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Acetylcholine participates in pain modulation by influencing endogenous opiate peptides in rat spinal cord

Author(s): Lu Lu | Daxin Wang | Jingcheng Wang | Guangzhou Lu | Jun Yang | Ying Zhao | Yanjuan Pan

Journal: Journal of Biophysical Chemistry
ISSN 2153-036X

Volume: 02;
Issue: 01;
Start page: 15;
Date: 2012;
Original page

Keywords: Achetylcholine | Endogenous Opiate Peptide | Pain Modulation | Spinal Cord

The spinal cord is a necessary pathway that transfers the body nociceptive inputs to the brain, and endo-genous opiate peptides (EOP) play an important role in pain modulation. Our previous work has proven that arginine vasopressin (AVP) antinociception in the caudate nucleus (CdN) relates with the acetylcholine (Ach) system mainly. The communication was de-signed to investigate the interrelations between Ach system and EOP system at the spinal level during pain process. The results showed that: 1) pain stimulation increased L-enkephalin (L-Ek), β-endorphin (β-Ep), dynorphin A1-13(DynA1-13), Ach and choline (Ch, an Ach metabolic product) concentrations in the spinal cord; 2) Ach increased L-Ek, β-Ep and DynA1-13 concentrations in the spinal cord; and 3) Atropine (M-receptor inhibitor) or hexahydric gallamine (N-receptor inhibitor) decreased L-Ek, β-Ep and DynA1-13 concentrations in the spinal cord. The data suggested that Ach antinociception was involved in the EOP system at the spinal level.
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