2013
DOI: 10.1016/j.brainres.2013.04.014
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Lactation exposure to BDE-153 damages learning and memory, disrupts spontaneous behavior and induces hippocampus neuron death in adult rats

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Cited by 29 publications
(16 citation statements)
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“…BDE-47 and BDE-153 changed hippocampus morphology and ultra structure in rats (He et al 2009; Zhang et al 2013). BDE-47 and BDE-99 damaged rats or mice’s neuron cytoskeletal formation and neuronal maturation by affecting Ca 2+ /calmodulin-dependent protein kinase II, synaptophysin and cytoskeletal protein expression, decreasing expressions of brain-derived neurotrophic factor and anti-apoptotic bcl-2 mRNA, and protein (Alm et al 2008; Blanco et al 2011; Viberg 2009).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…BDE-47 and BDE-153 changed hippocampus morphology and ultra structure in rats (He et al 2009; Zhang et al 2013). BDE-47 and BDE-99 damaged rats or mice’s neuron cytoskeletal formation and neuronal maturation by affecting Ca 2+ /calmodulin-dependent protein kinase II, synaptophysin and cytoskeletal protein expression, decreasing expressions of brain-derived neurotrophic factor and anti-apoptotic bcl-2 mRNA, and protein (Alm et al 2008; Blanco et al 2011; Viberg 2009).…”
Section: Discussionmentioning
confidence: 99%
“…Several mechanisms underlying PBDE-mediated developmental neurotoxicity have been suggested in rats and mice neonatal exposure to PBDE (Johansson et al 2008; Viberg et al 2003, 2005, 2007; Zhang et al 2013). BDE-47 and BDE-153 changed hippocampus morphology and ultra structure in rats (He et al 2009; Zhang et al 2013).…”
Section: Discussionmentioning
confidence: 99%
“…In another study it was observed that the brain tissue accumulated less than 0.5% of the ingested tetrabromobisphenol A (TBBPA) and BDE-99 (Viberg and Eriksson, 2011). These compounds show a drastically lower brain uptake than ATE, BATE and DPTE but nevertheless they caused severe neuronal dysfunctions in laboratory animals (Viberg and Eriksson, 2011;von der Recke and Vetter, 2007;Zhang et al, 2013). Thus, it may be that ATE, BATE and DPTE not only pass across the blood-brain barrier to a higher degree than the other BFRs but that they are also likely to affect neuronal functions.…”
Section: Introductionmentioning
confidence: 93%
“…Chronic exposure of LBDEs to organisms can lead to liver tumors, developmental neurotoxicity and thyroid dysfunctions [ 12 ]. LBDEs depress thyroid development as well as the long-term learning and memory capabilities in adult rats [ 13 , 14 ].…”
Section: Introductionmentioning
confidence: 99%