Animal study demonstrates brivaracetam reduces pain in vincristine-induced neuropathic pain, suggesting therapeutic potential.
Objectives: Neuropathic pain, characterised by abnormal pain processing, often arises due to nerve injury or chemotherapy-induced neurotoxicity. Current pharmacological interventions, including anticonvulsants and antidepressants, provide partial relief with adverse effects. Brivaracetam (BRV), a synaptic vesicle 2A ligand, has demonstrated neuroprotective effects in preclinical models. This study explores its potential analgesic properties in a vincristine-induced neuropathy model. Materials and Methods: Rats were administered vincristine (0.1 mg/kg, intraperitoneally) for 10 days to induce neuropathy. BRV (10 mg/kg and 20 mg/kg) was administered daily for 14 post-induction. Behavioural assessments, including the von Frey filament test and hot plate test, were performed to evaluate mechanical and thermal hyperalgesia. Results: Vincristine treatment resulted in significant hyperalgesia and nociceptive responses in the control group. BRV-treated rats exhibited significant improvement in pain thresholds compared to the control group ( P < 0.05). This demonstrates the substantial antinociceptive properties. Furthermore, the comparative analysis indicated that BRV provides similar levels of pain relief as gabapentin, supporting its potential utility in pain management. Conclusion: This study demonstrates BRV’s potential in mitigating vincristine-induced neuropathic pain, warranting further clinical investigations. Its multimodal action could offer a novel approach to neuropathic pain treatment.
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S. et al. (2026) studied this question.
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