Experimental Exposure to Tebuconazole Affects Metabolism and Body Condition in a Passerine Bird, the House Sparrow (Passer domesticus).

Agroecosystems Resting metabolic rate Sentinel species Sublethal effects Triazole fungicides

Journal

Environmental toxicology and chemistry
ISSN: 1552-8618
Titre abrégé: Environ Toxicol Chem
Pays: United States
ID NLM: 8308958

Informations de publication

Date de publication:
10 2022
Historique:
revised: 01 03 2022
received: 19 01 2022
accepted: 20 07 2022
pubmed: 29 7 2022
medline: 28 9 2022
entrez: 28 7 2022
Statut: ppublish

Résumé

Triazole compounds are among the most widely used fungicides in agroecosystems to protect crops from potential fungal diseases. Triazoles are suspected to have an impact on nontarget species due to their interactions with nonfungal sterol synthesis, and wild birds are likely to be contaminated by triazole fungicides because many of them live in agroecosystems. We experimentally tested whether exposure to environmental concentrations of a triazole could alter key integrative traits (metabolic rates and body condition) of an agroecosystem sentinel species, the house sparrow (Passer domesticus). Wild-caught adult sparrows were maintained in captivity and exposed (exposed group) or not (control group) for 7 continuous months to tebuconazole through drinking water. The metabolic rates of exposed and control sparrows were then measured at two different temperatures (12 °C and 25 °C), which correspond, respectively, to the thermoregulation and thermoneutrality temperatures of this species. We found that exposed sparrows had lower resting metabolic rates (i.e., measured at thermoneutrality, 25 °C) than controls. However, the thermoregulatory metabolic rates (i.e., measured at 12 °C) did not differ between exposed and control sparrows. Although the body mass and condition were not measured at the beginning of the exposure, sparrows at the time of the metabolic measurements 7 months after the onset of such exposure had a higher body condition than controls, supporting further the idea that tebuconazole affects metabolic functions. Our study demonstrates for the first time that the use of tebuconazole can alter metabolism and could potentially lead to adverse effects in birds. Environ Toxicol Chem 2022;41:2500-2511. © 2022 SETAC.

Identifiants

pubmed: 35899983
doi: 10.1002/etc.5446
doi:

Substances chimiques

Drinking Water 0
Fungicides, Industrial 0
Sterols 0
Triazoles 0
tebuconazole 401ATW8TRW

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2500-2511

Informations de copyright

© 2022 SETAC.

