The changes induced by cyclophosphamide in intestinal barrier and microflora in mice

被引:186
作者
Yang, Jin [1 ,2 ]
Liu, Kai-xiong [3 ]
Qu, Jie-ming [3 ]
Wang, Xiao-dan [1 ]
机构
[1] Fudan Univ, Dept Pulm Med, Zhongshan Hosp, Shanghai Med Coll, Shanghai 200032, Peoples R China
[2] Anhui Med Univ, Dept Resp Med, Hosp 2, Hefei 230601, Peoples R China
[3] Fudan Univ, Dept Pulm Med, Huadong Hosp, Shanghai Med Coll, Shanghai 200040, Peoples R China
关键词
Cyclophosphamide; Bacterial translocation; Tight junction; Intestinal microflora; BACTERIAL TRANSLOCATION; GUT; CHEMOTHERAPY; METHOTREXATE; INHIBITION; PROBIOTICS; SEPSIS; MODEL; FLORA; BURN;
D O I
10.1016/j.ejphar.2013.06.006
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Infection is one of the most commonly encountered complication during chemotherapy treatment, and recent studies showed that such infections are aroused primarily from the intestinal microflora through bacterial translocation. We aimed to investigate the alterations of mucosal barrier and colonization resistance in mouse treated with cyclophosphamide (CTX) to further understand the translocation mechanism. Male Balb/c mice were administered intraperitoneally with CTX at 25 mg/kg, 50 mg/kg and 100 mg/kg for 5 days. We found that pretreatment with CTX, especially at high dose, increased the potentially pathogenic bacteria counts (Escherichia coli, enterobacteraceae, Pseudomonas and enterococci) and the intestinal permeability, which was associated with the reduction of tight junctions and adherens junctions. Our results suggested that disruption of mucosal barrier and colonization resistance may be partly responsible for the bacterial translocation during chemotherapy. Thus, modulation of mechanical mucosal barrier and colonization resistance might represent a new opportunity for applications in cancer patients to reduce infectious complications. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 124
页数:5
相关论文
共 24 条
[1]
Bacterial translocation: Overview of mechanisms and clinical impact [J].
Balzan, Silvio ;
Quadros, Claudio de Almeida ;
de Cleva, Roberto ;
Zilberstein, Bruno ;
Cecconello, Ivan .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2007, 22 (04) :464-471
[2]
Acetaldehyde disrupts tight junctions and adherens junctions in human colonic mucosa: protection by EGF and L-glutamine [J].
Basuroy, S ;
Sheth, P ;
Mansbach, CM ;
Rao, RK .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 289 (02) :G367-G375
[3]
[4]
Reversal of the effect of albumin on gut barrier function in burn by the inhibition of inducible isoform of nitric oxide synthase [J].
Chen, LW ;
Wang, JS ;
Hwang, B ;
Chen, JS ;
Hsu, CM .
ARCHIVES OF SURGERY, 2003, 138 (11) :1219-1225
[5]
Probiotic Bacteria Regulate Intestinal Epithelial Permeability in Experimental Ileitis by a TNF-Dependent Mechanism [J].
Corridoni, Daniele ;
Pastorelli, Luca ;
Mattioli, Benedetta ;
Locovei, Silviu ;
Ishikawa, Dai ;
Arseneau, Kristen O. ;
Chieppa, Marcello ;
Cominelli, Fabio ;
Pizarro, Theresa T. .
PLOS ONE, 2012, 7 (07)
[6]
BURN-INDUCED GUT BARRIER INJURY IS ATTENUATED BY PHOSPHODIESTERASE INHIBITION: EFFECTS ON TIGHT JUNCTION STRUCTURAL PROTEINS [J].
Costantini, Todd W. ;
Loomis, William H. ;
Putnam, James G. ;
Drusinsky, Dana ;
Deree, Jessica ;
Choi, Sunghyuk ;
Wolf, Paul ;
Baird, Andrew ;
Eliceiri, Brian ;
Bansal, Vishal ;
Coimbra, Raul .
SHOCK, 2009, 31 (04) :416-422
[7]
Diversity of the human intestinal microbial flora [J].
Eckburg, PB ;
Bik, EM ;
Bernstein, CN ;
Purdom, E ;
Dethlefsen, L ;
Sargent, M ;
Gill, SR ;
Nelson, KE ;
Relman, DA .
SCIENCE, 2005, 308 (5728) :1635-1638
[8]
Berberine Ameliorates Intestinal Epithelial Tight-Junction Damage and Down-regulates Myosin Light Chain Kinase Pathways in a Mouse Model of Endotoxinemia [J].
Gu, Lili ;
Li, Ning ;
Gong, Jianfeng ;
Li, Qiurong ;
Zhu, Weiming ;
Li, Jieshou .
JOURNAL OF INFECTIOUS DISEASES, 2011, 203 (11) :1602-1612
[9]
Oral Administration of Heat-Killed Lactobacillus plantarum Strain b240 Protected Mice against Salmonella enterica Serovar Typhimurium [J].
Ishikawa, Hiroki ;
Kutsukake, Etsuko ;
Fukui, Toshie ;
Sato, Ikutaro ;
Shirai, Toshiaki ;
Kurihara, Tatsuya ;
Okada, Nobuhiko ;
Danbara, Hirofumi ;
Toba, Masamichi ;
Kohda, Noriyuki ;
Maeda, Yasuyuki ;
Matsumoto, Tetsuya .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2010, 74 (07) :1338-1342
[10]
Oral administration of Bifidobacterium longum prevents gut-derived Pseudomonas aeruginosa sepsis in mice [J].
Matsumoto, T. ;
Ishikawa, H. ;
Tateda, K. ;
Yaeshima, T. ;
Ishibashi, N. ;
Yamaguchi, K. .
JOURNAL OF APPLIED MICROBIOLOGY, 2008, 104 (03) :672-680