PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2012 | 42 | 3 |

Tytuł artykułu

Effects of the herbicide pendimethalin on hormone receptor expressions and dorsal fin biometrics in Thai medaka, Oryzias minutillus (Actinopterygii: Beloniformes: Adrianichthyidae)

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Background. Xeno-oestrogens have negative effects on the endocrine systems of wildlife including freshwater fish. Pendimethalin is a herbicide found in the environment which exerts some oestrogenic action in vivo. Dwarf medaka (known also as Thai medaka), Oryzias minutillus Smith, 1945, inhabit the natural aquatic environments. Dorsal fin of this species is a secondary sex character controlled by sex hormones and assumes as a sensitive bioindicator for testing of oestrogenic chemicals. In this study, we aimed to examine the pendimethalin effects on hormone receptor expressions and dorsal fin biometrics in adult Thai medaka. Materials and Methods. Pendimethalin effects on the androgen receptor (AR) and estrogen receptor (ER) β expressions in dorsal fins were determined by semi-quantitative RT-PCR. The fin biometry was presented as the values (%) of the dorsal fin length (DFL) divided by the standard length (SL). Results. In males, AR levels decreased when the fish were exposed to 0.1 µg · mL–1 pendimethalin for 60 days and were exposed to 1 µg · mL–1 for 30 and 60 days. In females, a 60-day treatment with 1 µg · mL–1 caused AR levels to decrease. Conversely, in males, ERβ levels increased after 30 and 60 days of treatment with 1 µg · mL–1. In females, ERβ levels increased after 30 days of treatment with 1 µg · mL–1 and 60 days of treatment with 0.1 µg · mL–1. In males, values of DFL/SL% decreased after exposure to 1 µg · mL–1 for 60 days. Additionally, we observed 4 testis-ova among 30 gonads from males treated with 1 µg · mL–1 for 60 days. Conclusion. Our results suggest that pendimethalin may interfere with endocrine processes via hormone receptors, leading to the feminisation of dorsal fins and gonads in Thai medaka

Słowa kluczowe

Wydawca

-

Rocznik

Tom

42

Numer

3

Opis fizyczny

p.239–246,fig.,ref.

Twórcy

autor
  • Faculty of Environmental Culture and Eco-tourism, Srinakharinwirot University, 10110, Bangkok, Thailand
  • Department of Anatomy Faculty of Medicine, Srinakharinwirot University, 10110, Bangkok, Thailandp

