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益生菌通过重建小鼠肠道微生物群来减轻氟诱导的记忆损伤。

Probiotic alleviate fluoride-induced memory impairment by reconstructing gut microbiota in mice.

作者信息

Xin Jinge, Wang Hesong, Sun Ning, Bughio Shamsuddin, Zeng Dong, Li Lianxin, Wang Yanyan, Khalique Abdul, Zeng Yan, Pan Kangcheng, Jing Bo, Ma Hailin, Bai Yang, Ni Xueqin

机构信息

Animal Microecology Institute, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, Sichuan, China.

Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastroenterology, Institute of Gastroenterology of Guangdong Province, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Ecotoxicol Environ Saf. 2021 Jun 1;215:112108. doi: 10.1016/j.ecoenv.2021.112108. Epub 2021 Mar 30.

DOI:10.1016/j.ecoenv.2021.112108
PMID:33799132
Abstract

Fluoride which is widespread in our environment and food due to its geological origin and industrial pollution has been identified as a developmental neurotoxicant. Gut-brain axis provides new insight into brain-derived injury. We previously found the psychoactive effects of a probiotic strain, Lactobacillus johnsonii BS15 against fluoride-induced memory dysfunction in mice by modulating the gut-brain axis. In this study, we aimed to detect the link between the reconstruction of gut microbiota and gut-brain axis through which probiotic alleviate fluoride-induced memory impairment. We also added an hour of water avoidance stress (WAS) before behavioral tests and sampling, aiming to demonstrate the preventive effects of the probiotic on fluoride-induced memory impairment after psychological stress. Mice were given fluoridated drinking water (sodium fluoride 100 ppm, corresponding to 37.8 ± 2.4 ppm F¯) for 70 days and administered with PBS or a probiotic strain, Lactobacillus johnsonii BS15 for 28 days prior to and throughout a 70 day exposure to sodium fluoride. Results showed that fluoride increases the hyperactivity of hypothalamic-pituitary-adrenal (HPA) axis and reduces the exploration ratio in novel object recognition (NOR) test and the spontaneous exploration during the T-maze test in mice following WAS, which were significantly improved by the probiotic. 16S rRNA sequencing showed a significant separation in ileal microbiota between the fluoride-treated mice and control mice. Lactobacillus was the main targeting bacteria and significantly reduced in fluoride-treated mice. BS15 reconstructed the fluoride-post microbiota and increased the relative abundance of Lactobacillus. D-lactate content and diamine oxidase (DAO) activity, two biomarkers of gut permeability were reduced in the serum of probiotic-inoculated mice. ZO-1, an intestinal tight junction protein was reduced by fluoride in mRNA, and its protein levels were increased by the probiotic treatment. Moreover, the hippocampus which is essential to learning and memory, down-regulated mRNA level of both the myelin-associated glycoprotein (MAG), and protein levels of brain-derived neurotrophic factor (BDNF), including the improvement of cAMP response element-binding protein (CREB) by BS15 in fluoride-exposed mice after WAS. Via spearman correlation analysis, Lactobacillus displayed significantly positive associations with the behavioral tests, levels of nerve development related factors, and intestinal tight junction proteins ZO-1, and negative association with TNF-α of the hippocampus, highlighting regulatory effects of gut bacteria on memory potential and gut barrier. These results suggested the psychoactive effects of BS15 on fluoride-induced memory dysfunction after psychological stress. In addition, there may be some correlations between fluoride-induced memory dysfunction and reconstruction of gut microbiota. AVAILABILITY OF DATA AND MATERIALS: 16S rRNA sequencing reads have uploaded to NCBI. The accession code of 16S rRNA sequencing reads in the National Center for Biotechnology Information (NCBI) BioProject database: PRJNA660154.

摘要

由于地质来源和工业污染,氟化物在我们的环境和食物中广泛存在,已被确定为一种发育神经毒物。肠-脑轴为脑源性损伤提供了新的见解。我们之前发现,益生菌约氏乳杆菌BS15通过调节肠-脑轴,对氟化物诱导的小鼠记忆功能障碍具有精神活性作用。在本研究中,我们旨在检测肠道微生物群重建与肠-脑轴之间的联系,益生菌通过该联系减轻氟化物诱导的记忆损伤。我们还在行为测试和取样前增加了一小时的避水应激(WAS),旨在证明益生菌对心理应激后氟化物诱导的记忆损伤的预防作用。小鼠饮用含氟饮用水(氟化钠100 ppm,相当于37.8±2.4 ppm F¯)70天,并在接触氟化钠的70天之前及期间,用PBS或益生菌约氏乳杆菌BS15处理28天。结果显示,氟化物会增加下丘脑-垂体-肾上腺(HPA)轴的活性,并降低WAS后小鼠在新物体识别(NOR)测试中的探索率以及T迷宫测试中的自发探索率,而益生菌可显著改善这些情况。16S rRNA测序显示,氟化物处理的小鼠与对照小鼠的回肠微生物群存在显著差异。乳酸杆菌是主要的靶向细菌,在氟化物处理的小鼠中显著减少。BS15重建了氟化物处理后的微生物群,并增加了乳酸杆菌的相对丰度。接种益生菌的小鼠血清中,两种肠道通透性生物标志物D-乳酸含量和二胺氧化酶(DAO)活性降低。肠道紧密连接蛋白ZO-1的mRNA水平因氟化物而降低,而益生菌处理可增加其蛋白水平。此外,对学习和记忆至关重要的海马体中,髓鞘相关糖蛋白(MAG)的mRNA水平下调,脑源性神经营养因子(BDNF)的蛋白水平下调,包括WAS后,BS15对氟化物暴露小鼠中cAMP反应元件结合蛋白(CREB)的改善。通过斯皮尔曼相关性分析,乳酸杆菌与行为测试、神经发育相关因子水平以及肠道紧密连接蛋白ZO-1呈显著正相关,与海马体的肿瘤坏死因子-α(TNF-α)呈负相关,突出了肠道细菌对记忆潜能和肠道屏障的调节作用。这些结果表明,BS15对心理应激后氟化物诱导的记忆功能障碍具有精神活性作用。此外,氟化物诱导的记忆功能障碍与肠道微生物群重建之间可能存在一些相关性。数据和材料的可用性:16S rRNA测序读数已上传至NCBI。国家生物技术信息中心(NCBI)生物项目数据库中16S rRNA测序读数的登录代码:PRJNA660154。

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