Koons J C, Long J P, Cannon J G
Naunyn Schmiedebergs Arch Pharmacol. 1984 Dec;328(2):180-5. doi: 10.1007/BF00512069.
The pharmacological effects of three ergoline fragments (BD-179, BD-271 and BD-214) were studied in vivo using the cat cardioaccelerator nerve preparation and in vitro using field stimulated isolated cat right atria. BD-179 and BD-271 produced dose dependent inhibition of tachycardia due to electrical stimulation of the right postganglionic cardioaccelerator nerve in anesthetized cats, BD-214 was inactive. BD-179 produced primarily hypotension, BD-271 produced a transient pressor response followed by hypotension and BD-214 produced only pressor effects. The tachycardia inhibitory effects and hypotension produced by BD-179 and BD-271 were antagonized by the dopamine receptor antagonist sulpiride. BD-179, BD-271 and BD-214 antagonized the presynaptic inhibitory effects of the dopamine receptor agonist apomorphine in vitro on field stimulated isolated cat right atria. All three ergoline fragments facilitated stimulation-induced increases in systolic tension development and BD-214 facilitated stimulation-induced tachycardia in isolated cat right atria.
使用猫心脏加速神经制备方法在体内以及使用场刺激离体猫右心房在体外研究了三种麦角灵片段(BD - 179、BD - 271和BD - 214)的药理作用。BD - 179和BD - 271对麻醉猫右侧节后心脏加速神经电刺激所致的心动过速产生剂量依赖性抑制,BD - 214无活性。BD - 179主要产生低血压,BD - 271产生短暂升压反应后出现低血压,而BD - 214仅产生升压作用。BD - 179和BD - 271所致的心动过速抑制作用和低血压被多巴胺受体拮抗剂舒必利拮抗。BD - 179、BD - 271和BD - 214在体外拮抗多巴胺受体激动剂阿扑吗啡对场刺激离体猫右心房的突触前抑制作用。所有三种麦角灵片段均促进刺激诱导的离体猫右心房收缩张力增加,且BD - 214促进刺激诱导的心动过速。