Stankeiwicz P J, Metz K R, Sassani J W, Briggs R W
Department of Radiology, Pennsylvania State University College of Medicine, Milton S. Hershey Medical Center, Hershey.
Invest Ophthalmol Vis Sci. 1989 Nov;30(11):2361-9.
Proton NMR relaxation times T1 and T2 were determined for normal lenses excised from sexually mature animals from seven different species. Lenses were immersed in physiological buffer during measurements, and suppression methods were employed to null the buffer signal. This enabled selective analysis of lenticular water. Observed relaxation times were correlated with protein and water content. At 37 degrees C and 1.89 Tesla, single-exponential spin-lattice relaxation was observed, but spin-spin relaxation was found to be double-exponential. It was shown that the short-T2 fraction is proportional to protein concentration; this fraction was attributed to water bound to protein. The long-T2 fraction was attributed to free lenticular water. The amounts of free and bound water thus obtained were used in the spin-lattice relaxation rate equation for rapid exchange in a two-component system to calculate the magnitudes of the two corresponding T1 relaxation components.
测定了从七个不同物种的性成熟动物身上摘除的正常晶状体的质子核磁共振弛豫时间T1和T2。在测量过程中,将晶状体浸入生理缓冲液中,并采用抑制方法消除缓冲液信号。这使得能够对晶状体水进行选择性分析。观察到的弛豫时间与蛋白质和水含量相关。在37摄氏度和1.89特斯拉的条件下,观察到单指数自旋晶格弛豫,但自旋自旋弛豫被发现是双指数的。结果表明,短T2部分与蛋白质浓度成正比;这部分归因于与蛋白质结合的水。长T2部分归因于晶状体中的自由水。由此获得的自由水和结合水的量被用于双组分系统中快速交换的自旋晶格弛豫速率方程,以计算两个相应T1弛豫分量的大小。