Effect of insulin therapy on nonglycemic variables during acute illness

Endocr Pract. Mar-Apr 2004;10 Suppl 2:63-70. doi: 10.4158/EP.10.S2.63.

Abstract

Objective: To review the possible mechanisms for the reported clinical finding of better outcomes for hospitalized and critically ill patients as the result of improved metabolic control.

Results: Insulin inhibits free fatty acids, proinflammatory cytokines, and inflammatory growth factors, all of which may be detrimental in critically ill patients. Furthermore, insulin enhances nitric oxide synthesis, which promotes vasodilation. The mechanisms of insulin regulation of these factors are complex, although insulin seems to have a direct effect on the transcriptional factor, nuclear factor-kappabeta (NF-kappabeta). In turn, NF-kappabeta modulates the proinflammatory cytokines, adhesion molecules, and chemokines. In a euglycemic or slightly hyperglycemic environment, NF-kappabeta is suppressed by insulin; however, with more profound hyperglycemia, NF-kappabeta is induced and the proinflammatory cytokines are thus increased.

Conclusion: Although considerable research must be completed to identify the apparent relationship between stringent metabolic control and improved outcomes in acutely ill patients, current evidence suggests that both the treatment (glucose-insulin-potassium infusion) and the resultant plasma glucose concentrations may be independent important components of the underlying mechanisms.

Publication types

  • Review

MeSH terms

  • Acute Disease / therapy*
  • Cytokines / antagonists & inhibitors
  • Drug Combinations
  • Fatty Acids, Nonesterified / metabolism
  • Glucose / therapeutic use
  • Growth Substances / metabolism
  • Humans
  • Inflammation Mediators / antagonists & inhibitors
  • Insulin / therapeutic use*
  • Nitric Oxide / metabolism
  • Potassium / therapeutic use

Substances

  • Cytokines
  • Drug Combinations
  • Fatty Acids, Nonesterified
  • Growth Substances
  • Inflammation Mediators
  • Insulin
  • Nitric Oxide
  • Glucose
  • Potassium