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多巴胺能药物对利血平诱导的大鼠海马θ波频率降低的影响。

Effect of dopaminergic drugs on the reserpine-induced lowering of hippocampal theta wave frequency in rats.

作者信息

Nakagawa T, Ukai K, Ohyama T, Gomita Y, Okamura H

机构信息

Central Research Institute, Kaken Pharmaceutical Co. Ltd., Kyoto, Japan.

出版信息

Nihon Shinkei Seishin Yakurigaku Zasshi. 2000 May;20(2):71-6.

Abstract

The effects of dopaminergic drugs on the lowering of hippocampal theta wave frequency induced by reserpine 1 mg/kg s.c. were examined. Sibutramine (monoamine reuptake inhibitor) 10 mg/kg p.o., methamphetamine (monoamine releaser) 1 mg/kg, quinpirole (dopamine D2 receptor agonist) 10 mg/kg i.p., and SKF 38393 (dopamine D1 receptor agonist) 10 mg/kg i.p. each antagonized the reserpine-induced lowering of hippocampal theta wave frequency in rats. Moreover, the combined administration of SKF 38393 1 mg/kg i.p. and quinpirole 1 mg/kg i.p. synergistically antagonized a reserpine-induced lowering of this frequency. Dosulepin, amitriptyline, and desipramine, which are weak inhibitors of dopamine reuptake, each had little effect on the reserpine-induced lowering of theta wave frequency at a dose of 40 mg/kg p.o. Furthermore, atropine (muscarinic anticholinergic drug) 20 mg/kg p.o. decreased theta wave power in the low-frequency range following a shift to the lower range by reserpine. A positive correlation was observed for each of the above drugs between a reversal of reserpine-induced lowering of theta wave frequency and a reversal of impairment of reserpine-induced conditioned avoidance responses (ACAR) in rats. These results suggest that the reserpine-induced lowering of hippocampal theta wave frequency plays a role in the impairment of reserpine-induced ACAR, and that dopamine D1 and D2 receptors play important roles in antagonizing this lowering of frequency.

摘要

研究了多巴胺能药物对1mg/kg皮下注射利血平所致海马θ波频率降低的影响。口服10mg/kg西布曲明(单胺再摄取抑制剂)、1mg/kg甲基苯丙胺(单胺释放剂)、腹腔注射10mg/kg喹吡罗(多巴胺D2受体激动剂)和腹腔注射10mg/kg SKF 38393(多巴胺D1受体激动剂)均可拮抗利血平引起的大鼠海马θ波频率降低。此外,腹腔注射1mg/kg SKF 38393和腹腔注射1mg/kg喹吡罗联合用药可协同拮抗利血平引起的该频率降低。多塞平、阿米替林和地昔帕明是多巴胺再摄取的弱抑制剂,口服40mg/kg剂量时,它们对利血平引起的θ波频率降低几乎没有影响。此外,口服20mg/kg阿托品(毒蕈碱抗胆碱能药物)可使利血平使低频范围的θ波功率降低后进一步向更低范围偏移。在大鼠中,上述每种药物使利血平引起的θ波频率降低的逆转与利血平引起的条件性回避反应(ACAR)损伤的逆转之间均观察到正相关。这些结果表明,利血平引起的海马θ波频率降低在利血平引起的ACAR损伤中起作用,并且多巴胺D1和D2受体在拮抗这种频率降低中起重要作用。

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