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. 2010 Apr;10(2):64-74.
doi: 10.4110/in.2010.10.2.64. Epub 2010 Apr 30.

Polybrominated Diphenyl Ethers Orally Administration to Mice Were Tansferred to Offspring during Gestation and Lactation with Disruptions on the Immune System

Affiliations

Polybrominated Diphenyl Ethers Orally Administration to Mice Were Tansferred to Offspring during Gestation and Lactation with Disruptions on the Immune System

Soon Keun Hong et al. Immune Netw. 2010 Apr.

Abstract

Background: The present study was undertaken to examine the immunological effects of pentabrominated diphenyl ether (penta-BDE) and decabrominated diphenyl ether (deca-BDE) on the immune system of the dams and the developmental immune system of the offsprings.

Methods: In this study, mated female C57BL/6J mice were orally administered penta-BDE, deca-BDE or corn oil for 5 weeks, from gestational day 6 to lactational day 21.

Results: The body weight of PND21 exposed to penta-BDE was significantly decreased relative to control mice, but that of post-natal day 63 (PND63) were recovered. Orally dosed dams with penta-BDE had significantly smaller absolute and relative spleen masses than control mice. Absolute and relative spleen and thymus masses of PND21 exposed to penta-BDE were significantly decreased over control. The exposure of dams and PND21 with penta-BDE reduced the number of splenocytes and thymocytes. As results of hematologic analysis, percentage WBC and percentage neutrophils increased in dams with deca-BDE. Splenic T cell proliferation in dams and PND21 exposed to penta-BDE was increased, and there were no significant difference in splenic B cell proliferation in all treatment groups. As results of flow cytometric analysis of splenocyte, percentage total T cell, Th cell and Tc cell in PND21 exposed to penta-BDE was slightly increased, and percentage macrophage in dams and PND21 exposed to deca-BDE was decreased. The ELISA results of antibody production show no significant difference in all treatment groups relative to controls.

Conclusion: These results imply that PBDEs given to the dam were transferred to the offspring during gestation and lactation, and PBDEs transferred from the dam affect immune system of offspring.

Keywords: Deca-BDE; Developing immune system; Penta-BDE.

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Conflict of interest statement

The authors declare no financial or commercial conflicts of interest.

Figures

Figure 1
Figure 1
A general structure of polybrominated diphenyl ether (PBDEs). (A) penta-BDE, (B) deca-BDE.
Figure 2
Figure 2
Body weight changes in dams.
Figure 3
Figure 3
Body weight changes in F1.
Figure 4
Figure 4
Effects of penta-BDE on splenic T cell proliferation responses. (A) Dam, (B) PND21, (C) PND63.
Figure 5
Figure 5
Effects of deca-BDE on splenic T cell proliferation responses. (A) Dam, (B) PND21, (C) PND63.
Figure 6
Figure 6
Effects of penta-BDE on splenic B cell proliferation responses. (A) Dam, (B) PND21, (C) PND63.
Figure 7
Figure 7
Effects of deca-BDE on splenic B cell proliferation responses. (A) Dam, (B) PND21, (C) PND63.
Figure 8
Figure 8
Effects on penta-BDE or deca-BDE on relative distribution of total T cell in spleen. (A) Dam, (B) PND21.
Figure 9
Figure 9
Effects on penta-BDE or deca-BDE on relative distribution of helper T cell subsets in spleen. (A) Dam, (B) PND21.
Figure 10
Figure 10
Effects on penta-BDE or deca-BDE on relative distribution of cytotoxic T cell subsets in spleen. (A) Dam, (B) PND21.
Figure 11
Figure 11
Effects on penta-BDE or deca-BDE on relative distribution of B cell in spleen. (A) Dam, (B) PND21.
Figure 12
Figure 12
Effects on penta-BDE or deca-BDE on relative distribution of macrophage in spleen. (A) Dam, (B) PND21.
Figure 13
Figure 13
The change of serum IgG1 level in mice exposed to penta-BDE or deca-BDE. (A) Dam, (B) PND21.
Figure 14
Figure 14
The change of serum IgM level in mice exposed to penta-BDE or deca-BDE. (A) Dam, (B) PND21.

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