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大鼠模型中老年与成年多器官功能障碍综合征的比较。

A comparison of elderly and adult multiple organ dysfunction syndrome in the rat model.

作者信息

Zhu Qinglei, Qian Xiaoshun, Wang Shiwen, Yin Tong, Yang Jie, Xue Qiao, Xu Bin

机构信息

Institute of Geriatric Cardiology, Chinese PLA General Hospital, Fuxing Road 28, Beijing 100853, China.

出版信息

Exp Gerontol. 2006 Aug;41(8):771-7. doi: 10.1016/j.exger.2006.05.010. Epub 2006 Jun 22.

DOI:10.1016/j.exger.2006.05.010
PMID:16797904
Abstract

Multiple organ dysfunction syndrome (MODS) in the elderly is the most common cause of mortality in critically ill elderly patients, and it is different from MODS in the adult in clinic. Rare studies have been done on its pathogenesis and the comparison between adult and elderly MODS animal models. This work aimed at exploring the mechanisms mediating elderly MODS and compared this with adult MODS. Male Sprague-Dawley aged and adult rats were intraperitoneally injected with zymosan for incitement of MODS. Aged rats receiving zymosan showed severer pulmonary, cardiac and renal dysfunctions than adult rats. Likewise, the tissue lesions under light microscope in major organs of zymosan treated aged rats were much worse than those of zymosan treated adult rats. Moreover, zymosan treated aged rats showed 142% and 64% greater increase in pulmonary alveolar macrophages (AMs) apoptotic rate and serum TNF-alpha level, respectively, whereas 43% smaller increase in serum IL-10 level compared to zymosan treated adult rats. Furthermore, lung injury was much worse than that in other organs in zymosan treated aged rats. Overall, these results suggest that zymosan can be used in aged rats to incite MODS in the elderly. In the animal model of elderly MODS, there are (1) severer injury in lung, heart and kidney vs adult; (2) easier to develop severe systemic inflammatory response syndrome (SIRS) instead of compensatory anti-inflammatory response syndrome (CARS) compared to the adult; and (3) severer inflammation in lung than other organs indicative of the possible roles of lung in triggering MODS in the elderly.

摘要

老年多器官功能障碍综合征(MODS)是危重症老年患者最常见的死亡原因,且在临床上与成人MODS有所不同。关于其发病机制以及成人与老年MODS动物模型之间的比较,相关研究较少。本研究旨在探讨介导老年MODS的机制,并将其与成人MODS进行比较。将雄性老年和成年Sprague-Dawley大鼠腹腔注射酵母聚糖以诱发MODS。接受酵母聚糖注射的老年大鼠比成年大鼠表现出更严重的肺、心脏和肾脏功能障碍。同样,酵母聚糖处理的老年大鼠主要器官在光镜下的组织损伤比酵母聚糖处理的成年大鼠严重得多。此外,与酵母聚糖处理的成年大鼠相比,酵母聚糖处理的老年大鼠肺泡巨噬细胞(AMs)凋亡率和血清TNF-α水平分别升高142%和64%,而血清IL-10水平升高幅度小43%。此外,酵母聚糖处理的老年大鼠肺损伤比其他器官严重得多。总体而言,这些结果表明酵母聚糖可用于老年大鼠以诱发老年MODS。在老年MODS动物模型中,存在以下情况:(1)与成年相比,肺、心脏和肾脏损伤更严重;(2)与成年相比,更容易发生严重的全身炎症反应综合征(SIRS)而非代偿性抗炎反应综合征(CARS);(3)肺炎症比其他器官更严重,表明肺在触发老年MODS中可能起作用。

相似文献

1
A comparison of elderly and adult multiple organ dysfunction syndrome in the rat model.大鼠模型中老年与成年多器官功能障碍综合征的比较。
Exp Gerontol. 2006 Aug;41(8):771-7. doi: 10.1016/j.exger.2006.05.010. Epub 2006 Jun 22.
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Altered chemokine response in an animal model of multiple organ dysfunction syndrome induced by zymosan.酵母聚糖诱导的多器官功能障碍综合征动物模型中趋化因子反应的改变
J Pediatr Surg. 2005 Mar;40(3):464-9. doi: 10.1016/j.jpedsurg.2004.11.042.
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[Apoptosis of pulmonary alveolar macrophages in aged and adult rats: a comparative study].[老年大鼠与成年大鼠肺泡巨噬细胞凋亡的比较研究]
Zhonghua Yi Xue Za Zhi. 2005 Jan 26;85(4):253-6.
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Interleukin 10 mitigates the development of the zymosan-induced multiple organ dysfunction syndrome in mice.白细胞介素10减轻小鼠中zymosan诱导的多器官功能障碍综合征的发展。
Cytokine. 1999 Sep;11(9):713-21. doi: 10.1006/cyto.1998.0476.
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Multiple organ dysfunction syndrome: end organ and systemic inflammatory response in a mouse model of nonseptic origin.多器官功能障碍综合征:非感染性来源小鼠模型中的终末器官与全身炎症反应
Shock. 1995 Dec;4(6):389-96.
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Role of the lung in the progression of multiple organ dysfunction syndrome in ageing rat model.肺在衰老大鼠多器官功能障碍综合征进展中的作用。
Chin Med J (Engl). 2012 Aug;125(15):2708-13.
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Interleukin-10 reduces morbidity and mortality in murine multiple organ dysfunction syndrome (MODS).白细胞介素-10可降低小鼠多器官功能障碍综合征(MODS)的发病率和死亡率。
J Surg Res. 1998 Jul 1;77(2):157-64. doi: 10.1006/jsre.1998.5372.
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[Effects of antithrombin-III on cytokines in rats with multiple organ dysfunction syndrome].抗凝血酶Ⅲ对多器官功能障碍综合征大鼠细胞因子的影响
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Etanercept reduces acute tissue injury and mortality associated to zymosan-induced multiple organ dysfunction syndrome.依那西普可减轻与酵母聚糖诱导的多器官功能障碍综合征相关的急性组织损伤和死亡率。
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Prenatal exposure to inflammation induced by zymosan results in activation of intrarenal renin-angiotensin system in adult offspring rats.
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