Pharmacokinetics-Biopharmaceutics Laboratory, Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland 21201, USA.
J Pharmacol Exp Ther. 2010 Jun;333(3):854-64. doi: 10.1124/jpet.109.165084. Epub 2010 Mar 12.
The recent discovery of novel high-affinity and selective dopamine D3 receptor (DA D3R) antagonists and partial agonists has provided tools with which to further elucidate the role DA D3R plays in substance abuse. The present study was conducted to evaluate the transport, metabolism, pharmacokinetics, and brain uptake of the DA D3R-selective fluorenyl amides, NGB 2904 [N-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butyl)-9H-fluorene-2-carboxamide] fumarate) and JJC 4-077 [N-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)-3-hydroxybutyl)-9H-fluorene-2-carboxamide hydrochloride], and the 2-pyridylphenyl amides, CJB 090 [N-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butyl)-4-(pyridine-2-yl)benzamide hydrochloride] and PG 01037 [N-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)-trans-but-2-enyl)-4-(pyridine-2-yl)benzamide hydrochloride], all of which have been studied in animal models of psychostimulant abuse. Additional screening with a panel of human and rat Supersomes was performed for NGB 2904 and PG 01037. Drug-stimulated ATPase activation assays and bidirectional transport and efflux assays were used to test for substrate specificity of NGB 2904 and PG 01037 for human and rat efflux transporters. All compounds exhibited moderate elimination half-lives, ranging from 1.49 to 3.27 h, and large volumes of distribution (5.95-14.19 l/kg). The brain-to-plasma ratios ranged from 2.93 to 11.81 and were higher than those previously reported for cocaine. Brain exposure levels of NGB 2904 and PG 01037 were significantly reduced after intraperitoneal administration compared with intravenous administration. The metabolism of these compounds was mediated primarily by CYP3A subfamilies. PG 01037 was a P-glycoprotein-transported substrate. Higher doses of these compounds are often required for in vivo action, suggesting decreased bioavailability via extravascular administration that may be attributed to high drug efflux and hepatic metabolism. These studies provide important preclinical information for optimization of next-generation D3R selective agents for the treatment of drug addiction.
最近发现了新型高亲和力和选择性多巴胺 D3 受体 (DA D3R) 拮抗剂和部分激动剂,为进一步阐明 DA D3R 在物质滥用中的作用提供了工具。本研究旨在评估 DA D3R 选择性氟苯酰胺 NGB 2904[ N-(4-(4-(2,3-二氯苯基)哌嗪-1-基)丁基)-9H-芴-2-甲酰胺]富马酸盐)和 JJC 4-077[N-(4-(4-(2,3-二氯苯基)哌嗪-1-基)-3-羟基丁基)-9H-芴-2-甲酰胺盐酸盐]以及 2-吡啶基苯甲酰胺 CJB 090[N-(4-(4-(2,3-二氯苯基)哌嗪-1-基)丁基)-4-(吡啶-2-基)苯甲酰胺盐酸盐]和 PG 01037[N-(4-(4-(2,3-二氯苯基)哌嗪-1-基)-反式-丁-2-烯基)-4-(吡啶-2-基)苯甲酰胺盐酸盐],这些化合物都在精神兴奋剂滥用的动物模型中进行了研究。还对 NGB 2904 和 PG 01037 进行了人类和大鼠 Supersomes 小组的额外筛选。使用药物刺激的 ATP 酶激活测定和双向转运和外排测定来测试 NGB 2904 和 PG 01037 对人和大鼠外排转运蛋白的底物特异性。所有化合物均表现出中等的消除半衰期,范围为 1.49 至 3.27 小时,并且分布体积较大(5.95-14.19 l/kg)。脑-血浆比范围为 2.93 至 11.81,高于先前报道的可卡因。与静脉内给药相比,腹腔内给予 NGB 2904 和 PG 01037 后,其脑暴露水平明显降低。这些化合物的代谢主要由 CYP3A 亚家族介导。PG 01037 是 P-糖蛋白转运的底物。这些化合物的体内作用通常需要更高的剂量,表明通过血管外给药导致生物利用度降低,这可能归因于高药物外排和肝脏代谢。这些研究为优化新一代 D3R 选择性药物治疗药物成瘾提供了重要的临床前信息。