[Protective mechanisms of radix salviae miltiorrhizae against chronic alcoholic liver injury in mice]

Zhongguo Zhong Xi Yi Jie He Za Zhi. 2005 May;25(5):425-8.
[Article in Chinese]

Abstract

Objective: To investigate the protective mechanisms of Radix Salviae miltiorrhizae (RSM) on chronic alcoholic liver injury in mice.

Methods: The chronic alcoholic liver injury mouse model was established. The morphologic change of hepatic tissue was observed with hematoxylin-eosin (HE) staining; the levels of toll-like receptor-4 (TLR-4) mRNA in hepatic tissue and hemeoxygenase-1 (HO-1) mRNA were determined using reverse transcription polymerase chain reaction (RT-PCR) technique; and the expression of TLR-4 protein was determined by immunohistochemistry method.

Results: RSM could alleviate the fatty degeneration and adiponecrosis of hepatic cells induced by alcohol, down-regulate the expressions of TLR-4 mRNA and HO-1 mRNA, and significantly decrease the number of TLR-4 positive cells.

Conclusion: RSM could prevent liver injury from alcohol by way of influencing TLR-4 signal transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drugs, Chinese Herbal / therapeutic use*
  • Female
  • Heme Oxygenase (Decyclizing) / biosynthesis
  • Heme Oxygenase (Decyclizing) / genetics
  • Heme Oxygenase-1
  • Hepatitis, Alcoholic / drug therapy*
  • Hepatitis, Alcoholic / pathology
  • Liver / metabolism
  • Male
  • Membrane Glycoproteins / biosynthesis*
  • Membrane Glycoproteins / genetics
  • Membrane Proteins
  • Mice
  • Phytotherapy*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptors, Cell Surface / biosynthesis*
  • Receptors, Cell Surface / genetics
  • Salvia miltiorrhiza*
  • Toll-Like Receptor 4
  • Toll-Like Receptors

Substances

  • Drugs, Chinese Herbal
  • Membrane Glycoproteins
  • Membrane Proteins
  • RNA, Messenger
  • Receptors, Cell Surface
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Heme Oxygenase (Decyclizing)
  • Heme Oxygenase-1
  • Hmox1 protein, mouse