von Zglinicki T, Rimmler M, Purz H J
J Microsc. 1986 Jan;141(Pt 1):79-90. doi: 10.1111/j.1365-2818.1986.tb02702.x.
The proposed cryofixation technique uses a tubule-shaped needle chilled in liquid propane for simultaneous excision and freezing of a tissue specimen. Due to this simultaneity, ionic shifts created by traumatic influences are avoided even in the outermost cells of the specimen. Moreover, it is shown here that stopping the blood flow for more than about 10 s results in notable ionic shifts between cells and extracellular space in rat heart and liver. Such preparative ischaemic injury is minimized by the Fast Cryofixation Technique because it can be easily performed on organs within the circulatory system, whilst the heart of the animal is still beating. Intracellular concentrations of the monovalent ions in rat heart and liver, obtained by this method, tally well with recent results from different independent techniques reported in the literature. As demonstrated by cross-sectioning and freeze-fracturing, the structural preservation of the freezing technique is sufficient for X-ray microanalytical work.
所提出的冷冻固定技术使用在液态丙烷中冷却的管状针,用于同时切除和冷冻组织标本。由于这种同步性,即使在标本的最外层细胞中,也能避免由创伤性影响产生的离子移位。此外,这里表明,在大鼠心脏和肝脏中,血流停止超过约10秒会导致细胞与细胞外空间之间出现明显的离子移位。快速冷冻固定技术可将这种制备性缺血损伤降至最低,因为它可以在循环系统内的器官上轻松进行,而此时动物的心脏仍在跳动。通过这种方法获得的大鼠心脏和肝脏中单价离子的细胞内浓度与文献中报道的不同独立技术的最新结果非常吻合。如通过切片和冷冻断裂所证明的,冷冻技术的结构保存足以用于X射线微分析工作。