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Sede: Claustro de San Agustín, Centro Histórico, Calle de la Universidad Cra. 6 #36-100
Colombia, Bolívar, Cartagena
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dc.contributor.advisor | Arroyo Salgado, Bárbara Julia (Director/a) | |
dc.contributor.author | Lozano Pineda, Juan Carlos | |
dc.date.accessioned | 2021-03-26T16:44:43Z | |
dc.date.available | 2021-03-26T16:44:43Z | |
dc.date.issued | 2020 | |
dc.description | Tesis (Magíster en Toxicología) -- Universidad de Cartagena. Facultad de Medicina. Departamento de Toxicología. Maestría en toxicología, 2020 | es |
dc.description.abstract | Tópicos para la alopecia androgénica son comúnmente utilizados para tratamientos estéticos, donde los residuos de estos mismos son vertidos por desagües sin ningún tipo de tratamiento previo, sin considerar los efectos adversos que esto pueda generar sobre el ambiente marino y terrestre al acumularse en fuentes hídricas, hogar de muchas especies de plantas y animales. El objetivo de este trabajo fue evaluar los efectos de tres tópicos diferentes para alopecia androgénica que contienen minoxidil, sobre el modelo biológico de Caenorhabditis elegans. Para ello se expusieron los nematodos C. elegans a diferentes concentraciones con los tópicos (0,01; 0,1; 1; y 10 ppm) y se evaluaron los puntos finales de mortalidad, crecimiento, reproducción, acumulación lipídica y genes relacionados con estrés oxidativo y shock térmico (sod-4, gpx-4, gpx-6, hsp-3). Los resultados mostraron mayores efectos adversos en las concentraciones más altas (1 y 10 ppm), al causar los porcentajes más altos de mortalidad y reducción de la longitud corporal, principalmente en aquellos gusanos expuestos al tópico 3. El estrés oxidativo fue más evidente en los tópicos que presentaron menos aditivos, mostrando sobreexpresión principalmente en los genes sod-4 y gpx-6. Además, la acumulación lipídica fue notoria principalmente en las concentraciones 0,01 y 0,1 ppm. Sin embargo, en todos los tratamientos se observó acumulación lipídica. Lo anterior indica que los tópicos para alopecia androgénica con presencia de minoxidil afectan la vitalidad del nematodo alterando funciones como el crecimiento y el metabolismo de lípidos, además actúan con agentes estresores al causar sobre expresión de genes reguladores de estrés oxidativo. La descarga de estos tópicos al ambiente puede generar un impacto negativo sobre los ecosistemas al afectar la vitalidad de seres vivos como C. elegans. | es |
dc.format.medium | application/pdf | es |
dc.identifier.citation | TM615.908 / L959 | es |
dc.identifier.uri | https://hdl.handle.net/11227/11672 | |
dc.identifier.uri | http://dx.doi.org/10.57799/11227/2093 | |
dc.language.iso | spa | es |
dc.publisher | Universidad de Cartagena | es |
dc.rights.access | openAccess | es |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0 | es |
dc.subject | Toxicología - Investigaciones | es |
dc.subject | Estrés oxidativo - Investigaciones | es |
dc.subject | Alopecia androgénica | es |
dc.subject | Alopecia - Tratamiento | es |
dc.subject | Minoxidil - Efectos toxicológicos | es |
dc.title | Evaluación del efecto toxicológico adverso de tópicos para la alopecia androgénica utilizando un modelo biológico de caenorhabditis elegans | es |
dc.type | Trabajo de grado - Maestría | spa |
dcterms.references | Abell, E. (1988) “Histologic response to topically applied minoxidil in male-pattern alopecia”, Clinics in Dermatology, 6(4), pp. 191–194. doi: 10.1016/0738- 081X(88)90086-7. Altun, Z. y Hall, D. (2012) “Handbook of C. elegans Anatomy”, WormAtlas, pp. 1– 16. Disponible en: http://www.wormatlas.org/hermaphrodite/hermaphroditehomepage.htm. | |
