Related Experiment Video
Updated: Jul 11, 2026

Procedure for Human Saphenous Veins Ex Vivo Perfusion and External Reinforcement
Published on: October 1, 2014
Paclitaxel treatment reduces neointimal hyperplasia in cultured human saphenous veins
Thomas Schachner1, Christina Steger, Simone Heiss
1Department of Cardiac Surgery, Innsbruck Medical University, Innsbruck, Austria. Thomas.Schachner@i-med.ac.at
Background:
Paclitaxel exerts antiproliferative properties by stabilizing microtubuli of the cell. The substance is in clinical use for drug-eluting coronary stents. We aimed to test the hypothesis that paclitaxel treatment can reduce neointimal hyperplasia in cultured human saphenous veins and thus might be useful for local pharmacologic treatment of vein grafts prior to coronary artery bypass grafting (CABG).
Methods:
The remnants of saphenous veins from 13 patients undergoing CABG were collected. The development of neointimal hyperplasia was induced using an established organ culture model (incubation time 2 weeks). In the treatment group, paclitaxel was added to the culture medium at different concentrations.
Results:
Veins treated with 1 micromol/l paclitaxel showed a median increase of intimal thickness of 2 microm (range -76 to 46) above baseline levels, whereas untreated control veins increased by 15 microm (range -3 to 142) (p=0.022). Treatment with 10 micromol/l paclitaxel resulted in a lower intimal thickness growth of 1 microm (range -82 to 212) above baseline levels (p=0.035 vs controls). Treatment with 25 or 50 micromol/l paclitaxel did not further inhibit intimal hyperplasia. The neointimal amount of the contractile protein smooth muscle actin (SMA) in paclitaxel 1 micromol/l treated veins was significantly higher than baseline values (p=0.037). The cytoskeletal protein desmin was predominant in the media, whereas it was less frequently found in the intima, and we observed no difference between controls and paclitaxel treated veins. The proliferation marker ki-67 was occasionally present in the circumferential media, whereas it was almost absent in both the (inner) longitudinal media and the intima. Elastic fibers were present in the media and intima before and after organ culture without significant differences between the groups. Collagen fibers (Masson's trichrome) were found abundantly (80%) in the inner longitudinal media, less commonly (20%) in the outer circumferential media, and they were absent in the intima without difference between the groups.
Conclusion:
Local paclitaxel treatment reduces neointimal hyperplasia in cultured human saphenous veins, without changing the amount of elastic or collagen fibers. Paclitaxel treatment leads to an increased amount of the contractile protein SMA and thus might have a therapeutic potential for the prevention of vein graft disease.
Insights
Paclitaxel treatment significantly reduced neointimal hyperplasia in cultured human saphenous veins. This finding suggests paclitaxel
Area of Science:
- Vascular Biology
- Pharmacology
- Regenerative Medicine
Background:
- Paclitaxel stabilizes microtubules and is used in drug-eluting coronary stents.
- Neointimal hyperplasia is a significant issue in vein grafts after coronary artery bypass grafting (CABG).
Purpose of the Study:
- To investigate the hypothesis that paclitaxel can reduce neointimal hyperplasia in cultured human saphenous veins.
- To evaluate paclitaxel's potential for local pharmacologic treatment of vein grafts before CABG.
Main Methods:
- Human saphenous veins from 13 CABG patients were cultured for 2 weeks to induce neointimal hyperplasia.
- Paclitaxel was added to the culture medium at varying concentrations (1, 10, 25, 50 µmol/l).
- Neointimal thickness, smooth muscle actin (SMA), desmin, ki-67, elastic, and collagen fibers were analyzed.
Main Results:
- 1 µmol/l paclitaxel reduced intimal thickness increase to 2 µm (vs. 15 µm in controls, p=0.022).
- 10 µmol/l paclitaxel further reduced intimal thickness increase to 1 µm (p=0.035 vs. controls).
- Higher paclitaxel concentrations did not show further inhibition; SMA levels increased significantly in treated veins (p=0.037).
Conclusions:
- Local paclitaxel treatment effectively reduces neointimal hyperplasia in cultured human saphenous veins.
- Paclitaxel treatment increased smooth muscle actin (SMA) levels without altering elastic or collagen fibers.
- Paclitaxel demonstrates therapeutic potential for preventing vein graft disease.
Related Concept Videos
Peripheral Artery Disease III: Interprofessional Care
Varicose Veins II: Diagnostic Studies and Interprofessional Care
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...