Bibliografia

  • Alister C.A., Gomez P.A., Rojas S., Kogan M. 2009.Pendimethalin and oxyfluorfen degradation under two irrigation conditions over four years application. Journal of Environmental Science and Health, Part B: Pesticides, Food Contaminants, and Agricultural Wastes 44 (4): 337–343.DOI: 10.1080/03601230902800986
  • Ankley G.T.,Benic D.C.,Breen M.S.,Collette T.W.,Conolly R.B.,Denslow N.D., Edwards S.W., Ekman D.R., Garcia-Reyero N., Jensen K.M., Lazorchak J.M., Martinović D.,Miller D.H., Perkins E.J., Orlando E.F., Villeneuve D.L.,Wang R.-L., Watanabe K.H. 2009. Endocrine disrupting chemicals in fish: Developing exposure indicators and predictive models of effects based on mechanism of action.Aquatic Toxicology 92 (3): 168–178DOI: 10.1016/j.aquatox.2009.01.013
  • Ankley G.T., Jensen K.M., Kahl M.D., Durhan E.J.,Makynen E.A., Cavallin J.E.,Martinović D.,Wehmas L.C.,Mueller N.D., Villeneuve D.L. 2010. Use of chemical mixtures to differentiate mechanisms of endocrine action in a small fish model. Aquatic Toxicology 99 (3): 389–396.DOI: 10.1016/j.aquatox.2010.05.020
  • Bandyopadhyay S., Choudhury P.P. 2009. Leaching behaviour of pendimethalin causes toxicity towards different cultivars of Brassica juncea and Brassica campestris in sandy loam soil. Interdisciplinary Toxicology 2 (4): 250–253.DOI: 10.2478/v10102-009-0025-z
  • Barbash J.E., and Resek, E.A. 1996. Pesticides in Grodnu water: Distribution, trends, and governing factors.Pp. 588–590. In: Gilliom R.J. (ed.) Pesticides in the hydrologic system. Ann Arbor Press, Chelsea, Michigan, USA.
  • Borg B. 1994. Androgens in teleost fishes. Comparative Biochemistry and Physiology, Part C: Pharmacology,Toxicology and Endocrinology 9 (3): 219–245.DOI: 10.1016/0742-8413(94)00063-G
  • Chang X., Kobayashi T., Todo T., Ikeuchi T., Yoshiura M.,Kajiura-Kobayashi H., Morrey C., Nagahama Y. 1999.Molecular cloning of estrogen receptors α and β the ovary of a teleost fish, the tilapia (Oreochromis niloticus). Zoological Science 16 (4): 653–658. DOI: 10.2108/zsj.16.653
  • Choi S.M., Yoo S.D., Lee B.M. 2004. Toxicological characteristics of endocrine-disrupting chemicals: Developmental toxicity, carcinogenicity, and mutagenicity. Journal of Toxicology and Environmental Health, Part B: Critical Reviews 7 (1): 1–23.DOI: 10.1080/10937400490253229
  • Danion M., Le Floch S., Kanan R., Lamour F., Quentel C.2012. Effects of in vivo chronic exposure to pendimethalin/Prowl 400® on sanitary status and the immune system in rainbow trout (Oncorhynchus mykiss).Science of the Total Environment 424: 143–152.DOI: 10.1016/j.scitotenv.2012.02.055
  • Donohoe R.M., Curtis L.R. 1996. Estrogenic activity of chlordecone,o,p’-DDT and o,p’-DDE in juvenile rainbow trout:Induction of vitellogenesis and interaction with hepatic estrogen binding sites. Aquatic Toxicology 36 (1–2): 31–52.DOI: 10.1016/S0166-445X(96)00799-0
  • Foran C.M., Bennett E.R., BensonW.H. 2000. Developmental evaluation of a potential non-steroidal estrogen: triclosan.Marine Environmental Research 50 (1–5): 153–156.DOI: 10.1016/S0141-1136(00)00080-5
  • Fusani L., Della Seta D., Dessě-Fulgheri F., Farabollini F.2007. Altered reproductive success in rat pairs after environmental-like exposure to xenoestrogen. Proceedings of the Royal Society, Part B: Biological Sciences 274 (1618):1631–1636.DOI: 10.1098/rspb.2007.0064
  • Gray M.A., Niimi A.J., Metcalfe C.D. 1990. Factors affecting the development of testis-ova in medaka, Oryzias latipes,exposed to octylphenol. Environmental Toxicology and Chemistry 18 (8): 1835–1842.DOI: 10.1002/etc.5620180834
  • Harbott L.K., Burmeister S.S., White R.B., Vagell M.,Fernald R.D. 2007. Androgen receptors in a cichlid fish,Astatotilapia burtoni: Structure, localization, and expression levels. Journal of Comparative Neurology and Psychology 504 (1): 57–73.DOI: 10.1002/cne.21435
  • Hawkins M.B., Thomas P. 2004. The unusual binding properties of the third distinct teleost estrogen receptor subtype ERa are accompanied by highly conserved amino acid changes in the ligand binding domain. Endocrinology 145 (6): 2968–2977.DOI: 10.1210/en.2003-0806
  • Hayashi H., Nishimoto A., Oshima N., Iwamuro S. 2007.Expression of the estrogen receptor alpha gene in the anal fin of Japanese medaka, Oryzias latipes, by environmental concentrations of bisphenol A. Journal of Toxicological Sciences 32 (1): 91–96.DOI: 10.2131/jts.32.91
  • Inui M., Adachi T., Takenaka S., Inui H., Nakazawa M.,Ueda M., Watanabe H., Mori C., Iguchi T., Miyatake K.2003. Effect of UV screens and preservatives on vitellogenin and choriogenin production in male medaka (Oryzias latipes). Toxicology 194 (1–2): 43–50.DOI: 10.1016/S0300-483X(03)00340-8
  • Islinger M.,Willimski D., Völkl A., Braunbeck T. 2003. Effects of 17a-ethinylestradiol on the expression of three estrogenresponsive genes and cellular ultrastructure of liver and testes in male zebrafish. Aquatic Toxicology 62 (2): 85–103.DOI: 10.1016/S0166-445X(02)00049-8
  • Iwamatsu T. 1999. Convenient method for sex reversal In a freshwater teleost, the medaka. Journal of Experimental Zoology 283 (2): 210–214.DOI: 10.1002/(SICI)1097-010X(19990201)283:2<210::AIDJEZ12>3.0.CO;2-F
  • Kidd H., James D.R. (eds.) 1991. The agrochemicals handbook.3rd edn. The Royal Society of Chemistry, Cambridge, UK.
  • Kojima H., Katsura E., Takeuchi S., Niiyama K., Kobayashi K.2004. Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays Rusing Chinese hamster ovary cells. Environmental Heath Perspectives 112 (5): 524–531.PMCID: PMC1241915
  • Lakshmipathi N., Gomathi D., Krishnamurthy G. 2008.Photocatalytic degradation of the herbicide pendimethalin using nanoparticles of BaTiO3/TiO2 prepared by gel to crystalline conversion method: A kinetic approach. Journal of Environmental Science and Health, Part B: Pesticides, Ford Contaminants, and Agricultural Wastes 43 (7): 553–561.DOI: 10.1080/03601230802234351
  • Leańos-Castańeda O., Van Der Kraak G. 2007. Functional characterization of estrogen receptor subtypes, ERα and ERβ, mediating vitellogenin production in the liver of rainbow trout. Toxicology and Applied Pharmacology 224 (2):116–125.DOI: 10.1016/j.taap.2007.06.017
  • Magtoon W., Nadee N., Higsdhitani T., Takaha K., Uwa H.1992. Karyotype evolution and geographical distribution of the Thai-medaka, Oryzias minutillus, in Thailand. Journal of Fish Biology 41 (3): 483–497.DOI: 10.1111/j.1095-8649.1992.tb02676.x
  • Menuet A., Pellegrini E., Anglade I., Blaise O., Laudet V.,Kah O., Pakdel F. 2002. Molecular characterization of three estrogen receptor forms in zebrafish: Binding characteristics,transactivation properties, and tissue distributions.Biology of Reproduction 66 (6): 1881–1892.DOI: 10.1095/biolreprod66.6.1881
  • Meucci V., Arukwe A. 2006. Transcriptional modulation of brain and hepatic estrogen receptor and P450arom isotypes in juvenile Atlantic salmon (Salmo salar) after waterborne exposure to the xenoestrogen, 4-nonylphenol. Aquatic Toxicology 77 (2): 167–177.DOI: 10.1016/j.aquatox.2005.11.008
  • Ngamniyom A., Magtoon W., Nagahama Y., Sasayama Y.2009. Expression levels of hormone receptors and bone morphogenic protein in fins of medaka. Zoological Science 26 (1): 74–79.DOI: 10.2108/zsj.26.74
  • Ngamniyom A., Panyarachun B. 2011. Expression levels of hormone receptor and vitellogenin mRNAs in livers of Tai medaka, Oryzias minutillus, inhabiting the suburbs of Bangkok, Thailand. Journal of Fisheries and Aquatic Science 6 (4): 438–446.DOI: 10.3923/jfas.2011.438.446
  • Ngamniyom A., Panyarachun B. 2012. Morphometry and hormone receptor expressions in dorsal and anal fins of Tai medaka, Oryzias minutillus, between breeding and nonbreeding seasons. Journal of Fisheries and Aquatic Science 7 (1): 39–48.DOI: 10.3923/jfas.2012.39.48
  • Ngamniyom A., Sasayama Y. 2011. Expression levels of sex hormone receptors in brains of Japanese medaka, Oryzias latipes (Actinopterygii: Beloniformes: Adrianichthyidae).Acta Ichtyologica et Piscatoria. 41 (1): 29–35.DOI: 10.3750/AIP2011.41.1.05
  • Ngamniyom A., Silprasit K., Panyarachun B. 2012. Effects of pharmaceutical Mestranol on estrogen receptor β mRNA expression levels and morphometry in the anal fins of adult Thai ricefish (Oryzias minutillus). Kasetsart Journal: Natura Science 43: 80–90.
  • Papoulias D.M., Villalobos S.A., Meadows J., Noltie D.B.,Giesy J.P., Tillitt D.E. 2003. In ovo exposure to o,p –DDE affects sexual development but not sexual differentiation In Japanese medaka (Oryzias latipes). Environmental Heath Perspectives 111 (1): 29–32.DOI: 10.1289/ehp.5540
  • Pinto A.P., Serrano C., Pires T., Mestrinho E., Dias L.,Martins Teixeira D., Caldeira A.T. 2012. Degradation of terbuthylazine, difenoconazole and pendimethalin pesticides by selected fungi cultures. Science of the Total Environment 435–436: 402–410.DOI: 10.1016/j.scitotenv.2012.07.027
  • Prado P.S., Souza C.C., Bazzoli N., Rizzo E. 2011.Reproductive disruption in lambari Astyanax fasciatus from a southeastern Brazilian reservoir. Ecotoxicology and Environmental Safety 74 (7): 1879–87.DOI: 10.1016/j.ecoenv.2011.07.017
  • Roca E., D’Errico E., Izzo A., Strumia S., Esposito A.,Fiorentino A. 2009. In vitro saprotrophic basidiomycetes tolerance to pendimethalin. International Biodeterioration and Biodegradation 63 (2): 182–186.DOI: 10.1016/j.ibiod.2008.08.004
  • Sabo-Attwood T., Kroll K.J., Denslow N.D. 2004. Differentia expression of largemouth bass (Micropterus salmoides) estrogen receptor isotypes alpha, beta, and gamma by estradiol. Molecular and Cellular Endocrinology 218 (1–2): 107–118.DOI: 10.1016/j.mce.2003.12.007
  • Scholz S., Kordes C., Hamann J., Gutzeit H.O. 2004.Induction of vitellogenin in vivo and in vitro in the model teleost medaka (Oryzias latipes): comparison of gene expression and protein levels. Marine Environmental Research 57 (3): 235–244. DOI: 10.1016/S0141-1136(03)00082-5
  • Socorro S., Power D.M., Olsson P.E., Canario A.V. 2000.Two estrogen receptors expressed in the teleost fish, Sparuj aurata: cDNA cloning, characterization and tissue distribution. Journal of Endocrinology 166 (2): 293–306.DOI: 10.1677/joe.0.1660293
  • Strandberg M., Scott-Fordsmand J.J. 2004. Effects of pendimethalin at lower trophic levels—a review.Ecotoxicology and Environmental Safety 57 (2): 190–201.DOI: 10.1016/j.ecoenv.2003.07.010
  • Todo T., Ikeuchi T., Kobayashi T., Nagahama Y. 1999. Fish androgen receptor: cDNA cloning, steroid activation of transcription in transfected mammalian cells, and tissue mRNA levels. Biochemical and Biophysical Research Communications 254 (2): 378–383.DOI: 10.1006/bbrc.1998.9919

Uwagi

PL
Rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-f6ff2d11-e5d5-43b8-abed-e3857b854fd9
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.