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. 2018 Feb 27;148(2):185–193. doi: 10.1093/jn/nxx032

TABLE 2.

Arginine, nitric oxide, ornithine, citrulline, and phenylalanine kinetics under euglycemic and hyperglycemic conditions prior to intravenous arginine bolus administration in 6 recent-onset KPD patients and 6 age-, gender-, and BMI-matched control participants1

Euglycemia Hyperglycemia
Kinetics,
μmol · kg LBM−1 · h−1 Control (n = 6) KPD (n = 6) Control (n = 6) KPD (n = 6)
Arginine flux2 55.2 ± 4.23 62.8 ± 3.70 44.5 ± 2.983 49.4 ± 2.203
Arginine synthesis2 (from citrulline) 7.83 ± 0.57 7.48 ± 0.28 5.30 ± 0.323 5.77 ± 0.673
Arginine flux from synthesis, % 14.4 ± 1.16 12.1 ± 0.78 13.1 ± 1.02 11.6 ± 1.09
Ornithine flux2 24.1 ± 3.46 16.3 ± 1.204 15.0 ± 1.483 13.5 ± 0.81
Nitric oxide synthesis 0.18 ± 0.05 0.19 ± 0.02 0.19 ± 0.03 0.28 ± 0.07
Citrulline flux2 9.17 ± 0.56 8.91 ± 0.45 7.16 ± 0.633 6.96 ± 0.813
Phenylalanine flux5 35.7 ± 2.46 45.6 ± 2.194 36.6 ± 2.61 43.9 ± 1.56

1All values are means ± SEMs. Cell means were compared by repeated-measures 2-factor ANOVA. KPD, ketosis-prone diabetes; LBM, lean body mass.

2Main effect of glycemic state (euglycemic compared with hyperglycemic), P < 0.05.

3Significantly different from corresponding group in euglycemic condition, P < 0.05 (post hoc Sidak multiple comparison test).

4Significantly different from control group in corresponding clinical condition, P < 0.05 (post hoc Sidak multiple comparison test).

5Main effect of group (control compared with KPD), P < 0.05.