Références

Allen, J. G., Gale, S., Zoeller, R. T., Spengler, J. D., Birnbaum, L., & McNeely, E. (2016). PBDE flame retardants, thyroid disease, and menopausal status in US women. Environmental Health, 15(1), 60. https://doi.org/10.1186/s12940-016-0141-0
Andreu-Sánchez, O., Paraíba, L. C., Jonsson, C. M., & Carrasco, J. M. (2012). Acute toxicity and bioconcentration of fungicide tebuconazole in zebrafish (Danio rerio). Environmental Toxicology, 27(2), 109-116. https://doi.org/10.1002/tox.20618
Asarian, L., & Geary, N. (2006). Modulation of appetite by gonadal steroid hormones. Philosophical Transactions of the Royal Society, B: Biological Sciences, 361(1471), 1251-1263. https://doi.org/10.1098/rstb.2006.1860
Ask, A. V., Jenssen, B. M., Tartu, S., Angelier, F., Chastel, O., & Gabrielsen, G. W. (2021). Per- and polyfluoroalkyl substances are positively associated with thyroid hormones in an arctic seabird. Environmental Toxicology and Chemistry, 40, 820-831. https://doi.org/10.1002/etc.4978
Astheimer, L. B., Buttemer, W. A., & Wingfield, J. C. (1992). Interactions of corticosterone with feeding, activity and metabolism in passerine birds. Ornis Scandinavica. Scandinavian Journal of Ornithology, 23(3), 355-365. https://doi.org/10.2307/3676661
Bartholomew, G. A., & Cade, T. J. (1963). The water economy of land birds. The Auk, 80(4), 504-539. https://doi.org/10.2307/4082856
Berenzen, N., Lentzen-Godding, A., Probst, M., Schulz, H., Schulz, R., & Liess, M. (2005). A comparison of predicted and measured levels of runoff-related pesticide concentrations in small lowland streams on a landscape level. Chemosphere, 58(5), 683-691. https://doi.org/10.1016/j.chemosphere.2004.05.009
Binev, R., Simeonov, R., Todorov, R., & Nikolov, Y. (2005). Pathomorphological studies following experimental acute intoxication with the triazole fungicide triticonazole in pigs. Bulgarian Journal of Veterinary Medicine, 8(3), 193-198.
Biro, P. A., & Stamps, J. A. (2010). Do consistent individual differences in metabolic rate promote consistent individual differences in behavior. Trends in Ecology & Evolution, 25(11), 653-659. https://doi.org/10.1016/j.tree.2010.08.003
Blévin, P., Angelier, F., Tartu, S., Ruault, S., Bustamante, P., Herzke, D., Moe, B., Bech, C., Gabrielsen, G. W., Bustnes, J. O., & Chastel, O. (2016). Exposure to oxychlordane is associated with shorter telomeres in arctic breeding kittiwakes. Science of the Total Environment, 563-564, 125-130. https://doi.org/10.1016/j.scitotenv.2016.04.096
Blévin, P., Tartu, S., Ellis, H. I., Chastel, O., Bustamante, P., Parenteau, C., Herzke, D., Angelier, F., & Gabrielsen, G. W. (2017). Contaminants and energy expenditure in an Arctic seabird: Organochlorine pesticides and perfluoroalkyl substances are associated with metabolic rate in a contrasted manner. Environmental Research, 157, 118-126. https://doi.org/10.1016/j.envres.2017.05.022
Bobek, S., Jastrzebski, M., & Pietras, M. (1977). Age-related changes in oxygen consumption and plasma thyroid hormone concentration in the young chicken. General and Comparative Endocrinology, 31(2), 169-174. https://doi.org/10.1016/0016-6480(77)90014-4
Bouwhuis, S., Sheldon, B. C., & Verhulst, S. (2011). Basal metabolic rate and the rate of senescence in the great tit. Functional Ecology, 25(4), 829-838. https://doi.org/10.1111/j.1365-2435.2011.01850.x
Braham, H. W., & Neal, C. M. (1974). The effects of DDT on energetics of the short-tailed shrew, Blarina brevicauda. Bulletin of Environmental Contamination and Toxicology, 12(1), 32-37. https://doi.org/10.1007/BF01713023
