苯对尾悬吊大鼠血细胞及脂质过氧化的影响 |
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引用本文: | 李曙光,何新星,吴大蔚,刘洪涛,肇海,许峰,高郁晨,彭远开,杨成佳. 苯对尾悬吊大鼠血细胞及脂质过氧化的影响[J]. 航空航天医药, 2012, 6(6): 694-697 |
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作者姓名: | 李曙光 何新星 吴大蔚 刘洪涛 肇海 许峰 高郁晨 彭远开 杨成佳 |
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作者单位: | 中国航天员科研训练中心,北京,100094 |
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基金项目: | 载人航天领域预先研究项目 |
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摘 要: | 目的:探讨苯吸入染毒对尾吊模拟失重大鼠血液系统、脂质过氧化水平及抗氧化酶的影响.方法:将20只雄性SD大鼠随机分为2组:对照组和染毒组.对照组吸入新鲜空气,染毒组吸入10 mg/m3的苯气体,每天24 h,连续7 d.结果:与对照组相比,染毒组中白细胞(WBC)显著低于对照组(P<0.05);血红蛋白(HGB)显著低于对照组(P<0.05);淋巴细胞(LYM)极显著低于对照组(P<0.01);嗜碱性粒细胞(BAS)显著高于对照组(P<0.05);T淋巴细胞亚群分类:CD4极显著降低(P<0.01)、CD8极显著升高(P<0.01).染毒组中血清超氧化物歧化酶SOD活力极显著低于对照组(P<0.01);血清谷胱甘肽过氧化酶GSH-PX活力极显著高于对照组(P<0.01).结论:苯吸入染毒7 d可导致尾吊SD大鼠血液学指标的改变,表现为WBC降低,HGB降低,淋巴细胞(LYM)降低,BAS升高;HGB明显降低,RDW明显升高.脂质过氧化及抗氧化酶指标的改变,表现为SOD活力降低和GSH-PX活力升高.
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关 键 词: | 尾吊 血液 毒性 脂质过氧化 抗氧化酶 |
Effects of Benzene Exposure on Blood System and Lipidperoxidation in Rats Weightlessness Simulated by Tail-suspension |
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Affiliation: | LI Shuguang,HE Xin-xing,WU Dawei,et al.(Chinese Astronaut Research Training Center,Beijing 100094,China) |
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Abstract: | Objective:To study effects of benzene exposure on blood systemand lipid peroxidation and activity of anti-exidase in rats weightlessness simulated by tail-suspension.Methods:Twenty Male SD rats ware divided randomly into two groups,control group with air and benzene group with breathed at the dose of 10 mg/m3 benzene for 7 days.Results:As compared with control group,white blood cell(WBC) decreased significantly(P0.05),blood hemoglobin(HGB) decreased significantly(P0.05),blood lymphocyte(LYM) decreased especial significantly(P0.01).basophil(BAS) increased significantly(P0.05),blood T-Lymphocytes subgroup typing:CD4 decreased especial significantly(P0.01),CD8 increased especial significantly(P0.01).Activity of superoxide dismutase(SOD) decreased especial significantly(P0.01),activity of glutathione peroxidase(GSH-PX) increased especial significantly(P0.01).Conclusions:The above results showed that benzene exposure could cause change in white blood cell differential count,blood lymphocyte(LYM) decreased especial significantly;SOD decreased especial significantly,and compensatively increase activity of GSH-PX. |
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Keywords: | tail-suspension blood toxicity lipid peroxidation Antioxidase |
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