Selhub J, Nakamura S, Carone F A
Am J Physiol. 1987 Apr;252(4 Pt 2):F757-60. doi: 10.1152/ajprenal.1987.252.4.F757.
Surface proximal convoluted tubules (PCT) in rats were microinfused in situ with [3H]folic acid to study the role of folate binding protein (FBP) in the kidney brush-border membrane for renal conservation and transport of folate [3H]folic acid absorption was linearly related to tubular length of PCT and occurred largely in this segment of the tubule. Unlabeled folate derivatives inhibited [3H]folic acid absorption, the extent of which was dependent on the type of unlabeled folate used and its concentration. At equivalent concentrations, inhibition was most effective with unlabeled folic acid, slightly lower than with 5-methyltetrahydrofolate and least effective with methotrexate. Comparisons between [3H]folic acid absorption before and after infusion of a saturating dose of unlabeled folic acid or repetitive injections of [3H]folic acid into the same tubular site revealed continuous and rapid regeneration of unsaturated folic acid uptake sites with an apparent half-life of 28.75 +/- 8.75 s. Determination of [3H] retained in the tubule at various periods after microinfusion of [3H]folic acid revealed slow cellular disappearance with an apparent half-life of 47.3 +/- 5.4 min. It is proposed that the brush-border FBP functions as a receptor of infused folic acid and that following the binding of the ligand the folic acid/FBP complex undergoes a rapid change that results in the internalization of folic acid and regeneration of unsaturated binding sites at the membrane surface. Internalized folic acid is slowly released into renal capillaries.
将[3H]叶酸原位微量注入大鼠的近端曲管(PCT),以研究叶酸结合蛋白(FBP)在肾刷状缘膜中对叶酸的肾脏保留和转运作用。[3H]叶酸的吸收与PCT的肾小管长度呈线性相关,且主要发生在该肾小管段。未标记的叶酸衍生物抑制[3H]叶酸的吸收,其抑制程度取决于所用未标记叶酸的类型及其浓度。在等效浓度下,未标记叶酸的抑制作用最有效,略低于5-甲基四氢叶酸,而甲氨蝶呤的抑制作用最弱。在注入饱和剂量的未标记叶酸前后或在同一肾小管部位重复注射[3H]叶酸后,比较[3H]叶酸的吸收情况,发现不饱和叶酸摄取位点能持续快速再生,表观半衰期为28.75±8.75秒。在微量注入[3H]叶酸后的不同时间段,测定肾小管中保留的[3H],结果显示细胞内的[3H]消失缓慢,表观半衰期为47.3±5.4分钟。有人提出,刷状缘FBP作为注入叶酸的受体,配体结合后,叶酸/FBP复合物会迅速发生变化,导致叶酸内化以及膜表面不饱和结合位点的再生。内化的叶酸会缓慢释放到肾毛细血管中。