CX3CR1 contributes to streptozotocin-induced mechanical allodynia in the mouse spinal cord

J Zhejiang Univ Sci B. 2020;21(2):166-171. doi: 10.1631/jzus.B1900439. Epub 2020 Feb 14.

Abstract

Patients with diabetic peripheral neuropathy experience debilitating pain that significantly affects their quality of life (Abbott et al., 2011), by causing sleeping disorders, anxiety, and depression (Dermanovic Dobrota et al., 2014). The primary clinical manifestation of painful diabetic neuropathy (PDN) is mechanical hypersensitivity, also known as mechanical allodynia (MA) (Callaghan et al., 2012). MA's underlying mechanism remains poorly understood, and so far, based on symptomatic treatment, it has no effective therapy (Moore et al., 2014).

Keywords: P2X7 receptor (P2X7R); Mechanical allodynia; Streptozotocin; Diabetic mice.

MeSH terms

  • Animals
  • CX3C Chemokine Receptor 1 / antagonists & inhibitors
  • CX3C Chemokine Receptor 1 / physiology*
  • Chemokine CX3CL1 / physiology
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Type 1 / complications*
  • Diabetic Neuropathies / etiology*
  • Hyperalgesia / etiology*
  • Mice
  • Mice, Inbred C57BL
  • Spinal Cord / physiology*
  • Streptozocin / pharmacology*

Substances

  • CX3C Chemokine Receptor 1
  • Chemokine CX3CL1
  • Cx3cl1 protein, mouse
  • Cx3cr1 protein, mouse
  • Streptozocin