Broggi, J., Hohtola, E., Koivula, K., Orell, M., Thomson, R. L., & Nilsson, J.-Å. (2007). Sources of variation in winter basal metabolic rate in the great tit. Functional Ecology, 21(3), 528-533. https://doi.org/10.1111/j.1365-2435.2007.01255.x
Brown, L. M., & Clegg, D. J. (2010). Central effects of estradiol in the regulation of food intake, body weight, and adiposity. The Journal of Steroid Biochemistry and Molecular Biology, 122(1), 65-73. https://doi.org/10.1016/j.jsbmb.2009.12.005
Bryant, D. M. (1997). Energy expenditure in wild birds. Proceedings of the Nutrition Society, 56(3), 1025-1039. https://doi.org/10.1079/PNS19970107
Burton, T., Killen, S. S., Armstrong, J. D., & Metcalfe, N. B. (2011). What causes intraspecific variation in resting metabolic rate and what are its ecological consequences? Proceedings of the Royal Society B: Biological Sciences, 278(1724), 3465-3473. https://doi.org/10.1098/rspb.2011.1778
Butera, P. C. (2010). Estradiol and the control of food intake. Physiology & Behavior, 99(2), 175-180. https://doi.org/10.1016/j.physbeh.2009.06.010
Cao, F., Souders, C. L., Li, P., Pang, S., Qiu, L., & Martyniuk, C. J. (2019). Developmental toxicity of the triazole fungicide cyproconazole in embryo-larval stages of zebrafish (Danio rerio). Environmental Science and Pollution Research, 26(5), 4913-4923. https://doi.org/10.1007/s11356-018-3957-z
Careau, V., Thomas, D., Humphries, M. M., & Réale, D. (2008). Energy metabolism and animal personality. Oikos, 117(5), 641-653. https://doi.org/10.1111/j.0030-1299.2008.16513.x
Careau, V., Thomas, D., Pelletier, F., Turki, L., Landry, F., Garant, D., & Réale, D. (2011). Genetic correlation between resting metabolic rate and exploratory behaviour in deer mice (Peromyscus maniculatus). Journal of Evolutionary Biology, 24(10), 2153-2163. https://doi.org/10.1111/j.1420-9101.2011.02344.x
Chappell, M. A., Bech, C., & Buttemer, W. A. (1999). The relationship of central and peripheral organ masses to aerobic performance variation in house sparrows. Journal of Experimental Biology, 202(17), 2269-2279. https://doi.org/10.1242/jeb.202.17.2269
Chastel, O., Lacroix, A., & Kersten, M. (2003). Pre-breeding energy requirements: Thyroid hormone, metabolism and the timing of reproduction in house sparrows Passer domesticus. Journal of Avian Biology, 34(3), 298-306. https://doi.org/10.1034/j.1600-048X.2003.02528.x
Daan, S., Masman, D., & Groenewold, A. (1990). Avian basal metabolic rates: Their association with body composition and energy expenditure in nature. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 259(2), R333-R340. https://doi.org/10.1152/ajpregu.1990.259.2.R333
Danforth, E., & Burger, A. (1984). The role of thyroid hormones in the control of energy expenditure. Clinics in Endocrinology and Metabolism, 13(3), 581-595. https://doi.org/10.1016/S0300-595X(84)80039-0
Daniele, G., Lafay, F., Pelosi, C., Fritsch, C., & Vulliet, E. (2018). Development of a method for the simultaneous determination of multi-class pesticides in earthworms by liquid chromatography coupled to tandem electrospray mass spectrometry. Analytical and Bioanalytical Chemistry, 410(20), 5009-5018. https://doi.org/10.1007/s00216-018-1151-2
Dupont, S. M., Grace, J. K., Lourdais, O., Brischoux, F., & Angelier, F. (2019). Slowing down the metabolic engine: Impact of early-life corticosterone exposure on adult metabolism in house sparrows (Passer domesticus). Journal of Experimental Biology, 222(22), jeb.211771. https://doi.org/10.1242/jeb.211771
European Food Safety Authority. (2016). The 2016 European Union report on pesticide residues in food. https://doi.org/10.2903/j.efsa.2018.5348
