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湿房和麦卡里-考夫曼培养基储存对角膜代谢状态的影响:一项31P磁共振分析。

Effects of moist-chamber and McCarey-Kaufman medium storage on the metabolic status of the cornea: a 31P-magnetic resonance analysis.

作者信息

Lass J H, Greiner J V, Medcalf S K, Kralik M R, Meneses P, Glonek T

机构信息

Division of Ophthalmology, Case Western Reserve University, Cleveland, Ohio, Boston.

出版信息

Ophthalmic Res. 1988;20(6):368-75. doi: 10.1159/000266754.

Abstract

The rate of change in concentration of corneal phosphatic metabolites of cat corneas stored in moist chamber and McCarey-Kaufman (M-K) medium was determined in order to provide a basis for prediction of the corneal metabolic status at a given storage time. Perchloric acid corneal extracts were examined by phosphorus-31 magnetic resonance after storage at 4 degrees C of whole globes under moist-chamber conditions up to 48 h and of excised corneas in M-K medium up to 168 h. A significant decline in the corneal concentrations of ATP and a significant increase in inorganic phosphate occurred for both storage methods; however, depending on the metabolite, the rate of decline or increase was significantly greater for the moist-chamber-stored corneas. The phosphorylated sugars significantly increased and the glycerophosphodiesters significantly decreased in the moist-chamber-stored corneas, whereas both metabolites remained unchanged in the M-K-medium-stored corneas. There was no significant change in the dinucleotides and nucleoside diphospho-sugars during the time course for both storage methods. A threefold greater rate of decline was noted in the tissue energy modulus for the moist-chamber-stored corneas than for the M-K-medium-stored corneas (-0.0465 vs. -0.0121 modulus values/h). M-K medium was significantly more effective in the maintenance of high-energy phosphatic metabolites. The mathematical model for these rate determinations provides a basis for prediction of the corneal metabolic status at a given time in moist-chamber or M-K medium storage.

摘要

为了为预测给定储存时间的角膜代谢状态提供依据,测定了储存在湿盒和麦卡雷 - 考夫曼(M-K)培养基中的猫角膜的角膜磷酸代谢物浓度变化率。在4℃下,将整个眼球在湿盒条件下储存长达48小时,将切除的角膜在M-K培养基中储存长达168小时后,用磷-31磁共振检查高氯酸角膜提取物。两种储存方法均使角膜ATP浓度显著下降,无机磷酸盐显著增加;然而,根据代谢物的不同,湿盒储存的角膜中下降或增加的速率显著更高。湿盒储存的角膜中磷酸化糖显著增加,甘油磷酸二酯显著减少,而在M-K培养基储存的角膜中这两种代谢物均保持不变。两种储存方法在整个时间过程中,二核苷酸和核苷二磷酸糖均无显著变化。湿盒储存的角膜的组织能量模量下降速率比M-K培养基储存的角膜快三倍(模量值分别为-0.0465和-0.0121 /小时)。M-K培养基在维持高能磷酸代谢物方面显著更有效。这些速率测定的数学模型为预测湿盒或M-K培养基储存中给定时间的角膜代谢状态提供了依据。

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