Huang J, Casida J E
Department of Environmental Science, Policy, and Management, University of California, Berkeley, USA.
J Pharmacol Exp Ther. 1996 Dec;279(3):1191-6.
[3H]Ethynylbicycloorthobenzoate ([3H]EBOB) is a recently developed specific radioligand for the noncompetitive blocker site of the gamma-aminobutyric acid (GABA) receptor, which is the target of many polychlorocycloalkane and heterocyclic insecticides. This study characterizes [3H]EBOB binding and the action of insecticides on the GABA-gated chloride channel of cerebellar granule neurons in primary culture. Specific [3H]EBOB binding increases rapidly between days 3 and 7 and then remains constant for days 7 to 12 in culture. A single, high-affinity and saturable binding site is involved with Kd = 0.51 nM and Bmax = 239 fmol/mg protein. GABA and muscimol are 6- to 12-fold more potent as inhibitors of [3H]EBOB binding to membranes from cultured cerebellar granule neurons than from cerebellar tissue, possibly because of localization of specific subunits in the granule cells. GABA-stimulated 36Cl- influx is also inhibited by seven insecticidal compounds (including EBOB, 12-ketoendrin and alpha-endosulfan) as well as picrotoxinin and t-butylbicyclophosphorothionate with IC50 levels ranging from 290 to 15300 nM, which correlate well (r = 0.92) with their inhibitory potencies for [3H]EBOB binding (1 to 773 nM). These findings validate the use of [3H]EBOB binding in cultured cerebellar granule cells for pharmacological studies on insecticides and other toxicants acting at the noncompetitive blocker or coupled site of the GABAA receptor/chloride channel complex.
[3H]乙炔基双环原苯甲酸酯([3H]EBOB)是一种最近开发的针对γ-氨基丁酸(GABA)受体非竞争性阻断位点的特异性放射性配体,该受体是许多多氯环烷和杂环杀虫剂的作用靶点。本研究对[3H]EBOB结合以及杀虫剂对原代培养的小脑颗粒神经元GABA门控氯离子通道的作用进行了表征。在培养的第3天到第7天之间,特异性[3H]EBOB结合迅速增加,然后在培养的第7天到第12天保持恒定。单一的高亲和力和可饱和结合位点参与其中,解离常数(Kd)=0.51 nM,最大结合容量(Bmax)=239 fmol/mg蛋白质。GABA和蝇蕈醇作为[3H]EBOB与培养的小脑颗粒神经元膜结合的抑制剂,其效力比与小脑组织膜结合时高6至12倍,这可能是由于颗粒细胞中特定亚基的定位。七种杀虫化合物(包括EBOB、12-酮异狄氏剂和α-硫丹)以及印防己毒素和叔丁基双环磷硫代酸酯也抑制GABA刺激的36Cl-内流,半数抑制浓度(IC50)水平范围为290至15300 nM,这与其对[3H]EBOB结合的抑制效力(1至773 nM)具有良好的相关性(r = 0.92)。这些发现验证了在培养的小脑颗粒细胞中使用[3H]EBOB结合来进行关于作用于GABAA受体/氯离子通道复合体非竞争性阻断剂或偶联位点的杀虫剂和其他毒物的药理学研究。