Puerarin blocks the signaling transmission mediated by P2X3 in SG and DRG to relieve myocardial ischemic damage

Brain Res Bull. 2014 Feb:101:57-63. doi: 10.1016/j.brainresbull.2014.01.001. Epub 2014 Jan 18.

Abstract

P2X₃ receptors in stellate ganglia (SG) and cervical dorsal root ganglia (DRG) neurons are involved in sympathoexcitatory reflex induced by myocardial ischemic damage. Puerarin, a major active ingredient extracted from the traditional Chinese plant medicine Ge-gen, has been widely used in treatment of myocardial and cerebral ischemia. The present study is aimed to observe the effects of puerarin on the signaling transmission mediated by P2X₃ receptor in SG and DRG after myocardial ischemic damage. Our results showed that systolic blood pressure and heart rate increased, and the expression levels of P2X₃ mRNA and protein in SG and DRG were up-regulated after myocardial ischemic damage. Puerarin reduced systolic blood pressure and heart rate, relieved pain and decreased up-regulated expression of P2X₃ mRNA and protein in SG and DRG after myocardial ischemia. Puerarin inhibited the up-regulated ATP-activated currents in DRG neurons after myocardial ischemia. Thus, puerarin can relieve myocardial ischemic damage through blocking the P2X₃ signaling transmission and then depressed the aggravated sympathoexcitatory reflex.

Keywords: Dorsal root ganglia; Myocardial ischemia; P2X(3) receptor; Puerarin; Stellate ganglia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Blood Pressure / drug effects
  • Blood Pressure / physiology
  • Female
  • Ganglia, Spinal / drug effects*
  • Ganglia, Spinal / physiopathology
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Isoflavones / pharmacology*
  • Male
  • Membrane Potentials / drug effects
  • Myocardial Ischemia / drug therapy*
  • Myocardial Ischemia / physiopathology
  • Neurons / drug effects
  • Neurons / physiology
  • Pain Management
  • Peripheral Nervous System Agents / pharmacology*
  • RNA, Messenger / metabolism
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Purinergic P2X3 / metabolism
  • Signal Transduction / drug effects*
  • Signal Transduction / physiology
  • Stellate Ganglion / drug effects*
  • Stellate Ganglion / physiopathology

Substances

  • Isoflavones
  • Peripheral Nervous System Agents
  • RNA, Messenger
  • Receptors, Purinergic P2X3
  • Adenosine Triphosphate
  • puerarin