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Toxicology and carcinogenesis studies of indium phosphide (CAS No. 22398-90-7) in F344/N rats and B6C3F1 mice (inhalation studies).磷化铟(CAS编号:22398-90-7)对F344/N大鼠和B6C3F1小鼠的毒理学和致癌性研究(吸入研究)
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Assessment of splenic function.脾脏功能评估。
Eur J Clin Microbiol Infect Dis. 2010 Dec;29(12):1465-73. doi: 10.1007/s10096-010-1049-1. Epub 2010 Sep 19.
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Microbial epidemiology and outcome of bloodstream infections in liver transplant recipients: an analysis of 259 episodes.肝移植受者血流感染的微生物流行病学和结局:259 例分析。
Liver Transpl. 2010 Mar;16(3):393-401. doi: 10.1002/lt.21991.
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Late acute celiac and hepatic artery thrombosis with portal vein thrombosis resulting in hepatic infarction 12 years post orthotopic liver transplantation.原位肝移植术后 12 年发生迟发性急性腹腔干和肝动脉血栓形成,并伴有门静脉血栓形成导致肝梗死。
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Childhood bacterial respiratory diseases: past, present, and future.儿童细菌性呼吸道疾病:过去、现在与未来。
Pediatr Infect Dis J. 2009 Oct;28(10 Suppl):S127-32. doi: 10.1097/INF.0b013e3181b6d800.
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Identification of splenic reservoir monocytes and their deployment to inflammatory sites.脾脏储备单核细胞的鉴定及其向炎症部位的募集
Science. 2009 Jul 31;325(5940):612-6. doi: 10.1126/science.1175202.
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Innate immunity and inflammation--two facets of the same anti-infectious reaction.固有免疫与炎症——同一抗感染反应的两个方面。
Clin Exp Immunol. 2009 May;156(2):194-8. doi: 10.1111/j.1365-2249.2009.03893.x. Epub 2009 Mar 2.
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Endotoxemia causes central downregulation of sympathetic vasomotor tone in healthy humans.内毒素血症会导致健康人体内交感神经血管运动张力的中枢性下调。
Am J Physiol Regul Integr Comp Physiol. 2008 Sep;295(3):R891-8. doi: 10.1152/ajpregu.90444.2008. Epub 2008 Jul 16.
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Lipopolysaccharide augments venous and arterial thrombosis in the mouse.脂多糖会加剧小鼠的静脉和动脉血栓形成。
Thromb Res. 2008;123(2):355-60. doi: 10.1016/j.thromres.2008.03.015. Epub 2008 Apr 29.
9
Sex differences in the impact of ozone on survival and alveolar macrophage function of mice after Klebsiella pneumoniae infection.肺炎克雷伯菌感染后臭氧对小鼠存活率和肺泡巨噬细胞功能影响的性别差异。
Respir Res. 2008 Feb 28;9(1):24. doi: 10.1186/1465-9921-9-24.
10
Environmental and occupational exposures: do they affect chronic obstructive pulmonary disease differently in women and men?环境与职业暴露:它们对男性和女性慢性阻塞性肺疾病的影响是否不同?
Proc Am Thorac Soc. 2007 Dec;4(8):692-4. doi: 10.1513/pats.200707-094SD.

在不同暴露条件下,对肺炎克雷伯菌感染小鼠的肺组织和肺外组织进行组织病理学评估,结果显示存在性别差异。

Histopathologic evaluation of lung and extrapulmonary tissues show sex differences in Klebsiella pneumoniae - infected mice under different exposure conditions.

作者信息

Mikerov Anatoly N, Cooper Timothy K, Wang Guirong, Hu Sanmei, Umstead Todd M, Phelps David S, Floros Joanna

出版信息

Int J Physiol Pathophysiol Pharmacol. 2011 Sep 30;3(3):176-90. Epub 2011 Sep 6.

PMID:21941609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3175744/
Abstract

It has been shown that female mice with pneumonia have a survival advantage over males, but this is reversed if ozone exposure precedes infection. The purpose of this study was to investigate factors that underlie these observations, by studying histopathologic changes in lung and extrapulmonary (spleen and liver) tissues after ozone or filtered air (FA) exposure followed by pulmonary bacterial infection. Male and female wild type C57BL/6J mice were exposed to ozone or FA, then anesthetized and infected intratracheally with Klebsiella pneumoniae bacteria. Tissues (lung, spleen, and liver) were subjected to histopathologic analysis at 48 h post-infection. We found that after infection, 1) the severity of inflammation was higher, the affected area of the lung was larger, and spleen red pulp myelopoiesis was lower in ozone-exposed mice compared to FA-exposed animals in both sexes; 2) more pronounced extrapulmonary lesions (in liver and spleen) were observed in FA-exposed males compared to FA-exposed females; and 3) excessive lung inflammatory response was detected in ozone-exposed females compared to ozone-exposed males. We concluded that different risk factors contribute to the differential outcome of pneumonia between sexes in the presence or absence of ozone-induced oxidative stress. In specific, the excessive lung inflammation and higher risk for extrapulmonary lesions in ozone-exposed infected females and in FA-exposed infected males appear to play, respectively, a dominant role in the previously observed respective survival outcomes.

摘要

研究表明,患肺炎的雌性小鼠比雄性小鼠具有生存优势,但如果在感染前暴露于臭氧中,这种优势就会逆转。本研究的目的是通过研究臭氧或过滤空气(FA)暴露后再进行肺部细菌感染,观察肺组织和肺外组织(脾脏和肝脏)的组织病理学变化,来探究这些观察结果背后的因素。将雄性和雌性野生型C57BL/6J小鼠暴露于臭氧或FA中,然后麻醉并经气管内注射肺炎克雷伯菌进行感染。在感染后48小时对组织(肺、脾脏和肝脏)进行组织病理学分析。我们发现,感染后,1)与暴露于FA的动物相比,暴露于臭氧的小鼠无论雌雄,炎症严重程度更高,肺的受累面积更大,脾脏红髓髓系造血更低;2)与暴露于FA的雌性相比,暴露于FA的雄性观察到更明显的肺外病变(肝脏和脾脏);3)与暴露于臭氧的雄性相比,暴露于臭氧的雌性检测到过度的肺部炎症反应。我们得出结论,在存在或不存在臭氧诱导的氧化应激的情况下,不同的风险因素导致了两性肺炎的不同结果。具体而言,暴露于臭氧的感染雌性小鼠中过度的肺部炎症和暴露于FA的感染雄性小鼠中更高的肺外病变风险,似乎分别在先前观察到的各自生存结果中起主导作用。