Elliott, K. H., Welcker, J., Gaston, A. J., Hatch, S. A., Palace, V., Hare, J. F., Speakman, J. R., & Anderson, W. G. (2013). Thyroid hormones correlate with resting metabolic rate, not daily energy expenditure, in two charadriiform seabirds. Biology Open, 2(6), 580-586. https://doi.org/10.1242/bio.20134358
Fernández-Vizcaíno, E., Fernández de Mera, I. G., Mougeot, F., Mateo, R., Ortiz-Santaliestra, M. E. (2020). Multi-level analysis of exposure to triazole fungicides through treated seed ingestion in the red-legged partridge. Environmental Research, 189, 109928. https://doi.org/10.1016/j.envres.2020.109928
Freake, H. C., & Oppenheimer, J. H. (1995). Thermogenesis and thyroid function. Annual Review of Nutrition, 15(1), 263-291. https://doi.org/10.1146/annurev.nu.15.070195.001403
French, J. B., Voltura, M. B., & Tomasi, T. E. (2001). Effects of pre- and postnatal polychlorinated biphenyl exposure on metabolic rate and thyroid hormones of white-footed mice. Environmental Toxicology and Chemistry, 20(8), 1704-1708. https://doi.org/10.1002/etc.5620200812
Goutte, A., Barbraud, C., Herzke, D., Bustamante, P., Angelier, F., Tartu, S., Clément-Chastel, C., Moe, B., Bech, C., Gabrielsen, G. W., Bustnes, J. O., & Chastel, O. (2015). Survival rate and breeding outputs in a high Arctic seabird exposed to legacy persistent organic pollutants and mercury. Environmental Pollution, 200, 1-9. https://doi.org/10.1016/j.envpol.2015.01.033
Grün, F., & Blumberg, B. (2009). Endocrine disrupters as obesogens. Molecular and Cellular Endocrinology, 304(1), 19-29. https://doi.org/10.1016/j.mce.2009.02.018
Hirschberg, A. L. (2012). Sex hormones, appetite and eating behaviour in women. Maturitas, 71(3), 248-256. https://doi.org/10.1016/j.maturitas.2011.12.016
Hulbert, A. J. (2000). Thyroid hormones and their effects: A new perspective. Biological Reviews, 75(4), 519-631. https://doi.org/10.1111/j.1469-185X.2000.tb00054.x
Hulbert, A. J., & Else, P. L. (2004). Basal metabolic rate: History, composition, regulation, and usefulness. Physiological and Biochemical Zoology, 77(6), 869-876. https://doi.org/10.1086/422768
Jenni, L., & Jenni-Eiermann, S. (1998). Fuel supply and metabolic constraints in migrating birds. Journal of Avian Biology, 29(4), 521-528. https://doi.org/10.2307/3677171
Jugan, M.-L., Levi, Y., & Blondeau, J.-P. (2010). Endocrine disruptors and thyroid hormone physiology. Biochemical Pharmacology, 79(7), 939-947. https://doi.org/10.1016/j.bcp.2009.11.006
Kahle, M., Buerge, I. J., Hauser, A., Müller, M. D., & Poiger, T. (2008). Azole fungicides: Occurrence and fate in wastewater and surface waters. Environmental Science & Technology, 42(19), 7193-7200. https://doi.org/10.1021/es8009309
Kim, B. (2008). Thyroid hormone as a determinant of energy expenditure and the basal metabolic rate. Thyroid, 18(2), 141-144. https://doi.org/10.1089/thy.2007.0266
Konarzewski, M., & Książek, A. (2013). Determinants of intra-specific variation in basal metabolic rate. Journal of Comparative Physiology B, 183(1), 27-41. https://doi.org/10.1007/s00360-012-0698-z
Lema Sean, C., Dickey Jon, T., Schultz Irvin, R., & Swanson, P. enny (2008). Dietary exposure to 2,2′,4,4′-tetrabromodiphenyl ether (pbde-47) alters thyroid status and thyroid hormone-regulated gene transcription in the pituitary and brain. Environmental Health Perspectives, 116(12), 1694-1699. https://doi.org/10.1289/ehp.11570
