Ferrari F, Mangiafico V, Tartoni P, Tampieri A
Institute of Pharmacology, University of Modena, Italy.
Pharmacol Res Commun. 1988 Sep;20(9):827-37. doi: 10.1016/s0031-6989(88)80720-3.
When the azepine derivative BHT 920, a putative agonist at dopamine autoreceptors, was injected i.p. into adult male rats at 100 micrograms/kg, it induced numerous penile erections, stretching and yawning and sedation, all considered typical signs of central DA autoreceptor stimulation, but did not elicit stereotyped behaviour. Imidazole (37.5-150 mg/kg i.p.) and the alpha 2 antagonist yohimbine (0.5-1 mg/kg i.p.) both antagonized the behavioural effects of BHT 920. In the light of the proposed selective action of the drugs used, the possible involvement of specific receptors for the modulation of these forms of behaviour, as well the possible relevance of the data presented, are briefly discussed.
当将氮杂环庚烷衍生物BHT 920(一种假定的多巴胺自身受体激动剂)以100微克/千克的剂量腹腔注射到成年雄性大鼠体内时,它诱发了多次阴茎勃起、伸展和打哈欠以及镇静作用,所有这些都被认为是中枢多巴胺自身受体刺激的典型迹象,但并未引发刻板行为。咪唑(37.5 - 150毫克/千克腹腔注射)和α2拮抗剂育亨宾(0.5 - 1毫克/千克腹腔注射)均拮抗了BHT 920的行为效应。鉴于所用药物的拟选择性作用,简要讨论了特定受体可能参与调节这些行为形式以及所呈现数据的可能相关性。