Wang De-Quan, Wang Xin-Ling, Wang Chong-Yang, Wang Yuan, Li Su-Xia, Liu Ke-Zhi
Department of Psychiatry, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China; National Institute on Drug Dependence, Peking University, Beijing, 100191, China.
National Institute on Drug Dependence, Peking University, Beijing, 100191, China; Savaid Medical School, University of Chinese Academy of Sciences, Beijing 100191, China.
Behav Brain Res. 2019 May 2;363:61-69. doi: 10.1016/j.bbr.2019.01.035. Epub 2019 Jan 22.
Drug addiction is a widespread social problem, which not only brings adverse consequences to the human body, but also causes great burden to the society. However, it's still unclear how the long-term and sustained cocaine exposure will affect clock genes' expression in the reward related brain areas. We hypothesize that chronic cocaine exposure causes changes in the circadian rhythmic expression of clock genes in brain regions associated with reward, since previous studies have shown that cocaine use causes circadian disorders. Sprague-Dawley male rats were administrated with cocaine 20 mg/kg at ZT4 through intraperitoneal injection for 21 consecutive days. Twenty-four hours after the last cocaine administration brain samples were collected at 4-h intervals for 24 h (every 4h: ZT 0; ZT 4; ZT 8; ZT 12; ZT 16; ZT 20) to examine expression of rPer1, rPer2, rPer3, rCry, rBmal1 and rClock by quantitative real-time reverse-transcription polymerase chain reaction (RT-PCR). We found that chronic cocaine exposure to rats resulted in significantly disturbances in expression of clock genes in reward related brain areas compared to saline - treated rats. In cocaine-treated rats, rPer1 expression in the suprachiasmatic nucleus (SCN), prefrontal cortex (PFC) and ventral tegmental area (VTA); rPer2 expression in the nucleus accumbens (NAc) shell and hippocampus; rPer3 expression in the NAc core; rCry expression in the SCN and PFC; rBmal1 expression in the SCN and NAc core showed robust circadian rhythms that were essentially identical to those in control rats. However, robust circadian rhythm in rPer1 expression in the SCN and rCry expression in the PFC was nearly completely phase - reversed in cocaine-treated rats. A blunting of circadian oscillations of rPer1 expression occurred in the NAc core and shell and hippocampus; of rPer2 expression occurred in the SCN, PFC, NAc core and hippocampus; of rPer3 expression occurred in the SCN, PFC, NAc shell, hippocampus and VTA; of rCry expression occurred in the NAc core and shell, hippocampus and VTA; of rBmal1 expression occurred in the PFC, NAc shell, hippocampus and VTA in cocaine - treated rats. These rhythm changes accompanied by significant increase in rPer1, rPer2, rPer3 and rBmal1 in the PFC, rPer1, rPer2 and rBmal1 in the hippocampus; significant decrease in rPer2, rPer3 and rCry in the SCN, rPer3, rCry, rBmal1 and rClock in the NAc core compared to control rats. rClock expression in cocaine - treated rats showed no rhythmic change, identical to control rats.These results suggest that chronic cocaine exposure results in disturbances in clock genes' expression in reward related areas.
药物成瘾是一个普遍存在的社会问题,它不仅给人体带来不良后果,也给社会造成巨大负担。然而,长期持续接触可卡因如何影响与奖赏相关脑区中生物钟基因的表达仍不清楚。我们推测,慢性可卡因暴露会导致与奖赏相关脑区中生物钟基因的昼夜节律表达发生变化,因为先前的研究表明使用可卡因会导致昼夜节律紊乱。通过腹腔注射,在ZT4给雄性Sprague-Dawley大鼠连续21天给予20mg/kg可卡因。在最后一次给予可卡因24小时后,每隔4小时收集脑样本,共收集24小时(每4小时:ZT 0;ZT 4;ZT 8;ZT 12;ZT 16;ZT 20),通过定量实时逆转录聚合酶链反应(RT-PCR)检测rPer1、rPer2、rPer3、rCry、rBmal1和rClock的表达。我们发现,与生理盐水处理的大鼠相比,慢性可卡因暴露导致大鼠与奖赏相关脑区中生物钟基因的表达出现明显紊乱。在可卡因处理的大鼠中,视交叉上核(SCN)、前额叶皮质(PFC)和腹侧被盖区(VTA)中的rPer1表达;伏隔核(NAc)壳和海马中的rPer2表达;NAc核心中的rPer3表达;SCN和PFC中的rCry表达;SCN和NAc核心中的rBmal1表达呈现出与对照大鼠基本相同的强劲昼夜节律。然而,在可卡因处理的大鼠中,SCN中rPer1的表达和PFC中rCry的表达的强劲昼夜节律几乎完全相位反转。在NAc核心、壳和海马中,rPer1表达的昼夜振荡减弱;在SCN、PFC、NAc核心和海马中,rPer2表达的昼夜振荡减弱;在SCN、PFC、NAc壳、海马和VTA中,rPer3表达的昼夜振荡减弱;在NAc核心、壳、海马和VTA中,rCry表达的昼夜振荡减弱;在PFC、NAc壳、海马和VTA中,rBmal1表达的昼夜振荡减弱。与对照大鼠相比,这些节律变化伴随着PFC中rPer1、rPer2、rPer3和rBmal1,海马中rPer1、rPer2和rBmal1的显著增加;SCN中rPer2、rPer3和rCry,NAc核心中rPer3、rCry、rBmal1和rClock的显著减少。可卡因处理的大鼠中rClock的表达没有节律变化,与对照大鼠相同。这些结果表明,慢性可卡因暴露导致与奖赏相关区域中生物钟基因的表达紊乱。