dcterms.references | Andersen, E. C. et al. (2012) “Chromosome-scale selective sweeps shape Caenorhabditis elegans genomic diversity”, HHS Public Access, 44(3), pp. 285–290. doi: 10.1038/ng.1050.Chromosome-scale. | |
dcterms.references | Avila, D. S. et al. (2016) “Involvement of heat shock proteins on Mn-induced toxicity in Caenorhabditis elegans”, BMC Pharmacology and Toxicology. BMC Pharmacology and Toxicology, 17(1), pp. 1–9. doi: 10.1186/s40360-016-0097-2. | |
dcterms.references | Campese, V. M. (1981) “Minoxidil: A Review of its Pharmacological Properties and Therapeutic Use”, Drugs, 22, pp. pages257–278. | |
dcterms.references | Clavijo, A. et al. (2016) “The nematode Caenorhabditis elegans as an integrated toxicological tool to assess water quality and pollution”, Science of the Total Environment. doi: 10.1016/j.scitotenv.2016.06.057. | |
dcterms.references | Delgado-Ciruelos, L. (2015) Mecanismos de acción implicados en la bioactividad de flavonoides. Caenorhabditis elegans y líneas celulares como sistemas modelo. UNIVERSIDAD DE SALAMANCA. | |
dcterms.references | Dengg, M. y Van Meel, J. C. A. (2004) “Caenorhabditis elegans as model system for rapid toxicity assessment of pharmaceutical compounds”, Journal of Pharmacological and Toxicological Methods. doi: 10.1016/j.vascn.2004.04.002. | |
dcterms.references | Dirksen, P. et al. (2016) “The native microbiome of the nematode Caenorhabditis elegans: Gateway to a new host-microbiome model”, BMC Biology. BMC Biology, 14(1), pp. 1–16. doi: 10.1186/s12915-016-0258-1. | |
dcterms.references | Dutilleul, M. et al. (2013) “Rapid phenotypic changes in Caenorhabditis elegans under uranium exposure”, Ecotoxicology. doi: 10.1007/s10646-013-1090-9. | |
dcterms.references | Earhart, R. N. et al. (1977) “Minoxidil-induced hypertrichosis: Treatment with calcium thioglycolate depilatory”, Southern Medical Journal. doi: 10.1097/00007611- 197704000-00023. | |
dcterms.references | Frézal, L. y Félix, M. A. (2015) “C. elegans outside the Petri dish”, eLife, 4, pp. 1– 14. doi: 10.7554/eLife.05849 | |
dcterms.references | Gao, A. W. et al. (2018) “Forward and reverse genetics approaches to uncover metabolic aging pathways in Caenorhabditis elegans”, Biochimica et Biophysica Acta - Molecular Basis of Disease. The Author(s). Published by Elsevier B.V, 1864(9), pp. 2697–2706. doi: 10.1016/j.bbadis.2017.09.006. | |
dcterms.references | García-Espiñeira, M. C., Tejeda-Benítez, L. P. y Olivero-Verbel, J. (2018) “Toxic effects of bisphenol A, propyl paraben, and triclosan on caenorhabditis elegans”, International Journal of Environmental Research and Public Health, 15(4). doi: 10.3390/ijerph15040684. | |
dcterms.references | García-Sancho, M. (2012) “From the genetic to the computer program: The historicity of ‘data’ and ‘computation’ in the investigations on the nematode worm C. elegans (1963-1998)”, Studies in History and Philosophy of Science Part C :Studies in History and Philosophy of Biological and Biomedical Sciences, 43(1), pp. 16–28. doi: 10.1016/j.shpsc.2011.10.002. | |
dcterms.references | Gogtay, J. A. y Panda, M. (2009) “Minoxidil topical foam: A new kid on the block”, International Journal of Trichology, 1(2), p. 142. doi: 10.4103/0974-7753.58560. | |
dcterms.references | Goussen, B. et al. (2013) “Consequences of a multi-generation exposure to uranium on Caenorhabditis elegans life parameters and sensitivity”, Ecotoxicology. doi: 10.1007/s10646-013-1078-5. | |
dcterms.references | Goussen, B. et al. (2015) “Transgenerational Adaptation to Pollution Changes Energy Allocation in Populations of Nematodes”, Environmental Science and Technology. doi: 10.1021/acs.est.5b03405. | |
dcterms.references | Han, X. et al. (2020) “An investigation of changes in water quality throughout the drinking water production/distribution chain using toxicological and fluorescence analyses”, Journal of Environmental Sciences (China). Elsevier B.V., 87, pp. 310– 318. doi: 10.1016/j.jes.2019.07.015. | |
