Periplocoside A, a pregnane glycoside from Periploca sepium Bge, prevents concanavalin A-induced mice hepatitis through inhibiting NKT-derived inflammatory cytokine productions

Int Immunopharmacol. 2008 Sep;8(9):1248-56. doi: 10.1016/j.intimp.2008.05.001. Epub 2008 Jun 2.

Abstract

Periploca sepium Bge, a traditional Chinese herb medicine, is widely used for treating rheumatoid arthritis in china. Periplocoside A (PSA), a pregnane glycoside, is a new nature product compound isolated from P. sepium Bge. We examined the protective effects of PSA, on concanavaline A (ConA)-induced hepatitis. Pretreatment with PSA dramatically ameliorated ConA-induced liver injury, which was characterized by reducing serum alanine transaminase (ALT), pathogenic cytokines of interleukin (IL)-4 and interferon (IFN)-gamma levels, impeding the liver necrosis, and thus elevating the survival rate. In vitro, PSA inhibited IL-4 and IFN-gamma productions of alpha-galactosylceramide (alpha-GalCer) or anti-CD3-activated Natural killer T (NKT) cells. Enzyme Linked Immunosorbent Assay (ELISA) and Reverse Transcription Polymerase Chain Reaction (RT-PCR) assays revealed PSA suppressed IL-4 transcription and IFN-gamma translation. In conclusion, PSA had significantly preventative effect on ConA-induced hepatitis, which was closely associated with inhibition of NKT-derived inflammatory cytokine productions. These findings suggested that PSA has the therapeutic potential for treatment of human autoimmune-related hepatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • CD3 Complex / pharmacology
  • Cell Proliferation / drug effects
  • Cell Separation
  • Cell Survival / drug effects
  • Chemical and Drug Induced Liver Injury / metabolism*
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Concanavalin A / antagonists & inhibitors*
  • Concanavalin A / toxicity*
  • Cytokines / biosynthesis*
  • Cytokines / physiology
  • Female
  • Flow Cytometry
  • Galactosylceramides / pharmacology
  • Glycosides / pharmacology*
  • Indicators and Reagents
  • Killer Cells, Natural / metabolism*
  • Liver Function Tests
  • Lymphocyte Culture Test, Mixed
  • Lymphocytes / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Oligosaccharides / pharmacology
  • Periploca / chemistry*
  • Pregnenes / pharmacology*

Substances

  • Antineoplastic Agents, Phytogenic
  • CD3 Complex
  • Cytokines
  • Galactosylceramides
  • Glycosides
  • Indicators and Reagents
  • Oligosaccharides
  • Pregnenes
  • alpha-galactosylceramide
  • periplocoside E
  • Concanavalin A
  • periplocoside A
  • Alanine Transaminase