2009
DOI: 10.1016/j.toxlet.2008.12.003
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Endocrine effects of hexabromocyclododecane (HBCD) in a one-generation reproduction study in Wistar rats

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Cited by 120 publications
(63 citation statements)
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“…Consistent with these effects by NCM, perinatal exposure to TCDD also reduced bone geometrical parameters in young developing rats (Miettinen et al 2005). In contrast to the observation of similarity in response pattern between genders in the present study, results of a recent perinatal exposure study to the brominated flame retardant hexabromocyclododecane revealed gender-related differences, with bone geometrical parameters decreased in young males at PND77, while bone mineral density was decreased in young females at PND77 (van der Ven et al 2009). …”
Section: Discussionsupporting
confidence: 71%
See 1 more Smart Citation
“…Consistent with these effects by NCM, perinatal exposure to TCDD also reduced bone geometrical parameters in young developing rats (Miettinen et al 2005). In contrast to the observation of similarity in response pattern between genders in the present study, results of a recent perinatal exposure study to the brominated flame retardant hexabromocyclododecane revealed gender-related differences, with bone geometrical parameters decreased in young males at PND77, while bone mineral density was decreased in young females at PND77 (van der Ven et al 2009). …”
Section: Discussionsupporting
confidence: 71%
“…Furthermore, alterations in bone quality were demonstrated for wildlife from organohalogencontaminated environments (Fox et al 2008;Johnson et al 2009;Lind et al 2003;Murtomaa et al 2007;RodriguezNavarro et al 2006;Roos et al 2010;Sonne et al 2004). Consistent with these observations, experimental studies with animal models revealed that single-chemical exposure to organohalogens induces changes in bone properties both in adult animals (Alvarez-Lloret et al 2009;Andrews et al 1990;Badraoui et al 2007;Herlin et al 2010;Jämsä et al 2001;Lind et al 2000a;2000b;van der Ven et al 2006) and in the offspring following maternal exposure (Hermsen et al 2008;van der Ven et al 2009). The most detailed toxicological bone studies were performed with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), the organohalogen pollutant model compound, which exerts most of its effects through activation of the aryl hydrocarbon receptor (AhR) (Denison and Nagy 2003;Herlin et al 2010;Jämsä et al 2001).…”
Section: Perinatal Exposure To Environmental Contaminants Detected Inmentioning
confidence: 85%
“…Long-term high-dose HBCDs exposure (30 mg/kg/day, 28 d) can result in increase of liver weight, [14] and 100 mg/kg/day continuous exposure for 90 d can cause liver nodules, fatty infiltration, liver necrosis and even liver carcinoma. [15] In addition, HBCDs exposure can also disrupt the thyroid function, [16] impact the immune system, [17,18] and lead to neurological disorders. [19,20] HBCDs have been included in the Priority Pollutants List of the OSPAR (No.793/93/EEC).…”
Section: Introductionmentioning
confidence: 99%
“…In Taiwan, the conducted research on breast milk in Taiwanese mothers found PBDE concentrations to be 1.6-2.3 times higher than those of Japanese mothers (Chao et al, 2007;Horng et al, 2010). The bio-accumulating effect in human bodies is of concern due to the fact that several toxicological effects of PBDE congeners have been detected in experimental animals, such as neurotoxicity, behavioral changes, and endocrine disruption (McDonald, 2002;Darnerud, 2003;Kuiper et al, 2008;van der Ven et al, 2009). The major sources of human PBDE exposure are through diet, accounting for 73% of daily intake (Bocio, et al, 2003).…”
Section: Introductionmentioning
confidence: 99%