Chignier E, Eloy R, Huc A, Gimeno R, Gleizal C
J Biomed Mater Res. 1985 Feb;19(2):115-31. doi: 10.1002/jbm.820190203.
The aim of the present study was to evaluate the sequence of the immediate and the mid/long-term organization of the blood interface of a collagenous membrane used as vascular substitute in rats. The implants were prepared from calf skin type I insoluble collagen, obtained after acidic dispersion, in absence of chemical or tanning treatment. They were used to patch an aortic defect by means of microsurgical techniques. The animals were sequentially sacrificed for immediate hemocompatibility studies at 10 s, 30 s, 10 min, 3 h, and 6 h, for long-term analyses of the organization of the blood material interface at the 7th, 15th, 45th, 60th, 90th day following the surgery and each month until 14 months after aortic replacement. The superficial immediate events at the blood patch interface demonstrated erythrocytes heavily engulfed in a thin but dense fibrin mesh both at the patch and at the adjacent aortic wall surfaces. Neither adherent platelet nor platelet aggregate were detectable on the collagen patch surface. This fibrinoerythrocytic membrane covered the patch completely at 60 s and at 3 h the deposit was limited to 5-6 erythrocyte layers as confirmed by histology. It did not further develop on the 7th day. At the blood-collagen interface there progressively developed a tissue composed of active myofibroblasts, collagen bundles, and elastic fibers. After 4 months, nests of fibroendothelial cells were present, and between 6 and 14 months surface cell differentiation, although complete on the adjacent aorta was still incomplete on the bovine collagen patch, amorphous fibers, and fibroendothelial cells coexisting. Heterologous patch debris were still present 14 months after implantation and were associated with macroscopic and ultrastructural calcification, which need further investigations concerning the exact nature and mechanism of mineralization of vascular substitutes of biological nature.
本研究的目的是评估在大鼠中用作血管替代物的胶原膜血液界面的即时和中长期组织序列。植入物由经酸性分散后获得的I型小牛皮不溶性胶原制备,未进行化学或鞣制处理。通过显微外科技术将它们用于修补主动脉缺损。依次处死动物,在10秒、30秒、10分钟、3小时和6小时进行即时血液相容性研究,在手术后第7天、15天、45天、60天、90天以及直至主动脉置换后14个月每月进行一次,以对血液材料界面的组织进行长期分析。血液贴片界面的表面即时事件显示,在贴片和相邻主动脉壁表面,红细胞都被大量吞噬在薄而致密的纤维蛋白网中。在胶原贴片表面未检测到粘附的血小板或血小板聚集体。这种纤维蛋白红细胞膜在60秒时完全覆盖贴片,3小时时沉积物限于5 - 6层红细胞,组织学证实了这一点。在第7天它没有进一步发展。在血液 - 胶原界面逐渐形成了由活跃的肌成纤维细胞、胶原束和弹性纤维组成的组织。4个月后,出现了纤维内皮细胞巢,在6至14个月之间,表面细胞分化虽然在相邻主动脉上已完成,但在牛胶原贴片上仍不完全,无定形纤维和纤维内皮细胞共存。植入14个月后仍存在异种贴片碎片,并与宏观和超微结构钙化相关,这需要进一步研究生物性质血管替代物矿化的确切性质和机制。