Tsukada Hideo, Miyasato Katsumasa, Kakiuchi Takeharu, Nishiyama Shingo, Harada Norihiro, Domino Edward F
Central Research Laboratory, Hamamatsu Photonics K.K., 5000 Hirakuchi, Hamakita, Shizuoka 434-8601, Japan.
Synapse. 2002 Sep 15;45(4):207-12. doi: 10.1002/syn.10102.
Although a very large literature exists on the in vitro, ex vivo, and in vivo effects of nicotine on dopamine release in rodents, similar data in primates are scant. This study was initiated to compare methamphetamine to nicotine given i.v. to normal unanesthetized monkeys using positron emission tomography (PET) techniques. Release of dopamine in the striatum using [(11)C]raclopride was determined indirectly in four nicotine-naïve adult Macaca mulatta monkeys under conscious and isoflurane-anesthetized conditions using high-resolution PET. [(11)C]Raclopride was given i.v. as a bolus injection followed by continuous infusion with steady state over 30-45 min. Nicotine bitartrate was then given as a bolus plus infusion for 30 min in doses of 32 microg/kg + 0.8 microg/kg/min or 100 microg/kg + 2.53 microg/kg/min as base. The larger doses of nicotine caused significant cardiovascular effects; these doses did not displace [(11)C]raclopride binding in either dorsal or ventral striatum under the anesthetized conscious condition. In contrast, isoflurane-anesthesia induced a slight but significant dose-dependent reduction of [(11)C]raclopride binding by nicotine even at the same doses used in the anesthetized condition. Methamphetamine in bolus doses of 0.1, 0.3, and 1.0 mg/kg i.v. under conscious condition caused a significant displacement of [(11)C]raclopride and isoflurane-anesthesia facilitated the displacement induced by nicotine. These results indicate that nicotine, in high tobacco-smoking-related doses, does not release sufficient brain dopamine to displace [(11)C]raclopride in the striatum in the awake and fully conscious state, in contrast to small doses of methamphetamine.
尽管关于尼古丁对啮齿动物多巴胺释放的体外、离体和体内效应已有大量文献,但灵长类动物的类似数据却很少。本研究旨在使用正电子发射断层扫描(PET)技术,将静脉注射甲基苯丙胺与尼古丁给予正常未麻醉的猴子进行比较。在清醒和异氟烷麻醉条件下,使用高分辨率PET间接测定了四只未接触过尼古丁的成年恒河猴纹状体中多巴胺的释放情况,方法是使用[(11)C]雷氯必利。[(11)C]雷氯必利通过静脉推注给药,随后在30 - 45分钟内持续输注以达到稳态。然后以32微克/千克 + 0.8微克/千克/分钟或100微克/千克 + 2.53微克/千克/分钟(以碱基计)的剂量静脉推注加输注酒石酸尼古丁30分钟。较大剂量的尼古丁会引起显著的心血管效应;在清醒麻醉条件下,这些剂量并未使[(11)C]雷氯必利在背侧或腹侧纹状体中的结合发生位移。相比之下,即使在麻醉条件下使用相同剂量,异氟烷麻醉也会导致尼古丁使[(11)C]雷氯必利的结合略有但显著的剂量依赖性降低。在清醒条件下,静脉注射0.1、0.3和1.0毫克/千克的甲基苯丙胺会显著取代[(11)C]雷氯必利,而异氟烷麻醉则促进了尼古丁诱导的取代作用。这些结果表明,与小剂量的甲基苯丙胺相比,与高吸烟量相关的尼古丁剂量在清醒和完全有意识的状态下,不会释放足够的脑内多巴胺来取代纹状体中的[(11)C]雷氯必利。