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益生菌诱导的结肠衰老抑制可促进小鼠长寿,这依赖于上调肠道细菌多胺的产生。

Longevity in mice is promoted by probiotic-induced suppression of colonic senescence dependent on upregulation of gut bacterial polyamine production.

机构信息

Dairy Science and Technology Institute, Kyodo Milk Industry Co. Ltd., Tokyo, Japan.

出版信息

PLoS One. 2011;6(8):e23652. doi: 10.1371/journal.pone.0023652. Epub 2011 Aug 16.

Abstract

BACKGROUND

Chronic low-grade inflammation is recognized as an important factor contributing to senescence and age-related diseases. In mammals, levels of polyamines (PAs) decrease during the ageing process; PAs are known to decrease systemic inflammation by inhibiting inflammatory cytokine synthesis in macrophages. Reductions in intestinal luminal PAs levels have been associated with intestinal barrier dysfunction. The probiotic strain Bifidobacterium animalis subsp. lactis LKM512 is known to increase intestinal luminal PA concentrations.

METHODOLOGY/PRINCIPAL FINDINGS: We supplemented the diet of 10-month-old Crj:CD-1 female mice with LKM512 for 11 months, while the controls received no supplementation. Survival rates were compared using Kaplan-Meier survival curves. LKM512-treated mice survived significantly longer than controls (P<0.001); moreover, skin ulcers and tumors were more common in the control mice. We then analyzed inflammatory and intestinal conditions by measuring several markers using HPLC, ELISA, reverse transcription-quantitative PCR, and histological slices. LKM512 mice showed altered 16S rRNA gene expression of several predominant intestinal bacterial groups. The fecal concentrations of PAs, but not of short-chain fatty acids, were significantly higher in LKM512-treated mice (P<0.05). Colonic mucosal function was also better in LKM512 mice, with increased mucus secretion and better maintenance of tight junctions. Changes in gene expression levels were evaluated using the NimbleGen mouse DNA microarray. LKM512 administration also downregulated the expression of ageing-associated and inflammation-associated genes and gene expression levels in 21-month-old LKM512-treated mice resembled those in 10-month-old untreated (younger) mice.

CONCLUSION/SIGNIFICANCE: Our study demonstrated increased longevity in mice following probiotic treatment with LKM512, possibly due to the suppression of chronic low-grade inflammation in the colon induced by higher PA levels. This indicates that ingestion of specific probiotics may be an easy approach for improving intestinal health and increasing lifespan. Further studies are required to clarify its effectiveness in humans.

摘要

背景

慢性低度炎症被认为是导致衰老和与年龄相关疾病的重要因素。在哺乳动物中,多胺(PAs)水平在衰老过程中降低;已知 PAs 通过抑制巨噬细胞中炎性细胞因子的合成来降低全身炎症。肠道腔 PAs 水平的降低与肠道屏障功能障碍有关。益生菌菌株双歧杆菌乳亚种 LKM512 已知可增加肠道腔 PA 浓度。

方法/主要发现:我们用 LKM512 补充 10 个月大的 Crj:CD-1 雌性小鼠的饮食 11 个月,而对照组则没有补充。使用 Kaplan-Meier 生存曲线比较存活率。LKM512 治疗组的小鼠存活时间明显长于对照组(P<0.001);此外,对照组的小鼠更容易出现皮肤溃疡和肿瘤。然后,我们通过使用 HPLC、ELISA、逆转录定量 PCR 和组织切片测量多个标志物来分析炎症和肠道状况。LKM512 小鼠显示出几种主要肠道细菌群的 16S rRNA 基因表达改变。LKM512 治疗组的粪便多胺浓度显著升高(P<0.05),但短链脂肪酸浓度没有升高。LKM512 小鼠的结肠黏膜功能也更好,黏液分泌增加,紧密连接保持更好。使用 NimbleGen 小鼠 DNA 微阵列评估基因表达水平的变化。LKM512 给药还下调了与衰老和炎症相关的基因的表达水平,并且 21 个月大的 LKM512 治疗组的基因表达水平类似于 10 个月大的未治疗(年轻)组的基因表达水平。

结论/意义:我们的研究表明,LKM512 益生菌治疗可使小鼠寿命延长,可能是由于较高的 PA 水平抑制了结肠的慢性低度炎症。这表明摄入特定的益生菌可能是改善肠道健康和延长寿命的一种简单方法。需要进一步的研究来阐明其在人类中的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba42/3156754/ad7c726a9ff1/pone.0023652.g001.jpg

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