Gholami Mohammadreza, Khayat Zahra Khanipour, Anbari Khatereh, Obidavi Zia, Varzi Alimohammad, Boroujeni Mandana Beigi, Alipour Mohsen, Niapoor Ali, Gharravi Anneh Mohammad
Razi Herbal Medicines Research Center and Department of Anatomy, Lorestan University of Medical Sciences, Khorramabad, Iran.
Department of Social Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Anat Sci Int. 2017 Jun;92(3):330-337. doi: 10.1007/s12565-016-0336-z. Epub 2016 Mar 14.
This study aimed to investigate the protective effect of quercetin against ischemia-reperfusion (IR) injury induced in the sciatic nerve of the rat. Quercetin (20 mg/kg) was given during ischemia just before reperfusion. Four groups of rats (Q+IR3, Q+IR7, Q+IR14, and Q+IR28) received 3, 7, 14, and 28 days of reperfusion, respectively, after the intraperitoneal injection of quercetin. After reperfusion, a behavioral test was performed and the sciatic functional index was calculated. Each sciatic nerve was stained to check for edema and ischemic fiber degeneration. Immunohistochemical staining was performed to detect TNF-alpha and NF-kappa B, and TUNEL staining was carried out to detect apoptosis. The Q+IR3, Q+IR7, and Q+IR14 groups showed significantly increased behavioral scores and ameliorated sciatic functional index values compared to IR-injured rats that received vehicle alone during ischemia and then the same period of reperfusion. The Q+IR3, Q+IR7, Q+IR14, and Q+IR28 groups presented significant ischemic fiber degeneration (IFD), TNF-alpha expression, and apoptosis as compared with the IR-injured and perfused rats that did not receive quercetin. The Q+IR3, Q+IR7, and Q+IR28 groups also exhibited significantly decreased NF-kappa B expression (p < 0.001, p = 0.001, p = 0.026) as compared with the IR-injured rats that were perfused but did not receive quercetin. These results imply that quercetin may be beneficial in the treatment of sciatic IR injury because of its antiapoptotic and antiinflammatory effects and its ability to decrease the expression of NF-kappa B.
本研究旨在探讨槲皮素对大鼠坐骨神经缺血再灌注(IR)损伤的保护作用。在再灌注前的缺血期间给予槲皮素(20mg/kg)。四组大鼠(Q+IR3、Q+IR7、Q+IR14和Q+IR28)在腹腔注射槲皮素后分别接受3、7、14和28天的再灌注。再灌注后,进行行为测试并计算坐骨神经功能指数。对每条坐骨神经进行染色以检查水肿和缺血性纤维变性。进行免疫组织化学染色以检测肿瘤坏死因子-α(TNF-α)和核因子-κB(NF-κB),并进行TUNEL染色以检测细胞凋亡。与在缺血期间仅接受赋形剂然后相同再灌注期的IR损伤大鼠相比,Q+IR3、Q+IR7和Q+IR14组的行为评分显著增加,坐骨神经功能指数值得到改善。与未接受槲皮素的IR损伤和再灌注大鼠相比,Q+IR3、Q+IR7、Q+IR14和Q+IR28组出现明显的缺血性纤维变性(IFD)、TNF-α表达和细胞凋亡。与灌注但未接受槲皮素的IR损伤大鼠相比,Q+IR3、Q+IR7和Q+IR28组的NF-κB表达也显著降低(p<0.001,p=0.001,p=0.026)。这些结果表明,槲皮素可能因其抗凋亡和抗炎作用以及降低NF-κB表达的能力而对坐骨神经IR损伤的治疗有益。