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首页> 外文期刊>Journal of Pharmacopuncture >Berberine Alleviates Paclitaxel-Induced Neuropathy
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Berberine Alleviates Paclitaxel-Induced Neuropathy

机译:小碱减轻紫杉醇诱发的神经病

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Objectives: Paclitaxel (PTX) as an anticancer drug used against solid cancers, possesses adverse reactions such as neuropathic pain which has confined its use. PTX-induced neuropathic pain is mediated via activation of oxidative stress. Berberine (BER), an isoquinoline phytochemical found in several plants, exerts strong antioxidant and painkilling properties. In the current study, we aimed to evaluate pain-relieving effect of BER in a mouse model of PTX-induced neuropathic pain. Methods: This study was done using 42 male albino mice that were randomly divided into 6 groups (n = 7) as follow: Sham-operated (not treated with PTX), negative control group (PTX-treated mice receiving normal saline), BER 5, 10, and 20 mg/kg (PTX-treated mice receiving BER) and positive control group (PTX-treated mice receiving imipramine 10 mg/kg). Neuropathic pain was induced by intraperitoneal administration of four doses of PTX (2 mg/kg/day) on days 1, 3, 5 and 7. Then, on day 7, hot plate test was done to assess latency to heat to measure possible anti-neuropathic pain effect of BER. Results: Four doses of PTX 2 mg/kg/day induced neuropathy that was reduced by BER at all time-points (i.e. 0, 30, 60, 90 and 120 min) after injection (P 0.001 in comparison to control). The statistical analysis of data showed significant differences between groups (P 0.001 in comparison to negative control), at 30, 60, 90 and 120 min after injection of BER 5, 10 and 20 mg/kg; in other words, 30, 60, 90 and 120 min after BER administration, neuropathic pain was significantly reduced as compared to normal saline-treated mice. Conclusion: Altogether, our results showed that PTX could induce neuropathic pain as reflected by hyperalgesia and BER could alleviate PTX-induced thermal hyperalgesia.
机译:目的:紫杉醇(PTX)作为抗实体癌的抗癌药,具有不良反应,例如神经性疼痛,因此已被限制使用。 PTX诱导的神经性疼痛是通过氧化应激的激活来介导的。小ber碱(BER)是在几种植物中发现的异喹啉植物化学成分,具有很强的抗氧化和止痛性能。在本研究中,我们旨在评估BER在PTX诱发的神经性疼痛小鼠模型中的镇痛作用。方法:本研究使用42只雄性白化病小鼠完成,将其随机分为6组(n = 7),分别为:假手术(未经PTX治疗),阴性对照组(PTX治疗的小鼠接受生理盐水),BER 5、10和20 mg / kg(接受BER的PTX处理的​​小鼠)和阳性对照组(接受imipramine 10 mg / kg的PTX处理的​​小鼠)。在第1、3、5和7天通过腹膜内施用四剂PTX(2 mg / kg /天)诱发神经性疼痛。然后,在第7天,进行热板测试以评估加热潜伏期,以测量可能的抗药性。 -BER的神经性疼痛作用。结果:四剂剂量为2 mg / kg / day的PTX引起的神经病在注射后的所有时间点(即0、30、60、90和120分钟)均通过BER降低(与对照组相比,P <0.001)。数据的统计分析表明,在注射BER 5、10和20 mg / kg后的30、60、90和120分钟时,组之间存在显着差异(与阴性对照相比,P <0.001)。换句话说,与正常生理盐水处理的小鼠相比,BER给药后30、60、90和120分钟,神经性疼痛明显减轻。结论:总的来说,我们的结果表明PTX可以引起痛觉过敏所反映的神经性疼痛,而BER可以减轻PTX引起的热痛觉过敏。

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