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长期吸入烟草烟雾对快速老化小鼠(SAM)-P/2衰老及氧化-抗氧化平衡的影响

Influences of chronic tobacco smoke inhalation on aging and oxidant-antioxidant balance in the senescence-accelerated mouse (SAM)-P/2.

作者信息

Teramoto S, Fukuchi Y, Uejima Y, Teramoto K, Orimo H

机构信息

Department of Geriatrics, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Exp Gerontol. 1993 Jan-Feb;28(1):87-95. doi: 10.1016/0531-5565(93)90023-7.

DOI:10.1016/0531-5565(93)90023-7
PMID:8436207
Abstract

We studied the influences of chronic tobacco exposure on aging and oxidant-antioxidant balance in two different strains of mice, hitherto called SAM (senescence-accelerated mice). One is a senescence-prone strain, "SAM-P/2," and another is a senescence-resistant strain, "SAM-R/1." We used 100 male mice--20 young (12 weeks of age) mice and 30 mature (24 weeks of age) mice from each strain. Half of each series were housed in a Hamburg II machine and exposed to tobacco smoke inhalation for five weeks. The result was that fewer of the mature SAM-P/2 survived compared with the mature SAM-R/1 after chronic tobacco inhalation. The grading of senility in the mature SAM-P/2 was also significantly higher than that in the mature SAM-R/1. The reduction of glutathione contents of blood and liver after tobacco exposure in the mature SAM-P/2 was greater than that in the young SAM-P/2 and the mature SAM-R/1. Moreover, oxygen radical generation of total blood cells stimulated by phorbol-myristate-acetate or opsonized zymosan showed a greater increase in the mature SAM-P/2 compared to the young SAM-P/2 and the mature SAM-R/1. These results indicate that the senescence-prone strain (SAM-P/2) was more susceptible to tobacco smoke exposure than the resistant strain (SAM-R/1). The impaired oxidant-antioxidant balance in the SAM-P/2 may therefore contribute to the process of senescence acceleration.

摘要

我们研究了长期烟草暴露对两种不同品系小鼠衰老及氧化-抗氧化平衡的影响,这两种品系小鼠迄今被称为SAM(衰老加速小鼠)。一种是易衰老品系“SAM-P/2”,另一种是抗衰老品系“SAM-R/1”。我们使用了100只雄性小鼠——每个品系各有20只年轻(12周龄)小鼠和30只成熟(24周龄)小鼠。每个组的一半小鼠被安置在一台Hamburg II机器中,吸入烟草烟雾5周。结果显示,长期吸入烟草后,成熟的SAM-P/2品系小鼠的存活数量比成熟的SAM-R/1品系小鼠少。成熟的SAM-P/2品系小鼠的衰老分级也显著高于成熟的SAM-R/1品系小鼠。成熟的SAM-P/2品系小鼠在烟草暴露后血液和肝脏中谷胱甘肽含量的降低幅度大于年轻的SAM-P/2品系小鼠和成熟的SAM-R/1品系小鼠。此外,与年轻的SAM-P/2品系小鼠和成熟的SAM-R/1品系小鼠相比,佛波酯-肉豆蔻酸酯-乙酸酯或调理酵母聚糖刺激的全血细胞氧自由基生成在成熟的SAM-P/2品系小鼠中增加得更多。这些结果表明,易衰老品系(SAM-P/2)比抗衰老品系(SAM-R/1)更容易受到烟草烟雾暴露的影响。因此,SAM-P/2品系小鼠中受损的氧化-抗氧化平衡可能导致衰老加速进程。

相似文献

1
Influences of chronic tobacco smoke inhalation on aging and oxidant-antioxidant balance in the senescence-accelerated mouse (SAM)-P/2.长期吸入烟草烟雾对快速老化小鼠(SAM)-P/2衰老及氧化-抗氧化平衡的影响
Exp Gerontol. 1993 Jan-Feb;28(1):87-95. doi: 10.1016/0531-5565(93)90023-7.
2
Influences of inhaled tobacco smoke on the senescence accelerated mouse (SAM).吸入烟草烟雾对衰老加速小鼠(SAM)的影响。
Eur Respir J. 1990 Oct;3(9):1029-36.
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A new murine model of aging lung: the senescence accelerated mouse (SAM)-P.一种新的衰老肺脏小鼠模型:衰老加速小鼠(SAM)-P。
Mech Ageing Dev. 1991 Dec 31;61(3):223-36. doi: 10.1016/0047-6374(91)90057-7.
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Effects of chronic cigarette smoke inhalation on the development of senile lung in senescence-accelerated mouse.
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Effect of age on alteration of glutathione metabolism following chronic cigarette smoke inhalation in mice.年龄对小鼠长期吸入香烟烟雾后谷胱甘肽代谢改变的影响。
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Age changes in visceral content of glutathione in the senescence accelerated mouse (SAM).快速老化小鼠(SAM)内脏中谷胱甘肽含量的年龄变化
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Biochemical characteristics of lungs in senescence-accelerated mouse (SAM).快速老化小鼠(SAM)肺脏的生化特性
Eur Respir J. 1995 Mar;8(3):450-6. doi: 10.1183/09031936.95.08030450.
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Grading score system: a method for evaluation of the degree of senescence in senescence accelerated mouse (SAM).评分系统:一种评估快速老化小鼠(SAM)衰老程度的方法。
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Age-associated changes in superoxide dismutase activity, thiobarbituric acid reactivity and reduced glutathione level in the brain and liver in senescence accelerated mice (SAM): a comparison with ddY mice.衰老加速小鼠(SAM)脑和肝脏中超氧化物歧化酶活性、硫代巴比妥酸反应性及还原型谷胱甘肽水平的年龄相关变化:与ddY小鼠的比较
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Cholinergic deficits in the septal-hippocampal pathway of the SAM-P/8 senescence accelerated mouse.SAM-P/8 加速衰老小鼠海马-隔区通路中的胆碱能缺陷
Brain Res. 2003 Mar 14;966(1):150-6. doi: 10.1016/s0006-8993(02)04192-6.

引用本文的文献

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Use of senescence-accelerated mouse model in bleomycin-induced lung injury suggests that bone marrow-derived cells can alter the outcome of lung injury in aged mice.衰老加速小鼠模型在博来霉素诱导的肺损伤中的应用表明,骨髓来源的细胞可改变老年小鼠肺损伤的结局。
J Gerontol A Biol Sci Med Sci. 2009 Jul;64(7):731-9. doi: 10.1093/gerona/glp040. Epub 2009 Apr 9.
2
Age-related changes in the antioxidant screen of the distal lung in mice.小鼠远端肺抗氧化指标的年龄相关性变化。
Lung. 1994;172(4):223-30. doi: 10.1007/BF00164439.