Machaerium hirtum (Vell.) Stellfeld Alleviates Acute Pain and Inflammation: Potential Mechanisms of Action

Biomolecules. 2020 Apr 11;10(4):590. doi: 10.3390/biom10040590.

Abstract

:Machaerium hirtum (Vell.) Stellfeld (Fabaceae) known in Brazil as "jacaranda de espinho" or "espinheira santa nativa" is a medicinal plant commonly used in folk medicine to treat ulcers, cough and diarrhea. This study aimed to investigate the anti-inflammatory and antinociceptive effects of hydroalcoholic extracts from M. hirtum twig (HEMh) using in vivo experimental models of nociception through the involvement of transient receptor potential channels, acid-sensing ion channel (ASIC), nitrergic, opioidergic, glutamatergic, and supraspinal pathways. Our results revealed an antinociceptive effect of HEMh mediated by the opioidergic, L-arginine-nitric oxide and glutamate systems, as well as by interactions with TRPA1/ASIC channels. The anti-inflammatory effect of HEMh evaluated with a xylene-induced ear edema and by the involvement of arachidonic acid and prostaglandin E2 (PGE2) showed involvement of the COX pathway, based on observed decreases in PGE2 levels. A phytochemical investigation of the HEMh led to the isolation of α-amyrin, β-amyrin, allantoin, apigenin-7-methoxy-6-C-β-D-glucopyranoside, and apigenin-6-C-β-D-glucopyranosyl-8-C-β-D-xylopyranoside. In conclusion, the acute oral administration of HEMh inhibits the nociceptive behavioral response in animals through the nitrergic, opioid, glutamatergic pathways, and by inhibition of the TRPA1 and ASIC channels, without causing locomotor dysfunction. In addition, its anti-inflammatory effect is associated with the COX pathway and decreased PGE2 levels.

Keywords: Machaerium hirtum; anti-inflammatory action; antinociceptive effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Pain / complications
  • Acute Pain / drug therapy*
  • Analgesics, Opioid / metabolism
  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use
  • Arachidonic Acid
  • Arginine / metabolism
  • Body Weight / drug effects
  • Dinoprostone / metabolism
  • Edema / drug therapy
  • Ethanol
  • Fabaceae / chemistry*
  • Female
  • Formaldehyde
  • Glutamates / metabolism
  • Indomethacin / adverse effects
  • Inflammation / complications
  • Inflammation / drug therapy*
  • Ion Channels / metabolism
  • Male
  • Mice
  • Motor Activity / drug effects
  • Nitric Oxide / metabolism
  • Nociception / drug effects
  • Phytochemicals / chemistry
  • Phytochemicals / pharmacology
  • Phytochemicals / therapeutic use
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use
  • Plant Extracts / toxicity
  • Toxicity Tests, Acute
  • Ulcer / chemically induced
  • Ulcer / complications
  • Ulcer / drug therapy
  • Xylenes

Substances

  • Analgesics, Opioid
  • Anti-Inflammatory Agents
  • Glutamates
  • Ion Channels
  • Phytochemicals
  • Plant Extracts
  • Xylenes
  • Formaldehyde
  • Arachidonic Acid
  • Nitric Oxide
  • Ethanol
  • Arginine
  • Dinoprostone
  • Indomethacin