{"title":"氨基酸输入率对灌注培养系统晶状体代谢的影响。","authors":"B Schwartz","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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)</p>","PeriodicalId":76972,"journal":{"name":"Acta ophthalmologica. 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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. 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引用次数: 0
摘要
建立了晶状体器官培养的灌注系统。该系统的设计是使流体的恒定流动通过透镜,同时有一个单独的流体通道绕过透镜。通过分析这两种液体样品之间的差异,可以确定晶状体的代谢活性。该系统还能维持与眼压相当的压力水平。用于观察和拍摄镜头的装置内置于系统中。这些研究的目的是为了确定这种灌注系统是否可以维持兔晶状体接近生理状态,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缺乏,并提供代谢底物来维持灌注条件下的晶状体。兔晶状体在33℃的温度下培养100 h。设计了一种完全合成的灌注培养基,不含蛋白质和抗生素。这种介质与后房水幽默相似,但不含抗坏血酸,因为发现抗坏血酸容易自动氧化并耗尽介质中的氧含量。调整灌注介质的氨基酸浓度,使其总氮含量与后房房水总氮含量相当。为了确定晶状体的代谢行为,分析了培养基中10种不同的代谢物质,分析了晶状体中15种不同的代谢物质。这些物质主要是代谢底物和最终产物。作为评价晶状体在灌注系统中的行为的参考,将灌注后的晶状体与家兔另一只眼的晶状体进行比较。在对照研究中制定了左右晶状体和从兔子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0 ~ 7.26倍后验氨基酸浓度的氨基酸浓度。共进行了7项实验,实验流速为2 g / h,每次实验持续80 ~ 100 h。
Effect of amino acid input rates on lens metabolism in a perfusion culture system.
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)