Involvement of inhibition of RhoA/Rho kinase signaling in simvastatin-induced amelioration of neuropathic pain

Neuroscience. 2016 Oct 1:333:204-13. doi: 10.1016/j.neuroscience.2016.07.029. Epub 2016 Jul 25.

Abstract

Small molecular G-protein plays a key role in several diseases. This study was designed to reveal the role of RhoA signaling in the pathophysiology of neuropathic pain in mice. Partial sciatic nerve injury caused thermal hyperalgesia, mechanical allodynia, and increased plasma membrane translocation of RhoA in the lumber spinal cord. GFAP-immunoreactivity (ir), Iba-1-ir, and Rho kinase 2 (ROCK2-ir) was also increased in the ipsilateral spinal dorsal horn of nerve-ligated mice. Moreover, partial nerve ligation increased the expression of phosphorylated myristoylated alanine-rich protein kinase C substrate (MARCKS)-ir in the ipsilateral spinal dorsal horn. Daily intrathecal administration of simvastatin, beginning 3days before nerve injury, completely blocked all these changes in nerve-ligated mice. Pharmacological inhibition of ROCK also attenuated the increased expression of GFAP-ir and phosphorylated MARCKS-ir. Together, it is suggested that astrogliosis initiated by the activation of RhoA/ROCK signaling results in MARCKS phosphorylation in nerve terminals, which leads to hyperalgesia in neuropathic pain. Furthermore, simvastatin exerts antihyperalgesic and antiallodynic effects through the inhibition of spinal RhoA activation.

Keywords: Rho kinase (ROCK); RhoA; astrocyte; myristoylated alanine-rich protein kinase C substrate (MARCKS); neuropathic pain; simvastatin.

MeSH terms

  • Analgesics / pharmacology*
  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism
  • Astrocytes / pathology
  • Calcium-Binding Proteins / metabolism
  • Disease Models, Animal
  • Glial Fibrillary Acidic Protein / metabolism
  • Gliosis / drug therapy
  • Gliosis / metabolism
  • Gliosis / pathology
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Hyperalgesia / drug therapy
  • Hyperalgesia / metabolism
  • Hyperalgesia / pathology
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Lumbar Vertebrae
  • Male
  • Membrane Proteins / metabolism
  • Mice, Inbred ICR
  • Microfilament Proteins / metabolism
  • Microglia / drug effects
  • Microglia / metabolism
  • Microglia / pathology
  • Myristoylated Alanine-Rich C Kinase Substrate
  • Neuralgia / drug therapy*
  • Neuralgia / metabolism*
  • Neuralgia / pathology
  • Protein Kinase Inhibitors / pharmacology
  • Sciatic Nerve / injuries
  • Simvastatin / pharmacology*
  • Spinal Cord / drug effects
  • Spinal Cord / metabolism
  • Spinal Cord / pathology
  • rho GTP-Binding Proteins / metabolism*
  • rho-Associated Kinases / antagonists & inhibitors
  • rho-Associated Kinases / metabolism*
  • rhoA GTP-Binding Protein

Substances

  • Aif1 protein, mouse
  • Analgesics
  • Calcium-Binding Proteins
  • Glial Fibrillary Acidic Protein
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Intracellular Signaling Peptides and Proteins
  • Marcks protein, mouse
  • Membrane Proteins
  • Microfilament Proteins
  • Protein Kinase Inhibitors
  • glial fibrillary astrocytic protein, mouse
  • Myristoylated Alanine-Rich C Kinase Substrate
  • Simvastatin
  • Rock2 protein, mouse
  • rho-Associated Kinases
  • RhoA protein, mouse
  • rho GTP-Binding Proteins
  • rhoA GTP-Binding Protein