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双歧杆菌婴儿 35624 的粪便排泄和口服包埋益生菌补充八周后粪便微生物群的变化。

Fecal excretion of Bifidobacterium infantis 35624 and changes in fecal microbiota after eight weeks of oral supplementation with encapsulated probiotic.

机构信息

Procter & Gamble, Cincinnati, OH, USA.

出版信息

Gut Microbes. 2013 May-Jun;4(3):201-11. doi: 10.4161/gmic.24196. Epub 2013 Apr 2.

Abstract

Certain randomized, placebo-controlled trials of oral supplementation with B. infantis 35624 have demonstrated the amelioration of symptoms of irritable bowel syndrome. Potential GI colonization by B. infantis 35624 or effects of supplementation on resident GI microbiota may pertain to these clinical observations. In this study, fecal excretion of B. infantis 35624 before, during and after 8 weeks of daily treatment was compared in subjects with IBS who received either the encapsulated oral supplement (n = 39) or placebo (n = 37) and in healthy subjects who received the supplement (n = 41). Secondarily, changes in assessed fecal microbiota and IBS symptoms were determined. Supplementation significantly increased fecal B. infantis 35624 excretion vs. placebo in IBS subjects; excretion in healthy subjects receiving supplement was quantitatively similar. Fecal levels of the probiotic declined and approached baseline once dosing ceased, documenting that colonization is transient. Although supplementation increased numbers of B infantis 35624 within the GI tract, limited changes in 10 other fecal taxa were observed either in healthy subjects or those with IBS. No impact on IBS symptoms was observed. Detection of bacterial DNA in fecal samples suggests that the probiotic is able to survive transit through the GI tract, although strain selective culture techniques were not performed to confirm viability of B. infantis 35624 in the feces. Continuous probiotic administration was necessary to maintain steady-state transit. Given the complex spectrum of GI microbiota, however, monitoring perturbations in selected taxa may not be not a useful indicator of probiotic function.

摘要

某些随机、安慰剂对照的口服补充 B. infantis 35624 的临床试验表明,该疗法可以改善肠易激综合征的症状。B. infantis 35624 对胃肠道的潜在定植或补充对常驻胃肠道微生物群的影响可能与这些临床观察有关。在这项研究中,比较了接受封装口服补充剂(n = 39)或安慰剂(n = 37)的 IBS 患者和接受补充剂的健康受试者(n = 41)在接受每日治疗 8 周前后粪便中 B. infantis 35624 的排泄情况。其次,确定了评估的粪便微生物群和 IBS 症状的变化。与安慰剂相比,补充剂显著增加了 IBS 患者粪便中 B. infantis 35624 的排泄量;接受补充剂的健康受试者的排泄量在数量上相似。一旦停止给药,粪便中益生菌的水平下降并接近基线,这表明定植是短暂的。尽管补充剂增加了 GI 道内 B infantis 35624 的数量,但在健康受试者或 IBS 患者中,其他 10 种粪便分类群的数量变化有限。未观察到对 IBS 症状的影响。粪便样本中细菌 DNA 的检测表明,益生菌能够在胃肠道中存活并通过,但未进行菌株选择性培养技术来确认 B. infantis 35624 在粪便中的活力。需要连续补充益生菌才能维持稳态转运。然而,鉴于胃肠道微生物群的复杂谱,监测选定分类群的扰动可能不是益生菌功能的有用指标。

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