dcterms.references | Hartung, T. (2009) “Toxicology for the twenty-first century”, Nature, 460(7252), pp 208–212. doi: 10.1038/460208a. | |
dcterms.references | Honnen, S. (2017) “Caenorhabditis elegans as a powerful alternative model organism to promote research in genetic toxicology and biomedicine”, Archives of Toxicology. doi: 10.1007/s00204-017-1944-7. | |
dcterms.references | Höss, S. et al. (1999) “GROWTH AND FERTILITY OF CAENORHABDITIS ELEGANS (NEMATODA) IN UNPOLLUTED FRESHWATER SEDIMENTS: RESPONSE TO PARTICLE SIZE DISTRIBUTION AND ORGANIC CONTENT”, Environmental Toxicology and Chemistry. doi: 10.1897/1551- 5028(1999)018<2921:gafoce>2.3.co;2. | |
dcterms.references | Hunt, P. R. (2017) “The C. elegans model in toxicity testing”, Journal of Applied Toxicology, 37(1), pp. 50–59. doi: 10.1002/jat.3357. | |
dcterms.references | Hutter, H. (2012) Fluorescent Protein Methods: Strategies and Applications. Second Edi, Methods in Cell Biology. Second Edi. Elsevier Inc. doi: 10.1016/B978-0-12- 394620-1.00003-5. | |
dcterms.references | Kvedar, J. C., Baden, H. P. y Levine, L. (1988) “Selective inhibition by minoxidil of prostacyclin production by cells in culture”, Biochemical Pharmacology, 37(5), pp. 867–874. doi: 10.1016/0006-2952(88)90174-8. | |
dcterms.references | Lachgar, S. et al. (1998) “Minoxidil upregulates the expression of vascular endothelial growth factor in human hair dermal papilla cells”, British Journal of Dermatology, 138(3), pp. 407–411. doi: 10.1046/j.1365-2133.1998.02115.x. | |
dcterms.references | Lenz, K. A., Pattison, C. y Ma, H. (2017) “Triclosan (TCS) and triclocarban (TCC) induce systemic toxic effects in a model organism the nematode Caenorhabditis elegans”, Environmental Pollution. doi: 10.1016/j.envpol.2017.08.036. | |
dcterms.references | Liu, H. et al. (2016) “Screening lifespan-extending drugs in Caenorhabditis elegans via label propagation on drug-protein networks”, BMC Systems Biology. doi: 10.1186/s12918-016-0362-4. | |
dcterms.references | Lowenthal, D. T. y Affrime, M. B. (1980) “Pharmacology and pharmacokinetics of minoxidil”, Journal of Cardiovascular Pharmacology. doi: 10.1097/00005344- 198000022-00002. | |
dcterms.references | Ma, L. et al. (2018) “Caenorhabditis elegans as a model system for target identification and drug screening against neurodegenerative diseases”, European Journal of Pharmacology. doi: 10.1016/j.ejphar.2017.11.051. | |
dcterms.references | Manfo, F., Nantia, E. y Mathur, P. (2015) “Effect of Environmental Contaminants on Mammalian Testis”, Current Molecular Pharmacology. doi: 10.2174/1874467208666150126155420. | |
dcterms.references | Messenger, A. G. y Rundegren, J. (2004) “Minoxidil: mecanisms of action on hair growth”, British Journald of dermatology, 150, pp. 186–194. doi: 10.1001/jama.1985.03350320055016. | |
dcterms.references | Michelet, J. F. et al. (1997) “Activation of cytoprotective prostaglandin synthase-1 by minoxidil as a possible explanation for its hair growth-stimulating effect”, Journal of Investigative Dermatology. doi: 10.1111/1523-1747.ep12334249. | |
dcterms.references | Nyström, J. et al. (2002) “Increased or decreased levels of Caenorhabditis elegans lon-3, a gene encoding a collagen, cause reciprocal changes in body length”, Genetics. | |
dcterms.references | Olsen, E. A. et al. (2002) “A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and placebo in the treatment of androgenetic alopecia in men”, Journal of the American Academy of Dermatology, 47(3), pp. 377–385. doi: 10.1067/mjd.2002.124088. | |
dcterms.references | Parada Ferro, L. K., Gualteros Bustos, A. V. y Sánchez Mora, M. R. (2017) “Caracterización fenotípica de la cepa N2 de Caenorhabditis elegans como un modelo en enfermedades neurodegenerativas”, Nova, 15(28), p. 69. doi: 10.22490/24629448.2080. | |
