Objective
In previous studies cholesterol-rich nanoemulsions (LDE) resembling low-density lipoprotein were shown to concentrate in atherosclerotic lesions of rabbits. Lesions were pronouncedly reduced by treatment with paclita
xel associated with LDE. This study aimed to test the hypothesis of whether LDE–paclita
xel is able to concentrate in grafted hearts of rabbits and to ameliorate coronary allograft vasculopathy after the transplantation procedure.
Methods
Twenty-one New Zealand rabbits fed 0.5 % cholesterol were submitted to heterotopic heart transplantation at the cervical position. All rabbits undergoing transplantation were treated with cyclosporin A (10 mg · kg−1 · d−1 by mouth). Eleven rabbits were treated with LDE–paclitaxel (4 mg/kg body weight paclitaxel per week administered intravenously for 6 weeks), and 10 control rabbits were treated with 3 mL/wk intravenous saline. Four control animals were injected with LDE labeled with [14C]-cholesteryl oleate ether to determine tissue uptake.
Results
Radioactive LDE uptake by grafts was 4-fold that of native hearts. In both groups the coronary arteries of native hearts showed no stenosis, but treatment with LDE–paclitaxel reduced the degree of stenosis in grafted hearts by 50 % . The arterial luminal area in grafts of the treated group was 3-fold larger than in control animals. LDE–paclitaxel treatment resulted in a 7-fold reduction of macrophage infiltration. In grafted hearts LDE–paclitaxel treatment reduced the width of the intimal layer and inhibited the destruction of the medial layer. No toxicity was observed in rabbits receiving LDE–paclitaxel treatment.
Conclusions
LDE–paclitaxel improved posttransplantation injury to the grafted heart. The novel therapeutic approach for heart transplantation management validated here is thus a promising strategy to be explored in future clinical studies.
