Dass P D, Lawson L R, Delaney V, Bourke E
Department of Medicine, Emory University School of Medicine, Atlanta, Ga.
Miner Electrolyte Metab. 1987;13(6):433-41.
The possible role of gamma-glutamyltransferase (gamma-GT) in renal ammonia production from glutamine remains controversial, prompting the current investigation. In rat proximal tubules, compounds known to activate the enzyme including the endogenously produced organic anion, hippurate, induced a significant increase in glutamine-ammoniagenesis both in nonacidosis and chronic metabolic acidosis although in absolute terms the increase was not more marked under the latter conditions. AT-125, which irreversibly inactivates gamma-GT, but not phosphate-dependent glutaminase, reduced the production of ammonia from glutamine in both acid-base states. In absolute terms, again, this reduction was similar under both acid-base conditions, implying an unimportant role for gamma-GT in vitro in the augmentation in renal ammoniagenesis induced by chronic metabolic acidosis. Maleate-stimulated glutamine-ammoniagenesis recently attributed to its intramitochondrial inhibitory effect in the dog is substantially due to the activation of gamma-GT in rat proximal tubules.
γ-谷氨酰转移酶(γ-GT)在谷氨酰胺生成肾脏氨的过程中可能发挥的作用仍存在争议,这促使了当前的研究。在大鼠近端肾小管中,已知能激活该酶的化合物,包括内源性产生的有机阴离子马尿酸盐,在非酸中毒和慢性代谢性酸中毒状态下均能显著增加谷氨酰胺生成氨的过程,尽管从绝对值来看,在后者情况下增加并不更明显。AT - 125能不可逆地使γ-GT失活,但不影响磷酸依赖性谷氨酰胺酶,在两种酸碱状态下均降低了谷氨酰胺生成氨的量。同样,从绝对值来看,这种降低在两种酸碱条件下相似,这意味着γ-GT在体外对慢性代谢性酸中毒诱导的肾脏氨生成增加作用不大。最近认为在犬中马来酸盐刺激谷氨酰胺生成氨是由于其线粒体内抑制作用,而在大鼠近端肾小管中主要是由于γ-GT的激活。