Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, United States.
Chem Biol Interact. 2010 Sep 6;187(1-3):142-7. doi: 10.1016/j.cbi.2010.01.036. Epub 2010 Jan 28.
Insecticides directed against acetylcholinesterase (AChE) are facing increased resistance among target species as well as increasing concerns for human toxicity. The result has been a resurgence of disease vectors, insects destructive to agriculture, and residential pests. We previously reported a free cysteine (Cys) residue at the entrance to the AChE active site in some insects but not higher vertebrates. We also reported Cys-targeting methanethiosulfonate molecules (AMTSn), which, under conditions that spared human AChE, caused total irreversible inhibition of aphid AChE, 95% inhibition of AChE from the malaria vector mosquito (Anopheles gambia), and >80% inhibition of activity from the yellow fever mosquito (Aedes aegypti) and northern house mosquito (Culex pipiens). We now find the same compounds inhibit AChE from cockroaches (Blattella germanica and Periplaneta americana), the flour beetle (Tribolium confusum), the multi-colored Asian ladybird beetle (Harmonia axyridis), the bed bug (Cimex lectularius), and a wasp (Vespula maculifrons), with IC(50) values of approximately 1-11muM. Our results support further study of Cys-targeting inhibitors as conceptually novel insecticides that may be free of resistance in a range of insect pests and disease vectors and, compared with current compounds, should demonstrate much lower toxicity to mammals, birds, and fish.
杀虫剂针对乙酰胆碱酯酶(AChE)面临着目标物种的抗药性增加以及对人类毒性的日益关注。结果是疾病载体、破坏农业的昆虫和住宅害虫的死灰复燃。我们之前报道了在一些昆虫但不是高等脊椎动物的 AChE 活性部位入口处存在游离半胱氨酸(Cys)残基。我们还报道了针对半胱氨酸的甲硫基磺酸盐分子(AMTSn),在不影响人类 AChE 的条件下,这些分子导致蚜虫 AChE 的完全不可逆抑制,疟疾传播媒介蚊子(冈比亚按蚊)的 AChE 抑制 95%,以及黄热病蚊子(埃及伊蚊)和北方家蚊(库蚊)的活性抑制>80%。我们现在发现相同的化合物抑制来自蟑螂(德国小蠊和美洲大蠊)、面粉甲虫(杂拟谷盗)、多色亚洲瓢虫(异色瓢虫)、臭虫(吸血臭虫)和黄蜂(胡蜂)的 AChE,IC50 值约为 1-11μM。我们的结果支持对半胱氨酸靶向抑制剂的进一步研究,这些抑制剂作为概念新颖的杀虫剂,可能在一系列害虫和疾病载体中没有抗药性,并且与现有化合物相比,对哺乳动物、鸟类和鱼类的毒性应该低得多。