(-)-Stepholidine enhances K+ depolarization-induced activation of synaptosomal tyrosine 3-monooxygenase from rat striatum

Zhongguo Yao Li Xue Bao. 1997 Jan;18(1):49-52.

Abstract

Aim: To study the mechanism of K+ depolarization-induced activation of synaptosomal tyrosine 3-monooxygenase (TM) in rat striatum and the effect of (-)-stepholidine (SPD) on this activation.

Methods: The TM was assayed for DOPA by HPLC-ECD; the activities of Ca2+/calmodulin (CaM)-dependent protein kinase (PK II) and Ca2+/phosphoinositide-dependent protein kinase (PKC) were assayed using histidine as substrate.

Results: The incubation of striatal synaptosomes in K(+)-riched (60 mmol.L-1) medium resulted in a marked activation of TM. PKC inhibitor polymyxin B (PMB) completely blocked the activation of K+ 60 mmol.L-1 on TM. Selective D2 receptor agonist quinpirole (QP), Ca2+ removal from incubation medium and CaM antagonist W7 failed to affect the activation. However, SPD enhanced the activation of K+ 60 mmol.L-1 on TM. Meanwhile, the incubation in K+ 60 mmol.L-1 also activated PKC. Neither QP nor SPD affected K+ depolarization-induced activation of PKC.

Conclusion: The activation of K+ depolarization on synaptosomal TM is enhanced by SPD and this activation is mediated by PKC rather than by PK II.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Berberine / analogs & derivatives*
  • Berberine / pharmacology
  • Corpus Striatum / enzymology*
  • Dopamine Antagonists / pharmacology*
  • Polymyxin B / pharmacology
  • Potassium / metabolism
  • Protein Kinase C / antagonists & inhibitors
  • Rats
  • Rats, Sprague-Dawley
  • Synaptosomes / enzymology
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • Dopamine Antagonists
  • Berberine
  • stepholidine
  • Tyrosine 3-Monooxygenase
  • Protein Kinase C
  • Polymyxin B
  • Potassium