de Souza Silva Maria A, Mattern Claudia, Decheva Cvetana, Huston Joseph P, Sadile Adolfo G, Beu Markus, Müller H-W, Nikolaus Susanne
Center for Behavioral Neuroscience, Institute of Experimental Psychology, Heinrich-Heine University Düsseldorf, Germany.
M et P Pharma AGEmmetten, Switzerland; Oceanographic Center, Nova Southeastern UniversityFort Lauderdale, FL, USA.
Front Behav Neurosci. 2016 Apr 22;10:80. doi: 10.3389/fnbeh.2016.00080. eCollection 2016.
Dopamine (DA), which does not cross the blood-brain barrier, has central and behavioral effects when administered via the nasal route. Neither the mechanisms of central action of intranasal dopamine (IN-DA), nor its mechanisms of diffusion and transport into the brain are well understood. We here examined whether IN-DA application influences dopamine transporter (DAT) binding in the dorsal striatum and assessed the extent of binding in relation to motor and exploratory behaviors. We hypothesized that, based on the finding of increased extracellular DA in the striatum induced by application of IN-DA, binding of [(123)I]FP-CIT to the DAT should be decreased due to competition at the receptor.
Rats were administered 3 mg/kg IN-DA and vehicle (VEH), with IN-DA injection either preceding or following VEH. Then motor and exploratory behaviors (traveled distance, velocity, center time, sitting, rearing, head-shoulder motility, grooming) were assessed for 30 min in an open field prior to administration of [(123)I]FP-CIT. DAT binding after IN-DA and VEH was measured with small animal SPECT 2 h following administration of the radioligand.
(1) After IN-DA application, striatal DAT binding was significantly lower as compared to VEH, indicating that the nasally delivered DA had central action and increased DA levels comparable to that found previously with L-DOPA administration; and (2) DAT binding in response to intranasal VEH was lower when IN-DA application preceded VEH treatment. This finding is suggestive of Pavlovian conditioning of DA at the level of the DAT, since the DA treatment modified (decreased) the binding in response to the subsequent VEH treatment. VEH treatment also reduced motor and exploratory behaviors more when applied before, as compared to when it followed IN-DA application, also indicative of behavioral Pavlovian conditioning akin to that found upon application of various psychostimulant drugs.
(a) demonstrate a direct central action of intranasally applied DA on the DAT in the dorsal striatum, indicating enhanced DA availability; and (b) provide first evidence of a Pavlovian conditioned DA response at the DAT. The latter results have relevance to understanding neurochemical mechanisms that underlie placebo action in the treatment of Parkinsonian patients.
多巴胺(DA)不能穿过血脑屏障,经鼻腔给药时具有中枢和行为效应。鼻内多巴胺(IN-DA)的中枢作用机制及其向脑内的扩散和转运机制均尚未完全明确。我们在此研究了应用IN-DA是否会影响背侧纹状体中多巴胺转运体(DAT)的结合,并评估了与运动和探索行为相关的结合程度。我们假设,基于应用IN-DA后纹状体细胞外DA增加的发现,由于在受体处的竞争,[(123)I]FP-CIT与DAT的结合应会减少。
给大鼠分别给予3 mg/kg的IN-DA和赋形剂(VEH),IN-DA注射可先于或后于VEH注射。然后在给予[(123)I]FP-CIT之前,在开放场中评估大鼠30分钟的运动和探索行为(行进距离、速度、在中央区域停留时间、静坐、站立、头肩活动、梳理毛发)。在给予放射性配体2小时后,用小动物单光子发射计算机断层扫描(SPECT)测量IN-DA和VEH处理后的DAT结合情况。
(1)应用IN-DA后,纹状体DAT结合显著低于VEH组,表明经鼻腔给药的DA具有中枢作用,且DA水平升高,与先前给予左旋多巴(L-DOPA)时的情况相当;(2)当IN-DA应用先于VEH处理时,对鼻内VEH的DAT结合较低。这一发现提示在DAT水平上存在多巴胺的巴甫洛夫条件反射,因为多巴胺处理改变了(降低了)对随后VEH处理的结合。与在IN-DA应用之后应用相比,在之前应用VEH时,VEH处理对运动和探索行为的抑制作用也更强,这也表明存在类似于应用各种精神兴奋剂药物时所发现的行为巴甫洛夫条件反射。
(a)证明了经鼻腔应用的多巴胺对背侧纹状体中的DAT具有直接中枢作用,表明多巴胺的可利用性增强;(b)提供了在DAT处存在巴甫洛夫条件性多巴胺反应的首个证据。后一结果对于理解帕金森病患者治疗中安慰剂作用的神经化学机制具有重要意义。