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止痛药物对神经酶的抑制作用:对其对水生动物潜在神经毒性的影响。

Inhibitory effects of pain relief drugs on neurological enzymes: implications on their potential neurotoxicity to aquatic animals.

作者信息

Wu Jui-Pin, Li Mei-Hui

机构信息

Environmental Toxicology Laboratory, Department of Geography, National Taiwan University, 1, Section 4, Roosevelt Road, Taipei 106, Taiwan.

Environmental Toxicology Laboratory, Department of Geography, National Taiwan University, 1, Section 4, Roosevelt Road, Taipei 106, Taiwan.

出版信息

Environ Toxicol Pharmacol. 2015 Mar;39(2):898-905. doi: 10.1016/j.etap.2015.02.022. Epub 2015 Mar 7.

Abstract

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 biomarkers 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 neurotransmission disturbance.

摘要

止痛药物在水生环境中通常以可测量的水平存在。虽然目前已知止痛剂对高等脊椎动物具有神经毒性,但对水生动物的影响却知之甚少。本研究调查了止痛剂对水生动物的神经毒性。我们使用来自淡水涡虫(日本三角涡虫)和绿色霓虹虾(锯齿新米虾)的三种神经酶,即胆碱酯酶(ChE)、三磷酸腺苷酶(ATPase)和单胺氧化酶(MAO)作为生物标志物,来检测止痛剂对体外活性的影响。对乙酰氨基酚显著抑制了MAO和ChE的活性,但未抑制ATPase的活性,而其他检测的止痛剂则没有这种作用。对乙酰氨基酚对虾神经酶的抑制作用可能比对涡虫更严重。这些发现表明,至少在神经传递干扰方面,对乙酰氨基酚对水生动物具有潜在的神经毒性。

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