Sophocarpine and matrine inhibit the production of TNF-alpha and IL-6 in murine macrophages and prevent cachexia-related symptoms induced by colon26 adenocarcinoma in mice

Int Immunopharmacol. 2008 Dec 20;8(13-14):1767-72. doi: 10.1016/j.intimp.2008.08.008. Epub 2008 Sep 5.

Abstract

The present study aims to access the effects of sophora alkaloids on the production of pro-inflammatory cytokines and evaluate their therapeutic efficiency on cachexia. The comparative study showed that all sophora alkaloids tested here, including matrine, oxymatrine, sophocarpine, sophoramine, and sophoridine, inhibited TNF-alpha and IL-6 production in both RAW264.7 cells and murine primary macrophages, and sophocarpine showed the most potent inhibitory effect among them. Quantification of TNF-alpha and IL-6 mRNA in RAW264.7 cells by real-time RT-PCR revealed that both sophocarpine and matrine suppressed TNF-alpha and IL-6 expression and sophocarpine has stronger suppressing potency than matrine. Inoculation (s.c.) of colon26 adenocarcinoma cells into BALB/c mice induced cachexia, as evidenced by progressive weight loss, reduction in food intake, wasting of gastrocnemius muscle and epididymal fat, and increase in serum levels of TNF-alpha and IL-6. Administration of 50 mg/kg/d sophocarpine or matrine for 5 days from the onset of cachexia did not inhibit the tumor growth but resulted in attenuation of cachexia symptoms. Furthermore, sophocarpine and matrine decreased the serum levels of TNF-alpha and IL-6, and sophocarpine showed a better therapeutic effect than matrine. These results suggest that sophocarpine and matrine exert anti-cachectic effects probably through inhibition of TNF-alpha and IL-6.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / complications*
  • Alkaloids / chemistry
  • Alkaloids / pharmacology
  • Alkaloids / therapeutic use*
  • Animals
  • Cachexia / etiology
  • Cachexia / prevention & control*
  • Cell Line
  • Colonic Neoplasms / complications*
  • Interleukin-6 / antagonists & inhibitors
  • Interleukin-6 / blood
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Macrophages / immunology
  • Male
  • Matrines
  • Mice
  • Mice, Inbred BALB C
  • Quinolizines / chemistry
  • Quinolizines / pharmacology
  • Quinolizines / therapeutic use*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Alkaloids
  • Interleukin-6
  • Lipopolysaccharides
  • Quinolizines
  • Tumor Necrosis Factor-alpha
  • sophocarpine
  • sophoramine
  • oxymatrine
  • Matrines