Role of endogenous interferon-gamma on the enhancement of splenic NK cell activity by electroacupuncture stimulation in mice

J Neuroimmunol. 1998 Oct 1;90(2):176-86. doi: 10.1016/s0165-5728(98)00143-x.

Abstract

Successive electro-acupuncture (EA) stimulation applied to bilateral anterior tibial muscles, where Zusanli (ST36) acupoints are located, once a day (30 min) for 3 successive days significantly enhanced splenic natural killer (NK) cell activity in BALB/c mice. The percentage of splenic NK cells, as measured by flow cytometry, was not affected in these mice. Interferon (IFN)-gamma level in splenic aqueous extract, prepared from the ST36 acupoint-stimulated mice, was significantly higher than that of the controls. In vivo treatment with neutralizing monoclonal antibody against mouse IFN-gamma completely abrogated the increase in splenic NK cell activity induced by ST36 acupoint stimulation. The same stimulation also significantly increased the concentration of splenic beta-endorphin, which coincided with the significant increase in splenic IFN-gamma production. Pre-administration of 10 mg/kg naloxone before initiation of EA stimulation every day reduced the enhancements of NK cell activity and IFN-gamma level. These observations strongly suggest that endogenous IFN-gamma mediates the up-regulation of NK cell activity by EA stimulation at the ST36 acupoints. Furthermore, endogenous beta-endorphin secreted by EA stimulation also plays an important role in the up-regulation of NK cell function, which may be realized through regulating IFN-gamma production.

MeSH terms

  • Animals
  • CD3 Complex / analysis
  • Catecholamines / blood
  • Electroacupuncture*
  • Interferon-gamma / analysis
  • Interferon-gamma / physiology*
  • Interleukin-12 / physiology
  • Killer Cells, Natural / immunology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred ICR
  • Naloxone / pharmacology
  • Rabbits
  • Receptors, Interleukin-2 / analysis
  • Spleen / immunology
  • beta-Endorphin / analysis

Substances

  • CD3 Complex
  • Catecholamines
  • Receptors, Interleukin-2
  • Interleukin-12
  • Naloxone
  • beta-Endorphin
  • Interferon-gamma