4.6 Article

Multi-Omics Characterization of Type 2 Diabetes Mellitus-Induced Cognitive Impairment in the db/db Mouse Model

Journal

MOLECULES
Volume 27, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27061904

Keywords

type 2 diabetes mellitus; cognitive impairment; transcriptome; metabolome; gut microbiota

Funding

  1. National Natural Science Foundation of China [81971014]
  2. Ministry of Science and Technology of the People's Republic of China [2016YFC1305804]

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This study investigated the potential mechanisms and interventions underlying T2DM-induced cognitive deficits by analyzing the brain transcriptome, plasma metabolome, and gut microbiota in db/db mice. The results suggest that disturbances in mitochondrial respiratory, glycolytic, and inflammatory pathways, as well as altered glucose, lipid, bile acid, and steroid metabolism, may contribute to cognitive impairment in these mice. The study also provides novel insights into the functional interactions among the brain, circulating metabolites, and gut microbiota.
Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder frequently accompanied by cognitive impairment. Contributing factors such as modern lifestyle, genetic predisposition, and gene environmental interactions have been postulated, but the pathogenesis remains unclear. In this study, we attempt to investigate the potential mechanisms and interventions underlying T2DM-induced cognitive deficits from the brain-gut axis perspective. A combined analysis of the brain transcriptome, plasma metabolome, and gut microbiota in db/db mice with cognitive decline was conducted. Transcriptome analysis identified 222 upregulated gene sets and 85 downregulated gene sets, mainly related to mitochondrial respiratory, glycolytic, and inflammation. In metabolomic analysis, a total of 75 significantly altered metabolites were identified, correlated with disturbances of glucose, lipid, bile acid, and steroid metabolism under disease state. Gut microbiota analysis suggested that the species abundance and diversity of db/db mice were significantly increased, with 23 significantly altered genus detected. Using the multi-omics integration, significant correlations among key genes (n = 33), metabolites (n = 41), and bacterial genera (n = 21) were identified. Our findings suggest that disturbed circulation and brain energy metabolism, especially mitochondrial-related disturbances, may contribute to cognitive impairment in db/db mice. This study provides novel insights into the functional interactions among the brain, circulating metabolites, and gut microbiota.

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