...
首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis
【24h】

Effect of strontium ranelate on pain behavior in an experimental model of osteoarthritis

机译:雷奈酸锶对骨关节炎实验模型疼痛行为的影响

获取原文

摘要

Strontium ranelate (SrRan) is a drug usually prescribed to treat osteoporosis, with proven effects of decreasing the risk of fractures and an indication of reducing the progression of osteoarthritis (OA). This study aimed to investigate the effects of SrRan as either a prophylactic or a treatment drug, using an OA rat model to assess pain behavior. A monoiodoacetate (MIA)-induced knee joint OA model in Wistar rats was used. Thirty Wistar rats (both sexes, 60 days old) were distributed in five groups of 6 rats each: the control group, that received no intervention; a prophylactic group, that received oral administration of 25 mg?·kg -1 ?·day -1 of SrRan for 28 days before induction of OA; a group treated with 25 mg?·kg -1 ?·day -1 of SrRan for 28 days after OA induction; a group treated with 50 mg?·kg -1 ?·day -1 during 28 days after OA induction; and a group that received oral saline for 28 days after induction. The assessment of pain behavior was performed considering articular incapacitation (weight-bearing test), mechanical hyperalgesia (Randall Selitto test) and motor activity (rotarod test), on days 0, 7, 14, 21, and 28. This experiment did not yield a significant difference when comparing the group that received SrRan prophylactically with the groups treated with 25 or 50 mg?·kg -1 ?·day -1 and the group that received oral saline. Thus, SrRan did not provide analgesia in either treated rats or as a prophylactic drug with the tested doses. Higher doses should be tested further to achieve possible significant results.
机译:雷奈酸锶(SrRan)是通常用于治疗骨质疏松症的药物,具有降低骨折风险和减少骨关节炎(OA)进展的迹象。这项研究旨在使用OA大鼠模型评估疼痛行为,以研究SrRan作为预防药物或治疗药物的作用。在Wistar大鼠中使用单碘乙酸盐(MIA)诱导的膝关节OA模型。将30只Wistar大鼠(性别均为60天)分成5组,每组6只大鼠:对照组,未干预;对照组,未干预。预防组,在诱导OA之前28天口服25 mg?·kg -1?·day -1的SrRan。 OA诱导后,用25 mg?·kg -1?·day -1的SrRan治疗28天。 OA诱导后28天,给予50 mg·kg -1 -1··天-1的治疗;诱导后28天接受口服盐水治疗的一组。在第0、7、14、21和28天时,考虑关节功能不全(负重测试),机械痛觉过敏(Randall Selitto测试)和运动活动(rotarod测试)进行疼痛行为评估。与预防性使用SrRan的组与接受25或50 mg?·kg -1 -1··day -1的组以及口服生理盐水的组相比,有显着差异。因此,SrRan在经治疗的大鼠中或作为测试剂量的预防药物均未提供镇痛作用。应进一步测试更高剂量,以获得可能的显着结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号