Effects and mechanisms of glucosides of chaenomeles speciosa on collagen-induced arthritis in rats

Int Immunopharmacol. 2003 Apr;3(4):593-608. doi: 10.1016/S1567-5769(03)00051-1.

Abstract

Effects of glucosides of chaenomeles speciosa (GCS)-a Chinese traditional herbal medicine (CTM) on inflammatory and immune responses and its mechanisms in collagen-induced arthritis (CIA) rat were studied. Hind paw volumes of rats were measured by volume meter; lymphocyte proliferation, interleukin-1, interleukin-2, TNF-alpha level was determined by 3-(4,5-2 dimethylthiazal-2yl)2,5-diphenyltetrazoliumbromide (MTT) assay; cAMP level in synoviocytes was analyzed by competitive protein binding assay (CPBA). mRNA expression of G(i,), G(s), and TNF-alpha of synoviocytes in CIA rats was measured by RT-PCR and antibodies to collagen type II (CII) were determined by enzyme-linked immunosorbent assay (ELISA), respectively. There was a marked secondary inflammatory response in CIA model, which accompanied with the decrease of body weight and the weight of immune organs simultaneously. The administration of GCS (30, 60, 120 mg x kg(-1), ig x 7 days) inhibited the inflammatory response and restored body weight and the weight of immune organs of CIA rats. Lymphocyte proliferation and IL-2 production of CIA rats increases, together with IL-1 and TNF-alpha in peritoneal macrophages and synoviocytes. The administration of GCS (30, 60, 120 mg x kg(-1), ig x 7 days) reduced above changes significantly. GCS at the concentration of 0.5, 2.5, 12.5, 62.5, 125 mg x l(-1) increased cAMP level of synoviocytes, which decreased in CIA rats in vitro. At the same time, GCS inhibited mRNA expression of G(i,) and TNF-alpha of synoviocytes and increased mRNA expression of G(s) of synoviocytes in CIA rats. GCS had no effect on the concentration of antibodies to CII. GCS possesses anti-inflammatory and immunoregulatory actions and has a therapeutic effect on CIA rats due to G protein-AC-cAMP transmembrane signal transduction of synoviocytes, which play a crucial role in pathogenesis of this disease.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Arthritis, Experimental / drug therapy*
  • Arthritis, Experimental / immunology
  • Cell Division / drug effects
  • Cell Division / immunology
  • Collagen
  • Collagen Type II / immunology
  • Cyclic AMP / biosynthesis
  • Cyclic AMP / immunology
  • Drugs, Chinese Herbal / therapeutic use*
  • Enzyme-Linked Immunosorbent Assay
  • Glucosides / therapeutic use*
  • Hypersensitivity, Delayed / immunology*
  • Interleukin-1 / biosynthesis
  • Interleukin-1 / immunology
  • Interleukin-2 / biosynthesis
  • Interleukin-2 / immunology
  • Joint Capsule / cytology
  • Joint Capsule / immunology
  • Joint Capsule / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rosaceae / chemistry*
  • Spleen / cytology
  • Spleen / immunology
  • Spleen / metabolism
  • Thymus Gland / cytology
  • Thymus Gland / immunology
  • Thymus Gland / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Collagen Type II
  • Drugs, Chinese Herbal
  • Glucosides
  • Interleukin-1
  • Interleukin-2
  • Tumor Necrosis Factor-alpha
  • Collagen
  • Cyclic AMP