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亚烷基连接的双新烟碱类化合物对美洲大蠊腹部末端神经节神经元表达的烟碱型乙酰胆碱受体的阻断作用。

Blocking actions of alkylene-tethered bis-neonicotinoids on nicotinic acetylcholine receptors expressed by terminal abdominal ganglion neurons of Periplaneta americana.

作者信息

Ihara Makoto, Hirata Koichi, Ishida Chiharu, Kagabu Shinzo, Matsuda Kazuhiko

机构信息

Department of Applied Biological Chemistry, School of Agriculture, Kinki University, Nakamachi 3327-204, Nara 631-8505, Japan.

出版信息

Neurosci Lett. 2007 Oct 2;425(3):137-40. doi: 10.1016/j.neulet.2007.05.065. Epub 2007 Jul 5.

Abstract

Neonicotinoid insecticides target nicotinic acetylcholine receptors (nAChRs), which, in both vertebrates and invertebrates, mediate fast-acting synaptic neurotransmission in the nervous system. Recently, Kagabu et al. synthesized bis-neonicotinoids. The neural activities of bis-neonicotinoids have been evaluated on the central nerve cord of American cockroaches. However, the action of bis-neonicotinoids on nAChRs expressed by dissociated insect neurons has not yet been studied. Thus, the actions of several alkylene-tethered bis-neonicotinoids on the terminal abdominal ganglion neurons of the American cockroach, Periplaneta americana, were investigated using whole-cell patch-clamp electrophysiology. All of the ligands tested did not induce membrane currents, but reduced the responses to ACh when bath applied prior to co-application with ACh. Of the compounds tested, HK-13, which possesses two imidacloprid units linked with a hexamethylene bridge, had the highest antagonist potency. The antagonist action was reduced, not only by elongating, but also by shortening the linker.

摘要

新烟碱类杀虫剂作用于烟碱型乙酰胆碱受体(nAChRs),该受体在脊椎动物和无脊椎动物中均介导神经系统中快速起效的突触神经传递。最近,加贺布等人合成了双新烟碱类化合物。已在美国蟑螂的中枢神经索上评估了双新烟碱类化合物的神经活性。然而,双新烟碱类化合物对解离的昆虫神经元所表达的nAChRs的作用尚未得到研究。因此,使用全细胞膜片钳电生理学方法研究了几种亚烷基连接的双新烟碱类化合物对美洲大蠊(Periplaneta americana)腹部末端神经节神经元的作用。所有测试的配体均未诱导膜电流,但在与乙酰胆碱(ACh)共同施加之前进行浴灌时,会降低对ACh的反应。在测试的化合物中,具有两个通过六亚甲基桥连接的吡虫啉单元的HK-13具有最高的拮抗效力。不仅延长连接子,而且缩短连接子都会降低拮抗作用。

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