Lograno M D, Reibaldi A, Camerino D C
Pharmacol Res Commun. 1987 Mar;19(3):209-21. doi: 10.1016/0031-6989(87)90064-6.
The effects of dapiprazole, a relatively new alpha 1-adrenolytic agent, on contractile responses and on spontaneous mechanical activity were studied in guinea pig isolated ileum. Dapiprazole (10(-10) to 10(-4) M) produced a concentration-dependent inhibition of high K+ (80 mM) -induced contractions. These inhibitory effects were observed with dapiprazole added either before or after the induced contractions. The Ca2+-induced contractions of K+-depolarized ileum were also inhibited by dapiprazole. Dapiprazole inhibited in a non competitive manner the responses of the ileum to: carbachol, histamine, 5-hydroxytryptamine, pentagastrin, angiotensin II and cholecystokinin. In order to analize whether dapiprazole exerts an intracellular effect on Ca2+-store, skinned preparations were used. The results suggest that dapiprazole might inhibit Ca2+ entry through both voltage-and receptor-operated channels of the smooth muscle membrane.
研究了一种相对较新的α1-肾上腺素能阻滞剂达哌唑对豚鼠离体回肠收缩反应和自发机械活动的影响。达哌唑(10^(-10)至10^(-4)M)对高钾(80mM)诱导的收缩产生浓度依赖性抑制。在诱导收缩之前或之后添加达哌唑均观察到这些抑制作用。达哌唑也抑制了钾离子去极化回肠的钙离子诱导收缩。达哌唑以非竞争性方式抑制回肠对以下物质的反应:卡巴胆碱、组胺、5-羟色胺、五肽胃泌素、血管紧张素II和胆囊收缩素。为了分析达哌唑是否对钙储存产生细胞内效应,使用了去皮标本。结果表明,达哌唑可能通过平滑肌膜的电压门控通道和受体操纵通道抑制钙离子内流。