Brazilian plant extract eases nerve pain in early mouse study

A phytotherapeutic candidate for neuropathic pain: Helicteres ovata (Lam.) extract shows antinociceptive effects and favorable acute toxicity profile.

Journal of ethnopharmacology β€’ β€’ Related
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AI Summary

Helicteres ovata, a Brazilian plant traditionally associated with pain and inflammatory disorders, showed pain-relieving effects in mice with paclitaxel-induced neuropathy. Its hydroethanolic extract reduced both mechanical sensitivity and heat-related pain responses in a dose-dependent manner. Chemical analysis identified flavonoids, xanthones, phenolic acids, and minerals such as potassium, magnesium, and phosphorus, but the abstract does not identify which compounds produced the effects.

The extract’s activity was weakened by drugs that block opioid and cannabinoid signaling, suggesting that both pathways may contribute to its effects. It also altered inflammatory markers and helped preserve the structure of nerves involved in pain transmission. Although the extract showed moderate toxicity in a laboratory Artemia salina assay after 48 hours, no adverse effects were observed in the acute mouse toxicity test at 2000 mg/kg. These findings are promising for future neuropathic-pain research, but they do not establish safety or effectiveness in cannabis users or humans.

πŸ’‘ Key Findings

1
The Helicteres ovata extract reduced mechanical allodynia and thermal hyperalgesia in mice with chemotherapy-induced neuropathic pain.
Limited
35%
2
The pain-relieving effect was weakened by opioid and cannabinoid pathway blockers, indicating involvement of both neuromodulatory systems.
Limited
35%
3
The extract modulated inflammatory signals and preserved the morphology of pain-related nerves in the tested mice.
Limited
35%
4
No adverse effects were detected in the acute mouse toxicity model at 2000 mg/kg, although moderate toxicity appeared in the Artemia salina assay after 48 hours.
Limited
35%

πŸ“„ Original Abstract

Helicteres ovata is a native Brazilian species belonging to a genus traditionally used for the treatment of inflammatory and pain-related disorders. However, its pharmacological studies remain scarce. This study investigated the phytochemical profile, inorganic composition, antinociceptive activity, and safety of a 60% hydroethanolic extract of Helicteres ovata in murine models of paclitaxel-induced neuropathic pain. Phytochemical dereplication was performed using UPLC-ESI-TOF-MS/MS, and elemental analysis via ICP-MS. Antinociceptive effects were evaluated using hot plate and von Frey assays in paclitaxel-sensitized mice. Opioid and cannabinoid pathways involvement was assessed using naltrexone and AM251, respectively. TNF-α and CXCL-1 modulation was determined in central and peripheral tissues. Histological and morphometric analyses were conducted on the sciatic nerve and dorsal root ganglia. Cytotoxicity was assessed via the Artemia salina lethality assay, and acute oral toxicity was evaluated in BALB/c mice (2000 mg/kg). The extract contained flavonoids, xanthones, phenolic acids, and essential minerals including potassium, magnesium, and phosphorus. It reduced mechanical allodynia and thermal hyperalgesia in a dose-dependent manner. Its antinociceptive effect was attenuated by naltrexone and AM251, indicating opioid and cannabinoid pathways involvment. The extract modulated pro-inflammatory cytokine and preserved neural morphology. Moderate cytotoxicity was observed at 48 h in A. salina, but no adverse effects were detected in acute toxicity model. Helicteres ovata extract exhibits significant antiallodynic effect in chemotherapy-induced neuropathic pain, mediated by inflammatory and neuromodulatory pathways. It is well tolerated in vivo and holds promise as a phytotherapeutic candidate for neuropathic pain management.

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