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作 者:王万铁[1] 戴雍月[1] 许益笑[1] 邱晓晓 汪洋[1] 郝卯林[1] 倪世容[1] 王方岩[1] 金可可[1] 王卫[1] 郑绿珍[1] 宋张娟[1] 王青[1]
机构地区:[1]温州医学院病理生理学教研室,浙江温州325053
出 处:《中国病理生理杂志》2007年第2期288-292,共5页Chinese Journal of Pathophysiology
基 金:浙江省教育厅科研基金资助项目(No.20000670);温州市科技计划重点资助项目(No.Y2005A080)
摘 要:目的:探讨L-精氨酸对肺缺血-再灌注损伤(PIR I)时bcl-2、bax基因表达的影响。方法:采用在体兔单肺原位缺血-再灌注模型。实验兔36只,随机分为假手术对照组(sham,12只)、肺缺血-再灌注组(I/R,12只)和肺缺血-再灌注加L-精氨酸组(L-Arg,12只)。分别于再灌注5 h取左肺组织,观察bcl-2、baxmRNA定位表达、凋亡指数(AI)、肺组织湿干重比(W/D)、肺损伤组织学定量评价指标(IQA)及光镜、电镜下的组织形态学改变。结果:在肺小动脉内(外)膜、肺小静脉内膜、肺泡上皮及细支气管上皮,L-Arg组bcl-2 mRNA的表达及bcl-2/baxmRNA的比值显著高于I/R组(均P<0.01),baxmRNA的表达明显低于I/R组(P<0.01);AI、W/D和IQA值显著低于I/R组(P<0.01和P<0.05);肺组织形态学异常改变不同程度减轻。结论:L-精氨酸可上调肺组织bcl-2 mRNA的表达、下调肺组织baxmRNA的表达、调控bcl-2/baxmRNA之间的平衡而减轻细胞凋亡,对PIR I发挥积极的防治作用。AIM : To investigate the effect of L - arginine ( L - Arg) on expression of bcl - 2, bax mRNA during pulmonary ischemia and reperfusion injury (PIRI) in rabbits. METHODS: Single lung ischemia and reperfusion animal model was used in vivo. The rabbits were randomly divided into three groups: sham operated group (sham, n = 12), ischemia - reperfusion group ( I/R, n = 12) and I/R + L - arginine group ( L - Arg, n = 12). Changes of several parameters, which included apoptotic index (AI), wet to dry ratio of lung tissue weight (W/D) and index of quantitative assessment of histologic lung injury ( IQA), were measured at 300 min after reperfusion in lung tissue. Meanwhile the location and expression of bcl - 2, bax mRNA as well as the ratio of bcl - 2 mRNA/bax mRNA were observed. The lung tissue was prepared for light microscopic and electron microscopic observation at 60, 180 and 300 min after reperfusion. RESULTS : As compared with I/R group, in intima and extima of small pulmonary artery, alveoli, and bronchiole epithelia, the expression of bcl - 2 mRNA and the ratio of bcl - 2 mRNA/bax mRNA were increased, and the expression of bax mRNA was decreased in L - Arg treatment group. The values of AI, W/D and IQA showed significantly lower than that in I/R group at 180 minutes after reperfusion in lung tissue (P 〈0. 01 and P 〈0. 05). Meanwhile, abnormal changes of the lung tissue in morphologically were markedly lessened in L - Arg treatment group. CONCLUSION: L - arginine produces a notable protective effect on PIRI in rabbits by up - regulating bcl - 2 mRNA expression, down - regulating bax mRNA expression in lung tissue and regulating the balance of bcl -2 mRNA and bax mRNA to decrease apoptosis.
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