Goiny M, Uvnäs-Moberg K
Naunyn Schmiedebergs Arch Pharmacol. 1987 Jul;336(1):16-9. doi: 10.1007/BF00177745.
Apomorphine (0.05 mg/kg intravenously) was given to conscious dogs, and gastrin levels were measured in peripheral venous blood with a radioimmunoassay. Apomorphine induced an increase of gastrin levels which peaked at 5 min. The peripheral dopamine D-2/DA2 receptor antagonist domperidone (0.2 mg/kg), but not halopemide (0.1-1 mg/kg) nor the D-1/DA1 receptor antagonist SCH 23,390 (0.1 mg/kg), blocked the gastrin response to apomorphine. Both domperidone and halopemide, but not SCH 23,390, blocked the apomorphine-induced vomiting. These results suggest that apomorphine increases gastrin levels by an action at D-2/DA2 receptors, which are situated outside the blood brain barrier and differ from the receptor inducing the vomiting.
将阿扑吗啡(0.05毫克/千克静脉注射)给予清醒的狗,并用放射免疫分析法测定外周静脉血中的胃泌素水平。阿扑吗啡诱导胃泌素水平升高,在5分钟时达到峰值。外周多巴胺D-2/DA2受体拮抗剂多潘立酮(0.2毫克/千克)可阻断阿扑吗啡引起的胃泌素反应,但氟哌酰胺(0.1 - 1毫克/千克)和D-1/DA1受体拮抗剂SCH 23,390(0.1毫克/千克)则不能。多潘立酮和氟哌酰胺均可阻断阿扑吗啡引起的呕吐,但SCH 23,390不能。这些结果表明,阿扑吗啡通过作用于位于血脑屏障之外且与诱导呕吐的受体不同的D-2/DA2受体来增加胃泌素水平。