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吡咯啉-5-羧酸还原酶对晶状体中磷酸己糖途径的刺激作用。

Stimulation of the hexose monophosphate pathway by pyrroline-5-carboxylate reductase in the lens.

作者信息

Shiono T, Kador P F, Kinoshita J H

出版信息

Exp Eye Res. 1985 Dec;41(6):767-75. doi: 10.1016/0014-4835(85)90185-x.

Abstract

Addition of pyrroline-5-carboxylate (P5C) or its precursors to rat lenses cultured for 24 hr in TC-199 medium containing 14C-glucose results in an apparent concentration-dependent increase in hexose monophosphate-pentose (HMP) pathway activity. Addition of proline, the reduction product of P5C, did not result in an increase, suggesting that stimulation of the HMP pathway is related to the reduction of P5C to proline by the enzyme P5C reductase. No apparent feedback inhibition on P5C reductase was observed. Stimulation of HMP pathway activity by P5C was also observed in the lenses of Philly and Nakano mouse, two models of congenital osmotic cataracts. Compared with its genetic control, the Swiss--Webster mouse, generally no difference in the lenticular levels of HMP pathway activity was observed in the Philly mouse--even after the onset of cataract. Stimulation of the HMP pathway in the Philly lens by P5C, however, was consistently lower than its control. In the lenses from the Nakano mouse and its genetic control, the Balb/c mouse, no difference in the percentage stimulation of the HMP pathway resulting from the addition of P5C was observed, but HMP pathway activity in the Nakano lens was consistently lower than that of the control.

摘要

在含有14C-葡萄糖的TC-199培养基中培养24小时的大鼠晶状体中添加吡咯啉-5-羧酸(P5C)或其前体,会导致磷酸己糖-戊糖(HMP)途径活性明显呈浓度依赖性增加。添加P5C的还原产物脯氨酸则不会导致活性增加,这表明HMP途径的刺激与P5C还原酶将P5C还原为脯氨酸有关。未观察到对P5C还原酶有明显的反馈抑制作用。在两种先天性渗透性白内障模型——菲利(Philly)和中野(Nakano)小鼠的晶状体中,也观察到了P5C对HMP途径活性的刺激作用。与基因对照瑞士-韦伯斯特(Swiss-Webster)小鼠相比,菲利小鼠晶状体中HMP途径活性水平通常没有差异——即使在白内障发病后也是如此。然而,P5C对菲利晶状体中HMP途径的刺激作用始终低于其对照。在中野小鼠及其基因对照Balb/c小鼠的晶状体中,添加P5C后HMP途径的刺激百分比没有差异,但中野晶状体中的HMP途径活性始终低于对照。

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