High-fat meal increases peripheral blood mononuclear cell pro-inflammatory cytokine expression in African-American women

Appl Physiol Nutr Metab. 2021 Jun;46(6):661-668. doi: 10.1139/apnm-2020-0873. Epub 2020 Dec 18.

Abstract

African-American (AA) women have elevated predominance of inflammatory diseases concurrent with local inflammation resulting in compromised metabolic function. The purpose of the study was 2-fold: 1) to examine the gene and protein expression of pro- and anti-inflammatory cytokine secretion by peripheral blood mononuclear cells (PBMC) obtained from AA and Caucasian-American (CA) women in response to an acute high-fat meal; and 2) to explore the influence of race (AA vs. CA) on PBMC reactivity. Ten AA and 11 CA women consumed a high-fat meal with baseline and 4 h postprandial venous blood draws. PBMCs were incubated for 3 h then messenger RNA expression and supernatant protein concentration was used to examine inflammatory profiles. All women had a postprandial increase in interleukin (IL)-8 gene expression, IL-8 protein concentration, and tumor necrosis factor alpha (TNF-α) protein concentration (P < 0.05). AA women had a postprandial increase in IL-6, IL-8, and TNF-α protein concentration (P < 0.05). AA women had higher postprandial IL-1β protein concentration and IL-8 gene expression compared with CA women (P < 0.05). Our data uncovers the specific impact of race and time on pro-inflammatory PBMC (IL-1β, IL-6, IL-8, and TNF-α) expression profiles in response to an acute high-fat meal challenge. Novelty: African Americans have higher predominance of inflammatory disease. We explored the potential race impact on peripheral blood mononuclear cell reactivity in response to a meal. A pro-inflammatory response to an acute high-fat meal with race impact was observed possibly contributing to health disparities impacting African-American women.

Keywords: African American; Afro-Américaine; PBMC; différences raciales; inflammation; metabolism; métabolisme; postprandial; racial differences.

MeSH terms

  • Adolescent
  • Adult
  • Black or African American*
  • Cytokines / blood*
  • Cytokines / genetics
  • Dietary Fats / administration & dosage*
  • Female
  • Gene Expression
  • Humans
  • Interleukin-1beta / blood
  • Interleukin-6 / blood
  • Interleukin-8 / blood
  • Interleukin-8 / genetics
  • Kentucky
  • Leukocytes, Mononuclear / metabolism*
  • Middle Aged
  • Postprandial Period
  • RNA, Messenger / blood
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Cytokines
  • Dietary Fats
  • IL1B protein, human
  • Interleukin-1beta
  • Interleukin-6
  • Interleukin-8
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha