Welsh M, Sener A, Malaisse-Lagae F, Malaisse W J
Mol Cell Biochem. 1984 Aug;63(1):33-7. doi: 10.1007/BF00230159.
Aminooxyacetate, an inhibitor of cytosolic transamination reactions, inhibited insulin release evoked by either 2-ketoisocaproate or L-leucine in rat pancreatic islets incubated in the presence of L-glutamine or L-asparagine. As a rule, aminooxyacetate also inhibited the oxidation of these nutrient secretagogues and impaired the respiratory response of the islets to the combinations of nutrients. However, the oxidative and secretory response to the combination of L-leucine and L-glutamine was less severely affected by aminooxyacetate than that evoked by the three other combinations of exogenous nutrients. These findings reinforce the view that the stimulus-secretion coupling of insulin release in response to L-leucine and 2-ketoisocaproate in association with either L-glutamine or L-asparagine tightly depends on the oxidation of these nutrient secretagogues, on their effect upon O2 uptake and, within limits, on the intracellular site of generation of reducing equivalents in the pancreatic islet cells.
氨基氧乙酸是一种胞质转氨反应抑制剂,在存在L-谷氨酰胺或L-天冬酰胺的情况下孵育的大鼠胰岛中,它抑制了由2-酮异己酸或L-亮氨酸诱发的胰岛素释放。通常,氨基氧乙酸也抑制这些营养性促分泌剂的氧化,并损害胰岛对营养物质组合的呼吸反应。然而,与其他三种外源营养物质组合相比,氨基氧乙酸对L-亮氨酸和L-谷氨酰胺组合的氧化和分泌反应影响较小。这些发现强化了这样一种观点,即胰岛细胞中,胰岛素释放对L-亮氨酸和2-酮异己酸与L-谷氨酰胺或L-天冬酰胺联合作用的刺激-分泌偶联紧密依赖于这些营养性促分泌剂的氧化、它们对氧气摄取的影响以及在一定限度内对还原当量产生的细胞内位点的依赖。