Department of Pharmacology and Toxicology, School of Medicine, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Integrative Life Sciences Doctoral Program, Virginia Commonwealth University, Richmond, VA, 23284, USA.
Psychopharmacology (Berl). 2023 Apr;240(4):969-981. doi: 10.1007/s00213-023-06340-8. Epub 2023 Feb 20.
Drug self-administration and intracranial self-stimulation (ICSS) are two preclinical behavioral procedures used to predict abuse potential of drugs, and abuse-related drug effects in both procedures are thought to depend on increased mesolimbic dopamine (DA) signaling. Drug self-administration and ICSS yield concordant metrics of abuse potential across a diverse range of drug mechanisms of action. The "rate of onset," defined as the velocity with which a drug produces its effect once administered, has also been implicated as a determinant of abuse-related drug effects in self-administration procedures, but this variable has not been systematically examined in ICSS. Accordingly, this study compared ICSS effects produced in rats by three DA transporter inhibitors that have different rates of onset (fastest to slowest: cocaine, WIN-35428, RTI-31) and that produced progressively weaker metrics of abuse potential in a drug self-administration procedure in rhesus monkeys. Additionally, in vivo photometry using the fluorescent DA sensor dLight1.1 targeted to the nucleus accumbens (NAc) was used to assess the time course of extracellular DA levels as a neurochemical correlate of behavioral effects. All three compounds produced ICSS facilitation and increased DA levels assessed by dLight. In both procedures, the rank order of onset rate was cocaine > WIN-35428 > RTI-31; however, in contrast to monkey drug self-administration results, maximum effects did not differ across compounds. These results provide additional evidence that drug-induced increases in DA drive ICSS facilitation in rats and illustrate the utility of both ICSS and photometry to evaluate the time course and magnitude of abuse-related drug effects in rats.
药物自我给药和颅内自我刺激(ICSS)是两种用于预测药物滥用潜力的临床前行为程序,这两种程序中的与滥用相关的药物效应被认为依赖于中脑边缘多巴胺(DA)信号的增加。药物自我给药和 ICSS 在广泛的药物作用机制下产生一致的滥用潜力指标。“起效速度”定义为药物一旦给药产生效果的速度,也被认为是自我给药程序中与滥用相关的药物效应的决定因素,但这一变量在 ICSS 中尚未得到系统研究。因此,本研究比较了三种具有不同起效速度(最快到最慢:可卡因、WIN-35428、RTI-31)的 DA 转运体抑制剂在大鼠中产生的 ICSS 效应,这些抑制剂在恒河猴的药物自我给药程序中产生了逐渐减弱的滥用潜力指标。此外,使用针对伏隔核(NAc)的荧光 DA 传感器 dLight1.1 的体内光度法评估了作为行为效应神经化学相关物的细胞外 DA 水平的时间过程。所有三种化合物均产生了 ICSS 促进作用,并增加了 dLight 评估的 DA 水平。在这两种程序中,起效速度的顺序为可卡因>WIN-35428>RTI-31;然而,与恒河猴药物自我给药结果相反,最大效应在化合物之间没有差异。这些结果提供了额外的证据,证明药物引起的 DA 增加驱动了大鼠的 ICSS 促进作用,并说明了 ICSS 和光度法在评估大鼠与滥用相关的药物效应的时间过程和幅度方面的实用性。