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Article: Modulation of steroidogenesis by coastal waters and sewage effluents of Hong Kong, China, using the H295R assay
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TitleModulation of steroidogenesis by coastal waters and sewage effluents of Hong Kong, China, using the H295R assay
 
AuthorsGracia, T4
Jones, PD4
Higley, EB4
Hilscherova, K1
Newsted, JL5
Murphy, MB6
Chan, AKY6
Zhang, X6 4
Hecker, M5 2
Lam, PKS6
Wu, RSS6
Giesy, JP6 2 4 3
 
KeywordsAquatic environment
China
Coastal waters
Endocrine disruptors
Environmental samples
H295R cell bioassay
Hong Kong
Hormones
Influents
Marine waters
Sewage effluents
Sex steroid hormones
Steroidogenesis
Wastewater treatment plants
 
Issue Date2008
 
PublisherSpringer. The Journal's web site is located at http://www.springer.com/environment/journal/11356
 
CitationEnvironmental Science And Pollution Research, 2008, v. 15 n. 4, p. 332-343 [How to Cite?]
DOI: http://dx.doi.org/10.1007/s11356-008-0011-6
 
AbstractBackground, aim, and scope: The presence of a variety of pollutants in the aquatic environment that can potentially interfere with the production of sex steroid hormones in wildlife and humans has been of increasing concern. The aim of the present study was to investigate the effects of extracts from Hong Kong marine waters, and influents and effluents from wastewater treatment plants on steroidogenesis using the H295R cell bioassay. After exposing H295R cells to extracts of water, the expression of four steroidogenic genes and the production of three steroid hormones were measured. Materials and methods: Water samples were collected during the summer of 2005 from 24 coastal marine areas and from the influents and effluents of two major waste water treatment plants (WWTPs) in Hong Kong, China. Samples were extracted by solid phase extraction (SPE). H295R cells were exposed for 48 h to dilutions of these extracts. Modulations of the expression of the steroidogenic genes CYP19, CYP17, 3βHSD2, and CYP11β2 were determined by measuring mRNA concentrations by real-time polymerase chain reaction (Q-RT-PCR). Production of the hormones progesterone (P), estradiol (E2), and testosterone (T) was quantified using enzyme linked immunosorbent assays (ELISA). Results: Extracts from samples collected in two fish culture areas inhibited growth and proliferation of H295R cells at concentrations greater or equal to 105 L equivalents. The cells were exposed to the equivalent concentration of active substances in 10,000 L of water. Thus, to observe the same level of effect as observed in vitro on aquatic organisms would require a bioaccumulation factor of this same magnitude. None of the other 22 marine samples affected growth of the cells at any dilution tested. Twelve of the marine water samples completely inhibited the expression of CYP19 without affecting E2 production; inhibition of CYP17 expression was observed only in one of the samples while expression of CYP11β2 was induced as much as five- and ninefold after exposure of cells to extracts from two locations. The expression of the progesterone gene 3βHSD2 was not affected by any of the samples; only one sample induced approximately fourfold the production of E2. Although more than twofold inductions were observed for P and T production, none of these values were statistically significant to conclude effects on the production of these two hormones. While influents from WWTPs did not affect gene expression, an approximately 30% inhibition in the production of E2 and a 40% increase in P occurred for the exposure with influents from the Sha Tin and Stonecutters WWTPs, respectively. Effluents from WWTPs did not affect the production of any of the studied hormones, but a decrement in the expression of the aldosterone gene CYP11β2 was observed for the Sha Tin WWTP exposure. No direct correlation could be established between gene expression and hormone production. Discussion: Observed cytotoxicity in the two samples from fish culture areas suggest the presence of toxic compounds; chemical analysis is required for their full identification. Although effluents from WWTPs did not affect hormone production, other types of endocrine activity such as receptor-mediated effects cannot be ruled out. Interactions due to the complexity of the samples and alternative steroidogenic pathways might explain the lack of correlation between gene expression and hormone production results. Conclusions: Changes observed in gene expression and hormone production suggest the presence in Hong Kong coastal waters of pollutants with endocrine disruption potential and others of significant toxic effects. The aromatase and aldosterone genes seem to be the most affected by the exposures, while E2 and P are the hormones with more significant changes observed. Results also suggest effectiveness in the removing of compounds with endocrine activity by the WWTPs studied, as effluent samples did not significantly affect hormone production. The H295R cell showed to be a valuable toll in the battery required for the analysis of endocrine disrupting activities of complex environmental samples. Recommendations and perspectives: Due to the intrinsic complexity of environmental samples, a combination of analytical tools is required to realistically assess environmental conditions, especially in aquatic systems. In the evaluation of endocrine disrupting activities, the H295R cell bioassay should be used in combination with other genomic, biological, chemical, and hydrological tests to establish viable modes for endocrine disruption and identify compounds responsible for the observed effects. © 2008 Springer-Verlag.
 
