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本文引用的文献

1
Bacterial diversity in aquatic and other environments: what 16S rDNA libraries can tell us.水生及其他环境中的细菌多样性:16S rDNA文库能告诉我们什么。
FEMS Microbiol Ecol. 2004 Feb 1;47(2):161-77. doi: 10.1016/S0168-6496(03)00257-5.
2
Molecular-phylogenetic analyses of human gastrointestinal microbiota.
Curr Opin Gastroenterol. 2001 Jan;17(1):52-7. doi: 10.1097/00001574-200101000-00010.
3
Unexpected diversity and complexity of the Guerrero Negro hypersaline microbial mat.格雷罗内格罗高盐度微生物垫出人意料的多样性和复杂性。
Appl Environ Microbiol. 2006 May;72(5):3685-95. doi: 10.1128/AEM.72.5.3685-3695.2006.
4
Risk of cardiovascular events and celecoxib: a systematic review and meta-analysis.心血管事件风险与塞来昔布:一项系统评价与荟萃分析
J R Soc Med. 2006 Mar;99(3):132-40. doi: 10.1177/014107680609900315.
5
Risk of adverse gastrointestinal outcomes in patients taking cyclo-oxygenase-2 inhibitors or conventional non-steroidal anti-inflammatory drugs: population based nested case-control analysis.服用环氧化酶-2抑制剂或传统非甾体抗炎药患者出现不良胃肠道后果的风险:基于人群的巢式病例对照分析。
BMJ. 2005 Dec 3;331(7528):1310-6. doi: 10.1136/bmj.331.7528.1310.
6
Composition and structure of microbial communities from stromatolites of Hamelin Pool in Shark Bay, Western Australia.西澳大利亚鲨鱼湾哈梅林池叠层石中微生物群落的组成与结构。
Appl Environ Microbiol. 2005 Aug;71(8):4822-32. doi: 10.1128/AEM.71.8.4822-4832.2005.
7
Obesity alters gut microbial ecology.肥胖会改变肠道微生物生态。
Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):11070-5. doi: 10.1073/pnas.0504978102. Epub 2005 Jul 20.
8
Risk of myocardial infarction in patients taking cyclo-oxygenase-2 inhibitors or conventional non-steroidal anti-inflammatory drugs: population based nested case-control analysis.服用环氧化酶-2抑制剂或传统非甾体抗炎药患者的心肌梗死风险:基于人群的巢式病例对照分析
BMJ. 2005 Jun 11;330(7504):1366. doi: 10.1136/bmj.330.7504.1366.
9
Geobiology of a microbial endolithic community in the Yellowstone geothermal environment.黄石地热环境中微生物内生岩群落的地质生物学
Nature. 2005 Apr 21;434(7036):1011-4. doi: 10.1038/nature03447.
10
Clostridium difficile toxins: mechanism of action and role in disease.艰难梭菌毒素:作用机制及在疾病中的作用
Clin Microbiol Rev. 2005 Apr;18(2):247-63. doi: 10.1128/CMR.18.2.247-263.2005.

非培养法分析吲哚美辛对大鼠胃肠道微生物群的影响

Culture-independent analysis of indomethacin-induced alterations in the rat gastrointestinal microbiota.

作者信息

Dalby Andrew B, Frank Daniel N, St Amand Allison L, Bendele Alison M, Pace Norman R

机构信息

Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO 80309-0347, USA.

出版信息

Appl Environ Microbiol. 2006 Oct;72(10):6707-15. doi: 10.1128/AEM.00378-06.

DOI:10.1128/AEM.00378-06
PMID:17021222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1610281/
Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly prescribed for a variety of inflammatory conditions; however, the benefits of this class of drugs are accompanied by deleterious side effects, most commonly gastric irritation and ulceration. NSAID-induced ulceration is thought to be exacerbated by intestinal microbiota, but previous studies have not identified specific microbes that contribute to these adverse effects. In this study, we conducted a culture-independent analysis of approximately 1,400 bacterial small-subunit rRNA genes associated with the small intestines and mesenteric lymph nodes of rats treated with the NSAID indomethacin. This is the first molecular analysis of the microbiota of the rat small intestine. A comparison of clone libraries and species-specific quantitative PCR results from rats treated with indomethacin and untreated rats revealed that organisms closely related to Enterococcus faecalis were heavily enriched in the small intestine and mesenteric lymph nodes of the treated rats. These data suggest that treatment of NSAID-induced ulceration may be facilitated by addressing the microbiological imbalances.

摘要

非甾体抗炎药(NSAIDs)常用于治疗各种炎症性疾病;然而,这类药物在带来益处的同时也伴有有害的副作用,最常见的是胃部刺激和溃疡。NSAID 诱导的溃疡被认为会因肠道微生物群而加剧,但先前的研究尚未确定导致这些不良反应的具体微生物。在本研究中,我们对约 1400 个与用 NSAID 消炎痛治疗的大鼠小肠和肠系膜淋巴结相关的细菌小亚基 rRNA 基因进行了非培养分析。这是对大鼠小肠微生物群的首次分子分析。对消炎痛治疗组大鼠和未治疗大鼠的克隆文库及物种特异性定量 PCR 结果进行比较后发现,与粪肠球菌密切相关的微生物在治疗组大鼠的小肠和肠系膜淋巴结中大量富集。这些数据表明,解决微生物失衡问题可能有助于治疗 NSAID 诱导的溃疡。