ORNITHINE ALPHA-KETOGLUTARATE MODULATES TISSUE PROTEIN-METABOLISM IN BURN-INJURED RATS

Citation
J. Leboucher et al., ORNITHINE ALPHA-KETOGLUTARATE MODULATES TISSUE PROTEIN-METABOLISM IN BURN-INJURED RATS, American journal of physiology: endocrinology and metabolism, 36(3), 1997, pp. 557-563
Citations number
43
Categorie Soggetti
Physiology
ISSN journal
01931849
Volume
36
Issue
3
Year of publication
1997
Pages
557 - 563
Database
ISI
SICI code
0193-1849(1997)36:3<557:OAMTPI>2.0.ZU;2-0
Abstract
Enterally administered ornithine alpha-ketoglutarate (OKG) displays wh ole body anabolic and anticatabolic properties in trauma situations, e specially after burn injury. The aim of this study was to get informat ion about the anabolic effect of OKG at tissue level. Thirty-six male Wistar rats (95 +/- 7 g) were allocated to four groups. Eighteen rats were burned by water (20% body surface area). After a 24-h fast (day 0 -day 1), rats were enterally refed for 48 h (day 1-day 3) by use of Os molite as a low-calorie, low-nitrogen regimen supplemented with either 5 g OKG.kg(-1).day(-1) (B-OKG) or an equivalent amount of nitrogen in the form of glycine (B-Gly). Nonburned pair-fed controls treated with glycine (C-Gly) and healthy rats fed ad libitum were also studied. On day 3, protein synthesis rates (large dose method), free glutamine co ncentrations, and total protein content were assessed in tissues. Myof ibrillar degradation was assessed by measuring urinary 3-methylhistidi ne excretion daily from day 0 to day 3. With regard to tissue protein synthesis rates, we demonstrate for the first time that OKG displays a nabolic properties in the jejunum [fractional synthesis rate (FSR) in %/day, ad libitum = 101.9 +/- 4.0; C-Gly = 84.7 +/- 3.1, P < 0.01 vs. ad libitum; B-Gly = 84.5 +/- 1.6, P < 0.01 vs. ad libitum; B-OKG = 97. 5 +/- 3.2, P < 0.05 vs. C-Gly and B-Gly] as well as in the liver (FSR in %/day, ad libitum = 75.9 +/- 3.7; C-Gly = 53.2 +/- 3.8, P < 0.01 vs . ad libitum; B-Gly = 70.2 +/- 2.0, P < 0.01 vs. C-Gly; B-OKG = 98.7 /- 4.6, P < 0.01 vs. ad libitum, C-Gly and B-Gly), the latter having p reviously been observed in vitro. Furthermore, we confirm that OKG inh ibits myofibrillar degradation, counteracts the trauma-induced fall of muscle glutamine pool, and induces an increase in glutamine concentra tion in the jejunum.