Systemic antihyperalgesic effect of a novel conotoxin from Californiconus californicus in an inflammatory pain model.

IF 2.5 Q2 CLINICAL NEUROLOGY
Frontiers in pain research (Lausanne, Switzerland) Pub Date : 2025-01-24 eCollection Date: 2024-01-01 DOI:10.3389/fpain.2024.1500789
Joaquín López-Carrillo, Johanna Bernáldez-Sarabia, Tushar J Pawar, Samanta Jiménez, Salvador Dueñas, Andrea Figueroa-Montiel, José L Olivares-Romero, Vinicio Granados-Soto, Alexei F Licea-Navarro, Nadia L Caram-Salas
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引用次数: 0

Abstract

Introduction: This study explores the analgesic potential of the novel conotoxin O1_cal6.4b, derived from Californiconus californicus, as a candidate for pain management in a model of inflammatory pain.

Methods: O1_cal6.4b was systemically administered to Wistar rats, and its effects on thermal hyperalgesia and motor coordination were evaluated. Comparative analyses were conducted against O1_cal6.4d, ω-MVIIA, and standard analgesics (morphine, dexamethasone, and diclofenac). Structural differences between O1_cal6.4b and O1_cal6.4d were examined using in silico modeling and molecular dynamics simulations.

Results: Systemic administration of O1_cal6.4b significantly reduced thermal hyperalgesia in a dose-dependent manner without impairing motor coordination. The analgesic effect of O1_cal6.4b was superior to that of O1_cal6.4d, ω-MVIIA, and standard analgesics. Structural analyses revealed notable differences between O1_cal6.4b and O1_cal6.4d, suggesting unique functional properties.

Discussion: The findings indicate that O1_cal6.4b exhibits a promising analgesic profile with advantages over traditional opioid-based therapies. These results underscore the molecular diversity of conotoxins and highlight their potential as innovative analgesic treatments. Further research is needed to elucidate the mechanism of action of this novel conotoxin.

一种来自加州锥虫的新型螺毒素在炎症性疼痛模型中的全身抗痛觉作用。
简介:本研究探讨了新型concontoxin O1_cal6.4b的镇痛潜力,该毒素来源于加州niconus californicus,作为炎症性疼痛模型疼痛管理的候选药物。方法:对Wistar大鼠系统给予O1_cal6.4b,观察其对热痛觉过敏和运动协调的影响。对比分析O1_cal6.4d、ω- mvia和标准镇痛药(吗啡、地塞米松、双氯芬酸)。利用硅模型和分子动力学模拟分析了O1_cal6.4b和O1_cal6.4d的结构差异。结果:全身给药O1_cal6.4b以剂量依赖的方式显著减少热痛觉过敏,而不损害运动协调。O1_cal6.4b的镇痛效果优于O1_cal6.4d、ω-MVIIA和标准镇痛药。结构分析显示O1_cal6.4b和O1_cal6.4d之间存在显著差异,表明它们具有独特的功能特性。讨论:研究结果表明,O1_cal6.4b具有比传统阿片类药物治疗更有前景的镇痛作用。这些结果强调了贝壳毒素的分子多样性,并强调了它们作为创新镇痛治疗的潜力。该新型螺毒素的作用机制有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.10
自引率
0.00%
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审稿时长
13 weeks
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