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Text
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URL Address
<a href="http://doi.org/10.1152/ajpgi.00223.2019" target="_blank" rel="noreferrer noopener">http://doi.org/10.1152/ajpgi.00223.2019</a>
Pages
G554-G573
Issue
3
Volume
318
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<a href="http://ezproxy.neomed.idm.oclc.org/login?url=http://doi.org/10.1152/ajpgi.00223.2019" target="_blank" rel="noreferrer noopener">NEOMED Full-text Holding (if available) - Proxy DOI: 10.1152/ajpgi.00223.2019</a>
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Update Year & Number
March 2020 Update
NEOMED College
NEOMED College of Medicine; NEOMED College of Graduate Studies
NEOMED Department
Department of Integrative Medical Sciences
Dublin Core
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Title
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Bile acid receptors FXR and TGR5 signaling in fatty liver diseases and therapy.
Publisher
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American journal of physiology. Gastrointestinal and liver physiology
Date
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2020
2020-03
Subject
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bile acid metabolism; liver diseases; farnesoid X receptor; alcoholic and nonalcoholic fatty; bile acid therapies; Takeda G protein-coupled receptor 5
Creator
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Chiang John Y L; Ferrell Jessica M
Description
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Bile acid synthesis is the most significant pathway for catabolism of cholesterol and for maintenance of whole body cholesterol homeostasis. Bile acids are physiological detergents that absorb, distribute, metabolize, and excrete nutrients, drugs, and xenobiotics. Bile acids also are signal molecules and metabolic integrators that activate nuclear farnesoid X receptor (FXR) and membrane Takeda G protein-coupled receptor 5 (TGR5; i.e., G protein-coupled bile acid receptor 1) to regulate glucose, lipid, and energy metabolism. The gut-to-liver axis plays a critical role in the transformation of primary bile acids to secondary bile acids, in the regulation of bile acid synthesis to maintain composition within the bile acid pool, and in the regulation of metabolic homeostasis to prevent hyperglycemia, dyslipidemia, obesity, and diabetes. High-fat and high-calorie diets, dysbiosis, alcohol, drugs, and disruption of sleep and circadian rhythms cause metabolic diseases, including alcoholic and nonalcoholic fatty liver diseases, obesity, diabetes, and cardiovascular disease. Bile acid-based drugs that target bile acid receptors are being developed for the treatment of metabolic diseases of the liver.
Identifier
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<a href="http://doi.org/10.1152/ajpgi.00223.2019" target="_blank" rel="noreferrer noopener">10.1152/ajpgi.00223.2019</a>
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Journal Article
2020
alcoholic and nonalcoholic fatty
American journal of physiology. Gastrointestinal and liver physiology
Bile acid metabolism
bile acid therapies
Chiang John Y L
Department of Integrative Medical Sciences
Farnesoid X receptor
Ferrell Jessica M
Liver Diseases
NEOMED College of Graduate Studies
NEOMED College of Medicine
Takeda G protein-coupled receptor 5