Lietz T, Bryła J
Institute of Biochemistry, University of Warsaw, Poland.
Arch Biochem Biophys. 1995 Aug 20;321(2):501-9. doi: 10.1006/abbi.1995.1423.
In renal tubules isolated from fed rabbits, 1 mM aspartate is mainly utilized for production of glutamine, glutamate, alanine, and serine, while it is not used for glucose synthesis. However, the addition of either 2 mM glycerol or 2 mM lactate, which are poor gluconeogenic substrates in renal tubules, results in acceleration of both glucose formation and incorporation of [14C]aspartate into glucose by several fold, accompanied by about a twofold decrease in glutamine synthesis and marked accumulation of glutamate and alanine. Ammonium release in renal tubules incubated with aspartate in the presence of methionine sulfoximine, an inhibitor of glutamine synthetase, is also decreased on the addition of glycerol and lactate by about two- and threefold, respectively. Since intracellular [glyceraldehyde 3-phosphate]/[3-phosphoglycerate], [glycerol 3-phosphate]/[dihydroxyacetone phosphate], [lactate]/[pyruvate], and intramitochondrial [glutamate]/[2-oxoglutarate] x [NH4+] ratios are increased in comparison with control values determined with aspartate alone, it is likely that the stimulatory effect of lactate and glycerol on glucose formation from aspartate may be due to (i) an increased availability of reducing equivalents in the cytosol resulting in an enhancement of glyceraldehyde-3-phosphate dehydrogenase activity and (ii) elevation of the mitochondrial NADH/NAD- ratio causing a decrease in glutamate dehydrogenase activity resulting in a diminished glutamine synthesis and enhanced provision of carbon skeleton of aspartate for gluconeogenesis. Stimulation of glucose formation in the presence of 1 mM aspartate + glycerol is not related to cell volume changes. However, an increase for about 30% of intracellular water space induced by 10 mM aspartate + glycerol is accompanied by both diminished gluconeogenesis and enhanced glutamine synthesis, compared with values measured with 1 mM aspartate plus glycerol.
在从喂食后的兔子分离出的肾小管中,1 mM天冬氨酸主要用于生成谷氨酰胺、谷氨酸、丙氨酸和丝氨酸,而不用于葡萄糖合成。然而,添加2 mM甘油或2 mM乳酸(它们是肾小管中较差的糖异生底物)会导致葡萄糖生成加速以及[14C]天冬氨酸掺入葡萄糖的量增加数倍,同时谷氨酰胺合成减少约两倍,谷氨酸和丙氨酸显著积累。在谷氨酰胺合成酶抑制剂甲硫氨酸亚砜亚胺存在下,用天冬氨酸孵育的肾小管中,添加甘油和乳酸后,铵释放也分别减少约两倍和三倍。由于与仅用天冬氨酸测定的对照值相比,细胞内[甘油醛3-磷酸]/[3-磷酸甘油酸]、[3-磷酸甘油]/[二羟丙酮磷酸]、[乳酸]/[丙酮酸]以及线粒体内[谷氨酸]/[2-氧代戊二酸]×[NH4+]的比值增加,乳酸和甘油对从天冬氨酸生成葡萄糖的刺激作用可能是由于:(i) 胞质中还原当量的可用性增加,导致甘油醛-3-磷酸脱氢酶活性增强;(ii) 线粒体NADH/NAD+比值升高,导致谷氨酸脱氢酶活性降低,从而使谷氨酰胺合成减少,并增强了用于糖异生的天冬氨酸碳骨架的供应。在1 mM天冬氨酸 + 甘油存在下葡萄糖生成的刺激与细胞体积变化无关。然而,与用1 mM天冬氨酸加甘油测量的值相比,10 mM天冬氨酸 + 甘油诱导的细胞内水空间增加约30%,同时伴有糖异生减少和谷氨酰胺合成增强。