Li Hongwu, Scuppa Giulia, Shen Qianwei, Masi Alessio, Nasuti Cinzia, Cannella Nazzareno, Ciccocioppo Roberto
College of Chemical Engineering, Changchun University of Technology, Changchun, China.
Pharmacology Unit, School of Pharmacy, University of Camerino, Camerino, Italy.
Front Psychiatry. 2019 Mar 29;10:176. doi: 10.3389/fpsyt.2019.00176. eCollection 2019.
Cocaine dependence is a psychiatric condition for which effective medications are still lacking. Published data indicate that an increase in nociceptin/orphanin FQ (N/OFQ) transmission by NOP receptor activation attenuates cocaine-induced place conditioning and the locomotor sensitization effects of cocaine. This suggests that the activation of the N/OFQ receptor (NOP) may attenuate the motivation for psychostimulants. To further explore this possibility, we investigated the effect of the potent and selective NOP receptor agonist Ro 64-6198 on cocaine intake under 1 h short access (ShA) and 6 h long access (LgA) operant self-administration conditions in rats. We used Marchigian Sardinian alcohol-preferring (msP) rats and Wistar control rats. msP rats were used because we recently found that this rat line, originally selected for excessive alcohol drinking and preference, exhibits a greater propensity to escalate cocaine self-administration following LgA training. msP rats are also characterized by innate overexpression of the N/OFQ-NOP system compared with Wistar rats. Wistar and msP rats both exhibited an increase in cocaine self-administration under LgA conditions, with a higher trend toward escalation in msP rats. In Wistar rats, the intraperitoneal administration of Ro 64-6198 (0. 1 and 3 mg/kg) significantly decreased ShA cocaine self-administration. In Wistar rats that underwent LgA cocaine self-administration training, Ro 64-6198 induced no significant effect either during the first hour of self-administration or after the entire 6 h session. In msP rats, Ro 64-6198 significantly reduced cocaine self-administration both under ShA conditions and in the first hour of the LgA session. At the end of the 6 h session, the effect of Ro 64-6198 was no longer observed in msP rats. The highest dose of Ro 64-6198 (3 mg/kg) did not affect saccharin self-administration in msP rats but reduced saccharin self-administration in Wistar rats. Altogether, these data suggest that NOP receptor activation attenuates cocaine self-administration, and this effect tends to be more pronounced in a rat line with innately higher NOP receptor expression and that more robustly escalates cocaine intake.
可卡因成瘾是一种仍缺乏有效药物治疗的精神疾病。已发表的数据表明,通过NOP受体激活增加痛敏肽/孤啡肽FQ(N/OFQ)传递可减弱可卡因诱导的条件性位置偏爱以及可卡因的运动敏化作用。这表明N/OFQ受体(NOP)的激活可能会减弱对精神兴奋剂的动机。为了进一步探究这种可能性,我们研究了强效选择性NOP受体激动剂Ro 64-6198在1小时短时间接触(ShA)和6小时长时间接触(LgA)操作性自身给药条件下对大鼠可卡因摄入量的影响。我们使用了马尔基安撒丁岛嗜酒(msP)大鼠和Wistar对照大鼠。使用msP大鼠是因为我们最近发现,该大鼠品系最初是因过度饮酒和偏爱酒精而被选育出来的,在LgA训练后表现出更强的可卡因自身给药量增加倾向。与Wistar大鼠相比,msP大鼠的特征还在于N/OFQ-NOP系统的先天性过表达。Wistar大鼠和msP大鼠在LgA条件下可卡因自身给药量均增加,msP大鼠的增加趋势更高。在Wistar大鼠中,腹腔注射Ro 64-6198(0.1和3mg/kg)显著降低了ShA可卡因自身给药量。在接受LgA可卡因自身给药训练的Wistar大鼠中,Ro 64-6198在自身给药的第一个小时或整个6小时实验过程中均未产生显著影响。在msP大鼠中,Ro 64-6198在ShA条件下以及LgA实验的第一个小时均显著降低了可卡因自身给药量。在6小时实验结束时,msP大鼠中不再观察到Ro 64-6198的作用。Ro 64-6198的最高剂量(3mg/kg)对msP大鼠的糖精自身给药量没有影响,但降低了Wistar大鼠的糖精自身给药量。总之,这些数据表明NOP受体激活可减弱可卡因自身给药,并且这种作用在具有先天性较高NOP受体表达且更强烈地增加可卡因摄入量的大鼠品系中往往更为明显。