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大鼠肺纤维化形成中内源性一氧化氮对肺泡上皮细胞凋亡的影响
引用本文:陈晓玲,沈铁宝,赵松,李英敏,张爱子,李文斌,艾洁. 大鼠肺纤维化形成中内源性一氧化氮对肺泡上皮细胞凋亡的影响[J]. 中国病理生理杂志, 2004, 20(12): 2307-2310
作者姓名:陈晓玲  沈铁宝  赵松  李英敏  张爱子  李文斌  艾洁
作者单位:1. 河北医科大学基础所病理生理研究室, 河北 石家庄 050017;
2. 河北医科大学病理学教研室, 河北 石家庄 050017;
3. 河北医科大学组织胚胎学教研室, 河北 石家庄 050017
基金项目:河北省教育厅博士科研基金资助项目(No.B2002215)
摘    要:目的:研究大鼠肺纤维化形成过程中异常增多的肺内源性一氧化氮对肺泡上皮细胞凋亡的影响。方法:气管内滴注博莱霉素,用硝酸还原法检测出肺血NO2-/NO3-含量;TdT介导的dUTP缺口末端标记法(TUNEL)和透射电镜观察肺泡上皮细胞凋亡。分别观察注BLMA5后14 d和30 d以及用氨基胍(AG)阻断iNOS合成NO后上述指标的变化。结果:(1)注BLMA5后14 d,出肺血NO2-/NO3-含量分别高于正常对照组和注BLMA5后30 d组(均P<0.01);凋亡的肺泡上皮细胞数亦分别多于正常对照和注BLMA5后30 d组(均P<0.01)。(2)AG阻止出肺血NO2-/NO3-含量增高的同时,亦抑制了肺泡上皮细胞的凋亡。结论:在肺纤维化形成过程中,内源性NO的增多,有诱导肺泡上皮细胞凋亡的作用。

关 键 词:肺纤维化  肺泡上皮细胞  细胞凋亡  一氧化氮  大鼠  
文章编号:1000-4718(2004)12-2307-04
收稿时间:2003-06-18

Role of endogenous nitric oxide in apoptosis of alveolar epithelial cells in the development of pulmonary fibrosis in rats
CHEN Xiao-ling,SHEN Tie-bao,ZHAO Song,LI Ying-min,ZHANG Ai-zi,LI Wen-bin,AI Jie. Role of endogenous nitric oxide in apoptosis of alveolar epithelial cells in the development of pulmonary fibrosis in rats[J]. Chinese Journal of Pathophysiology, 2004, 20(12): 2307-2310
Authors:CHEN Xiao-ling  SHEN Tie-bao  ZHAO Song  LI Ying-min  ZHANG Ai-zi  LI Wen-bin  AI Jie
Affiliation:1. Department of Pathophysiology, Institute of Basic Medicine, Hebei Medical University, Shijiazhuang 050017, China;
2. Department of Pathology, Hebei Medical University, Shijiazhuang 050017, China;
3. Department of Histology & Embryology, Hebei Medical University, Shijiazhuang 050017, China
Abstract:AIM: To study the role of high level of endogenous nitric oxide (NO) in apoptosis of alveolar epithelial cells in the development of pulmonary fibrosis in rats. METHODS: The content of nitrite/nitrate (NO 2-/NO 3-) in out-flowing pulmonary blood (OPB) was assayed by nitric acid reduction method. The apoptosis of alveolar epithelial cells was observed by TdT-mediated dUTP nick-end labeling (TUNEL) and electron microscopy, respectively. The above indices were observed on the day 14 and the day 30 after intratracheal administration of BLMA 5 alone or along with blockade of iNOS by aminoguanidine (AG) in rats. RESULTS: (1) Both the content of NO 2-/NO 3- in OPB and the number of apoptotic alveolar epithelial cells in lung were increased in BLMA 5 14 d group, compared with normal control group and BLMA 5 30 d group, respectively (P<0.05). The high level of NO 2-/NO 3-in OPB and the apoptosis of alveolar epithelial cells were ameliorated by AG. CONCLUSION: The apoptosis of alveolar epithelial cell is induced by high level of endogenous NO in the development of pulmonary fibrosis. [
Keywords:Pulmonary fibrosis  Alveolar epithelial cells  Apoptosis  Nitric oxide  Rats
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