Some pharmacological effects of 17(S) methyl-ω-honiytrans-Δ2-PGE1 (ONO 1206)

P.G. Adaikan, S.M.M. Karim
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引用次数: 8

Abstract

17(s) methyl-ω-hamo-trans-Δ2-PGE, (ONO 1206) produced qualitatively similar effects to PGE1 in several systems.It was 18.4 and 25.6 times respectively more potent than PGE1 in inhibiting ADP-induced baboon and human platelet aggregation in vitro. Intravenous infusion of ONO 1206 in baboon also produced ex-vivo inhibition of ADP-induced platelet aggregation.However, this was accompanied by a significant fall in blood pressure and an increase in heart rate. The potent relaxant effect of ONO 1206 on human respiratory tract smooth muscle in vitro suggests that this compound may be a bronchodilator in man.

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17(S) methyl-ω-honiytrans-Δ2-PGE1 (ONO 1206)的药理作用
17(s) methyl-ω-hamo-trans-Δ2-PGE, (ONO 1206)在几个体系中产生与PGE1质量相似的效果。对adp诱导的狒狒和人体外血小板聚集的抑制作用分别是PGE1的18.4倍和25.6倍。在狒狒体内静脉输注ONO 1206也对adp诱导的血小板聚集产生体外抑制作用。然而,这伴随着血压的显著下降和心率的增加。ONO 1206在体外对人呼吸道平滑肌的有效松弛作用表明该化合物可能是人支气管扩张剂。
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