• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

细菌战:益生菌对早产儿肠道的保护作用

Germ warfare: probiotics in defense of the premature gut.

作者信息

Hammerman Cathy, Bin-Nun Alona, Kaplan Michael

机构信息

Ben-Gurion University of the Negev, Beersheva, Israel.

出版信息

Clin Perinatol. 2004 Sep;31(3):489-500. doi: 10.1016/j.clp.2004.04.015.

DOI:10.1016/j.clp.2004.04.015
PMID:15325534
Abstract

The potential benefits of a predominantly lactic acid bacterial flora include an improved balance of gut microbial ecology and decreased susceptibility of the gut mucosa to bacterial translocation via adherence to the intestinal mucosa, strengthening mucosal barrier function. These properties should be especially beneficial to the premature neonate with (1) delayed establishment of nor-mal flora, increasing the potential for proliferation of pathogenic bacteria and (2) immature development of the intestinal mucosa, rendering it more susceptible to the translocation of these pathogenic bacteria and leading to extra-intestinal spread and systemic disease. Early probiotic supplementation in preterm infants is theoretically sound and associated with minimal risk. Clinical data remain preliminary but are supportive of a reduction in feeding intolerance and NEC in this high-risk group.

摘要

以乳酸菌为主的菌群的潜在益处包括改善肠道微生物生态平衡,以及通过黏附于肠黏膜降低肠道黏膜对细菌易位的敏感性,从而增强黏膜屏障功能。这些特性对于早产新生儿尤其有益,原因在于:(1)正常菌群建立延迟,增加了病原菌增殖的可能性;(2)肠道黏膜发育不成熟,使其更容易受到这些病原菌易位的影响,进而导致肠外扩散和全身性疾病。理论上,对早产儿早期补充益生菌是合理的,且风险极小。临床数据仍然初步,但支持降低这一高危群体的喂养不耐受和坏死性小肠结肠炎的发生率。

相似文献

1
Germ warfare: probiotics in defense of the premature gut.细菌战:益生菌对早产儿肠道的保护作用
Clin Perinatol. 2004 Sep;31(3):489-500. doi: 10.1016/j.clp.2004.04.015.
2
Probiotics: role in pathophysiology and prevention in necrotizing enterocolitis.益生菌:在坏死性小肠结肠炎的病理生理学及预防中的作用
Semin Perinatol. 2008 Apr;32(2):127-37. doi: 10.1053/j.semperi.2008.01.006.
3
The role of the intestinal barrier in the pathogenesis of necrotizing enterocolitis.肠道屏障在坏死性小肠结肠炎发病机制中的作用。
Shock. 2007 Feb;27(2):124-33. doi: 10.1097/01.shk.0000239774.02904.65.
4
Probiotics and neonatal necrotizing enterocolitis.益生菌与新生儿坏死性小肠结肠炎。
Anaerobe. 2011 Aug;17(4):180-5. doi: 10.1016/j.anaerobe.2011.02.004. Epub 2011 Mar 3.
5
Probiotics as modulators of the gut flora.益生菌作为肠道菌群的调节剂。
Br J Nutr. 2002 Sep;88 Suppl 1:S39-49. doi: 10.1079/BJN2002628.
6
Protective nutrients and bacterial colonization in the immature human gut.未成熟人类肠道中的保护性营养素与细菌定植
Adv Pediatr. 1999;46:353-82.
7
Probiotics and neonatal intestinal infection.益生菌与新生儿肠道感染
Curr Opin Infect Dis. 2006 Jun;19(3):277-82. doi: 10.1097/01.qco.0000224823.73223.29.
8
Probiotics and the mechanism of necrotizing enterocolitis.益生菌与坏死性小肠结肠炎的发病机制
Semin Pediatr Surg. 2013 May;22(2):94-100. doi: 10.1053/j.sempedsurg.2013.01.006.
9
Enteral feeding induces diet-dependent mucosal dysfunction, bacterial proliferation, and necrotizing enterocolitis in preterm pigs on parenteral nutrition.肠内喂养会在接受肠外营养的早产仔猪中引发饮食依赖性的黏膜功能障碍、细菌增殖和坏死性小肠结肠炎。
Am J Physiol Gastrointest Liver Physiol. 2008 Nov;295(5):G1092-103. doi: 10.1152/ajpgi.00414.2007. Epub 2008 Sep 25.
10
What next in necrotizing enterocolitis?坏死性小肠结肠炎接下来该如何治疗?
Turk J Pediatr. 2008 Jan-Feb;50(1):1-11.

