Tauroursodeoxycholic acid

Tauroursodeoxycholic acid is a lipid of Sterol Lipids (ST) class. Tauroursodeoxycholic acid is associated with abnormalities such as Hyperglycemia, Obesity, Wiskott-Aldrich Syndrome, neurogenic hypertension and Cholestatic liver disease. The involved functions are known as Cell Death, Apoptosis, Homeostasis, Process and mRNA Expression. Tauroursodeoxycholic acid often locates in Body tissue, Endoplasmic Reticulum, Hepatic, Blood and Protoplasm. The associated genes with Tauroursodeoxycholic acid are Homologous Gene and Mutant Proteins. The related lipids are cholanic acid, taurolithocholic acid 3-sulfate, Sterols, 7-dehydrocholesterol and tauromuricholic acid. The related experimental models are Disease model.

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Introduction

To understand associated biological information of Tauroursodeoxycholic acid, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Tauroursodeoxycholic acid?

Tauroursodeoxycholic acid is suspected in Endothelial dysfunction, Hyperglycemia, Obesity, neurogenic hypertension, Cholestatic liver disease, Heart failure and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Tauroursodeoxycholic acid

MeSH term MeSH ID Detail
Hypertension D006973 115 associated lipids
Insulin Resistance D007333 99 associated lipids
Total 2

PubChem Associated disorders and diseases

What pathways are associated with Tauroursodeoxycholic acid

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Tauroursodeoxycholic acid?

Related references are published most in these journals:

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What functions are associated with Tauroursodeoxycholic acid?


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What lipids are associated with Tauroursodeoxycholic acid?

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What genes are associated with Tauroursodeoxycholic acid?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Tauroursodeoxycholic acid?

Disease model

Disease model are used in the study 'Bile Acids Reduce Prion Conversion, Reduce Neuronal Loss, and Prolong Male Survival in Models of Prion Disease.' (Cortez LM et al., 2015).

Related references are published most in these journals:

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NCBI Entrez Crosslinks

All references with Tauroursodeoxycholic acid

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Authors Title Published Journal PubMed Link
Shen S et al. Ursolic acid induces autophagy in U87MG cells via ROS-dependent endoplasmic reticulum stress. 2014 Chem. Biol. Interact. pmid:24802810
Lee ES et al. Chemical chaperones reduce ionizing radiation-induced endoplasmic reticulum stress and cell death in IEC-6 cells. 2014 Biochem. Biophys. Res. Commun. pmid:24973711
Penno CA et al. 11β-Hydroxysteroid dehydrogenase-1 is involved in bile acid homeostasis by modulating fatty acid transport protein-5 in the liver of mice. 2014 Mol Metab pmid:25061560
Cheng X et al. Decreased bile-acid synthesis in livers of hepatocyte-conditional NADPH-cytochrome P450 reductase-null mice results in increased bile acids in serum. 2014 J. Pharmacol. Exp. Ther. pmid:25034404
Cho EJ et al. Tauroursodeoxycholic acid attenuates progression of steatohepatitis in mice fed a methionine-choline-deficient diet. 2014 Dig. Dis. Sci. pmid:24865256
Xavier JM et al. Tauroursodeoxycholic acid increases neural stem cell pool and neuronal conversion by regulating mitochondria-cell cycle retrograde signaling. 2014 Cell Cycle pmid:25483094
Ishimura S et al. Reduction of endoplasmic reticulum stress inhibits neointima formation after vascular injury. 2014 Sci Rep pmid:25373918
Debattisti V et al. Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletion. 2014 J. Cell Biol. pmid:24469638
Myronovych A et al. Vertical sleeve gastrectomy reduces hepatic steatosis while increasing serum bile acids in a weight-loss-independent manner. 2014 Obesity (Silver Spring) pmid:23804416
Hamano M et al. Lipid overloading during liver regeneration causes delayed hepatocyte DNA replication by increasing ER stress in mice with simple hepatic steatosis. 2014 J. Gastroenterol. pmid:23512345
Simoni P et al. A new point-of-care portable immunosensor for non-invasive assessment of oro-ileal transit time by oral fluid tauroursodeoxycholate measurement after its oral load. 2013 Jul-Aug J Pharm Biomed Anal pmid:23587552
Pan XL et al. Efficacy and safety of tauroursodeoxycholic acid in the treatment of liver cirrhosis: a double-blind randomized controlled trial. 2013 J. Huazhong Univ. Sci. Technol. Med. Sci. pmid:23592128
Belaidi E et al. Endoplasmic reticulum stress contributes to heart protection induced by cyclophilin D inhibition. 2013 Basic Res. Cardiol. pmid:23744057
Omura T et al. Sodium tauroursodeoxycholate prevents paraquat-induced cell death by suppressing endoplasmic reticulum stress responses in human lung epithelial A549 cells. 2013 Biochem. Biophys. Res. Commun. pmid:23416354
Beuers U β1 integrin is a long-sought sensor for tauroursodeoxycholic acid. 2013 Hepatology pmid:23456677
Cai Z et al. Endoplasmic reticulum stress participates in aortic valve calcification in hypercholesterolemic animals. 2013 Arterioscler. Thromb. Vasc. Biol. pmid:23928865
Gaspar JM et al. Tauroursodeoxycholic acid protects retinal neural cells from cell death induced by prolonged exposure to elevated glucose. 2013 Neuroscience pmid:24012838
Xu H et al. The ER luminal binding protein (BiP) alleviates Cd(2+)-induced programmed cell death through endoplasmic reticulum stress-cell death signaling pathway in tobacco cells. 2013 J. Plant Physiol. pmid:23867017
Takeda N et al. Altered unfolded protein response is implicated in the age-related exacerbation of proteinuria-induced proximal tubular cell damage. 2013 Am. J. Pathol. pmid:23871833
Fang L et al. Involvement of endoplasmic reticulum stress in albuminuria induced inflammasome activation in renal proximal tubular cells. 2013 PLoS ONE pmid:23977286