Risquez A, Slemmer Gaydos D, Preuss H G
Ren Physiol. 1983;6(5):218-25. doi: 10.1159/000172903.
The concentration of renal 2-oxoglutarate has been proposed as an important regulator of ammoniagenesis in dog kidneys. In the present study, canine kidney slices produced less ammonia from glutamine and glutamate when 2-oxoglutarate was present in the incubation medium. However, the addition of arsenite, a metabolic blocker known to block 2-oxoglutarate metabolism and lead to its accumulation, overcame 2-oxoglutarate inhibition of ammoniagenesis when glutamine and glutamate were the ammonia precursors. Therefore, metabolism of 2-oxoglutarate, rather than its concentration, governed ammonia production from glutamine and glutamate in incubating dog renal tissue. In contrast to the results with 2-oxoglutarate, inhibition of glutamine ammoniagenesis by glutamate was not overcome by arsenite. The results suggest that renal ammonia adaptation in acidotic dogs cannot be ascribed to a theory based upon 2-oxoglutarate concentrations controlling the direction of the glutamate dehydrogenase pathway (GDH), decreasing glutamine transport, or directly inhibiting GDH enzyme activity.
肾中2-氧代戊二酸的浓度被认为是犬肾中氨生成的重要调节因子。在本研究中,当孵育培养基中存在2-氧代戊二酸时,犬肾切片从谷氨酰胺和谷氨酸产生的氨较少。然而,添加亚砷酸盐(一种已知可阻断2-氧代戊二酸代谢并导致其积累的代谢阻滞剂),当谷氨酰胺和谷氨酸是氨的前体时,可克服2-氧代戊二酸对氨生成的抑制作用。因此,在孵育的犬肾组织中,2-氧代戊二酸的代谢而非其浓度决定了谷氨酰胺和谷氨酸产生氨的过程。与2-氧代戊二酸的结果相反,亚砷酸盐不能克服谷氨酸对谷氨酰胺氨生成的抑制作用。结果表明,酸中毒犬的肾氨适应性不能归因于基于2-氧代戊二酸浓度控制谷氨酸脱氢酶途径(GDH)方向、减少谷氨酰胺转运或直接抑制GDH酶活性的理论。