Redzic Z B, Markovic I D, Vidovic V P, Vranic V P, Gasic J M, Duricic B M, Pokrajac M, Dordevic J B, Segal M B, Rakic L M
Institute of Biochemistry, Faculty of Medicine, Belgrade, Yugoslavia.
Exp Eye Res. 1998 Mar;66(3):315-25. doi: 10.1006/exer.1997.0424.
This study investigates the transport of endogenous nucleosides and deoxynucleosides from the capillaries of the eye into the aqueous humour and the lens using the in situ vascular eye perfusion technique in the guinea-pig. The transport of [3H] adenosine and [3H] thymidine across the blood-aqueous barrier proved to be very rapid with a volume of distribution after 4 minutes perfusion reaching 11.9+/-3.0% and 9.93+/-1.1%, respectively. However, the transport of [3H] guanosine and [3H] cytidine was slower, with volumes of distribution reaching only 3.38+/-0.58% and 4.8+/-1.41%. The values for the entry of deoxyadenosine and deoxyguanosine were not significantly different from the values obtained for corresponding ribonucleosides (adenosine and guanosine) so that a change in the pentose sugar does not change the affinity of the nucleoside for the transport protein. Perfusion with a low sodium medium inhibited the transport of [3H] adenosine and [3H] thymidine into the aqueous humour. The presence of 800 nM NBTI also caused a decrease in adenosine transport into the aqueous humour, so that the volume of distribution after 2 minutes reached only 3.78+/-1.87%. These findings suggest that the transfer of adenosine across the blood-aqueous barrier has both concentrative and equilibrative components. The presence of 0.1 mM thymidine had no effect on the [3H] adenosine transport, whereas 0.1 mM of adenosine resulted in a marked decrease on the [3H] thymidine transport which suggests that the concentrative nucleotide transport is probably mediated by both cif and cit transport systems. The cellular uptake of nucleosides into the lens was very rapid and the volume of distribution of purine nucleosides was within the range of 30-50% whereas that for thymidine uptake was somewhat lower, reaching 20-30%. HPLC analysis of the eye structures in the guinea-pig showed that lens, vitreous body and the rest of the eye do not contain either free nucleosides or purine bases in detectable quantities, except for xanthine which was detected in aqueous humour at a concentration of 2.51+/-0.51 mM. However, serum of the anaesthetised guinea-pig did not contain xanthine in detectable amount so it seems that the metabolic degradation of the nucleosides in the guinea-pig eye progresses as far as xanthine, which is then accumulated in the aqueous humour.
本研究采用豚鼠原位血管眼灌注技术,研究内源性核苷和脱氧核苷从眼毛细血管向房水和晶状体的转运。[3H]腺苷和[3H]胸苷跨血-房水屏障的转运非常迅速,灌注4分钟后的分布容积分别达到11.9±3.0%和9.93±1.1%。然而,[3H]鸟苷和[3H]胞苷的转运较慢,分布容积仅达到3.38±0.58%和4.8±1.41%。脱氧腺苷和脱氧鸟苷的进入值与相应核糖核苷(腺苷和鸟苷)获得的值无显著差异,因此戊糖的变化不会改变核苷对转运蛋白的亲和力。用低钠培养基灌注可抑制[3H]腺苷和[3H]胸苷向房水的转运。800 nM NBTI的存在也导致腺苷向房水的转运减少,因此2分钟后的分布容积仅达到3.78±1.87%。这些发现表明腺苷跨血-房水屏障的转运既有浓缩成分又有平衡成分。0.1 mM胸苷的存在对[3H]腺苷转运无影响,而0.1 mM腺苷导致[3H]胸苷转运显著降低,这表明浓缩核苷酸转运可能由cif和cit转运系统介导。核苷进入晶状体的细胞摄取非常迅速,嘌呤核苷的分布容积在30-50%范围内,而胸苷摄取的分布容积略低,达到20-30%。豚鼠眼结构的HPLC分析表明,除了在房水中以2.51±0.51 mM的浓度检测到黄嘌呤外,晶状体、玻璃体和眼的其余部分均未含有可检测量的游离核苷或嘌呤碱基。然而,麻醉豚鼠的血清中未检测到可检测量的黄嘌呤,因此似乎豚鼠眼中核苷的代谢降解进展到黄嘌呤,然后黄嘌呤在房水中积累。