Bromophenols, both present in marine organisms and in industrial flame retardants, disturb cellular Ca2+ signaling in neuroendocrine cells (PC12)

被引:67
作者
Hassenklöver, T
Predehl, S
Pilli, J
Ledwolorz, J
Assmann, M
Bickmeyer, U [1 ]
机构
[1] Alfred Wegener Inst Polar & Meeresforsch Helmholt, Biol Anstalt Helgoland, D-27498 Helgoland, Germany
[2] Univ Hamburg, Hamburg, Germany
[3] Alfred Wegener Inst Polar & Meeresforsch Helmholt, D-27570 Bremerhaven, Germany
关键词
calcium signaling; neurotoxicology; flame retardant; algae; 2,4-dibromophenol; 2,4,6-tribromophenol;
D O I
10.1016/j.aquatox.2005.09.004
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Bromophenols are present in polychaetes as well as in algae in marine environments including the North Sea. They are thought to cause the typical sea-like taste and flavour. The ecological function of brominated phenols is not clear yet, but they may play a role in chemical defence and deterrence [Kicklighter, C.E., Kubaneck, J., Hay, M.E., 2004. Do brominated natural products defend marine worms from consumers? Some do, most don't. Limnol. Oceanogr. 49, 430-441]. Some brominated phenols are commercially used as industrial flame retardants as, e.g., 2,4,6-tfibromophenol and are suspected to disrupt the Immoral system by showing tyroid hormone-like activity [Legler, I., Brouwer, A., 2003. Are brominated flame retardants endocrine disruptors? Environ. Int. 29, 879-885]. In this study 2-bromophenol (2-BP), 4-bromophenol (4-BP), 2,4-dibromophenol (2,4-DBP), 2,6-dibrornophenol (2,6-DBP) and 2,4,6-tribromophenol (2,4,6-TBP), all of which are present in marine organisms, were tested. Especially 2,4-DBP and 2,4,6-TBP showed a significant effect on the Ca2+ homeostasis in endocrine cells (PC 12). The reduction of depolarization induced Ca2+ elevations by 2,4-DBP and 2,4,6-TBP and the increase of intracellular Ca2+ by both substances, partly released from intracellular stores, may suggest a link to the disrupting effect of endocrine systems by brominated phenols. 2,4-DBP was the most potent substance we tested in respect to inhibition of voltage dependent Ca2+ currents as revealed in whole cell patch clamp experiments. Brominated phenols disturb cellular Ca2+ signaling with differential efficacy, depending on the number and position of bromine. (c) 2005 Elsevier B.V. All rights reserved.
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页码:37 / 45
页数:9
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