Influence of postangioplasty beta-irradiation on endothelial function in porcine coronary arteries

Article

关键词: INHIBITS NEOINTIMA FORMATION;    RABBIT EAR ARTERY;    RADIATION-THERAPY;    BALLOON INJURY;    X-IRRADIATION;    SMOOTH-MUSCLE;    RESTENOSIS;    ANGIOPLASTY;    CONDUCTANCE;    SEROTONIN;   

DOI  :  10.1161/01.CIR.101.12.1430

来源: SCIE

【 摘 要 】

Background-Postangioplasty (PTCA) intracoronary radiation therapy (ICRT) has been demonstrated to limit restenosis. The consequences of these procedures on coronary reactivity are unknown. Methods and Results-Porcine coronary arteries were studied after PTCA immediately (n=5) and 6 weeks (n=5) after ICRT (n=5 and 5, respectively), after combined PTCA+ICRT (n=5 and 7, respectively), and after no intervention (n=11). A 3-cm-long source train of Sr/Y-90 was used in vivo to deliver 16 Gy at a depth of 2 mm from the source center, as used in clinical trials. Arterial rings were mounted on myographs to record isometric tension. After achieving steady-state contraction to depolarizing physiological solution containing 40 mmol/L KCl, measured baseline tension was significantly elevated immediately after all interventions. It returned to normal levels 6 weeks after PTCA and ICRT alone but was significantly reduced if combined. Active contractions induced by 40 mmol/L KCL were maintained after combined therapy both immediately after and at 6 weeks. In these depolarizing conditions, nitric oxide-dependent relaxation to substance P was trivial after PTCA+ICRT and reduced after ICRT, whereas in the presence of physiological solution and N-omega-nitro-L-arginine, substance P-induced relaxation was reduced after PTCA and abolished after PTCA + ICRT 6 weeks after intervention. In rings without endothelium, the relaxation mediated by sodium nitroprusside (0.1 mu mol/L) was reduced immediately after PTCA and at 6 weeks. Conclusions-PTCA+ ICRT altered the passive mechanical properties of porcine coronary arterial wall. Furthermore, at 6 weeks, receptor-operated release of endothelium-derived nitric oxide and endothelium-derived hyperpolarizing factor was reduced by ICRT and PTCA alone, respectively, and was prevented by their combination.

【 授权许可】

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