Byers James P, Masters Karilane, Sarver Jeffrey G, Hassoun Ezdihar A
College of Pharmacy, The University of Toledo, 2801 W. Bancroft Street, Toledo, OH 43606, USA.
Toxicology. 2006 Dec 7;228(2-3):291-8. doi: 10.1016/j.tox.2006.09.009. Epub 2006 Sep 29.
The effects of TCDD on the distribution of biogenic amines and production of superoxide anion (SA) in different brain regions of rats have been studied after subchronic exposure. Groups of females Sprague-Dawley rats were administered daily dose of 46ng TCDD/(kgday) (treated groups), or the vehicle used to dissolve TCDD (control group), for 90 days. The rats were sacrificed at the end of the exposure period and their brains were dissected into different regions including, hippocampus (H), cerebral cortex (Cc), cerebellum (C), and brain stem (Bs). The levels of different biogenic amines and some of their metabolites, including, norepinephrine (NE), dopamine (DA), 3,4-dihydroxy phenyl acetic acid (DOPAC), 4-hydroxy-3-methoxy-phenyl acetic acid (HVA), 5-hydroxy tryptamine (5-HT), and 5-hydroxy indole 3-acetic acid (5-HIAA), were determined in those brain regions, using a high performance liquid chromatography (HPLC) system with an electrochemical detector. SA production was also determined in those regions, using the cytochrome c reduction method. Results of analyses indicate significant increases in the levels of DA, NE and DOPAC in H, NE and HVA in Cc, NE and DA in Bs and NE in C. SA production was significantly increased in H and Cc, but not in Bs or C. The results also indicated strong correlations between DA and DOPAC, and SA and NE in all of the brain regions, and also between SA and 5-HT/HIAA in H and Cc. These results may indicate the contribution of biogenic amines, especially NE and 5-HT/HIAA to SA overproduction in some brain regions and may also indicate the potential of long term neurotoxic effects of those biogenic amines, in response to subchronic exposure to TCDD.
在亚慢性暴露后,研究了2,3,7,8-四氯二苯并对二恶英(TCDD)对大鼠不同脑区生物胺分布和超氧阴离子(SA)产生的影响。将雌性斯普拉格-道利大鼠分组,每天给予46纳克TCDD/(千克·天)的剂量(处理组),或用于溶解TCDD的赋形剂(对照组),持续90天。在暴露期结束时处死大鼠,将其大脑解剖成不同区域,包括海马体(H)、大脑皮层(Cc)、小脑(C)和脑干(Bs)。使用配备电化学检测器的高效液相色谱(HPLC)系统测定这些脑区中不同生物胺及其一些代谢产物的水平,包括去甲肾上腺素(NE)、多巴胺(DA)、3,4-二羟基苯乙酸(DOPAC)、4-羟基-3-甲氧基苯乙酸(HVA)、5-羟色胺(5-HT)和5-羟基吲哚-3-乙酸(5-HIAA)。还使用细胞色素c还原法在这些区域测定SA的产生。分析结果表明,海马体中DA、NE和DOPAC的水平显著升高,大脑皮层中NE和HVA的水平显著升高,脑干中NE和DA的水平显著升高,小脑中NE的水平显著升高。海马体和大脑皮层中SA的产生显著增加,但脑干和小脑中没有。结果还表明,在所有脑区中,DA与DOPAC之间、SA与NE之间以及海马体和大脑皮层中SA与5-HT/5-HIAA之间存在强相关性。这些结果可能表明生物胺,尤其是NE和5-HT/5-HIAA在某些脑区SA过量产生中的作用,也可能表明这些生物胺在亚慢性暴露于TCDD后的长期神经毒性作用潜力。