dcterms.references | Peralta-Mocha, M. y Cango-Diaz, L. (2017) “La investigación universitaria y los proyectos de vinculación con los sectores productivos: Caso UTMACH”, Conference Proceedings UTMACH, 2, pp. 301–310. | |
dcterms.references | Perez-Mora, N., Velasco, C. y Bermúdez, F. (2015) “Oral finasteride presents with sexual-unrelated withdrawal in long-term treated androgenic alopecia in men”, SKINmed. | |
dcterms.references | Price, V. H., Menefee, E. y Strauss, P. C. (1999) “Changes in hair weight and hair count in men with androgenetic alopecia, after application of 5% and 2% topical minoxidil, placebo, or no treatment”, Journal of the American Academy of Dermatology, 41(5 I), pp. 717–721. doi: 10.1016/S0190-9622(99)70006-X. | |
dcterms.references | Radomski, S. B., Herschorn, S. y Rangaswamy, S. (1994) “Topical minoxidil in the treatment of male erectile dysfunction”, Journal of Urology. doi: 10.1016/S0022- 5347(17)35217-5. | |
dcterms.references | Shin, H. R. et al. (2010) “Identification of transcriptional targets of Wnt/β-catenin signaling in dermal papilla cells of human scalp hair follicles: EP2 is a novel transcriptional target of Wnt3a”, Journal of Dermatological Science. Japanese Society for Investigative Dermatology, 58(2), pp. 91–96. doi: 10.1016/j.jdermsci.2010.02.011. | |
dcterms.references | Sorathia, N. y S. Rajadhyaksha, M. (2016) “Caenorhabditis elegans: A Model for Studying Human Pathogen Biology”, Recent Patents on Biotechnology. doi: 10.2174/1872208310666160727151853. | |
dcterms.references | Suchonwanit, P., Thammarucha, S. y Leerunyakul, K. (2019) “Minoxidil and its use in hair disorders: A review”, Drug Design, Development and Therapy, 13, pp. 2777– 2786. doi: 10.2147/DDDT.S214907. | |
dcterms.references | Sulston, J. E. et al. (1983) “The embryonic cell lineage of the nematode {\lcel}”, Developmental Biology, 100(1), pp. 64–119. | |
dcterms.references | Tain, L. S. et al. (2008) “Dietary regulation of hypodermal polyploidization in C. elegans”, BMC Developmental Biology. doi: 10.1186/1471-213X-8-28. | |
dcterms.references | Tejeda-Benitez, L. et al. (2016) “Pollution by metals and toxicity assessment using Caenorhabditis elegans in sediments from the Magdalena River, Colombia”, Environmental Pollution. Elsevier Ltd, 212, pp. 238–250. doi: 10.1016/j.envpol.2016.01.057. | |
dcterms.references | Tejeda, L. et al. (2015) Caenorhabditis elegans, a Biological Model for Research in Toxicology Article in Reviews of environmental contamination and toxicology. doi: 10.1007/978-3-319-23573-8. | |
dcterms.references | Wählby, C. et al. (2014) “High- and low-throughput scoring of fat mass and body fat distribution in C. elegans”, Methods. doi: 10.1016/j.ymeth.2014.04.017. | |
dcterms.references | Wang, H. et al. (2018) “Blueberry extract promotes longevity and stress tolerance via DAF-16 in Caenorhabditis elegans”, Food and Function. doi: 10.1039/c8fo01680a. | |
dcterms.references | Wu, M., Yu, Q. y Li, Q. (2016) “Differences in reproductive toxicology between alopecia drugs: An analysis on adverse events among female and male cases”, Oncotarget, 7(50), pp. 82074–82084. doi: 10.18632/oncotarget.12617. | |
dcterms.references | Yano, K., Brown, L. F. y Detmar, M. (2001) “Control of hair growth and follicle size by VEGF-mediated angiogenesis”, Journal of Clinical Investigation, 107(4), pp. 409– 417. doi: 10.1172/JCI11317. | |
dcterms.references | Yum, S. et al. (2018) “Minoxidil induction of VEGF is mediated by inhibition of HIFprolyl hydroxylase”, International Journal of Molecular Sciences, 19(1). doi: 10.3390/ijms19010053. | |
dspace.entity.type | Publication |
Sede: Claustro de San Agustín, Centro Histórico, Calle de la Universidad Cra. 6 #36-100
Colombia, Bolívar, Cartagena
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