Inhibitory Effect of OP-41483·α-CD, a Prostacyclin Analog, on Peripheral Vascular Lesion Models in Rats

[摘要] References(13)Cited-By(9)The effect of a chemically stable prostacyclin analog, OP-41483 α-cyclodextrin clathrate (OP-41483·α-CD), on vascular lesions, platelet aggregation and blood pressure were examined and compared with those of prostaglandin E1 α-cyclodextrin clathrate (PGE1·CD) in in vivo rat models. 1) In the laurate (1 mg/leg, i.a.)-induced arterial thrombotic model, OP-41483·α-CD (1 μg/kg/min, i.v.) prevented the progression of femoral arterial vascular lesions and enhanced the development of collaterals in the femoral artery. PGE1·CD did not inhibit the progression of vascular damages. 2) In the model of vasoconstriction induced by epinephrine (0.05 mg/tail, s.c.) and ergotamine (2 mg/kg, s.c.), OP-41483·α-CD and PGE1·CD, at 1 μg/kg/min, inhibited the progress of tail gangrene and lessened the decrease in tail cutaneous blood flow. 3) OP-41483·α-CD (1 μg/kg/min) suppressed the ADP (0.1 mg/kg/min, i.v.)-induced decrease in the number of circulating platelets without affecting the change in blood pressure. In contrast, PGE1·CD (3 μg/kg/min) inhibited ADP-induced thrombocytopenia with a decrease in blood pressure. These results indicate that OP-41483·α-CD has antiplatelet and cutaneous blood flow improving activities that are greater than its hypotensive effect and may be of therapeutic potential in peripheral vascular diseases.

[学科分类] 药理学

[关键词] OP-41483;Prostacyclin analog;Peripheral vascular lesion;Antiplatelet activity;Prostaglandin E1.