Li, S., Wu, Q., Sun, Q., Coffin, S., Gui, W., & Zhu, G. (2019). Parental exposure to tebuconazole causes thyroid endocrine disruption in zebrafish and developmental toxicity in offspring. Aquatic Toxicology, 211, 116-123. https://doi.org/10.1016/j.aquatox.2019.04.002
Liu, C., Zhang, X., Deng, J., Hecker, M., Al-Khedhairy, A., Giesy, J. P., & Zhou, B. (2011). Effects of prochloraz or propylthiouracil on the cross-talk between the HPG, HPA, and HPT axes in zebrafish. Environmental Science & Technology, 45(2), 769-775. https://doi.org/10.1021/es102659p
Lopez-Antia, A., Feliu, J., Camarero, P. R., Ortiz-Santaliestra, M. E., & Mateo, R. (2016). Risk assessment of pesticide seed treatment for farmland birds using refined field data. Journal of Applied Ecology, 53(5), 1373-1381. https://doi.org/10.1111/1365-2664.12668
Lopez-Antia, A., Ortiz-Santaliestra, M. E., Mougeot, F., Camarero, P. R., & Mateo, R. (2018). Brood size is reduced by half in birds feeding on flutriafol-treated seeds below the recommended application rate. Environmental Pollution, 243, 418-426. https://doi.org/10.1016/j.envpol.2018.08.078
Lopez-Antia, A., Ortiz-Santaliestra, M. E., Mougeot, F., Camarero, P. R., & Mateo, R. (2021). Birds feeding on tebuconazole treated seeds have reduced breeding output. Environmental Pollution, 271, 116292. https://doi.org/10.1016/j.envpol.2020.116292
Lopez-Antia, A., Ortiz-Santaliestra, M. E., Mougeot, F., & Mateo, R. (2013). Experimental exposure of red-legged partridges (Alectoris rufa) to seeds coated with imidacloprid, thiram and difenoconazole. Ecotoxicology, 22(1), 125-138. https://doi.org/10.1007/s10646-012-1009-x
Mahmood, I., Imadi, S. R., Shazadi, K., Gul, A., & Hakeem, K. R. (2016). Effects of pesticides on environment, Plant, soil and microbes: Volume 1: Implications in crop science (pp. 253-269). Springer International Publishing. https://doi.org/10.1007/978-3-319-27455-3_13
McNab, B. K. (2002). The physiological ecology of vertebrates: A view from energetics. Cornell University Press.
Misso, M. L., Murata, Y., Boon, W. C., Jones, M. E. E., Britt, K. L., & Simpson, E. R. (2003). Cellular and molecular characterization of the adipose phenotype of the aromatase-deficient mouse. Endocrinology, 144(4), 1474-1480. https://doi.org/10.1210/en.2002-221123
Mozo, J., Emre, Y., Bouillaud, F., Ricquier, D., & Criscuolo, F. (2005). Thermoregulation: What role for UCPs in mammals and birds. Bioscience Reports, 25(3-4), 227-249. https://doi.org/10.1007/s10540-005-2887-4
Nagy, K. A., Girard, I. A., & Brown, T. K. (1999). Energetics of free-ranging mammals, reptiles, and birds. Annual Review of Nutrition, 19(1), 247-277. https://doi.org/10.1146/annurev.nutr.19.1.247
Nilsson, J. (2002). Metabolic consequences of hard work. Proceedings of the Royal Society of London. Series B: Biological Sciences, 269(1501), 1735-1739. https://doi.org/10.1098/rspb.2002.2071
Nzama, S. N., Downs, C. T., & Brown, M. (2010). Seasonal variation in the metabolism-temperature relation of house sparrows (Passer domesticus) in KwaZulu-Natal, South Africa. Journal of Thermal Biology, 35(2), 100-104. https://doi.org/10.1016/j.jtherbio.2009.12.002
Ortiga-Carvalho, T. M., Chiamolera, M. I., Pazos-Moura, C. C., & Wondisford, F. E. (2011). Hypothalamuspituitary-thyroid axis. Comprehensive Physiology, 6(3), 1387-1428. https://doi.org/10.1002/cphy.c150027
Pelosi, C., Bertrand, C., Daniele, G., Coeurdassier, M., Benoit, P., Nélieu, S., & Fritsch, C. (2021). Residues of currently used pesticides in soils and earthworms: A silent threat? Agriculture, Ecosystems & Environment, 305, 107167. https://doi.org/10.1016/j.agee.2020.107167
