Staley J K, Hearn W L, Ruttenber A J, Wetli C V, Mash D C
Department of Neurology, University of Miami School of Medicine, Florida.
J Pharmacol Exp Ther. 1994 Dec;271(3):1678-85.
Cocaine mediates its powerful reinforcement by binding to recognition sites on the dopamine (DA) transporter. The pharmacological identity of cocaine recognition sites and their relevance to dopamine transport function has remained unclear. Ligand binding studies with transport inhibitors and cocaine congeners have provided evidence for multiple sites or "states" of the DA transporter. The potent cocaine congener [3H]WIN 35,428 ((CFT), 2B-carbomethoxy-3 beta-(4-fluorophenyl)-tropane) has been shown to recognize high and low affinity binding sites on the DA transporter. We have used [3H]WIN 35,428 to map and quantify the high affinity cocaine recognition site on the DA transporter in victims of fatal cocaine overdose. Region-of-interest densitometric analysis of the autoradiograms demonstrated a 2- to 3-fold elevation in the apparent density of [3H]WIN 35,428 binding in particular sectors of the striatum from victims of cocaine overdose as compared to age-matched and drug-free control subjects. The most marked increase in [3H]WIN 35,428 binding was seen in the nucleus accumbens. The apparent increase in the density of high affinity sites was confirmed by saturation binding analysis of [3H]WIN 35,428 to putamen membranes. Saturation analysis revealed high and low affinity binding components with affinities (KD values) of 4.3 +/- 1.2 and 84.7 +/- 19.7 nM (mean +/- S.E.) and densities of 9.9 +/- 4.0 and 193.0 +/- 28.6 pmol/g of tissue, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
可卡因通过与多巴胺(DA)转运体上的识别位点结合来介导其强大的强化作用。可卡因识别位点的药理学特性及其与多巴胺转运功能的相关性仍不清楚。使用转运抑制剂和可卡因同系物进行的配体结合研究为DA转运体的多个位点或“状态”提供了证据。强效可卡因同系物[3H]WIN 35,428((CFT),2B-甲氧羰基-3β-(4-氟苯基)-托烷)已被证明可识别DA转运体上的高亲和力和低亲和力结合位点。我们使用[3H]WIN 35,428对致命可卡因过量受害者的DA转运体上的高亲和力可卡因识别位点进行定位和定量。对放射自显影片进行感兴趣区域光密度分析表明,与年龄匹配且无药物的对照受试者相比,可卡因过量受害者纹状体特定区域中[3H]WIN 35,428结合的表观密度升高了2至3倍。[3H]WIN 35,428结合增加最明显的是伏隔核。通过对[3H]WIN 35,428与壳核膜进行饱和结合分析,证实了高亲和力位点密度的明显增加。饱和分析显示高亲和力和低亲和力结合成分,其亲和力(KD值)分别为4.3±1.2和84.7±19.7 nM(平均值±标准误),密度分别为9.9±4.0和193.0±28.6 pmol/g组织。(摘要截断于250字)