AI Article Synopsis

  • Casearia sylvestris is commonly used in folk medicine for pain relief and this study explores its effects on chronic pain in a mouse model.
  • The research involved administering a hydroalcoholic extract of Casearia sylvestris and pro-resolving mediators to mice after inducing pain through ischemia and reperfusion.
  • Results showed that the extract and certain natural and synthetic compounds effectively reduced mechanical hyperalgesia, suggesting that the anti-pain effects are linked to the ALX/FPR2 receptor pathway involved in resolving inflammation.

Article 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.

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Source
http://dx.doi.org/10.1016/j.jep.2017.03.059DOI Listing

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Center for Studies in Stem Cells, Cell Therapy and Toxicological Genetics (CeTroGen), Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, 79070-900, MS, Brazil; Postgraduate Program in Health and Development of the Midwest Region, School of Medicine (FAMED), Federal University of Mato Grosso Do Sul (UFMS), Campo Grande, 79070-900, MS, Brazil. Electronic address:

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