引用本文的文献

1
Identification and evaluation of probiotic potential of Bifidobacterium breve AHC3 isolated from chicken intestines and its effect on necrotizing enterocolitis (NEC) in newborn SD rats.从鸡肠道中分离出的短双歧杆菌 AHC3 的益生菌潜力的鉴定和评估及其对新生 SD 大鼠坏死性小肠结肠炎 (NEC) 的影响。
PLoS One. 2023 Nov 2;18(11):e0287799. doi: 10.1371/journal.pone.0287799. eCollection 2023.
2
subsp. lactis A6 Alleviates Obesity Associated with Promoting Mitochondrial Biogenesis and Function of Adipose Tissue in Mice.植物乳杆菌 A6 可通过促进脂肪组织中线粒体生物发生和功能减轻肥胖。
Molecules. 2020 Mar 25;25(7):1490. doi: 10.3390/molecules25071490.
3
Bifidobacterium and Lactobacillus for preventing necrotizing enterocolitis in very-low-birth-weight preterm infants: a systematic review and meta-analysis.
双歧杆菌和乳酸杆菌预防极低出生体重早产儿坏死性小肠结肠炎的系统评价和荟萃分析。
World J Pediatr. 2020 Apr;16(2):135-142. doi: 10.1007/s12519-019-00297-5. Epub 2019 Sep 4.
4
Probiotic strategies to prevent necrotizing enterocolitis in preterm infants: a meta-analysis.预防早产儿坏死性小肠结肠炎的益生菌策略:一项荟萃分析。
Pediatr Surg Int. 2019 Oct;35(10):1143-1162. doi: 10.1007/s00383-019-04547-5. Epub 2019 Aug 16.
5
Lactobacillus rhamnosus GG Ameliorates Liver Injury and Hypoxic Hepatitis in Rat Model of CLP-Induced Sepsis.鼠盲肠结扎穿孔术诱导脓毒症模型中罗伊氏乳杆菌 GG 改善肝损伤和缺氧性肝炎。
Dig Dis Sci. 2019 Oct;64(10):2867-2877. doi: 10.1007/s10620-019-05628-0. Epub 2019 Apr 30.
6
Efficacy of Bifidobacterium Species in Prevention of Necrotizing Enterocolitis in Very-Low Birth Weight Infants. A Systematic Review.双歧杆菌属对极低出生体重儿坏死性小肠结肠炎的预防效果:一项系统评价
J Pediatr Pharmacol Ther. 2019 Jan-Feb;24(1):10-15. doi: 10.5863/1551-6776-24.1.10.
7
Protective Effects of Bifidobacterium on Intestinal Barrier Function in LPS-Induced Enterocyte Barrier Injury of Caco-2 Monolayers and in a Rat NEC Model.双歧杆菌对脂多糖诱导的Caco-2单层细胞肠上皮细胞屏障损伤及大鼠坏死性小肠结肠炎模型肠道屏障功能的保护作用
PLoS One. 2016 Aug 23;11(8):e0161635. doi: 10.1371/journal.pone.0161635. eCollection 2016.
8
Lactobacillus rhamnosus GG and Bifidobacterium longum attenuate lung injury and inflammatory response in experimental sepsis.鼠李糖乳杆菌GG和长双歧杆菌减轻实验性脓毒症中的肺损伤和炎症反应。
PLoS One. 2014 May 15;9(5):e97861. doi: 10.1371/journal.pone.0097861. eCollection 2014.
9
Lactobacillus rhamnosus GG improves outcome in experimental pseudomonas aeruginosa pneumonia: potential role of regulatory T cells.鼠李糖乳杆菌 GG 改善实验性铜绿假单胞菌肺炎的结局:调节性 T 细胞的潜在作用。
Shock. 2013 Dec;40(6):496-503. doi: 10.1097/SHK.0000000000000066.
10
Probiotic administration reduces mortality and improves intestinal epithelial homeostasis in experimental sepsis.益生菌给药可降低实验性脓毒症的死亡率并改善肠道上皮细胞的稳态。
Anesthesiology. 2013 Jul;119(1):166-77. doi: 10.1097/ALN.0b013e318291c2fc.