Treadmill exercise in mice increases intestinal lymphocyte loss via apoptosis

Acta Physiol Scand. 2003 Nov;179(3):289-97. doi: 10.1046/j.1365-201X.2003.01176.x.

Abstract

Strenuous exercise is associated with a transient decline in circulating lymphocytes, possibly through increased apoptosis. Intestinal lymphocytes are important effector cells of intestinal immune function but have not been studied in relation to exercise.

Aim: The purpose of the present study was to examine the effect of exercise on intestinal lymphocyte phenotypes and apoptosis.

Methods: Female C57BL/6 mice (n = 112) were randomized to: (1) treadmill running (90 min, 32 m min-1, 8 degrees grade) and killed immediately after exercise, (2) treadmill running and killed 2 h after exercise, (3) treadmill running and killed 24 h after exercise or (4) a non-exercised control condition with exposure to treadmill noise and vibration without running.

Results: Flow cytometry indicated that the total intestinal CD3+T (P < 0.01), CD4+T (P < 0.005), CD8+T (P < 0.05), pan-NK (P < 0.005) and CD19+B (P < 0.05) lymphocytes were significantly lower 24 h after exercise compared with non-exercised controls. Significantly more CD3+T (P < 0.05) and CD8+T (P < 0.05) intestinal lymphocytes stained positive for annexin V, a marker of apoptosis, at 24 h after exercise compared with intestinal lymphocytes from non-exercised controls. Plasma corticosterone and 8-isoprostane concentrations were also significantly higher immediately after exercise compared with other exercise conditions.

Conclusion: Acute strenuous exercise increases intestinal T (CD3+ and CD8+) lymphocyte loss and apoptosis. The extent to which the exercise-induced apoptosis in intestinal lymphocytes is mediated by increased glucocorticoid concentrations in the gastrointestinal tract will require further studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / analysis
  • Apoptosis / physiology*
  • Corticosterone / blood
  • Dinoprost* / analogs & derivatives*
  • F2-Isoprostanes / blood
  • Female
  • Flow Cytometry / methods
  • Intestines / cytology*
  • Lymphocyte Count
  • Lymphocyte Subsets / physiology
  • Lymphocytes / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Phenotype
  • Physical Conditioning, Animal / physiology*

Substances

  • Antigens, CD
  • F2-Isoprostanes
  • 8-epi-prostaglandin F2alpha
  • Dinoprost
  • Corticosterone