Nucleo de Pós-graduação, Instituto de Ensino e Pesquisa Santa Casa de Belo Horizonte, Belo Horizonte, MG, Brazil.
Graduate Program in Health Sciences, University of the Extreme South of Santa Catarina (UNESC), Criciuma, SC, Brazil.
Toxicon. 2021 May;195:104-110. doi: 10.1016/j.toxicon.2021.03.012. Epub 2021 Mar 19.
This study investigated the effects of intravenous (iv) administration of recombinant Phα1β toxin, pregabalin, and diclofenac by the intrathecal route using an animal model fibromyalgia (FM). The reserpine administration (0.25 mg/kg s. c) once daily for three consecutive days significantly induced hyperalgesia, immobility time, and sucrose consumption in mice on the 4th day. Reserpine caused hyperalgesia on the mechanical and thermal hyperalgesia on the 4th day was reverted by recombinant Phα1β (0.2 mg/kg iv) and pregabalin (1.25 μmol/site i. t) treatments. In contrast, diclofenac (215 nmol/site i. t) was ineffective. Recombinant Phα1β toxin, pregabalin, and diclofenac did not affect the depressive-like behavioural effect induced by reserpine on mice during the forced swim and sucrose consumption tests. The data confirmed the analgesic effect of the recombinant Phα1β toxin administered intravenously in a fibromyalgia mouse model.
本研究通过动物纤维肌痛模型调查了静脉注射(iv)重组 Phα1β 毒素、普瑞巴林和双氯芬酸,鞘内给药的效果。连续三天每天一次给予利血平(0.25mg/kg sc)可显著诱导小鼠在第 4 天产生痛觉过敏、不动时间和蔗糖消耗。第 4 天,利血平引起机械性和热痛觉过敏,重组 Phα1β(0.2mg/kg iv)和普瑞巴林(1.25μmol/部位 it)治疗可逆转这种痛觉过敏。相比之下,双氯芬酸(215nmol/部位 it)无效。重组 Phα1β 毒素、普瑞巴林和双氯芬酸均不影响利血平在强迫游泳和蔗糖消耗试验中对小鼠产生的抑郁样行为效应。数据证实了重组 Phα1β 毒素在纤维肌痛小鼠模型中静脉给药的镇痛效果。