Fonseca M I, Lunt G G, Aguilar J S
Department of Biochemistry, Bath University, U.K.
Biochem Pharmacol. 1991 Mar 1;41(5):735-42. doi: 10.1016/0006-2952(91)90074-f.
Muscarinic receptors are altered by sulfhydryl reagents. Arsenic compounds, which have been used as insecticides, exert their toxic effects by combining with sulfhydryl groups. We compared the action of arsenicals and other sulfhydryl reagents on the muscarinic receptor from invertebrate and vertebrate species (locust and rat). Disulfide-reducing reagents dithiothreitol (DTT) and British Anti-Lewisite (BAL), but not arsenicals, inhibited [3H]quinuclidinyl benzilate ([3H]QNB) binding. However, after disulfide reduction, arsenicals caused a further inhibition of muscarinic binding. The effect of DTT + arsenicals was largely irreversible. The locust receptors were more sensitive to the action of both disulfide reagents either in the absence or presence of arsenicals than the rat receptors. The sulfhydryl reagent p-chloromercuric benzoate (PCMB) was more effective at inhibiting the locust receptors than the rat receptors, but addition of arsenicals did not cause further inhibition in either the locust or rat receptors. In locust, DTT + cacodylate and DTT + arsenite caused a reduction in the number of sites without modifying the affinity of [3H]QNB binding. In rat, DTT + arsenite caused a decrease in the affinity, while DTT + cacodylate caused a decrease in the affinity of [3H]QNB binding and its number of sites. Competition experiments after DTT + cacodylate showed that the IC50 and the Hill coefficient (nH) remained unchanged in the locust. In the rat, the IC50 for atropine was increased without alteration in the nH, and both parameters were increased for carbachol. These results are explained assuming that the binding site of the locust receptor has a disulfide group similar to that of the mammalian receptor, but that the hydrophobic interactions within the binding site are weaker in the locust receptor. The higher sensitivity of the insect receptor to sulfhydryl reagents could be of interest for developing methods of pest control.
毒蕈碱受体可被巯基试剂改变。曾用作杀虫剂的砷化合物通过与巯基结合发挥其毒性作用。我们比较了砷制剂和其他巯基试剂对无脊椎动物和脊椎动物(蝗虫和大鼠)毒蕈碱受体的作用。二硫键还原试剂二硫苏糖醇(DTT)和二巯基丙醇(BAL),而非砷制剂,抑制了[3H]喹核醇基苯甲酸酯([3H]QNB)结合。然而,在二硫键还原后,砷制剂导致毒蕈碱结合进一步受到抑制。DTT + 砷制剂的作用在很大程度上是不可逆的。无论是在不存在还是存在砷制剂的情况下,蝗虫受体对这两种二硫键试剂的作用都比大鼠受体更敏感。巯基试剂对氯汞苯甲酸(PCMB)在抑制蝗虫受体方面比抑制大鼠受体更有效,但添加砷制剂在蝗虫或大鼠受体中均未引起进一步抑制。在蝗虫中,DTT + 二甲胂酸和DTT + 亚砷酸盐导致位点数量减少,而未改变[3H]QNB结合的亲和力。在大鼠中,DTT + 亚砷酸盐导致亲和力降低,而DTT + 二甲胂酸导致[3H]QNB结合的亲和力及其位点数量降低。DTT + 二甲胂酸后的竞争实验表明,蝗虫中的半数抑制浓度(IC50)和希尔系数(nH)保持不变。在大鼠中,阿托品的IC50增加而nH未改变,对于卡巴胆碱,这两个参数均增加。假设蝗虫受体的结合位点具有与哺乳动物受体类似的二硫键基团,但结合位点内的疏水相互作用在蝗虫受体中较弱,这些结果就可以得到解释。昆虫受体对巯基试剂的更高敏感性可能对开发害虫防治方法具有重要意义。