Electroacupuncture alleviates retrieval of pain memory and its effect on phosphorylation of cAMP response element-binding protein in anterior cingulate cortex in rats

Behav Brain Funct. 2015 Mar 4:11:9. doi: 10.1186/s12993-015-0055-y.

Abstract

Background: Recent evidence suggests that persistent pain and recurrent pain are due to the pain memory which is related to the phosphorylation of cAMP response element-binding protein (p-CREB) in anterior cingulate cortex (ACC). Eletroacupuncture (EA), as a complementary Chinese medical procedure, has a significant impact on the treatment of pain and is now considered as a mind-body therapy.

Methods: The rat model of pain memory was induced by two injections of carrageenan into the paws, which was administered separately by a 14-day interval, and treated with EA therapy. The paw withdrawal thresholds (PWTs) of animals were measured and p-CREB expressions in ACC were detected by using immunofluorescence (IF) and electrophoretic mobility shift assay (EMSA). Statistical comparisons among different groups were made by one-way, repeated-measures analysis of variance (ANOVA).

Results: The second injection of carrageenan caused the decrease of PWTs in the non-injected hind paw. EA stimulation applied prior to the second injection, increased the values of PWTs. In ACC, the numbers of p-CREB positive cells were significantly increased in pain memory model rats, which were significantly reduced by EA. EMSA results showed EA also down-regulated the combining capacity of p-CREB with its DNA. Furthermore, the co-expression of p-CREB with GFAP, OX-42, or NeuN in ACC was strengthened in the pain memory model rats. EA inhibited the co-expression of p-CREB with GFAP or OX-42, but not NeuN in ACC.

Conclusions: The present results suggest the retrieval of pain memory could be alleviated by the pre-treatment of EA, which is at least partially attributed to the down-regulated expression and combining capacity of p-CREB and the decreased expression of p-CREB in astrocytes and microglia cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Nuclear / metabolism
  • Brain Chemistry
  • CD11b Antigen / metabolism
  • Carrageenan
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • Electroacupuncture / methods*
  • Glial Fibrillary Acidic Protein / metabolism
  • Gyrus Cinguli / metabolism*
  • Hyperalgesia / therapy
  • Male
  • Memory*
  • Nerve Tissue Proteins / metabolism
  • Pain / chemically induced
  • Pain / psychology
  • Pain Management / methods*
  • Pain Measurement
  • Pain Threshold / drug effects
  • Phosphorylation
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Antigens, Nuclear
  • CD11b Antigen
  • Cyclic AMP Response Element-Binding Protein
  • Glial Fibrillary Acidic Protein
  • Nerve Tissue Proteins
  • Rbfox3 protein, rat
  • Carrageenan