Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 May;76(2):294-303.
doi: 10.1007/s12020-022-03002-1. Epub 2022 Mar 4.

Changes of gut microbiota in diabetic nephropathy and its effect on the progression of kidney injury

Affiliations

Changes of gut microbiota in diabetic nephropathy and its effect on the progression of kidney injury

Kedan Cai et al. Endocrine. 2022 May.

Abstract

Purpose: We aimed to illustrate gut microbiota and short chain fatty acid (SCFA) levels in diabetic nephropathy (DN) patients, and investigate the mechanism of sodium butyrate in diabetic mellitus (DM) rats.

Methods: Gut microbiota and serum SCFA levels were measured by 16S rDNA and GC-MS. After being built by streptozotocin (DM rats), the DM rats were administered 300 mg/kg sodium butyrate for 12 weeks (DM + BU rats). Gut microbiota, serum and fecal butyrate level were measured. RT-PCR, WB and transmission electron microscopy were performed to explore LC3mRNA or LC3B protein expression, and autophagosomes in kidney tissues. AMPK/mTOR protein expression in renal tissue were also measured.

Results: The gut microbial dysbiosis was found in DM and DN groups, and some SCFAs-producing bacteria were decreased in DN group. The serum butyrate concentrations were lower in SCFA-DN group compared with SCFA-HC group and SCFA-DM group in the other cohort. Serum butyrate level was positively correlated with eGFR. Sodium butyrate increased serum and fecal butyrate levels, and improved the enlargement of glomerular area and fibronectin and collagen IV expressions in renal tissues in DM + BU rats. The LC3 mRNA, LC3BII/I ratio and number of autophagosomes were increased in renal tissue of DM + BU rats. Higher p-AMPK/AMPK ratio and lower p-mTOR/ mTOR ratio were shown in renal tissue of DM + BU rats compared with DM rats.

Conclusions: We found the decrease in SCFAs-producing bacteria and low SCFAs concentrations in DN patients. Oral butyrate supplementation may improve kidney injury in DM rats, possibly by increasing autophagy via activating AMPK/mTOR pathway.

Keywords: Autophagy; Butyrate; Diabetic nephropathy; Gut microbiome; Short chain fatty acid.

PubMed Disclaimer

References

    1. Y.Z. Li, T. Di, X.G. Shi et al. Prevalence of diabetes recorded in mainland China using 2018 diagnostic criteria from the American Diabetes Association: national cross sectional study. BMJ. 369, m997 (2020) - PubMed - PMC - DOI
    1. R.T. Demmer, A.M. Zuk, M. Rosenbaum, M. Desvarieux, Prevalence of diagnosed and undiagnosed type 2 diabetes mellitus among us adolescents: results from the continuous NHANES, 1999–2010. Am J Epidemiol 178(7), 1106–1113 (2013) - PubMed - PMC - DOI
    1. R.Z. Alicic, E.J. Johnson, K.R. Tuttle, SGLT2 Inhibition for the prevention and treatment of diabetic kidney disease: a review. Am J Kidney Dis 72(2), 267–277 (2018) - PubMed - DOI
    1. R.Z. Alicic, M.T. Rooney, K.R. Tuttle, Diabetic kidney disease challenges, progress, and possibilities. Clin J Am Soc Nephrol 12(12), 2032–2045 (2017) - PubMed - PMC - DOI
    1. H.J. Anders, K. Andersen, B. Stecher, The intestinal microbiota, a leaky gut, and abnormal immunity in kidney disease. Kidney Int 83(6), 1010–1016 (2013) - PubMed - DOI

LinkOut - more resources