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D1 或 D2 受体刺激对小鼠记忆检索的影响。

Effect of D-1 or D-2 receptor stimulation on memory retrieval in mice.

机构信息

Department of Pharmacology, Medical Faculty, University of Tehran, and Department of Physiology, Medical Faculty, Shaheed-Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

J Psychopharmacol. 1992 Jan;6(4):526-31. doi: 10.1177/026988119200600409.

Abstract

Mice were trained in one-way active avoidance procedure and retention was tested at 4, 8, 16 and 24 h after training of animals and compared with non-shocked or untrained animals. The effect of drugs was tested on retrieval 24 h after training in other groups of mice. High doses of apomorphine or bromocriptine impaired, while low doses of the drugs improved, retrieval of avoidance. High doses of sulpiride reversed the impairment induced by high doses of these dopamine agonists. Low doses of sulpiride antagonized the improvement of retrieval induced by low doses of apomorphine. SKF 38393 treatment of animals also improved the retrieval. The retrieval impairment induced by higher doses of apomorphine or the improvement induced by different doses of SKF 38393 was antagonized by SCH 23390 pre-treatment. Single administration of SCH 23390 or low doses of sulpiride also impaired retrieval. It is concluded that stimulating post-synaptic D-2 dopamine receptors impairs retrieval whilst activation of pre-synaptic D-2 or post-synaptic D-1 receptors improves memory retrieval.

摘要

小鼠在单向主动回避程序中接受训练,并在动物训练后 4、8、16 和 24 小时进行保留测试,与未受电击或未经训练的动物进行比较。在其他组小鼠训练后 24 小时进行检索时,测试药物的作用。高剂量的阿朴吗啡或溴隐亭损害,而低剂量的药物改善回避的检索。高剂量的舒必利逆转了这些多巴胺激动剂高剂量引起的损害。低剂量的舒必利拮抗了低剂量阿朴吗啡引起的检索改善。SKF 38393 治疗动物也改善了检索。SCH 23390 预处理可拮抗高剂量阿朴吗啡引起的检索损害或不同剂量 SKF 38393 引起的检索改善。单次给予 SCH 23390 或低剂量舒必利也损害了检索。结论是,刺激突触后 D-2 多巴胺受体损害检索,而激活突触前 D-2 或突触后 D-1 受体改善记忆检索。

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