Perez-Rodriguez, V., Souders, C. L., Tischuk, C., & Martyniuk, C. J. (2019). Tebuconazole reduces basal oxidative respiration and promotes anxiolytic responses and hypoactivity in early-staged zebrafish (Danio rerio). Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 217, 87-97. https://doi.org/10.1016/j.cbpc.2018.11.017
Pesticide Properties DataBase. (2022). Tebuconazole. University of Hertfordshire, UK. http://sitem.herts.ac.uk/aeru/ppdb/en/Reports/610.htm
Peters, R. H., & Peters, R. H. (1986). The ecological implications of body size. Cambridge University Press.
Polledri, E., Mercadante, R., Nijssen, R., Consonni, D., Mol, H., & Fustinoni, S. (2019). Hair as a matrix to evaluate cumulative and aggregate exposure to pesticides in winegrowers. Science of the Total Environment, 687, 808-816. https://doi.org/10.1016/j.scitotenv.2019.06.061
Poulsen, R., Luong, X., Hansen, M., Styrishave, B., & Hayes, T. (2015). Tebuconazole disrupts steroidogenesis in Xenopus laevis. Aquatic Toxicology, 168, 28-37. https://doi.org/10.1016/j.aquatox.2015.09.008
Prouteau, L. (2021). Caractérisation de la contamination en pesticides azoles et néonicotinoïdes chez les espèces d'intérêt localisées en région Nouvelle-Aquitaine: Développement de méthodes analytiques et applications [Doctoral dissertation, Université de La Rochelle (ULR) La Rochelle, France]. https://www.theses.fr/2021LAROS019
Quagliariello, V., Rossetti, S., Cavaliere, C., Di Palo, R., Lamantia, E., Castaldo, L., Nocerino, F., Ametrano, G., Cappuccio, F., Malzone, G., Montanari, M., Vanacore, D., Romano, J. F., Piscitelli, R., Iovane, G., Pepe, M. F., Berretta, M., D'Aniello, C., Perdonà, S.,… Facchini, G. (2017). Metabolic syndrome, endocrine disruptors and prostate cancer associations: Biochemical and pathophysiological evidences. Oncotarget, 8(18), 30606. https://doi.org/10.18632/oncotarget.16725
Raby, M., Maloney, E., Poirier, D. G., & Sibley, P. K. (2019). Acute effects of binary mixtures of imidacloprid and tebuconazole on 4 freshwater invertebrates. Environmental Toxicology and Chemistry, 38(5), 1093-1103. https://doi.org/10.1002/etc.4386
Rico, A., Sabater, C., & Castillo, M.-Á. (2016). Lethal and sub-lethal effects of five pesticides used in rice farming on the earthworm Eisenia fetida. Ecotoxicology and Environmental Safety, 127, 222-229. https://doi.org/10.1016/j.ecoenv.2016.02.004
Rodríguez, P., Tortosa, F. S., & Villafuerte, R. (2005). The effects of fasting and refeeding on biochemical parameters in the red-legged partridge (Alectoris rufa). Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 140(1), 157-164. https://doi.org/10.1016/j.cbpb.2004.11.014
Rokbani, O., Fattouch, S., Chakir, A., & Roth, E. (2019). Heterogeneous oxidation of two triazole pesticides (diniconazole and tebuconazole) by OH-radicals and ozone. Science of the Total Environment, 694, 133745. https://doi.org/10.1016/j.scitotenv.2019.133745
Rønning, B., Broggi, J., Bech, C., Moe, B., Ringsby, T. H., Pärn, H., Hagen, I. J., Saether, B.-E., & Jensen, H. (2016). Is basal metabolic rate associated with recruit production and survival in free-living house sparrows? Functional Ecology, 30(7), 1140-1148. https://doi.org/10.1111/1365-2435.12597
Sancho, E., Villarroel, M. J., Fernández, C., Andreu, E., & Ferrando, M. D. (2010). Short-term exposure to sublethal tebuconazole induces physiological impairment in male zebrafish (Danio rerio). Ecotoxicology and Environmental Safety, 73(3), 370-376. https://doi.org/10.1016/j.ecoenv.2009.09.020
Saxena, A. K., Devillers, J., Bhunia, S. S., & Bro, E. (2015). Modelling inhibition of avian aromatase by azole pesticides. SAR and QSAR in Environmental Research, 26(7-9), 757-782. https://doi.org/10.1080/1062936X.2015.1090749
