Differential effects of glucose and alcohol on reactive oxygen species generation and intranuclear nuclear factor-kappaB in mononuclear cells

Metabolism. 2004 Mar;53(3):330-4. doi: 10.1016/j.metabol.2003.10.013.

Abstract

It has previously been shown that oral intake of 300 calories of glucose (75 g), lipid, or protein increases reactive oxygen species (ROS) generation by polymorphonuclear cells (PMNL) and mononuclear cells (MNCs). We investigated the effects of 75 g glucose on proinflammatory transcription factor, nuclear factor-kappaB (NFkappaB), in mononuclear cells. To further investigate whether the effects of macronutrient-induced oxidative stress are due to consumption of calories or are nutrient specific, we investigated the effects of acute oral challenge of equicaloric amounts of alcohol (300 calories) on ROS generation and NF-kappaB activation in MNCs and PMNL and compared them with those of glucose and water (control). Sixteen normal healthy adult volunteers were given either vodka (10 subjects), glucose solution (10 subjects), or 300 mL water (7 subjects). Vodka and glucose drinks were equivalent to 300 calories. We measured ROS generation and intranuclear NF-kappaB activation by PMNL cells and MNCs at 1 hour, 2 hours, and 3 hours following ingestion. ROS generation by both MNC and PMNL increased significantly (P <.05 for MNC and P <.01 for PMNL) following intake of glucose solution, but did not change significantly following alcohol or water. NF-kappaB binding activity in MNC nuclear extracts also increased (P <.001) following ingestion of glucose solution, but did not change after the administration of alcohol or water. We conclude that (1) 75 g oral glucose increases NF-kappaB binding activity in MNCs. (2) While 75 g glucose (300 calories) induces an increase in ROS generation and intranuclear NF-kappaB, equicaloric amounts of alcohol did not produce these effects.

MeSH terms

  • Adult
  • Blood Glucose / metabolism
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism*
  • Cell Separation
  • Central Nervous System Depressants / blood
  • Central Nervous System Depressants / pharmacology*
  • Electrophoretic Mobility Shift Assay
  • Ethanol / blood
  • Ethanol / pharmacology*
  • Female
  • Glucose / pharmacology*
  • Humans
  • Inflammation Mediators / blood
  • Insulin / blood
  • Male
  • Monocytes / drug effects
  • Monocytes / metabolism*
  • NF-kappa B / metabolism*
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Reactive Oxygen Species / metabolism*

Substances

  • Blood Glucose
  • Central Nervous System Depressants
  • Inflammation Mediators
  • Insulin
  • NF-kappa B
  • Reactive Oxygen Species
  • Ethanol
  • Glucose