Horio M
First Department of Surgery, Asahikawa Medical College, Japan.
Nihon Geka Gakkai Zasshi. 1991 Jul;92(7):867-73.
Preparation for preserving endothelial cells (ECs) of autogenous vein grafts (AVGs) and the process of de-endothelialization (de-E) and re-endothelialization (re-E) were studied. Jugular veins (n = 31) from mongrel dogs were immersed in saline solution (SS), heparinized blood (HB), and other three kinds of solution. Then jugular veins (n = 26) immersed in SS for 3 hours, were used for AVGs to the abdominal aorta. Intimal changes were observed by scanning electron microscopy. ECs showed irreversible changes about 60 minutes after immersion in SS and about 150 minutes in HB. Eleven (92%) of 12 graft specimens within 1 day after implantation showed wide areas of de-E, while ECs on the venous valve were satisfactorily preserved in 6 (55%) of 11 valves. Re-E was observed predominantly around the valve from 3 days after implantation, and completed within 3 weeks. Clinically, specimens in 35 AVGs were collected before anastomosis. Severe EC damage was observed in 23 (66%) of them. Long-term observation revealed graft stenosis in 2 due to intimal hyperplasia (IH) in grafts with severely damaged EC. These results suggest that venous valves are an important source of re-E, and that the preservation of ECs in graft preparation is an important factor to prevent IH.
研究了自体静脉移植物(AVG)内皮细胞(EC)的保存准备以及去内皮化(de-E)和再内皮化(re-E)过程。将杂种犬的颈静脉(n = 31)浸入盐溶液(SS)、肝素化血液(HB)和其他三种溶液中。然后将浸入SS 3小时的颈静脉(n = 26)用于与腹主动脉的AVG。通过扫描电子显微镜观察内膜变化。EC在浸入SS后约60分钟和浸入HB后约150分钟显示出不可逆变化。植入后1天内,12个移植标本中有11个(92%)显示出大面积的去内皮化,而11个瓣膜中有6个(55%)的静脉瓣膜上的EC保存良好。植入后3天起主要在瓣膜周围观察到再内皮化,并在3周内完成。临床上,在35个AVG中收集了吻合前的标本。其中23个(66%)观察到严重的EC损伤。长期观察发现,2个因严重EC损伤的移植物中内膜增生(IH)导致移植狭窄。这些结果表明,静脉瓣膜是再内皮化的重要来源,并且在移植物制备中保存EC是预防IH的重要因素。