Daly S A, Waddington J L
Department of Clinical Pharmacology, Royal College of Surgeons in Ireland, Dublin.
Psychopharmacology (Berl). 1993;113(1):45-50. doi: 10.1007/BF02244332.
The full efficacy, high potency isochroman D-1 agonist A 68930 demonstrated greater than 220-fold selectivity for D-1 over D-2 receptors. A 68930 (0.06 and 0.25 mg/kg) readily induced intense grooming, together with vacuous chewing; these responses became less evident following higher doses (1.0 and 4.0 mg/kg) and sniffing became prominent. Intense grooming was blocked by three D-1 antagonists, the benzazepines SCH 23390 (0.01-1.0 mg/kg) and NNC-756 (0.01-1.0 mg/kg), and the isoquinoline BW 737C (0.2-5.0 mg/kg); however, vacuous chewing was not antagonised by SCH 23390 and NNC-756, but was blocked by BW 737C. Intense grooming was attenuated by the D-2 antagonist YM 09151 (0.005-0.5 mg/kg) while vacuous chewing was enhanced. These data suggest that intense grooming is mediated by a "D-1 like" receptor that recognises all known chemical classes of D-1-selective compounds, while vacuous chewing may be mediated by a pharmacologically distinct subtype of "D-1-like" receptor that recognises preferentially the isochromans and isoquinolines.
高效能异苯并二氢吡喃D-1激动剂A 68930对D-1受体的选择性比对D-2受体高220倍以上。A 68930(0.06和0.25毫克/千克)很容易诱发强烈的理毛行为以及空嚼;在较高剂量(1.0和4.0毫克/千克)时,这些反应变得不那么明显,而嗅探变得突出。三种D-1拮抗剂可阻断强烈的理毛行为,即苯并氮杂卓类的SCH 23390(0.01 - 1.0毫克/千克)和NNC - 756(0.01 - 1.0毫克/千克),以及异喹啉类的BW 737C(0.2 - 5.0毫克/千克);然而,SCH 23390和NNC - 756不能拮抗空嚼行为,但BW 737C可阻断。D-2拮抗剂YM 09151(0.005 - 0.5毫克/千克)可减弱强烈的理毛行为,同时增强空嚼行为。这些数据表明,强烈的理毛行为是由一种“类D-1”受体介导的,该受体能识别所有已知化学类别的D-1选择性化合物,而空嚼行为可能由一种药理学上不同的“类D-1”受体亚型介导,该亚型优先识别异苯并二氢吡喃和异喹啉类化合物。