Slotkin Theodore A, Tate Charlotte A, Ryde Ian T, Levin Edward D, Seidler Frederic J
Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Environ Health Perspect. 2006 Oct;114(10):1542-6. doi: 10.1289/ehp.9337.
In the developing brain, serotonin (5HT) systems are among the most sensitive to disruption by organophosphates.
We exposed neonatal rats to daily doses of diazinon or parathion on postnatal days (PND)1-4 and evaluated 5HT receptors and the 5HT transporter in brainstem and forebrain on PND5, focusing on doses of each agent below the maximum tolerated dose and spanning the threshold for cholinesterase inhibition: 0.5, 1, or 2 mg/kg for diazinon, and 0.02, 0.05, and 0.1 mg/kg for parathion.
Diazinon evoked up-regulation of 5HT1A and 5HT2 receptor expression even at doses devoid of effects on cholinesterase activity, a pattern similar to that seen earlier for another organophosphate, chlorpyrifos. In contrast, parathion decreased 5HT1A receptors, again at doses below those required for effects on cholinesterase. The two agents also differed in their effects on the 5HT transporter. Diazinon evoked a decrease in the brainstem and an increase in the forebrain, again similar to that seen for chlorpyrifos; this pattern is typical of damage of nerve terminals and reactive sprouting. Parathion had smaller, nonsignificant effects.
Our results buttress the idea that, in the developing brain, the various organophosphates target specific neurotransmitter systems differently from each other and without the requirement for cholinesterase inhibition, their supposed common mechanism of action.
在发育中的大脑中,血清素(5-羟色胺,5HT)系统是对有机磷酸酯破坏最为敏感的系统之一。
我们在新生大鼠出生后第1至4天每天给予其一定剂量的二嗪农或对硫磷,并在出生后第5天评估其脑干和前脑中的5HT受体及5HT转运体,重点关注每种药剂低于最大耐受剂量且跨越胆碱酯酶抑制阈值的剂量:二嗪农为0.5、1或2毫克/千克,对硫磷为0.02、0.05和0.1毫克/千克。
即使在对胆碱酯酶活性无影响的剂量下,二嗪农也能引起5HT1A和5HT2受体表达上调,这一模式与之前另一种有机磷酸酯毒死蜱的情况相似。相比之下,对硫磷则会降低5HT1A受体,同样是在低于对胆碱酯酶有影响所需的剂量下。这两种药剂对5HT转运体的影响也有所不同。二嗪农会使脑干中的5HT转运体减少,前脑中的增加,同样与毒死蜱的情况相似;这种模式是神经末梢损伤和反应性芽生的典型表现。对硫磷的影响较小且无统计学意义。
我们的结果支持了这样一种观点,即在发育中的大脑中,各种有机磷酸酯对特定神经递质系统的靶向作用彼此不同,且无需胆碱酯酶抑制这一它们所谓的共同作用机制。