De Vry Jean, Rüdiger Jentzsch Klaus
CNS Research, Bayer Health Care, Aprather Weg 18a, D-42096 Wuppertal, Germany.
Eur J Pharmacol. 2002 Dec 20;457(2-3):147-52. doi: 10.1016/s0014-2999(02)02697-3.
BAY 38-7271 [(-)-(R)-3-(2-hydroxymethylindanyl-4-oxy)phenyl-4,4,4-trifluoro-1-sulfonate] is a novel, highly potent and selective cannabinoid CB(1)/CB(2) receptor agonist with neuroprotective properties. It was the aim of the present study to further confirm its cannabinoid CB(1) receptor agonist properties in a highly sensitive in vivo assay. Male Wistar rats (n=24) were trained to discriminate BAY 38-7271 (0.05 mg/kg, i.p., t-30 min) from vehicle in a fixed-ratio:10, food-reinforced two-lever standard procedure. The animals acquired the discrimination after a median number of 52 training sessions. BAY 38-7271 generalized dose-dependently when tested after different routes of administration (ED(50): 0.018 mg/kg, i.p.; 0.001 microg/kg, i.v.; 0.18 mg/kg, p.o.). A time-dependency study indicated that the cue (0.05 mg/kg, i.p.) was detectable between 15 min and 4 h, with a maximum of generalization obtained at 30 min after administration. Pretreatment with the selective cannabinoid CB(1) receptor antagonist SR 141716A [N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide hydrochloride] completely antagonized the effects of BAY 38-7271 (ID(50): 1.1 mg/kg, i.p.). Dose-dependent and complete generalization was also obtained after i.p. administration of the reference cannabinoid CB(1) receptor agonists HU-210 [(-)-11-OH-Delta(8)-tetrahydrocannabinol-dimethylheptyl, ED(50): 0.003 mg/kg], CP 55,940 [(-)-cis-3-[2-hydroxy-4(1,1-dimethyl-heptyl)phenyl]-trans-4-(3-hydroxypropyl)cyclohexanol, 0.007 mg/kg], WIN 55,212-2 [(R)-4,5-dihydro-2-methyl-4(4-morpholinylmethyl)-1-(1-naphtalenylcarbonyl)-6H-pyrrolo [3,2,1-ij] quinolin-6-one, 0.28 mg/kg] and (-)-Delta(9)-tetrahydrocannabinol (0.34 mg/kg). The present study confirms that BAY 38-7271 is a highly potent cannabinoid CB(1) receptor agonist in vivo.
BAY 38 - 7271 [(-)-(R)-3-(2 - 羟甲基茚满基 - 4 - 氧基)苯基 - 4,4,4 - 三氟 - 1 - 磺酸盐]是一种新型、高效且具有神经保护特性的选择性大麻素CB(1)/CB(2)受体激动剂。本研究的目的是在一项高灵敏度的体内试验中进一步确认其大麻素CB(1)受体激动剂特性。选用雄性Wistar大鼠(n = 24),通过固定比率为10、食物强化的双杠杆标准程序,训练它们区分BAY 38 - 7271(0.05 mg/kg,腹腔注射,提前30分钟给药)和溶剂。动物在经过中位数为52次训练后获得了辨别能力。不同给药途径后进行测试时,BAY 38 - 7271呈现出剂量依赖性的泛化现象(半数有效剂量:腹腔注射为0.018 mg/kg;静脉注射为0.001 μg/kg;口服为0.18 mg/kg)。一项时间依赖性研究表明,提示剂量(0.05 mg/kg,腹腔注射)在给药后15分钟至4小时内可检测到,给药后30分钟时泛化程度最高。用选择性大麻素CB(1)受体拮抗剂SR 141716A [N - (哌啶 - 1 - 基)-5 - (4 - 氯苯基)-1 - (2,4 - 二氯苯基)-4 - 甲基 - 1H - 吡唑 - 3 - 甲酰胺盐酸盐]进行预处理,可完全拮抗BAY 38 - 7271的作用(半数拮抗剂量:腹腔注射为1.1 mg/kg)。腹腔注射参考大麻素CB(1)受体激动剂HU - 210 [(-)-11 - 羟基 - Δ(8)-四氢大麻酚 - 二甲基庚基,半数有效剂量:0.003 mg/kg]、CP 55,940 [(-)-顺式 - 3 - [2 - 羟基 - 4(1,1 - 二甲基 - 庚基)苯基]-反式 - 4 - (3 - 羟丙基)环己醇,0.007 mg/kg]、WIN 55,212 - 2 [(R)-4,5 - 二氢 - 2 - 甲基 - 4(4 - 吗啉基甲基)-1 - (1 - 萘甲酰基)-6H - 吡咯并[3,2,1 - ij]喹啉 - 6 - 酮,0.28 mg/kg]和(-)-Δ(9)-四氢大麻酚(0.34 mg/kg)后,也获得了剂量依赖性和完全泛化现象。本研究证实BAY 38 - 7271在体内是一种高效的大麻素CB(1)受体激动剂。