Hydroalcoholic crude extract of Casearia sylvestris Sw. reduces chronic post-ischemic pain by activation of pro-resolving pathways

J Ethnopharmacol. 2017 May 23:204:179-188. doi: 10.1016/j.jep.2017.03.059. Epub 2017 Apr 13.

Abstract

Ethnopharmacological relevance: Casearia sylvestris Sw. is widely used in popular medicine to treat conditions associated with pain.

Aim of the study: The present study investigated the influence of hydroalcoholic crude extract of Casearia sylvestris (HCE-CS) and contribution of pro-resolving mediators on mechanical hyperalgesia in a mouse model of chronic post-ischemia pain (CPIP).

Methods and results: Male Swiss mice were subjected to ischemia of the right hind paw (3h), then reperfusion was allowed. At 10min, 24h or 48h post-ischemia/reperfusion (I/R), different groups of animals were treated with HCE-CS (30mg/Kg, orally [p.o]), selected agonists at the pro-resolving receptor ALX/FPR2 (natural molecules like resolvin D1 and lipoxin A4 or the synthetic compound BML-111; 0.1-1µg/animal) or vehicle (saline, 10mL/Kg, s.c.), in the absence or presence of the antagonist WRW4 (10µg, s.c.). Mechanical hyperalgesia (paw withdrawal to von Frey filament) was asseseed together with histological and immunostainning analyses. In these settings, pro-resolving mediators reduced mechanical hyperalgesia and HCE-CS or BML-111 displayed anti-hyperalgesic effects which was markedly attenuated in animals treated with WRW4. ALX/FPR2 expression was raised in skeletal muscle or neutrophils after treatment with HCE-CS or BML-111.

Conclusion: These results reveal significant antihyperalgesic effect of HCE-CS on CPIP, mediated at least in part, by the pathway of resolution of inflammation centred on the axis modulated by ALX/FPR2.

Keywords: ALX/FPR2; Casearia sylvestris; Chronic post-ischemia pain; Inflammation; Salicaceae.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Analgesics / pharmacology
  • Analgesics / therapeutic use*
  • Animals
  • Annexin A1 / genetics
  • Casearia*
  • Chronic Pain / drug therapy*
  • Chronic Pain / metabolism
  • Hyperalgesia / drug therapy*
  • Hyperalgesia / metabolism
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use*
  • Plant Leaves
  • Receptors, Formyl Peptide / metabolism
  • Reperfusion Injury / drug therapy*
  • Reperfusion Injury / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Analgesics
  • Annexin A1
  • HSH2 protein, mouse
  • Plant Extracts
  • Receptors, Formyl Peptide
  • annexin A1, mouse
  • formyl peptide receptor 2, mouse