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Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer's Disease

Title: Metabolic Network Analysis Reveals Altered Bile Acid Synthesis and Metabolism in Alzheimer's Disease
Authors: Baloni, P; Funk, CC; Yan, J; Yurkovich, JT; Kueider-Paisley, A; Nho, K; Heinken, A; Jia, W; Mahmoudiandehkordi, S; Louie, G; Saykin, AJ; Arnold, M; Kastenmüller, G; Griffiths, WJ; Thiele, I; Kaddurah-Daouk, R; Doraiswamy, PM; Blach, C; Moseley, A; Thompson, JW; Mahmoudiandehkhordi, S; Welsh-Balmer, K; Plassman, B; Bhattacharyya, S; Han, X; Baillie, R; Fiehn, O; Barupal, D; Meikle, P; Mazmanian, S; Kling, M; Shaw, L; Trojanowski, J; Toledo, J; van Duijin, C; Hankemier, T; Wishart, D; Brinton, R; Chang, R; Farrer, L; Au, R; Qiu, W; Würtz, P; Mangravite, L; Krumsiek, J; Newman, J; Zhang, B; Moreno, H; Price, ND
Publisher Information: CELL PRESS
Publication Year: 2020
Collection: The University of Melbourne: Digital Repository
Description: Increasing evidence suggests Alzheimer's disease (AD) pathophysiology is influenced by primary and secondary bile acids, the end product of cholesterol metabolism. We analyze 2,114 post-mortem brain transcriptomes and identify genes in the alternative bile acid synthesis pathway to be expressed in the brain. A targeted metabolomic analysis of primary and secondary bile acids measured from post-mortem brain samples of 111 individuals supports these results. Our metabolic network analysis suggests that taurine transport, bile acid synthesis, and cholesterol metabolism differ in AD and cognitively normal individuals. We also identify putative transcription factors regulating metabolic genes and influencing altered metabolism in AD. Intriguingly, some bile acids measured in brain tissue cannot be explained by the presence of enzymes responsible for their synthesis, suggesting that they may originate from the gut microbiome and are transported to the brain. These findings motivate further research into bile acid metabolism in AD to elucidate their possible connection to cognitive decline.
Document Type: article in journal/newspaper
Language: English
ISSN: 2666-3791
Relation: https://hdl.handle.net/11343/304523
Availability: https://hdl.handle.net/11343/304523
Rights: https://creativecommons.org/licenses/by-nc-nd/4.0 ; CC BY-NC-ND
Accession Number: edsbas.87AAB268
Database: BASE