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氨基甲酸酯类杀虫剂靶向人类褪黑素受体。

Carbamate Insecticides Target Human Melatonin Receptors.

作者信息

Popovska-Gorevski Marina, Dubocovich Margarita L, Rajnarayanan Rajendram V

机构信息

Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo , Buffalo, New York 14221, United States.

出版信息

Chem Res Toxicol. 2017 Feb 20;30(2):574-582. doi: 10.1021/acs.chemrestox.6b00301. Epub 2017 Jan 11.

Abstract

Carbaryl (1-naphthyl methylcarbamate) and carbofuran (2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate) are among the most toxic insecticides, implicated in a variety of diseases including diabetes and cancer among others. Using an integrated pharmacoinformatics based screening approach, we have identified these insecticides to be structural mimics of the neurohormone melatonin and were able to bind to the putative melatonin binding sites in MT and MT melatonin receptors in silico. Carbaryl and carbofuran then were tested for competition with 2-[I]-iodomelatonin (300 pM) binding to hMT or hMT receptors stably expressed in CHO cells. Carbaryl and carbofuran showed higher affinity for competition with 2-[I]-iodomelatonin binding to the hMT compared to the hMT melatonin receptor (33 and 35-fold difference, respectively) as predicted by the molecular modeling. In the presence of GTP (100 μM), which decouples the G-protein linked receptors to modulate signaling, the apparent efficacy of carbaryl and carbofuran for 2-[I]-iodomelatonin binding for the hMT melatonin receptor was not affected but significantly decreased for the hMT melatonin receptor compatible with receptor antagonist/inverse agonist and agonist efficacy, respectively. Altogether, our data points to a potentially new mechanism through which carbamate insecticides carbaryl and carbofuran could impact human health by altering the homeostatic balance of key regulatory processes by directly binding to melatonin receptors.

摘要

西维因(1-萘基甲基氨基甲酸酯)和克百威(2,3-二氢-2,2-二甲基-7-苯并呋喃基甲基氨基甲酸酯)是毒性最强的杀虫剂之一,与包括糖尿病和癌症在内的多种疾病有关。通过基于整合药物信息学的筛选方法,我们已确定这些杀虫剂是神经激素褪黑素的结构模拟物,并且能够在计算机模拟中与褪黑素MT1和MT2褪黑素受体中的假定褪黑素结合位点结合。然后测试了西维因和克百威与2-[I]-碘褪黑素(300 pM)竞争结合稳定表达于CHO细胞中的hMT1或hMT2受体的能力。正如分子模拟所预测的,与hMT2褪黑素受体相比,西维因和克百威在与2-[I]-碘褪黑素竞争结合hMT1时表现出更高的亲和力(分别相差33倍和35倍)。在存在GTP(100 μM)的情况下,GTP可使G蛋白偶联受体解偶联以调节信号传导,西维因和克百威对2-[I]-碘褪黑素结合hMT2褪黑素受体的表观效力未受影响,但对hMT1褪黑素受体的表观效力则显著降低,这分别与受体拮抗剂/反向激动剂和激动剂的效力相符。总之,我们的数据表明了一种潜在的新机制,通过该机制,氨基甲酸酯类杀虫剂西维因和克百威可能通过直接结合褪黑素受体来改变关键调节过程的稳态平衡,从而影响人类健康。

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