Ranaldi R, Pocock D, Zereik R, Wise R A
Center for Studies in Behavioral Neurobiology, Concordia University, Montreal, Québec, Canada H3G 1M5.
J Neurosci. 1999 May 15;19(10):4102-9. doi: 10.1523/JNEUROSCI.19-10-04102.1999.
Moment-to-moment fluctuations of nucleus accumbens dopamine (DA) were determined in rats self-administering or passively receiving "yoked" intravenous infusions of D-amphetamine. The initial lever presses of each session caused elevations in DA concentration, usually to an initial peak that was not maintained throughout the rest of the session. As the initial ("loading") injections were metabolized, DA levels dropped toward baseline but were sustained at elevated plateaus by subsequent lever pressing that was spaced throughout the remainder of the 3 hr sessions. During this period, DA levels fluctuated phasically, time-locked to the cycle of periodic lever pressing. Consistent with the known pharmacological actions and dynamics of amphetamine, peak DA elevations were seen approximately 10-15 min after each injection, and the mean DA level was at a low point in the phasic cycle at the time of each new lever press. During extinction periods when saline was substituted for amphetamine, DA levels dropped steadily toward baseline levels despite a dramatic increase in (now-unrewarded) lever pressing. Noncontingent injections during extinction reinstated lever-pressing behavior and increased nucleus accumbens DA concentrations. These data are consistent with the hypothesis that under the conditions of this experiment-during periods of amphetamine intoxication in well-trained animals-the timing of amphetamine self-administration comes primarily under the control of extracellular DA concentrations. The probability of lever pressing during the maintenance phase is highest when DA concentrations fall near a characteristic trigger point, a trigger point that is significantly elevated above baseline, and falls as DA concentrations fall below or increase above that trigger point.
在自行给药或被动接受“配对”静脉注射右旋苯丙胺的大鼠中,测定了伏隔核多巴胺(DA)的实时波动情况。每次实验开始时的杠杆按压会导致DA浓度升高,通常会达到一个初始峰值,但在实验剩余时间内该峰值无法持续保持。随着初始(“加载”)注射药物的代谢,DA水平降至基线附近,但随后在整个3小时实验剩余时间内间隔进行的杠杆按压使DA水平维持在升高的平台期。在此期间,DA水平呈现相位性波动,与周期性杠杆按压的周期时间锁定。与已知的苯丙胺药理作用和动力学一致,每次注射后约10 - 15分钟可观察到DA峰值升高,并且在每次新的杠杆按压时,平均DA水平处于相位周期的低点。在消退期,用生理盐水替代苯丙胺后,尽管(此时无奖励的)杠杆按压显著增加,但DA水平仍稳步降至基线水平。在消退期进行非条件注射可恢复杠杆按压行为并增加伏隔核DA浓度。这些数据与以下假设一致:在本实验条件下——在训练有素的动物苯丙胺中毒期间——苯丙胺自我给药的时间主要受细胞外DA浓度的控制。在维持阶段,当DA浓度降至接近一个特征触发点时,杠杆按压的概率最高,该触发点显著高于基线,并且随着DA浓度降至该触发点以下或升至该触发点以上而下降。