Department of Pharmaceutics, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Microvasc Res. 2011 Nov;82(3):385-90. doi: 10.1016/j.mvr.2011.06.009. Epub 2011 Jun 29.
Nicotinic acid is a constituent of the coenzymes NAD and NADP. It also serves as an agonist for the G-protein-coupled receptor GPR109A. Nicotinic acid is widely used at high doses as a lipid-lowering drug, which is associated with an ocular side effect known as niacin maculopathy. Here we investigated the mechanism by which nicotinate is transferred into retina across the inner blood-retinal barrier (BRB). In vivo the blood-to-retina transport of [(3)H]-nicotinate was studied using the carotid artery injection technique. The characteristics of nicotinate transport at the inner BRB were examined in a conditionally immortalized rat retinal capillary endothelial cell line (TR-iBRB2), an in vitro model of inner BRB. The expression of transporters in TR-iBRB2 cells was determined by reverse transcription-polymerase chain reaction. In vivo [(3)H]-nicotinate uptake by the retina was 5.4-fold greater than that of [(14)C]-sucrose, a BRB impermeable vascular space marker. Excess amounts of unlabeled nicotinate and salicylate significantly decreased the in vivo retinal uptake of [(3)H]-nicotinate. [(3)H]-Nicotinate was taken up by TR-iBRB2 cells via an H(+)-dependent saturable process with a Michaelis constant of ~7 mM. Na(+) had minimal effect on the uptake. The H(+)-dependent uptake was significantly inhibited by endogenous monocarboxylates such as lactate and pyruvate, and monocarboxylic drugs such as valproate, salicylate, and ibuprofen. These characteristics are consistent with those of H(+)-coupled monocarboxylate transporters (MCTs). MCT1, MCT2, and MCT4 mRNAs were expressed in TR-iBRB2 cells. The Na(+)-dependent monocarboxylate transporters SMCT1 and SMCT2 were not expressed in these cells. In conclusion, transfer of nicotinate from blood to retina across the inner BRB occurs primarily via H(+)-coupled monocarboxylate transporters.
烟酸是辅酶 NAD 和 NADP 的组成部分。它也作为 G 蛋白偶联受体 GPR109A 的激动剂。烟酸被广泛用作高剂量的降脂药物,其与一种称为烟酸黄斑病的眼部副作用有关。在这里,我们研究了烟酸盐通过内血视网膜屏障(BRB)转移到视网膜的机制。在体内,使用颈动脉注射技术研究了[(3)H]-烟酸盐的血液到视网膜的转运。在条件性永生化大鼠视网膜毛细血管内皮细胞系(TR-iBRB2)中,一种内 BRB 的体外模型中,检查了烟酸盐在内 BRB 处的转运特性。通过逆转录聚合酶链反应确定了 TR-iBRB2 细胞中的转运体表达。与 BRB 不可渗透的血管空间标记物[(14)C]-蔗糖相比,体内[(3)H]-烟酸盐对视网膜的摄取增加了 5.4 倍。过量的未标记的烟酸盐和水杨酸盐显著降低了体内[(3)H]-烟酸盐的视网膜摄取。[(3)H]-烟酸盐通过 TR-iBRB2 细胞的摄取是通过依赖 H(+)的饱和过程进行的,米氏常数约为 7 mM。Na(+)对摄取的影响最小。内源性单羧酸如乳酸盐和丙酮酸以及单羧酸药物如丙戊酸盐、水杨酸盐和布洛芬显著抑制 H(+)-依赖性摄取。这些特征与 H(+)-偶联的单羧酸转运体(MCTs)一致。MCT1、MCT2 和 MCT4 mRNA 在 TR-iBRB2 细胞中表达。这些细胞中未表达 Na(+)-依赖性单羧酸转运体 SMCT1 和 SMCT2。总之,烟酸盐从血液到内 BRB 内的视网膜的转运主要通过 H(+)-偶联的单羧酸转运体发生。