LASSBio-1586, an N-acylhydrazone derivative, attenuates nociceptive behavior and the inflammatory response in mice

PLoS One. 2018 Jul 30;13(7):e0199009. doi: 10.1371/journal.pone.0199009. eCollection 2018.

Abstract

Pain and inflammation are complex clinical conditions that are present in a wide variety of disorders. Most drugs used to treat pain and inflammation have potential side effects, which makes it necessary to search for new sources of bioactive molecules. In this paper, we describe the ability of LASSBio-1586, an N-acylhydrazone derivative, to attenuate nociceptive behavior and the inflammatory response in mice. Antinociceptive activity was evaluated through acetic acid-induced writhing and formalin-induced nociception tests. In these experimental models, LASSBio-1586 significantly (p<0.05) reduced nociceptive behavior. Several methods of acute and chronic inflammation induced by different chemical (carrageenan, histamine, croton oil, arachidonic acid) and physical (cotton pellet) agents were used to evaluate the anti-inflammatory effect of LASSBio-1586. LASSBio-1586 exhibited potent anti-inflammatory activity in all tests (p<0.05). Study of the mechanism of action demonstrated the possible involvement of the nitrergic, serotonergic and histamine signaling pathways. In addition, a molecular docking study was performed, indicating that LASSBio-1586 is able to block the COX-2 enzyme, reducing arachidonic acid metabolism and consequently decreasing the production of prostaglandins, which are important inflammatory mediators. In summary, LASSBio-1586 exhibited relevant antinociceptive and anti-inflammatory potential and acted on several targets, making it a candidate for a new multi-target oral anti-inflammatory drug.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetic Acid
  • Analgesics / chemical synthesis
  • Analgesics / pharmacology*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Arachidonic Acid / administration & dosage
  • Carrageenan / administration & dosage
  • Croton Oil / administration & dosage
  • Cyclooxygenase 2 / chemistry
  • Cyclooxygenase 2 / metabolism
  • Cyclooxygenase 2 Inhibitors / chemical synthesis
  • Cyclooxygenase 2 Inhibitors / pharmacology*
  • Dexamethasone / pharmacology
  • Disease Models, Animal
  • Edema / chemically induced
  • Edema / drug therapy*
  • Edema / metabolism
  • Edema / pathology
  • Formaldehyde
  • Hindlimb
  • Histamine / administration & dosage
  • Hydrazones / chemical synthesis
  • Hydrazones / pharmacology*
  • Indomethacin / pharmacology
  • Inflammation
  • Male
  • Mice
  • Molecular Docking Simulation
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nociception / drug effects*
  • Nociceptive Pain / chemically induced
  • Nociceptive Pain / drug therapy*
  • Nociceptive Pain / metabolism
  • Nociceptive Pain / physiopathology
  • Ondansetron / pharmacology
  • Prostaglandins / biosynthesis

Substances

  • Analgesics
  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Hydrazones
  • Prostaglandins
  • Formaldehyde
  • Arachidonic Acid
  • Ondansetron
  • Dexamethasone
  • Croton Oil
  • Histamine
  • Carrageenan
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Acetic Acid
  • NG-Nitroarginine Methyl Ester
  • Indomethacin

Grants and funding

The authors received specific funding of Conselho Nacional de Desenvolvimento Científico e Tecnológico (Process CNPq 465249/2014-0), INCT-INOFAR (Instituto Nacional de Ciência e Tecnologia de Fármacos e Medicamentos) for this work. The project is coordinated by Prof. Eliezer Jesus de Lacerda Barreiro. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.