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针刺调节 mPFC-LHb 通路抑制可卡因的精神运动活性。

Mediation of mPFC-LHb pathway in acupuncture inhibition of cocaine psychomotor activity.

机构信息

Department of Physiology, College of Korean Medicine, Daegu Haany University, Daegu, South Korea.

Department of Oral Physiology, School of Dentistry, Kyungpook National University, Daegu, South Korea.

出版信息

Addict Biol. 2023 Oct;28(10):e13321. doi: 10.1111/adb.13321.

Abstract

The medial prefrontal cortex (mPFC) and the lateral habenula (LHb) play roles in drug addiction and cognitive functions. Our previous studies have suggested that acupuncture at Shenmen (HT7) points modulates mesolimbic reward system in order to suppress drug-induced addiction behaviours. To explore whether an mPFC-LHb circuit mediates the inhibitory effects of acupuncture on addictive behaviours, we examined the projection from mPFC to LHb, excitation of mPFC neurons during acupuncture stimulation, the effects of optogenetic modulation of mPFC-LHb on HT7 inhibition of cocaine-induced locomotion and the effect of mPFC lesion on HT7 inhibition of nucleus accumbens (NAc) dopamine release. Acupuncture was applied at bilateral HT7 points for 20 s, and locomotor activity was measured in male Sprague-Dawley rats. Although cocaine injection significantly increased locomotor activity, HT7 acupuncture suppressed the cocaine-induced locomotion. The inhibitory effect of HT7 on cocaine-enhanced locomotion was blocked by optogenetic silencing of the mPFC-LHb circuit. In vivo extracellular recordings showed that HT7 acupuncture evoked an increase in the action potentials of mPFC neurons. Optopatch experiment proved glutamatergic projections from mPFC to LHb. HT7 acupuncture suppressed NAc dopamine release following cocaine injection, which was blocked by electrolytic lesion of mPFC. These results suggest the mediation of mPFC-LHb circuit in the inhibitory effects of acupuncture on cocaine psychomotor activity in rats.

摘要

内侧前额叶皮层(mPFC)和外侧缰核(LHb)在药物成瘾和认知功能中发挥作用。我们之前的研究表明,针刺神门(HT7)穴位调节中脑边缘奖赏系统,以抑制药物引起的成瘾行为。为了探讨 mPFC-LHb 回路是否介导针刺对成瘾行为的抑制作用,我们检查了 mPFC 投射到 LHb 的情况,针刺刺激时 mPFC 神经元的兴奋情况,mPFC-LHb 的光遗传调节对 HT7 抑制可卡因诱导的运动的影响,以及 mPFC 损伤对 HT7 抑制伏隔核(NAc)多巴胺释放的影响。双侧 HT7 点针刺 20s,测量雄性 Sprague-Dawley 大鼠的运动活性。尽管可卡因注射显著增加了运动活性,但 HT7 针刺抑制了可卡因诱导的运动。HT7 对可卡因增强运动的抑制作用被 mPFC-LHb 回路的光遗传沉默所阻断。在体细胞外记录显示,HT7 针刺引起 mPFC 神经元动作电位的增加。光贴实验证明了 mPFC 到 LHb 的谷氨酸能投射。HT7 针刺抑制了可卡因注射后 NAc 多巴胺的释放,而 mPFC 损伤则阻断了这一释放。这些结果表明,mPFC-LHb 回路介导了针刺对大鼠可卡因精神运动活动的抑制作用。

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