Sebastiano, M., Jouanneau, W., Blévin, P., Angelier, F., Parenteau, C., Gernigon, J., Lemesle, J. C., Robin, F., Pardon, P., Budzinski, H., Labadie, P., & Chastel, O. (2021). High levels of fluoroalkyl substances and potential disruption of thyroid hormones in three gull species from SouthWestern France. Science of the Total Environment, 765, 144611. https://doi.org/10.1016/j.scitotenv.2020.144611
Smits, J. E., Fernie, K. J., Bortolotti, G. R., & Marchant, T. A. (2002). Thyroid hormone suppression and cell-mediated immunomodulation in American Kestrels (Falco sparverius) exposed to PCBs. Archives of Environmental Contamination and Toxicology, 43(3), 338-344. https://doi.org/10.1007/s00244-002-1200-9
Souders, C. L., Perez-Rodriguez, V., Ahmadie, N. E., Zhang, X., Tischuk, C., & Martyniuk, C. J. (2020). Investigation into the sub-lethal effects of the triazole fungicide triticonazole in zebrafish (Danio rerio) embryos/larvae. Environmental Toxicology, 35(2), 254-267. https://doi.org/10.1002/tox.22862
Souders, C. L., Xavier, P., Perez-Rodriguez, V., Ector, N., Zhang, J.-L., & Martyniuk, C. J. (2019). Sub-lethal effects of the triazole fungicide propiconazole on zebrafish (Danio rerio) development, oxidative respiration, and larval locomotor activity. Neurotoxicology and Teratology, 74, 106809. https://doi.org/10.1016/j.ntt.2019.106809
Suzuki, K., Simpson, K. A., Minnion, J. S., Shillito, J. C., & Bloom, S. R. (2010). The role of gut hormones and the hypothalamus in appetite regulation. Endocrine Journal, 57(5), 359-372. https://doi.org/10.1507/endocrj.K10E-077
Takeda, K., Toda, K., Saibara, T., Nakagawa, M., Saika, K., Onishi, T., & Shizuta, Y. (2003). Progressive development of insulin resistance phenotype in male mice with complete aromatase (CYP19) deficiency. Journal of Endocrinology, 176(2), 237-246.
Taxvig, C., Hass, U., Axelstad, M., Dalgaard, M., Boberg, J., Andeasen, H. R., & Vinggaard, A. M. (2007). Endocrine-disrupting activities in vivo of the fungicides tebuconazole and epoxiconazole. Toxicological Sciences, 100(2), 464-473. https://doi.org/10.1093/toxsci/kfm227
Teng, M., Zhu, W., Wang, D., Qi, S., Wang, Y., Yan, J., Dong, K., Zheng, M., & Wang, C. (2018). Metabolomics and transcriptomics reveal the toxicity of difenoconazole to the early life stages of zebrafish (Danio rerio). Aquatic Toxicology, 194, 112-120. https://doi.org/10.1016/j.aquatox.2017.11.009
Toni, C., Ferreira, D., Kreutz, L. C., Loro, V. L., & Barcellos, L. J. G. (2011). Assessment of oxidative stress and metabolic changes in common carp (Cyprinus carpio) acutely exposed to different concentrations of the fungicide tebuconazole. Chemosphere, 83(4), 579-584. https://doi.org/10.1016/j.chemosphere.2010.12.022
Tori, G. M., & Mayer, L. P. (1981). Effects of polychlorinated biphenyls on the metabolic rates of mourning doves exposed to low ambient temperatures. Bulletin of Environmental Contamination and Toxicology, 27(1), 678-682. https://doi.org/10.1007/BF01611081
Verreault, J., Bech, C., Letcher, R. J., Ropstad, E., Dahl, E., & Gabrielsen, G. W. (2007). Organohalogen contamination in breeding glaucous gulls from the Norwegian Arctic: Associations with basal metabolism and circulating thyroid hormones. Environmental Pollution, 145(1), 138-145. https://doi.org/10.1016/j.envpol.2006.03.049
Vinggaard, A. M., Hnida, C., Breinholt, V., & Larsen, J. C. (2000). Screening of selected pesticides for inhibition of CYP19 aromatase activity in vitro. Toxicology In Vitro, 14(3), 227−234. https://doi.org/10.1016/S0887-2333(00)00018-7
