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首页> 外文期刊>Environmental toxicology and pharmacology >Inhibitory effects of pain relief drugs on neurological enzymes: Implications on their potential neurotoxicity to aquatic animals
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Inhibitory effects of pain relief drugs on neurological enzymes: Implications on their potential neurotoxicity to aquatic animals

机译:止痛药对神经酶的抑制作用:对水生动物潜在神经毒性的影响

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摘要

Pain relief medications commonly occur in the aquatic environment at measurable levels. While the neurotoxicity of pain relievers to higher vertebrates is currently known, little is known about their effects on aquatic animals. This study investigated the neurotoxicity of pain relievers to aquatic animals. We used three neurological enzymes, cholinesterase (ChE), adenosine triphosphatase (ATPase), and monoamine oxidase (MAO), from a freshwater planarian (Dugesia japonica) and green neon shrimp (Neocaridina denticulata) as biomark-ers to examine the effects of pain relievers on in vitro activity. The activity of MAO and ChE, but not ATPase, was significantly inhibited by acetaminophen, but not by other pain relievers examined. It was likely that the inhibitory effects of acetaminophen on shrimp neurological enzymes were more severe than on the planarian. These findings suggest that acetaminophen is potentially neurotoxic to aquatic animals, at least in terms of neurotrans-mission disturbance.
机译:止痛药通常在水生环境中以可测量的水平出现。虽然目前已知止痛药对高等脊椎动物的神经毒性,但对其对水生动物的影响知之甚少。这项研究调查了止痛药对水生动物的神经毒性。我们使用来自淡水浮游动物(Dugesia japonica)和绿色霓虹虾(Neocaridina denticulata)的三种神经学酶胆碱酯酶(ChE),腺苷三磷酸酶(ATPase)和单胺氧化酶(MAO)作为生物标志物来研究疼痛的影响对体外活性的缓解作用。对乙酰氨基酚显着抑制MAO和ChE的活性,但不抑制ATPase的活性,但所检查的其他止痛药则没有。对乙酰氨基酚对虾神经系统酶的抑制作用可能比对涡虫的抑制作用更严重。这些发现表明,至少在神经传递障碍方面,对乙酰氨基酚对水生动物具有潜在的神经毒性。

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