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作 者:杨进国[1] 夏中元[1] 赵博[1] 江莹[1] 胡兴云[1] 孟庆涛[1]
出 处:《中华实验外科杂志》2012年第11期2234-2236,F0004,共4页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(81170768、81000027)
摘 要:目的探讨人参皂甙Rbl对肠缺血/再灌注致急性肺损伤的保护效应及核因子NF-E2相关因子2(Nrf2)/血红素氧合酶-1(HO-1)通路参与该效应的分子机制。方法成年雄性C57BL/6J小鼠随机分为5组:假手术组(S组);肠缺血/再灌注组(I/R组);再灌注+Rbl组(I/R+Rbl组);全反式维甲酸(ATRA)+再灌注组(ATRA+I/R组);ATRA+再灌注+Rbl组(ATRA+I/R+Rbl组)。采用肠缺血/再灌注模型,Westernblot检测肺组织Nrf2、HO-1表达变化;酶联免疫吸附试验(ELISA)法检测肺组织肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6、IL-10水平;检测超氧化物歧化酶(SOD)活性及丙二醛(MDA)含量;检测肺湿/干比及肺组织病理损伤评分。结果与S组比较,其他4组Nrf2、HO-1蛋白表达,TNF-α、IL-6、MDA含量,肺组织湿/干重比及肺组织病理评分增高(P〈0.05);与I/R组比较,I/R+Rbl组Nrf2,HO-1蛋白表达,TNF-α,IL-6,MDA含量,肺组织彤干重比及肺组织病理评分降低(P〈0.05);与1/R+Rbl组比较,ATRA+I/R组,ATRA+I/R+Rbl组Nrf2、HO-1蛋白表达,TNF-α、IL-6、MDA含量,肺组织湿/干重比及肺组织病理评分增高(P〈0.05)。SOD活性、IL-10水平与上述变化相反。结论肠缺St/再灌注可引起急性肺损伤,人参皂甙Rbl后处理能通过激活Nrf2/HO-1通路减轻肠缺血/再灌注所致肺损伤。Objective To investigate the effectsof ginsenosi-de Rbl on acute lung injury induced by intestinal ischemia reperfusion in mice and role of nuclear factor erythroid 2-related factor 2 (Nri2) / heme oxygenase-1 (HO-1) pathway in the pathophysiologic process. Methods Male C57BL/6J mice were randomly divided into 5 groups : ( 1 ) Sham group ( S group) ; ( 2 ) Intestinal Ischemia Reperfusion group (I/R group) ; ( 3 ) Intestinal Isehemia Reperfusion + 60 mg/kg ginsenoside Rbl ( I/R + Rb 1 group) ; (4) all-trans retinoic acid (ATRA) + I/R group ( ATRA + I/R group) ; (5) ATRA + I/R + 60 mg/kg ginseuoside Rbl ( ATRA + I/R + Rbl group). The Western blotting analysis were performed to ob- serve the expression of Nrf2 and HO-1 ; tumor necrosis factor-α (TNF-ct), interleukin (IL)-6, IL-10, su- peroxide dismutase (SOD) and malondialdehyde (MDA) were measured;Lung histology was observed and evaluated. Results Intestinal ischemia reperfusion can increase lung injury which was characterized by Nrf2, HO-1, TNF-α, IL-6, MDA, edema (P 〈 0. 05). Rbl can reduce the Intestinal ischemia reperfusion which decreased by Nrl2, HO-1, TNF-α, IL-6, MDA, edema (P 〈 0. 05). After administration of ATRA, which was an antagonists of Nrf2, Nrf2, HO-I, TNF-α, IL-6, MDA, edema were increased ( P 〈 0. 05 ). SOD was opposite as well as IL-10. Conclusion Ginsenoside Rbl attenuates acute lung injury induced by intestinal ischemia reperfusion by activating Nrf2/HO-1 pathway.
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