ISSN0944-1344
2012 Impact Factor: 2.618
2012 SCImago Journal Rankings: 0.878
 
DOIhttp://dx.doi.org/10.1007/s11356-008-0011-6
 
ISI Accession Number IDWOS:000256910500008
 
ReferencesReferences in Scopus
 
DC FieldValue
dc.contributor.authorGracia, T
 
dc.contributor.authorJones, PD
 
dc.contributor.authorHigley, EB
 
dc.contributor.authorHilscherova, K
 
dc.contributor.authorNewsted, JL
 
dc.contributor.authorMurphy, MB
 
dc.contributor.authorChan, AKY
 
dc.contributor.authorZhang, X
 
dc.contributor.authorHecker, M
 
dc.contributor.authorLam, PKS
 
dc.contributor.authorWu, RSS
 
dc.contributor.authorGiesy, JP
 
dc.date.accessioned2010-09-17T10:57:05Z
 
dc.date.available2010-09-17T10:57:05Z
 
dc.date.issued2008
 
dc.description.abstractBackground, aim, and scope: The presence of a variety of pollutants in the aquatic environment that can potentially interfere with the production of sex steroid hormones in wildlife and humans has been of increasing concern. The aim of the present study was to investigate the effects of extracts from Hong Kong marine waters, and influents and effluents from wastewater treatment plants on steroidogenesis using the H295R cell bioassay. After exposing H295R cells to extracts of water, the expression of four steroidogenic genes and the production of three steroid hormones were measured. Materials and methods: Water samples were collected during the summer of 2005 from 24 coastal marine areas and from the influents and effluents of two major waste water treatment plants (WWTPs) in Hong Kong, China. Samples were extracted by solid phase extraction (SPE). H295R cells were exposed for 48 h to dilutions of these extracts. Modulations of the expression of the steroidogenic genes CYP19, CYP17, 3βHSD2, and CYP11β2 were determined by measuring mRNA concentrations by real-time polymerase chain reaction (Q-RT-PCR). Production of the hormones progesterone (P), estradiol (E2), and testosterone (T) was quantified using enzyme linked immunosorbent assays (ELISA). Results: Extracts from samples collected in two fish culture areas inhibited growth and proliferation of H295R cells at concentrations greater or equal to 105 L equivalents. The cells were exposed to the equivalent concentration of active substances in 10,000 L of water. Thus, to observe the same level of effect as observed in vitro on aquatic organisms would require a bioaccumulation factor of this same magnitude. None of the other 22 marine samples affected growth of the cells at any dilution tested. Twelve of the marine water samples completely inhibited the expression of CYP19 without affecting E2 production; inhibition of CYP17 expression was observed only in one of the samples while expression of CYP11β2 was induced as much as five- and ninefold after exposure of cells to extracts from two locations. The expression of the progesterone gene 3βHSD2 was not affected by any of the samples; only one sample induced approximately fourfold the production of E2. Although more than twofold inductions were observed for P and T production, none of these values were statistically significant to conclude effects on the production of these two hormones. While influents from WWTPs did not affect gene expression, an approximately 30% inhibition in the production of E2 and a 40% increase in P occurred for the exposure with influents from the Sha Tin and Stonecutters WWTPs, respectively. Effluents from WWTPs did not affect the production of any of the studied hormones, but a decrement in the expression of the aldosterone gene CYP11β2 was observed for the Sha Tin WWTP exposure. No direct correlation could be established between gene expression and hormone production. Discussion: Observed cytotoxicity in the two samples from fish culture areas suggest the presence of toxic compounds; chemical analysis is required for their full identification. Although effluents from WWTPs did not affect hormone production, other types of endocrine activity such as receptor-mediated effects cannot be ruled out. Interactions due to the complexity of the samples and alternative steroidogenic pathways might explain the lack of correlation between gene expression and hormone production results. Conclusions: Changes observed in gene expression and hormone production suggest the presence in Hong Kong coastal waters of pollutants with endocrine disruption potential and others of significant toxic effects. The aromatase and aldosterone genes seem to be the most affected by the exposures, while E2 and P are the hormones with more significant changes observed. Results also suggest effectiveness in the removing of compounds with endocrine activity by the WWTPs studied, as effluent samples did not significantly affect hormone production. The H295R cell showed to be a valuable toll in the battery required for the analysis of endocrine disrupting activities of complex environmental samples. Recommendations and perspectives: Due to the intrinsic complexity of environmental samples, a combination of analytical tools is required to realistically assess environmental conditions, especially in aquatic systems. In the evaluation of endocrine disrupting activities, the H295R cell bioassay should be used in combination with other genomic, biological, chemical, and hydrological tests to establish viable modes for endocrine disruption and identify compounds responsible for the observed effects. © 2008 Springer-Verlag.
 
