The analgesic effects of β-elemene in rats with neuropathic pain by inhibition of spinal astrocytic ERK activation

Mol Pain. 2022 Apr:18:17448069221121562. doi: 10.1177/17448069221121562.

Abstract

Neuropathic pain takes a heavy toll on individual well-being, while current therapy is far from desirable. Herein, we assessed the analgesic effect of β-elemene, a chief component in the traditional Chinese medicine Curcuma wenyujin, and explored the underlying mechanisms at the level of spinal dorsal horn (SDH) under neuropathic pain. A spared nerve injury (SNI)-induced neuropathic pain model was established in rats. Intraperitoneal injection (i.p.) of β-elemene was administered for 21 consecutive days. Mechanical allodynia was explored by von Frey filaments. The activation of the mitogen-activated protein kinase (MAPK) family (including ERK, p38, and JNK) in spinal neurons, astrocytes, and microglia was evaluated using immunostaining 29 days after SNI surgery. The expression of GFAP, Iba-1, p-ERK, p-JNK, and p-p38 within the SDH was measured using immunoblotting. The levels of proinflammatory cytokines (including TNF-α, IL-1β, and IL-6) were measured with ELISA. The levels of oxidative stress indicators (including MDA, SOD, and GSH-PX) were detected using biochemical tests. Consecutive i.p. administration of β-elemene relieved SNI-induced mechanical allodynia (with an EC50 of 16.40 mg/kg). SNI significantly increased the expression of p-ERK in spinal astrocytes but not microglia on day 29. β-elemene reversed spinal astrocytic ERK activation and subsequent upregulation of proinflammatory cytokines in SNI rats, with no effect on the expression of p38 and JNK in spinal glia. β-elemene also exerted antioxidative effects by increasing the levels of SOD and GSH-PX and decreasing the level of MDA. Our results suggest that SNI induces robust astrocytic ERK activation within the SDH in the late phase of neuropathic pain. β-elemene exerts remarkable analgesic effects on neuropathic pain, possibly by inhibiting spinal astrocytic ERK activation and subsequent neuroinflammatory processes. Our findings suggest that β-elemene might be a promising analgesic for the treatment of chronic pain.

Keywords: ERK; astrocytes; neuroinflammation; neuropathic pain; spinal dorsal horn; β-elemene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics / metabolism
  • Analgesics / pharmacology
  • Analgesics / therapeutic use
  • Animals
  • Enzyme Activation
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Hyperalgesia* / complications
  • Hyperalgesia* / drug therapy
  • Hyperalgesia* / metabolism
  • Neuralgia* / drug therapy
  • Neuralgia* / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sesquiterpenes
  • Spinal Cord / metabolism
  • Spinal Cord Dorsal Horn / metabolism
  • Superoxide Dismutase / metabolism

Substances

  • Analgesics
  • Sesquiterpenes
  • beta-elemene
  • Superoxide Dismutase
  • Extracellular Signal-Regulated MAP Kinases