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Preventing morphine reinforcement with high-frequency deep brain stimulation of the lateral hypothalamic area

机译:用高频深脑刺激侧面下丘脑区域预防吗啡增强

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Deep brain stimulation (DBS) has been proposed as a promising intervention for patients with treatment-refractory substance use disorder. Here, we investigated if high-frequency DBS in the lateral hypothalamic area (LHA) could affect drug-induced reinforcement. Rats were bilaterally implanted with bipolar stimulation electrodes in the LHA and trained to the morphine conditioned place preference. DBS (monophasic square pulses, 130 Hz, 100-microsecond pulse duration and 150 mu A) was applied during the morphine-pairing trials (30 minutes daily for 4 days) or drug-free postconditioning test (15 minutes) to determine its effect on the acquisition or expression of morphine reward, respectively. LHA DBS during morphine-conditioning trials blocked subsequent preference for the drug-associated context. In contrast, DBS in the postconditioning phase failed to inhibit expression of morphine-induced conditioned place preference. These results were further controlled by ruling out significant changes by DBS in physical performance and anxiety-like behavior as measured by an open field test and by precluding anhedonia-like behavior as measured by sucrose consumption test. Our results suggest that LHA DBS can prevent development of morphine reward without diminishing the motivation for naturally rewarding stimuli. Therefore, the LHA could be a potential target for research in the field of DBS-based treatment of intractable substance use disorder. Further studies will be necessary to assess the translatability of these findings to the clinic.
机译:已经提出了深脑刺激(DBS)作为治疗难治物质使用障碍患者的有希望的干预。在这里,我们研究了侧丘脑区域(LHA)中的高频DBS,可能会影响药物诱导的增强。大鼠在LHA中双侧植入双极刺激电极并培养到吗啡条件的地方偏好。在吗啡配对试验期间(每天30分钟为4天)或无药后处理试验(15分钟),施用DBS(单级方脉冲,130Hz,100微秒脉冲持续时间和150μma),以确定其对其效果Myphine奖励的收购或​​表达。吗啡调节试验期间的LHA DBS阻止了随后对药物相关背景的偏好。相反,后后处理阶段的DBS未能抑制吗啡诱导的条件偏好的表达。通过通过开放场测试测量的物理性能和焦虑形式的DBS在物理性能和焦虑的行为中的显着变化以及通过蔗糖消耗测试测量的抑制厌氧样行为来进一步控制这些结果。我们的研究结果表明,LHA DBS可以防止Muphine奖励的发展,而不会减少自然有益刺激的动机。因此,LHA可以是在顽固物质使用障碍的基于DBS的治疗领域研究的潜在目标。进一步的研究是必要的,以评估这些发现对诊所的可相互性。

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