Voltura, M. B., & French, J. B. (2000). Effects of dietary polychlorinated biphenyl exposure on energetics of white-footed mouse, Peromyscus leucopus. Environmental Toxicology and Chemistry, 19(11), 2757-2761. https://doi.org/10.1002/etc.5620191121
Welcker, J., Chastel, O., Gabrielsen, G. W., Guillaumin, J., Kitaysky, A. S., Speakman, J. R., Tremblay, Y., & Bech, C. (2013). Thyroid hormones correlate with basal metabolic rate but not field metabolic rate in a wild bird species. PLoS One, 8(2), e56229. https://doi.org/10.1371/journal.pone.0056229
Yang, J.-D., Liu, S.-H., Liao, M.-H., Chen, R.-M., Liu, P.-Y., & Ueng, T.-H. (2018). Effects of tebuconazole on cytochrome P450 enzymes, oxidative stress, and endocrine disruption in male rats. Environmental Toxicology, 33(8), 899-907. https://doi.org/10.1002/tox.22575
Yu, L., Chen, M., Liu, Y., Gui, W., & Zhu, G. (2013). Thyroid endocrine disruption in zebrafish larvae following exposure to hexaconazole and tebuconazole. Aquatic Toxicology, 138-139, 35-42. https://doi.org/10.1016/j.aquatox.2013.04.001
Zarn, J. A., Brüschweiler, B. J., & Schlatter, J. R. (2003). Azole fungicides affect mammalian steroidogenesis by inhibiting sterol 14 alpha-demethylase and aromatase. Environmental Health Perspectives, 111(3), 255−261. https://doi.org/10.1289/ehp.5785
Zgirski, T., Legagneux, P., Chastel, O., Regimbald, L., Prouteau, L., Le Pogam, A., & Vézina, F. (2021). Early life neonicotinoid exposure results in proximal benefits and ultimate carryover effects. Scientific Reports, 11(1), 1-10. https://doi.org/10.1038/s41598-021-93894-2
Zhang, W. (2018). Global pesticide use: Profile, trend, cost/benefit and more. Proceedings of the International Academy of Ecology and Environmental Sciences, 8(1), 1.
Zhang, W., Ramamoorthy, Y., Kilicarslan, T., Nolte, H., Tyndale, R. F., & Sellers, E. M. (2002). Inhibition of cytochromes P450 by antifungal imidazole derivatives. Drug Metabolism and Disposition, 30(3), 314-318. https://doi.org/10.1124/dmd.30.3.314
Zheng, W.-H., Lin, L., Liu, J.-S., Xu, X.-J., & Li, M. (2013). Geographic variation in basal thermogenesis in little buntings: Relationship to cellular thermogenesis and thyroid hormone concentrations. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 164(3), 483-490. https://doi.org/10.1016/j.cbpa.2012.12.004

Auteurs

Pauline Bellot (P)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.

Sophie Marie Dupont (SM)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.

François Brischoux (F)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.

Hélène Budzinski (H)

University of Bordeaux, CNRS-EPOC, UMR 5805, LPTC Research Group, Talence, France.

Olivier Chastel (O)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.

Clémentine Fritsch (C)

Laboratoire Chrono-Environnement, UMR 6249 CNRS/Université Bourgogne Franche-Comté, Besançon, France.

Olivier Lourdais (O)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.
School of Life Sciences, Arizona State University, Tempe, Arizona, USA.

Louise Prouteau (L)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.
University of Bordeaux, CNRS-EPOC, UMR 5805, LPTC Research Group, Talence, France.

Steffi Rocchi (S)

Laboratoire Chrono-Environnement, UMR 6249 CNRS/Université Bourgogne Franche-Comté, Besançon, France.
Service de Parasitologie-Mycologie, CHU Jean Minjoz, Besançon, France.

Frédéric Angelier (F)

Centre d'Etudes Biologiques de Chizé, CNRS-La Rochelle Université, UMR 7372, Villiers en Bois, France.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH