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dc.contributor.author
Rodriguez, Enrique Marcelo  
dc.contributor.author
Medesani, Daniel Alberto  
dc.contributor.author
López Greco, Laura S.  
dc.contributor.other
Luppi, Tomas Atilio  
dc.contributor.other
Rodriguez, Enrique Marcelo  
dc.date.available
2024-06-05T18:01:18Z  
dc.date.issued
2020  
dc.identifier.citation
Rodriguez, Enrique Marcelo; Medesani, Daniel Alberto; López Greco, Laura S.; Endocrine disruption by pollutants and effects on progeny; Cambridge Scholars Publishing; 2; 2020; 339-356  
dc.identifier.isbn
978-1-5275-5003-2  
dc.identifier.uri
http://hdl.handle.net/11336/237210  
dc.description.abstract
As mentioned in Chapter 10, hormonally-regulated functions of crustaceans have been reviewed during the last years by several authors. Main endocrine-regulated processes of crustaceans involve moulting, reproduction, glycemia levels, and pigment migration, among others. Several pollutants, such as pesticides, alkylphenols, polychlorinated biphenyls, hydrocarbons, and heavy metals, can interfere with these processes, therefore acting as endocrine-disrupting compounds (ECDs) on crustaceans, as reviewed by several authors (LeBlanc 2007, Rodríguez et al. 2007, deFur et al. 1999). The hyperglycemic crustacean hormone (CHH) belongs to a highly diversified family of peptide hormones, secreted by the sinus gland at the eyestalks (Nagaraju 2011, Fingerman 1997). This hormone has been considered as the “stress hormone” of crustaceans (Chang et al. 1999). In some cases, a hyperglycemic response has been observed following exposure to cadmium (Reddy et al. 2009), but an eventual inhibition of the CHH synthesis has also been reported (Reddy et al. 1996). Hyperglycemia caused by heavy metals in shrimps also showed dependence on both the time of exposure and concentration (Lorenzon et al. 2000). An inhibition of moulting by several estrogenic compounds, as well as by testosterone, antiandrogens, antiestrogens, and some pesticides, has been reported in daphnids and copepods (LeBlanc 2007, Andersen et al. 2001, Zou and Fingerman 1997). Besides, evidence about a possible antagonism of these compounds with the transductional pathway of ecdysone at target tissues has been provided (Mu and LeBlanc 2002a). Juvenoid compounds, such as methoprene and JHIII have also inhibited moulting, perhaps interfering with the stimulating effect of the juvenoid hormone methyl farnesoate (Olmstead and LeBlanc 2001). Regarding reproduction, several estrogenic compounds, both natural and synthetic, as well as some juvenoids and ecdysteroids, have shown to exert an abnormal stimulation on several aspects of crustacean reproduction. Observed effects were mainly the abnormal development of secondary sexual characters in both sexes, and a shift to all-female or allmale broods. These effects were observed in daphnids (Dodson et al. 1999, Olmstead and LeBlanc 2000), copepods (Andersen et al. 1999), and amphipods (Brown et al. 1999, Watts et al. 2002).  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Cambridge Scholars Publishing  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
NEOHELICE GRANULATA  
dc.subject
ENDOCRINE DISRUPTORS  
dc.subject
POLLUTANTS  
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PROGENY  
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Otras Ciencias Biológicas  
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Ciencias Biológicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Endocrine disruption by pollutants and effects on progeny  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.type
info:eu-repo/semantics/bookPart  
dc.type
info:ar-repo/semantics/parte de libro  
dc.date.updated
2021-09-07T18:27:12Z  
dc.journal.volume
2  
dc.journal.pagination
339-356  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Cambridge  
dc.description.fil
Fil: Rodriguez, Enrique Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Biodiversidad y Biología Experimental y Aplicada. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Biodiversidad y Biología Experimental y Aplicada; Argentina. Universidad de Buenos Aires. Facultad de Cs.exactas y Naturales. Departamento de Biodiversidad y Biologia Experimental. Laboratorio de Fisiologia de Crustáceos; Argentina  
dc.description.fil
Fil: Medesani, Daniel Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Biodiversidad y Biología Experimental y Aplicada. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Biodiversidad y Biología Experimental y Aplicada; Argentina. Universidad de Buenos Aires. Facultad de Cs.exactas y Naturales. Departamento de Biodiversidad y Biologia Experimental. Laboratorio de Fisiologia de Crustáceos; Argentina  
dc.description.fil
Fil: López Greco, Laura S.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Biodiversidad y Biología Experimental y Aplicada. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Biodiversidad y Biología Experimental y Aplicada; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Biodiversidad y Biología Experimental. Laboratorio de Biología de la Reproducción y Crecimiento de Crustáceos Decápodos; Argentina  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.cambridgescholars.com/product/978-1-5275-5003-2  
dc.conicet.paginas
413  
dc.source.titulo
Neohelice granulata, a Model Species for Studies on Crustaceans