Taylor P M, Rennie M J
FEBS Lett. 1987 Sep 14;221(2):370-4. doi: 10.1016/0014-5793(87)80958-4.
Periportal and perivenous hepatocytes differ in their metabolism of blood glutamate (Glu). Uncertainty about the mechanisms of Glu blood-liver exchange led us to characterise, by paired-tracer dilution, a sodium-dependent dicarboxylate transporter (resembling system X-ag) in sinusoidal membranes of perfused rat liver (Vmax = 0.18 mumol Glu/g per min, Km = 0.29 mM Glu). Tracer Glu transport was depressed 65% after necrosis of perivenous hepatocytes by acute CCl4 treatment, indicating that X-ag transporter activity is located mainly in these cells, the sites of glutamine (Gln) synthesis from glutamate and ammonia. Modulation of Glu transport may influence the extent of hepatic Gln release.
汇管区和肝静脉周围的肝细胞在血液谷氨酸(Glu)代谢方面存在差异。由于Glu在血液与肝脏之间交换的机制尚不确定,我们通过成对示踪剂稀释法对灌注大鼠肝脏的窦状隙膜中的一种钠依赖性二羧酸转运体(类似于X-ag系统)进行了表征(Vmax = 0.18 μmol Glu/g每分钟,Km = 0.29 mM Glu)。急性四氯化碳处理导致肝静脉周围肝细胞坏死后,示踪剂Glu转运降低了65%,这表明X-ag转运体活性主要位于这些细胞中,这些细胞是由谷氨酸和氨合成谷氨酰胺(Gln)的部位。Glu转运的调节可能会影响肝脏Gln释放的程度。