Andrographolide relieved pathological pain generated by spared nerve injury model in mice

Pharm Biol. 2018 Dec;56(1):124-131. doi: 10.1080/13880209.2018.1426614.

Abstract

Context: Andrographolide (Andro), found in large quantities in Andrographis paniculata Nees (Acanthaceae), is anti-inflammatory, especially in the central nervous system (CNS) glia.

Objective: The objective of this study is to test Andro's ability to reduce allodynia in a spared nerve injury model.

Material and methods: Male 30 g BalbC mice were divided into four groups: (1) Sham-operated control (Sham-group); (2) nerve injured and treated with saline (Saline-group); (3) nerve injured and treated with Andro (Andro-group); (4) nerve injured and treated with non-steroidal anti-inflammatory drugs (NSAIDS) (NSAIDS-group). Andro or NSAIDS (diclofenac salt) were injected intraperitoneally at 5 mg/kg body weight daily. Mechanical allodynia was assessed by von Frey tests at 3, 7, and 14 d. For immunohistochemical analysis, samples were collected at 7 d.

Results: The threshold for inducing allodynia increased and the response percentage reduced in the Andro-group when compared with the Saline-group, as well as when compared with NSAIDS groups throughout 3-14 d. The ratio of threshold for OP-Andro/OP-saline and for OP-Andro/OP-NSAIDS groups was 20.42 and 11.67 at 14 d, respectively. The ratio of response percentage for OP-Andro/OP-saline and for OP-Andro/OP-NSAIDS was 0.32 and 0.39 at 14 d, respectively. Interleukin-1 (IL-1) immunostaining in the spinal cord was reduced in the Andro-group. Astrocytic activities were not significantly reduced in the Andro-group compared with the Saline-group at 7 d post-operation (PO) Conclusions: Andro reduced mechanical allodynia more than NSAIDS at the same concentration, and the observed behaviour was associated with a reduction in inflammatory cytokine produced in the spinal cord.

Keywords: Allodynia; Andrographis paniculata; IL-1; astrocytes; von Frey test.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / therapeutic use*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Disease Models, Animal*
  • Diterpenes / therapeutic use*
  • Hyperalgesia / drug therapy*
  • Hyperalgesia / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Pain / drug therapy*
  • Pain / pathology
  • Sciatic Neuropathy / drug therapy
  • Sciatic Neuropathy / pathology

Substances

  • Anti-Inflammatory Agents
  • Anti-Inflammatory Agents, Non-Steroidal
  • Diterpenes
  • andrographolide

Grants and funding

This study was supported by Ministry of Science and Technology (formerly National Science Council) of Taiwan (NSC 101-2320-B-324 -001; MOST 106-2632-B-324-001).