Higa Diez, M., Kado, Y., Sanada, S., & Doi, H. (2016). Prenatal Exposure to Traffic-related Air Pollution and Child Behavioral Development Milestone Delays in Japan: Epidemiology, 27(1), 57-65. https://doi.org/10.1097/EDE.0000000000000361

Yu, C., Fan, X., Sha, Q.-Q., Wang, H.-H., Li, B.-T., Dai, X.-X., Shen, L., Liu, J., Wang, L., Liu, K., Tang, F., & Fan, H.-Y. (2017). CFP1 Regulates Histone H3K4 Trimethylation and Developmental Potential in Mouse Oocytes. Cell Reports, 20(5), 1161-1172. https://doi.org/10.1016/j.celrep.2017.07.011

Zhang, M., Miao, Y., Chen, Q., Cai, M., Dong, W., Dai, X., Lu, Y., Zhou, C., Cui, Z., & Xiong, B. (2018). BaP exposure causes oocyte meiotic arrest and fertilization failure to weaken female fertility. The FASEB Journal, 32(1), 342-352. https://doi.org/10.1096/fj.201700514r

Zhang, W., Liu, Y., An, Z., Huang, D., Qi, Y., & Zhang, Y. (2011). Mediating effect of ROS on mtDNA damage and low ATP content induced by arsenic trioxide in mouse oocytes. Toxicology in Vitro, 25(4), 979-984. https://doi.org/10.1016/j.tiv.2011.03.009

Zhou, N., Cui, Z., Yang, S., Han, X., Chen, G., Zhou, Z., Zhai, C., Ma, M., Li, L., Cai, M., Li, Y., Ao, L., Shu, W., Liu, J., & Cao, J. (2014). Air pollution and decreased semen quality: A comparative study of Chongqing urban and rural areas. Environmental Pollution, 187, 145-152. https://doi.org/10.1016/j.envpol.2013.12.030

Zhu, J., Lee, R. W., Twum, C., & Wei, Y. (2019). Exposure to ambient PM2.5 during pregnancy and preterm birth in metropolitan areas of the state of Georgia. Environmental Science and Pollution Research, 26(3), 2492-2500. https://doi.org/10.1007/s11356-018-3746-8

Zorrilla, G., Adonis E., Eirez, M., & Izquierdo, M. (2004). Papel de los radicales libres sobre el ADN: Carcinogénesis y terapia antioxidante. Revista Cubana de Investigaciones Biomédicas, 23(1), 51-57. http://scielo.sld.cu/scielo.php?script=sci_abstract&pid=S0864-03002004000100008&lng=es&nrm=iso&tlng=es

Publicado

2022-11-17

Cómo citar

Guerra-Rangel, Y., & Torres-Osorio, V. (2022). Contaminantes atmosféricos y su incidencia sobre la reproducción en murinos y humanos. Actualidades Biológicas, 45(118), 1–13. https://doi.org/10.17533/udea.acbi/v45n118a02

Número

Sección

Artículos de revisión