ABSTRACT
Twenty patients with obliterative atherosclerosis in the lower extremities arteries (Fontaine's stage II) were treated with nitrendipine (Bayotensin) given in the dose of 20 mg daily for 6 weeks. This therapy with nitrendipine produced improvement manifested by the prolongation of the distance of intermittent claudication, shortening of pain duration, increase in blood flow in the ischemic extremity, and increase in pressure index. At the same time, nitrendipine decreased ADP-produced platelet aggregation and activated fibrinolytic system. Clinical trials have shown that nitrendipine is effective in the obliterative atherosclerosis in the lower extremities.
Subject(s)
Arteriosclerosis/drug therapy , Leg/blood supply , Nitrendipine/therapeutic use , Adult , Aged , Arteriosclerosis/complications , Drug Administration Schedule , Female , Humans , Intermittent Claudication/drug therapy , Intermittent Claudication/etiology , Ischemia/drug therapy , Ischemia/etiology , Male , Middle AgedSubject(s)
Circadian Rhythm , Pituitary Hormones, Anterior/metabolism , Testosterone/metabolism , Adult , Humans , Male , Mathematics , Middle Aged , Models, BiologicalABSTRACT
Infusion of PGI2 at a dose of 5 or 10 ng/kg/min during 72 hours into patients with peripheral vascular disease was followed by increased susceptibility of platelets to proaggregatory action of ADP and collagen but not that of arachidonate. The above effects were observed 24 hours after termination of infusion of PGI2. A tendency to an increased formation of TXA2 in PRP aggregated by arachidonate was also noticed. Infusion of PGI2 at a dose of 2 mg/kg/min during 72 hours into the patients caused the decreased platelet aggregability to ADP and arachidonate but not to collagen, and a decreased tendency to production of TXA2 in PRP aggregated by arachidonate. The existence of a "rebound effect" in platelets after a long term PGI2 therapy is suggested.
