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粪菌移植在 2 型糖尿病、肥胖和糖尿病肾病的临床前模型中的应用。

Fecal Microbiota Transplant in a Pre-Clinical Model of Type 2 Diabetes Mellitus, Obesity and Diabetic Kidney Disease.

机构信息

Hospital Israelita Albert Einstein, São Paulo 05652-900, SP, Brazil.

BiomeHub, Santa Catarina 88040-900, SC, Brazil.

出版信息

Int J Mol Sci. 2022 Mar 31;23(7):3842. doi: 10.3390/ijms23073842.

Abstract

Diabetes mellitus (DM) burden encompasses diabetic kidney disease (DKD), the leading cause of end-stage renal disease worldwide. Despite compelling evidence indicating that pharmacological intervention curtails DKD progression, the search for non-pharmacological strategies can identify novel targets for drug development against metabolic diseases. One of those emergent strategies comprises the modulation of the intestinal microbiota through fecal transplant from healthy donors. This study sought to investigate the benefits of fecal microbiota transplant (FMT) on functional and morphological parameters in a preclinical model of type 2 DM, obesity, and DKD using BTBR mice. These animals develop hyperglycemia and albuminuria in a time-dependent manner, mimicking DKD in humans. Our main findings unveiled that FMT prevented body weight gain, reduced albuminuria and tumor necrosis factor-α (TNF-α) levels within the ileum and ascending colon, and potentially ameliorated insulin resistance in BTBR mice. Intestinal structural integrity was maintained. Notably, FMT was associated with the abundance of the succinate-consuming bacteria family throughout the intestine. Collectively, our data pointed out the safety and efficacy of FMT in a preclinical model of type 2 DM, obesity, and DKD. These findings provide a basis for translational research on intestinal microbiota modulation and testing its therapeutic potential combined with current treatment for DM.

摘要

糖尿病(DM)负担包括糖尿病肾病(DKD),这是全球范围内导致终末期肾病的主要原因。尽管有令人信服的证据表明药物干预可以减缓 DKD 的进展,但寻找非药物策略可以为针对代谢疾病的药物开发确定新的靶点。其中一种新兴策略包括通过来自健康供体的粪便移植来调节肠道微生物群。本研究旨在使用 BTBR 小鼠研究粪便微生物群移植(FMT)对 2 型糖尿病、肥胖和 DKD 临床前模型的功能和形态参数的益处。这些动物会在一定时间内出现高血糖和白蛋白尿,模拟人类的 DKD。我们的主要发现揭示了 FMT 可预防体重增加、减少回肠和升结肠中的白蛋白尿和肿瘤坏死因子-α(TNF-α)水平,并可能改善 BTBR 小鼠的胰岛素抵抗。肠道结构完整性得以维持。值得注意的是,FMT 与肠道中整个肠道中消耗琥珀酸盐的细菌家族的丰度有关。总的来说,我们的数据表明 FMT 在 2 型糖尿病、肥胖和 DKD 的临床前模型中是安全有效的。这些发现为肠道微生物群调节的转化研究提供了基础,并测试了其与当前 DM 治疗相结合的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f96/8998923/00ba6b6d6ff4/ijms-23-03842-g001.jpg

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