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生物人工猪瓣膜的体外动态钙化:磷灰石结晶的证据。

Dynamic in vitro calcification of bioprosthetic porcine valves: evidence of apatite crystallization.

作者信息

Pettenazzo E, Deiwick M, Thiene G, Molin G, Glasmacher B, Martignago F, Bottio T, Reul H, Valente M

机构信息

Department of Pathology, University of Padua Medical School, Padua, Italy.

出版信息

J Thorac Cardiovasc Surg. 2001 Mar;121(3):500-9. doi: 10.1067/mtc.2001.112464.

Abstract

OBJECTIVE

Calcification is the most important cause of structural deterioration of glutaraldehyde-fixed bioprosthetic valves. Devitalization of tissue favors calcium deposits in the shape of apatite crystals. Host factors influence the extent and progression of calcification, but the phenomenon can also occur in vitro in the absence of a viable milieu. Whether calcific deposits obtained in vitro are similar to those found in vivo is unknown.

METHODS

Four porcine frame-mounted bioprostheses (St Jude Medical Bioimplant; St Jude Medical, Inc, St Paul, Minn) were tested in vitro by using a pulsatile accelerated calcification testing device at a frequency of 300 cycles per minute at 37 degrees C for 19 x 10(6) cycles with a rapid synthetic calcification solution (final product [calcium x phosphate], 130 mg/dL(2)). Three of the same type of xenografts explanted from human subjects because of calcific failure (time in place, 108 +/- 25.63 mo) served as control grafts. Each sample underwent gross and x-ray examination, histology, transmission and scanning electron microscopy, atomic absorption spectroscopy, electron microprobe analysis, and x-ray powder diffraction methods.

RESULTS

All in vitro bioprostheses were heavily calcific, with intrinsic Von Kossa stain-positive deposits and a mean calcium content of 205.285 +/- 64.87 mg/g dry weight. At transmission electron microscopy, nuclei of calcification involved mostly collagen fibers and interfibrillar spaces and, more rarely, cell debris and nuclei. Electron microprobe analysis showed a Ca/P atoms ratio of 4.5:3, a value intermediate between hydroxyapatite and its precursor, octacalciumphosphate. X-ray powder diffraction showed a well-separated and sharp peak, which is typical of hydroxyapatite. Aggregates of plate-like crystals up to 8 microm in size were observed at scanning electron microscopy, with a typical tabular hexagonal shape consistent with apatite. The morphologic and chemical findings in human explants were similar.

CONCLUSIONS

Intrinsic calcification of glutaraldehyde-fixed porcine valves was induced in vitro. Electron microprobe analysis and x-ray powder diffraction findings were in keeping with apatite crystallization, such as that occurring in valve xenografts implanted in vivo. The model may be of value to accelerate the screening of anticalcific agents and may reduce the need for animal experiments.

摘要

目的

钙化是戊二醛固定生物瓣膜结构退变的最重要原因。组织失活有利于磷灰石晶体形式的钙沉积。宿主因素影响钙化的程度和进展,但在没有活细胞环境的体外条件下也会出现这种现象。体外获得的钙化沉积物是否与体内发现的相似尚不清楚。

方法

使用脉动加速钙化测试装置,在37℃、每分钟300次循环的频率下,用快速合成钙化溶液(最终产物[钙×磷],130mg/dL(2))对4个猪支架生物瓣膜(圣犹达医疗生物植入物;圣犹达医疗公司,明尼苏达州圣保罗)进行19×10(6)次循环的体外测试。从因钙化失败而取出的人体受试者身上获取的3个相同类型的异种移植物(在位时间,108±25.63个月)作为对照移植物。每个样本都进行了大体和X线检查、组织学检查、透射和扫描电子显微镜检查、原子吸收光谱分析、电子微探针分析以及X线粉末衍射分析。

结果

所有体外生物瓣膜均有严重钙化,有内在的Von Kossa染色阳性沉积物,钙平均含量为205.285±64.87mg/g干重。在透射电子显微镜下,钙化核主要累及胶原纤维和纤维间间隙,较少累及细胞碎片和细胞核。电子微探针分析显示钙/磷原子比为4.5:3,该值介于羟基磷灰石及其前体磷酸八钙之间。X线粉末衍射显示有一个分离良好且尖锐的峰,这是羟基磷灰石的典型特征。在扫描电子显微镜下观察到尺寸达8微米的板状晶体聚集体,具有与磷灰石一致的典型板状六边形形状。人体移植物中的形态学和化学发现相似。

结论

体外诱导了戊二醛固定猪瓣膜的内在钙化。电子微探针分析和X线粉末衍射结果与磷灰石结晶一致,如体内植入的瓣膜异种移植物中发生的那样。该模型可能有助于加速抗钙化剂的筛选,并可能减少动物实验的需求。

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