dc.description.natureLink_to_subscribed_fulltext
 
dc.identifier.citationEnvironmental Science And Pollution Research, 2008, v. 15 n. 4, p. 332-343 [How to Cite?]
DOI: http://dx.doi.org/10.1007/s11356-008-0011-6
 
dc.identifier.doihttp://dx.doi.org/10.1007/s11356-008-0011-6
 
dc.identifier.epage343
 
dc.identifier.isiWOS:000256910500008
 
dc.identifier.issn0944-1344
2012 Impact Factor: 2.618
2012 SCImago Journal Rankings: 0.878
 
dc.identifier.issue4
 
dc.identifier.pmid18493807
 
dc.identifier.scopuseid_2-s2.0-45849087643
 
dc.identifier.spage332
 
dc.identifier.urihttp://hdl.handle.net/10722/92785
 
dc.identifier.volume15
 
dc.languageeng
 
dc.publisherSpringer. The Journal's web site is located at http://www.springer.com/environment/journal/11356
 
dc.publisher.placeGermany
 
dc.relation.ispartofEnvironmental Science and Pollution Research
 
dc.relation.referencesReferences in Scopus
 
dc.subjectAquatic environment
 
dc.subjectChina
 
dc.subjectCoastal waters
 
dc.subjectEndocrine disruptors
 
dc.subjectEnvironmental samples
 
dc.subjectH295R cell bioassay
 
dc.subjectHong Kong
 
dc.subjectHormones
 
dc.subjectInfluents
 
dc.subjectMarine waters
 
dc.subjectSewage effluents
 
dc.subjectSex steroid hormones
 
dc.subjectSteroidogenesis
 
dc.subjectWastewater treatment plants
 
dc.titleModulation of steroidogenesis by coastal waters and sewage effluents of Hong Kong, China, using the H295R assay
 
dc.typeArticle
 
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<contributor.author>Higley, EB</contributor.author>
<contributor.author>Hilscherova, K</contributor.author>
<contributor.author>Newsted, JL</contributor.author>
<contributor.author>Murphy, MB</contributor.author>
<contributor.author>Chan, AKY</contributor.author>
<contributor.author>Zhang, X</contributor.author>
<contributor.author>Hecker, M</contributor.author>
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Author Affiliations
  1. Masaryk University
  2. University of Saskatchewan
  3. Nanjing University
  4. Michigan State University
  5. ENTRIX Inc.
  6. City University of Hong Kong