Greenberg R, Smorong K, Bagli J F
Prostaglandins. 1976 Jun;11(6):961-80. doi: 10.1016/0090-6980(76)90005-8.
The bronchodilator activity of (+/-) 11-deoxy prostaglandin E1 was compared to the activity of its (+/-) 15-methyl analogue, (doxaprost). Both compounds inhibited histamine-induced bronchoconstriction in the anesthetized guinea pig where changes in tracheal pressure were measured. Doxaprost was 73 and 32 times more potent that (+/-) 11-deoxy PGE1 by the aerosol and i.v. routes, respectively. Doxaprost also demonstrated a longer duration of effect. Both compounds decreased pulmonary resistance in the 5HT tonal cat. There was no difference in the potency of the two compounds. However, doxaprost had a longer duration of effect. Both compounds caused a fall in mean arterial blood pressure after i.v. administration in the guinea pig but not after aerosol administration in the guinea pig and cat. Both compounds caused relaxation of the isolated guinea pig tracheal strip when tone was induced with carbachol. There was no difference in the potency of the two compounds. The increased activity in vivo but not in vitro of the 15-methyl analogue doxaprost is consistent with a lack of enzyme inactivation.
将(±)11-脱氧前列腺素E1的支气管扩张活性与其(±)15-甲基类似物(多沙普仑)的活性进行了比较。在麻醉的豚鼠中测量气管压力变化时,两种化合物均抑制组胺诱导的支气管收缩。通过气雾剂和静脉注射途径,多沙普仑的效力分别比(±)11-脱氧PGE1强73倍和32倍。多沙普仑的作用持续时间也更长。两种化合物均降低了5-羟色胺张力猫的肺阻力。两种化合物的效力没有差异。然而,多沙普仑的作用持续时间更长。在豚鼠中静脉注射后,两种化合物均导致平均动脉血压下降,但在豚鼠和气雾剂给药后,在猫中则不然。当用卡巴胆碱诱导张力时,两种化合物均使离体豚鼠气管条松弛。两种化合物的效力没有差异。15-甲基类似物多沙普仑在体内而非体外活性增加与缺乏酶失活一致。