Table 3.
Type of lens | Cortex | Nucleus | ||
---|---|---|---|---|
| ||||
Specific activity (nmoles/mg protein/h) | Total activity in cortex (nmoles/h) | Specific activity (nmoles/h) protein/h) | Total activity in nucleus (nmoles/mg | |
Human young (20 years) | 0.28 ± 0.04** | 7.86 ± 0.89 | 0.043 ± 0.003** | 0.98 ± 0.07 |
Human middle aged (40 years) | 0.37 ± 0.04*** | 6.50 ± 0.78 | 0.032 ± 0.001*** | 0.76 ± 0.05 |
Human old aged (60 years) | 0.29 ± 0.02** | 4.92 ± 0.27 | 0.037 ± 0.001** | 0.57 ± 0.02 |
Bovine young | 0.68 ± 0.07*** | 95.87 ± 3.26 | 0.035 ± 0.001*** | 7.53 ± 0.31 |
Water-soluble cortical and nuclear extracts (1 mg protein) of young, middle-aged and old human lenses were incubated with MCA-62-70 substrate (25 μg) at 37 °C for 2 h. Difference in fluorescence intensity was measured before and after incubation in a spectrofluorometer after excitation at 326 nm and emission at 398 nm. The amount of MCA-62-70 hydrolyzed was calculated by extrapolation of standard graph prepared by tryptic digestion of different concentrations of MCA-62-70 substrate. The values presented are average ± SE of four independent experiments. The data was analyzed by one-way ANOVA followed by Tukey’s multiple comparison test where **p<0.001 and ***p<0.0001, compared within lens groups of cortex and nucleus. Differences between lens groups of different ages were not significant.