Rao Kalyan N, Sentir Alena M, Engleman Eric A, Bell Richard L, Hulvershorn Leslie A, Breier Alan, Chambers R Andrew
Department of Psychiatry, Indiana University School of Medicine, Indianapolis, IN, USA.
IU Neuroscience Research Center, Indianapolis, IN, USA.
Psychopharmacology (Berl). 2016 Dec;233(23-24):3933-3945. doi: 10.1007/s00213-016-4421-8. Epub 2016 Sep 17.
Prefrontal cortical (PFC)-hippocampal-striatal circuits, interconnected via glutamatergic signaling, are dysfunctional in mental illnesses that involve addiction vulnerability.
In healthy and neurodevelopmentally altered rats, we examined how Radial Arm Maze (RAM) performance estimates addiction vulnerability, and how starting a glutamatergic modulating agent, N-acetyl cysteine (NAC) in adolescence alters adult mental illness and/or addiction phenotypes.
Rats with neonatal ventral hippocampal lesions (NVHL) vs. SHAM-operated controls were randomized to NAC vs. saline in adolescence followed by cognitive testing (RAM) in early adulthood and then cocaine behavioral sensitization (experiment 1; n = 80) or nicotine self-administration (experiment 2; n = 12).
In experiment 1, NVHL rats showed over-consumption of food (Froot-Loops (FL)) baiting the RAM with poor working memory (low-arm entries to repeat (ETR)), producing an elevated FL to ETR ratio ("FLETR"; p < 0.001). FLETR was the best linear estimator (compared to FL or ETR) of magnitude of long-term cocaine sensitization (R = 0.14, p < 0.001). NAC treatment did not alter FL, ETR, FLETR, or cocaine sensitization. In experiment 2, FLETR also significantly and uniquely correlated with subsequent drug seeking during nicotine-induced reinstatement after extinction of nicotine self-administration (R = 0.47, p < 0.01). NAC did not alter RAM performance, but significantly reversed NVHL-induced increases in nicotine seeking during extinction and reinstatement.
These findings demonstrate the utility of animal models of mental illness with addiction vulnerability for developing novel diagnostic measures of PFC-hippocampal-striatal circuit dysfunction that may reflect addiction risk. Such tests may direct pharmacological treatments prior to adulthood and addictive drug exposure, to prevent or treat adult addictions.
前额叶皮质(PFC)-海马体-纹状体回路通过谷氨酸能信号相互连接,在涉及成瘾易感性的精神疾病中功能失调。
在健康大鼠和神经发育改变的大鼠中,我们研究了放射状臂迷宫(RAM)任务表现如何评估成瘾易感性,以及在青春期开始使用谷氨酸能调节剂N-乙酰半胱氨酸(NAC)如何改变成年期精神疾病和/或成瘾表型。
将新生期腹侧海马损伤(NVHL)大鼠与假手术对照组随机分为青春期接受NAC或生理盐水处理,随后在成年早期进行认知测试(RAM),然后进行可卡因行为敏化实验(实验1;n = 80)或尼古丁自我给药实验(实验2;n = 12)。
在实验1中,NVHL大鼠表现出对食物(水果圈(FL))的过度消耗,在RAM任务中工作记忆较差(低臂重复进入次数(ETR)),导致FL与ETR比值升高(“FLETR”;p < 0.001)。FLETR是长期可卡因敏化程度的最佳线性估计指标(与FL或ETR相比)(R = 0.14,p < 0.001)。NAC处理未改变FL、ETR、FLETR或可卡因敏化。在实验2中,FLETR也与尼古丁自我给药消退后尼古丁诱导的复吸期间随后的觅药行为显著且独特相关(R = 0.47,p < 0.01)。NAC未改变RAM任务表现,但显著逆转了NVHL诱导的尼古丁消退和复吸期间觅药行为的增加。
这些发现证明了具有成瘾易感性的精神疾病动物模型在开发可能反映成瘾风险的PFC-海马体-纹状体回路功能障碍新诊断措施方面的实用性。此类测试可在成年期和成瘾药物暴露之前指导药物治疗,以预防或治疗成人成瘾。