首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Protective effect of hesperetin In rat model of partial sciatic nerve ligation induced painful neuropathic pain: an evidence of anti-inflammatory and anti-oxidative activity
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Protective effect of hesperetin In rat model of partial sciatic nerve ligation induced painful neuropathic pain: an evidence of anti-inflammatory and anti-oxidative activity

机译:橙皮素的保护作用在部分坐骨神经结扎所致的痛性神经性疼痛大鼠模型中:抗炎和抗氧化活性的证据

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Behavioral, biochemical and gene expression changes were investigated in a rat model of partial sciatic nerve ligation (PSNL) after administration of hesperetin (20,50 mg/kg; p.o.), pregabalin (10 mg/kg; p.o.) or vehicle (1 ml/kg, p.o.). Thirty-six animals were randomly divided into six groups. Left sciatic nerve was exposed and ligated, animals in the control and test groups were treated orally with respective drugs for fifteen days. Nociceptive threshold was assessed on 0 day and thereafter every three days. Three weeks later, sciatic nerve tissue homogenate was prepared and subjected for estimation of oxidative markers namely total protein, nitric oxide, lipid peroxidase, interleukins (IL-1beta and IL-6) and TNF-alpha. Administration of hesperetin resulted in a dose dependent attenuation in PSNL-induced mechanical and thermal hyperalgesia, mechanical allodynia as well as down regulation of IL-1beta, IL-6 and TNF-a, and biochemical markers. Consequently, it can be concluded that anti-hyperalgesic effect of hesperetin in rats after PSNL may be attributed to various oxidative markers as well as the pro-inflammatory mediators secreted at the injury site. Hesperetin appears to be a promising candidate for the development as a novel therapeutic for the patients suffering from the neuropathic pain.
机译:在给予橙皮素(20,50 mg / kg; po),普瑞巴林(10 mg / kg; po)或赋形剂(1 ml)后,在部分坐骨神经结扎(PSNL)的大鼠模型中研究了行为,生化和基因表达的变化。 / kg,po)。将三十六只动物随机分为六组。暴露并结扎左坐骨神经,将对照组和测试组的动物分别用药物口服治疗十五天。在0天和此后每三天评估一次伤害阈值。三周后,准备坐骨神经组织匀浆并进行氧化标记的评估,即总蛋白,一氧化氮,脂质过氧化物酶,白介素(IL-1β和IL-6)和TNF-α。服用橙皮素会导致PSNL诱导的机械和热痛觉过敏,机械异常性疼痛以及IL-1beta,IL-6和TNF-a的下调以及生物化学标记物的剂量依赖性减弱。因此,可以得出结论,橙皮苷在PSNL后对大鼠的抗痛觉过敏作用可能归因于各种氧化标记以及损伤部位分泌的促炎介质。橙皮素似乎是发展为患有神经性疼痛的患者的新型疗法的有希望的候选者。

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