P. Fitscha et al., ISRADIPINE DECREASES ARTERIAL THROMBOGENICITY IN RABBITS - A MORPHOMETRIC AND RADIOISOTOPIC STUDY, Thrombosis research, 74(3), 1994, pp. 175-183
The effect of isradipine, a calcium antagonist, on aortic and iliac wa
ll thrombogenicity was examined in rabbits. After one week of dosing,
the abdominal aortic and iliac artery endothelium was abraded using a
Fogarthy catheter; One group of animals (n=8) was dosed for one week w
ith isradipine 0.3 mg/kg. A second group of animals received 10 mg ace
tylsalicylic acid (ASA)/kg daily in addition, while a third group rece
ived the vehicle only. Finally, a fourth group of animals (n=8) was tr
eated with ASA only. The percentage denuded surface covered with conta
ct (unspread) platelets decreased significantly (p<0.01) from 14.7+/-
2.0 to 9.3+/-2.1 (6.2+/-0.8 to 3.7+/-0.4*). The amount of contact and
spread platelets was diminished from 84.9+/-5.6 to 71.4+/-4.4 (91.8/-5.3 to 75.2+/-4.6). Platelet thrombi decreased from 7.4+/-0.9 to 4.
6+/-1.4 (9.4+/-1.9 to 5.2+/-0.7*) in the aortic and the iliac artery,
respectively. In-111-platelet deposition decreased by 39.9 and 41.9%.
Concomitant ASA -therapy not only abolished the effect of isradipine
but enhanced thrombogenicity, probably as a result of almost complete
blockade of vascular PGI(2)-production.