Leclercq-Meyer V, Marchand J, Leclercq R, Malaisse W J
Diabetologia. 1979 Aug;17(2):121-6. doi: 10.1007/BF01222213.
The effects of alpha-ketoisocaproate (KIC, 10 mmol/l) on glucagon and insulin release were studied in the in vitro perfused rat pancreas. The experiments were performed at low glucose concentration (3.3 mmol/l) in the absence or presence of arginine (10 mmol/l). In all the experiments KIC induced a marked and not rapidly reversible inhibition of glucagon release. This inhibition was more pronounced in the absence (76 percent) than presence of arginine (61 percent). These inhibitory patterns closely duplicated those which were seen in parallel experiments which included a rise in the concentration of glucose (from 3.3 to 11.1 mmol/l). KIC was also a potent stimulator of insulin release. The results are compatible with the view that the intracellular metabolism of KIC and glucose plays an essential role in the regulation of glucagon release by exogenous substrates.
在体外灌注大鼠胰腺中研究了α-酮异己酸(KIC,10 mmol/L)对胰高血糖素和胰岛素释放的影响。实验在低葡萄糖浓度(3.3 mmol/L)下进行,有无精氨酸(10 mmol/L)存在。在所有实验中,KIC均诱导胰高血糖素释放出现显著且非快速可逆的抑制。在无精氨酸时这种抑制更为明显(76%),而有精氨酸时为61%。这些抑制模式与平行实验中观察到的模式非常相似,平行实验包括葡萄糖浓度升高(从3.3 mmol/L升至11.1 mmol/L)。KIC也是胰岛素释放的有效刺激剂。这些结果与以下观点相符,即KIC和葡萄糖的细胞内代谢在外源性底物对胰高血糖素释放的调节中起重要作用。