Weiss F, Paulus M P, Lorang M T, Koob G F
Department of Neuropharmacology, Scripps Research Institute, La Jolla, California 92037.
J Neurosci. 1992 Nov;12(11):4372-80. doi: 10.1523/JNEUROSCI.12-11-04372.1992.
Repeated administration of cocaine enhances several of the behavioral and neurochemical responses to subsequent cocaine injections, an effect that has been attributed, in part, to decreased somatodendritic autoreceptor sensitivity of mesocorticolimbic dopamine (DA) neurons. Such changes in autoregulation may not only modify the direct effects of cocaine on extracellular DA levels but also result in tonically increased basal DA release in the terminal areas of the mesocorticolimbic DA system. The present study was therefore designed to investigate the effects of repeated cocaine administration on basal extracellular DA concentrations in the nucleus accumbens (NAC) using in vivo microdialysis procedures in halothane-anesthetized rats. We subsequently examined the relationship between basal DA levels and the increase in extracellular DA produced by an acute injection of cocaine, and determined whether this relationship was altered by prior, repeated exposure to cocaine. Rats received one daily intraperitoneal injection of cocaine (30 mg/kg) or its vehicle (saline) for 10 consecutive days. On days 1, 3, or 7 after termination of the repeated cocaine treatment, extracellular DA levels in the NAC were determined under basal conditions and following a single intraperitoneal cocaine challenge injection (10 mg/kg) in separate groups of rats. Repeated cocaine administration produced a substantial increase in basal DA release in the NAC that was most prominent on day 1 post-cocaine (mean +/- SEM: 10.7 +/- 2.55 nM vs 3.55 +/- 0.56 nM) but was no longer apparent on day 7 post-cocaine. Higher extracellular DA levels were also observed after cocaine challenge in rats that received repeated cocaine treatments. Similar to the increase in basal release, this effect was most pronounced on day 1 post-cocaine (23.6 +/- 4.36 nM vs 12.61 +/- 1.76 nM) but did not persist through day 7 post-cocaine.(ABSTRACT TRUNCATED AT 250 WORDS)
重复给予可卡因会增强对后续可卡因注射的多种行为和神经化学反应,这种效应部分归因于中脑皮质边缘多巴胺(DA)神经元的树突体自身受体敏感性降低。这种自身调节的变化不仅可能改变可卡因对细胞外DA水平的直接影响,还可能导致中脑皮质边缘DA系统终末区域的基础DA释放持续性增加。因此,本研究旨在使用体内微透析程序,研究在氟烷麻醉的大鼠中重复给予可卡因对伏隔核(NAC)基础细胞外DA浓度的影响。我们随后检查了基础DA水平与急性注射可卡因引起的细胞外DA增加之间的关系,并确定这种关系是否因先前重复接触可卡因而改变。大鼠连续10天每天腹腔注射一次可卡因(30mg/kg)或其溶媒(生理盐水)。在重复可卡因治疗终止后的第1、3或7天,在基础条件下以及在单独的大鼠组中腹腔注射一次可卡因激发剂量(10mg/kg)后,测定NAC中的细胞外DA水平。重复给予可卡因导致NAC中的基础DA释放大幅增加,在可卡因注射后第1天最为明显(平均值±标准误:10.7±2.55nM对3.55±0.56nM),但在可卡因注射后第7天不再明显。在接受重复可卡因治疗的大鼠中,可卡因激发后也观察到较高的细胞外DA水平。与基础释放增加相似,这种效应在可卡因注射后第1天最为明显(23.6±4.36nM对12.61±1.76nM),但在可卡因注射后第7天不再持续。(摘要截断于250字)