beta2-Integrin and lipid modifications indicate a non-antioxidant mechanism for the anti-atherogenic effect of dietary coenzyme Q10

Biochem Biophys Res Commun. 2002 Aug 16;296(2):255-60. doi: 10.1016/s0006-291x(02)00871-9.

Abstract

Dietary supplementation with coenzyme Q (CoQ) has been proposed to have anti-atherogenic effects by virtue of its antioxidant capacity. To investigate this question, the leukocyte status of 5 males and 5 females (52-68 years) was evaluated before and after supplementation with 200mg CoQ/day for 5 and 10 weeks. CoQ was selectively taken up by mononuclear cells and alpha-tocopherol increased in polynuclear and mononuclear cells. The expression of beta2-integrin CD11b and complement receptor CD35 on the plasma membrane of resting and stimulated monocytes was significantly decreased upon dietary CoQ. Fatty acid and aldehyde analysis revealed that there was a selective increase of arachidonic acid and plasmalogens in only mononuclear cells. These selective lipid changes are not consistent with a general improvement in antioxidant status and indicate that CoQ most likely inhibits a phospholipase A2. Thus, these results strongly suggest that the anti-atherogenic effects of CoQ be mediated by other mechanisms beside its antioxidant protection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Antioxidants / metabolism*
  • CD18 Antigens / metabolism*
  • Coenzymes
  • Cytoprotection
  • Diet, Atherogenic
  • Dietary Supplements*
  • Female
  • Humans
  • Leukocytes / metabolism
  • Macrophage-1 Antigen / metabolism
  • Male
  • Middle Aged
  • Phospholipids / metabolism*
  • Receptors, Complement 3b / metabolism
  • Ubiquinone / administration & dosage*
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / metabolism
  • alpha-Tocopherol / metabolism

Substances

  • Antioxidants
  • CD18 Antigens
  • Coenzymes
  • Macrophage-1 Antigen
  • Phospholipids
  • Receptors, Complement 3b
  • Ubiquinone
  • coenzyme Q10
  • alpha-Tocopherol