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芪地糖肾颗粒调节糖尿病肾病小鼠肠道微生物组成并改善胆汁酸谱。

QiDiTangShen granules modulated the gut microbiome composition and improved bile acid profiles in a mouse model of diabetic nephropathy.

机构信息

Department of Endocrinology and Nephrology, Renal Research Institute of Beijing University of Chinese Medicine, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Haiyuncang Road No. 5, Beijing, 100700, China.

Department of Endocrinology and Nephrology, Renal Research Institute of Beijing University of Chinese Medicine, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Haiyuncang Road No. 5, Beijing, 100700, China; Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Haiyuncang Road No. 5, Beijing, 100700, China.

出版信息

Biomed Pharmacother. 2021 Jan;133:111061. doi: 10.1016/j.biopha.2020.111061. Epub 2020 Nov 28.

Abstract

QiDiTangShen granules (QDTS), a traditional Chinese herbal medicine, have been used in clinical practice for treating diabetic kidney disease for several years. In our previous study, we have demonstrated that QDTS displayed good efficacy on reducing proteinuria in mice with diabetic nephropathy (DN). However, the exact mechanism by which QDTS exerts its reno-protection remains largely unknown. To ascertain whether QDTS could target the gut microbiota-bile acid axis, the db/db mice were adopted as a mouse model of DN. After a 12-week of treatment, we found that QDTS significantly reduced urinary albumin excretion (UAE), and attenuated the pathological injuries of kidney in the db/db mice, while the body weight and blood glucose levels of those mice were not affected. In addition, we found that QDTS significantly altered the gut microbiota composition, and decreased serum levels of total bile acid (TBA) and BA profiles such as β-muricholic acid (β-MCA), taurocholic acid (TCA), tauro β-muricholic acid (Tβ-MCA) and deoxycholic acid (DCA). These BAs are associated with the activation of farnesoid X receptor (FXR), which is highly expressed in kidney. However, there was no significant difference between QDTS-treated and -untreated db/db mice regarding the renal expression of FXR, indicating that other mechanisms may be involved. Conclusively, our study revealed that QDTS significantly alleviated renal injuries in mice with DN. The gut microbiota-bile acid axis may be an important target for the reno-protection of QDTS in DN, but the specific mechanism merits further study.

摘要

芪地糖肾颗粒(QDTS)是一种中药,已在临床实践中用于治疗糖尿病肾病多年。在我们之前的研究中,我们已经证明 QDTS 对减少糖尿病肾病(DN)小鼠的蛋白尿具有良好的疗效。然而,QDTS 发挥其肾脏保护作用的确切机制在很大程度上尚不清楚。为了确定 QDTS 是否可以靶向肠道微生物群-胆汁酸轴,我们采用 db/db 小鼠作为 DN 的小鼠模型。经过 12 周的治疗,我们发现 QDTS 可显著降低 db/db 小鼠的尿白蛋白排泄(UAE),并减轻其肾脏的病理损伤,而小鼠的体重和血糖水平不受影响。此外,我们发现 QDTS 可显著改变肠道微生物群组成,并降低血清总胆汁酸(TBA)水平和 BA 谱,如β-鼠胆酸(β-MCA)、牛磺胆酸(TCA)、牛磺-β-鼠胆酸(Tβ-MCA)和脱氧胆酸(DCA)。这些 BA 与法尼醇 X 受体(FXR)的激活有关,FXR 在肾脏中高度表达。然而,QDTS 处理和未处理的 db/db 小鼠之间的肾脏 FXR 表达没有明显差异,这表明可能涉及其他机制。总之,我们的研究表明,QDTS 可显著减轻 DN 小鼠的肾脏损伤。肠道微生物群-胆汁酸轴可能是 QDTS 在 DN 中肾脏保护的重要靶点,但具体机制值得进一步研究。

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