Daegu Haany University, Daegu, South Korea.
Alcohol Clin Exp Res. 2010 Dec;34(12):2137-46. doi: 10.1111/j.1530-0277.2010.01310.x. Epub 2010 Sep 22.
Withdrawal from chronic ethanol enhances ventral tegmental area (VTA) GABA neuron excitability and reduces mesolimbic dopamine (DA) neurotransmission, which is suppressed by acupuncture at Shenmen (HT7) points (Zhao et al., 2006). The aim of this study was to evaluate the effects of HT7 acupuncture on VTA GABA neuron excitability, ethanol inhibition of VTA GABA neuron firing rate, and ethanol self-administration. A role for opioid receptors (ORs) in ethanol and acupuncture effects is also explored.
Using electrophysiological methods in mature rats, we evaluated the effects of HT7 stimulation and opioid antagonists on VTA GABA neuron firing rate. Using behavioral paradigms in rats, we evaluated the effects of HT7 stimulation and opioid antagonists on ethanol self-administration using a modification of the sucrose-fading procedure.
HT7 stimulation produced a biphasic modulation of VTA GABA neuron firing rate characterized by transient enhancement followed by inhibition and subsequent recovery in 5 minutes. HT7 inhibition of VTA GABA neuron firing rate was blocked by systemic administration of the nonselective μ-opioid receptor antagonist naloxone. HT7 stimulation significantly reduced ethanol suppression of VTA GABA neuron firing rate, which was also blocked by naloxone. HT7 acupuncture reduced ethanol self-administration without affecting sucrose consumption. Systemic administration of the δ-opioid receptor (DOR) antagonist naltrindole blocked ethanol suppression of VTA GABA neuron firing rate and significantly reduced ethanol self-administration without affecting sucrose consumption.
These findings suggest that DOR-mediated opioid modulation of VTA GABA neurons may mediate acupuncture's role in modulating mesolimbic DA release and suppressing the reinforcing effects of ethanol.
慢性乙醇戒断会增强腹侧被盖区(VTA)GABA 神经元的兴奋性,并减少中脑边缘多巴胺(DA)神经传递,而针刺神门(HT7)穴位会抑制这种作用(Zhao 等人,2006 年)。本研究旨在评估 HT7 针刺对 VTA GABA 神经元兴奋性、乙醇抑制 VTA GABA 神经元放电频率以及乙醇自身给药的影响。还探讨了阿片受体(ORs)在乙醇和针刺作用中的作用。
在成熟大鼠中使用电生理方法,我们评估了 HT7 刺激和阿片受体拮抗剂对 VTA GABA 神经元放电频率的影响。在大鼠行为范式中,我们使用蔗糖消退程序的修改来评估 HT7 刺激和阿片受体拮抗剂对乙醇自身给药的影响。
HT7 刺激对 VTA GABA 神经元放电频率产生双相调制作用,表现为短暂增强,随后抑制,5 分钟后恢复。HT7 抑制 VTA GABA 神经元放电频率被系统给予非选择性 μ 阿片受体拮抗剂纳洛酮阻断。HT7 刺激显著降低了乙醇对 VTA GABA 神经元放电频率的抑制作用,纳洛酮也阻断了这种作用。HT7 针刺降低了乙醇自身给药,而不影响蔗糖消耗。系统给予 δ 阿片受体(DOR)拮抗剂纳曲吲哚阻断了乙醇对 VTA GABA 神经元放电频率的抑制作用,并显著降低了乙醇自身给药,而不影响蔗糖消耗。
这些发现表明,DOR 介导的 VTA GABA 神经元阿片调节可能介导针刺在调节中脑边缘 DA 释放和抑制乙醇的强化作用中的作用。