Department of Pharmaceutical Care and Health Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka, Kita-ku, Okayama 700-8530, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 2010 Aug;382(2):151-8. doi: 10.1007/s00210-010-0521-x. Epub 2010 Jun 6.
The dopamine reuptake inhibitor bupropion has clinically been proven to improve depression and treatment-resistant depression. We examined its influence on the duration of immobility during the forced swim test in adrenocorticotropic hormone (ACTH)-treated rats and further analyzed the possible role of dopamine receptors in this effect. Additionally, the mechanism by which bupropion acts in this model was explored specifically in relation to the site of action through the use of microinjections into the medial prefrontal cortex and nucleus accumbens. Bupropion significantly decreased the duration of immobility in normal and ACTH-treated rats. This effect was blocked by D2 and D3 receptor antagonists in normal rats. Furthermore, infusions of bupropion into the nucleus accumbens, but not medial prefrontal cortex, decreased the immobility of normal and ACTH-treated rats during the forced swim test. Bupropion treatment plus repeated ACTH treatment significantly increased the extracellular dopamine concentration. These findings suggest the antidepressant-like effect of bupropion to be related to levels of dopamine in the rat nucleus accumbens.
多巴胺再摄取抑制剂安非他酮已被临床证明可改善抑郁和治疗抵抗性抑郁。我们研究了它对促肾上腺皮质激素(ACTH)处理的大鼠强迫游泳试验中不动时间的影响,并进一步分析了多巴胺受体在这种作用中的可能作用。此外,通过将微注射到伏隔核和前额叶皮质中来专门研究安非他酮在该模型中的作用机制,以探讨其作用部位。安非他酮可显著缩短正常和 ACTH 处理大鼠的不动时间。该作用在正常大鼠中被 D2 和 D3 受体拮抗剂阻断。此外,安非他酮输注到伏隔核而不是前额叶皮质可减少正常和 ACTH 处理大鼠在强迫游泳试验中的不动时间。安非他酮治疗加重复 ACTH 治疗可显著增加细胞外多巴胺浓度。这些发现表明,安非他酮的抗抑郁样作用与大鼠伏隔核中的多巴胺水平有关。