Recent development in studies of tetrahydroprotoberberines: Mechanism in antinociception and drug addiction

Hongyuan Chu, Guozhang Jin, Eitan Friedman, Xuechu Zhen*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

105 Scopus citations

Abstract

The tetrahydroprotoberberines (THPBs) are compounds isolated from Chinese herbs that possess a unique pharmacological profile as D2 dopamine receptor antagonists and D1 receptor agonists. l-Tetrahydropalmatine (l-THP) and l-stepholidine (SPD), members of the THPB family, were shown to have potential clinical use in the treatment of pain. However, their mechanism of action is not clear. In the past decades, Chinese scientists have made a great deal of effort to explore the mechanisms by which the THPBs and its analogues elicit antinociception and their potential utility in treating drug abuse. It is now clear that the antinociception produced by l-THP is related to inhibition of D2 dopamine receptors. The present review focuses on the recent progress made in understanding the mechanisms of l-THP- and l-SPD-mediated antinociception and the sequel of drug addiction.

Original languageEnglish (US)
Pages (from-to)491-499
Number of pages9
JournalCellular and molecular neurobiology
Volume28
Issue number4
DOIs
StatePublished - Jun 2008

Keywords

  • Antinociception
  • Dopamine receptor
  • Drug addiction
  • Tetrahydroprotoberberines
  • l-Stepholidine
  • l-Tetrahydropalmatine

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology

Fingerprint Dive into the research topics of 'Recent development in studies of tetrahydroprotoberberines: Mechanism in antinociception and drug addiction'. Together they form a unique fingerprint.

Cite this