Leclercq-Meyer V, Marchand J, Malaisse W J
Laboratory of Experimental Medicine, Brussels Free University, Belgium.
Biochem Pharmacol. 1990 Feb 1;39(3):537-47. doi: 10.1016/0006-2952(90)90061-o.
In the isolated perfused rat pancreas, D,L-difluoromethylornithine, tested at a concentration of 3 mmol/L, failed to affect the release of glucagon and insulin caused, over 15 min stimulation, by either L-arginine or L-ornithine (2.0, 5.0 or 10.0 mmol/L) in the presence of either 3.3 or 5.6 mmol/L D-glucose. The inhibition of ornithine decarboxylase also failed to affect the release of glucagon provoked by either L-leucine (2 or 3 mmol/L) or L-glutamine (2 mmol/L) and the secretion of insulin stimulated by a rise in glucose concentration from 5.6 to 10.6 mmol/L. These data are interpreted to suggest that the rapid generation of polyamines from either L-arginine or L-ornithine does not play any significant role in the immediate glucagonotropic and insulinotropic action of these cationic amino acids.
在离体灌注大鼠胰腺中,浓度为3 mmol/L的D,L-二氟甲基鸟氨酸未能影响在3.3或5.6 mmol/L D-葡萄糖存在下,由L-精氨酸或L-鸟氨酸(2.0、5.0或10.0 mmol/L)经15分钟刺激所引起的胰高血糖素和胰岛素释放。鸟氨酸脱羧酶的抑制作用也未能影响由L-亮氨酸(2或3 mmol/L)或L-谷氨酰胺(2 mmol/L)所引发的胰高血糖素释放,以及由葡萄糖浓度从5.6 mmol/L升高至10.6 mmol/L所刺激的胰岛素分泌。这些数据被解读为表明从L-精氨酸或L-鸟氨酸快速生成多胺在这些阳离子氨基酸的即时促胰高血糖素和促胰岛素作用中未发挥任何显著作用。