Enteral infusion of sodium 2-ketoisocaproate in endotoxic rats

Citation
M. Hirokawa et M. Walser, Enteral infusion of sodium 2-ketoisocaproate in endotoxic rats, CRIT CARE M, 27(2), 1999, pp. 373-379
Citations number
54
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
27
Issue
2
Year of publication
1999
Pages
373 - 379
Database
ISI
SICI code
0090-3493(199902)27:2<373:EIOS2I>2.0.ZU;2-2
Abstract
Objective: In view of our previous finding that the intravenous infusion of 2-ketoisocaproate (KIC) improved survival in septic rats, we endeavored to determine whether the enteral infusion of KIC improves survival in endotox ic rats, and, if so, the mechanism of this effect, Subjects: Eighty-five rats were given 15 mg/kg of Escherichia coli lipopoly saccharide(026:B6). Interventions: KIC, sodium pyruvate (PYR), or sodium bicarbonate (HCO,) was infused continuously intragastrically at 18.75 mmol/kg/day. Measurements and Main Results: KIC administration increased circulating con centrations of KIC and ketone bodies, Survival rates were: KIC 17/32; PYR 2 /22; and HCO3 8/31. The significant improvement in survival with KIC, in co ntrast with HCO3 (p<.04) or PYR (p <.002), points to an effect specific to KIC rather than to ketoacids generally, and argues against an antioxidant m echanism to explain improved survival with enteral administration, To deter mine whether altered nitric oxide production was responsible, plasma nitrit e plus nitrate concentrations were measured sequentially in rats given a lo wer dose of lipopolysaccharide plus continuous intragastric KIC, PYR, or HC O3, All rats exhibited pronounced increases in plasma nitrite plus nitrate concentrations, peaking at 8 hrs, but both KIC and PYR caused greater incre ases than HCO3. Thus, differences in nitric oxide production cannot account for the different effects of PYR and KIC on survival, However, KIC infusio n for 8 hrs substantially increased ketone bodies in blood and liver, in co mparison with the infusion of HCO3 or PYR, Conclusion: Continuous enteral infusion of KIC improves survival in endotox emia, probably by its conversion to ketone bodies, which serve as an altern ative energy substrate.