Schwartz B
Acta Ophthalmol Suppl (1985). 1986;177:3-55.
A perfusion system has been established for the organ culture of the lens. The system is designed so that a constant flow of fluid occurs past the lens and a separate channel of fluid simultaneously bypasses the lens. Lens metabolic activity can be determined by analyzing differences between these two samples of fluid. The system also maintains a level of pressure comparable to intraocular pressure. Apparatus for observation and photography of the lens is built into the system. The purpose of these studies was to determine if this perfusion system could maintain the rabbit lens close to the physiological state, to study the metabolic behavior of the lens under steady state conditions, and to determine the effect of increasing amino acid concentrations on the metabolic activity of the lens under steady state conditions. By increasing the amino acid concentrations in the medium we hoped to compensate for the lack of protein in the medium and to provide metabolic substrate to maintain the lens under perfusion conditions. The rabbit lens was cultured at a temperature of 33 degrees C for periods up to 100 h. A totally synthetic perfusion medium without proteins or antibiotics was devised. This medium imitates posterior chamber aqueous humour, except that it does not contain ascorbic acid because it was found that ascorbic acid readily auto-oxidizes and depletes the oxygen content of the medium. The amino acid concentration of the perfusion medium was adjusted so that its total nitrogen content was equivalent to the total nitrogen content of posterior chamber aqueous humour. To determine the metabolic behavior of the lens, 10 different metabolic substances were analyzed in the medium and 15 were analyzed in the lens. These substances are mainly metabolic substrates and end products. As a reference for the evaluation of the behavior of the lens in the perfusion system, the perfused lens was compared to the lens in the other eye of the rabbit. Standards for differences between the right and left lens and the first or second lens removed from the rabbit were developed in control studies. A series of experiments was devised to determine the effect of increased amino acid concentration in the medium on the metabolic behavior of the lens. Concentrations of amino acids from 0 to 7.26 times the posterior concentration of amino acids in chamber aqueous humour were studied. Seven studies were done with a flow rate of medium of about 2 g per h, with each experiment lasting from 80 to 100 h.(ABSTRACT TRUNCATED AT 400 WORDS)
已建立一种用于晶状体器官培养的灌注系统。该系统的设计使得恒定的流体流经过晶状体,同时一个单独的流体通道绕过晶状体。通过分析这两种流体样本之间的差异,可以确定晶状体的代谢活性。该系统还能维持与眼内压相当的压力水平。系统内置了用于观察和拍摄晶状体的设备。这些研究的目的是确定这种灌注系统能否使兔晶状体维持接近生理状态,研究晶状体在稳态条件下的代谢行为,以及确定在稳态条件下增加氨基酸浓度对晶状体代谢活性的影响。通过增加培养基中的氨基酸浓度,我们希望弥补培养基中蛋白质的不足,并提供代谢底物以在灌注条件下维持晶状体。兔晶状体在33摄氏度的温度下培养长达100小时。设计了一种完全不含蛋白质或抗生素的合成灌注培养基。这种培养基模仿后房房水,只是它不含抗坏血酸,因为发现抗坏血酸容易自动氧化并耗尽培养基中的氧气含量。调整灌注培养基的氨基酸浓度,使其总氮含量与后房房水的总氮含量相当。为了确定晶状体的代谢行为,在培养基中分析了10种不同的代谢物质,在晶状体中分析了15种。这些物质主要是代谢底物和终产物。作为评估灌注系统中晶状体行为的参考,将灌注的晶状体与兔另一只眼中的晶状体进行比较。在对照研究中制定了左右晶状体之间以及从兔身上取出的第一或第二晶状体之间差异的标准。设计了一系列实验来确定培养基中氨基酸浓度增加对晶状体代谢行为的影响。研究了氨基酸浓度为后房房水中氨基酸浓度的0至7.26倍的情况。以约每小时2克的培养基流速进行了七项研究,每项实验持续80至100小时。(摘要截断于400字)