3alpha,7alpha,12beta-Trihydroxy-5beta-cholanoic acid (BioDeep_00000017798)

Main id: BioDeep_00000000134

Secondary id: BioDeep_00000871727

human metabolite PANOMIX_OTCML-2023 Endogenous Bile acids BioNovoGene_Lab2019


代谢物信息卡片


(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R,16R)-5,9,16-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid

化学式: C24H40O5 (408.2876)
中文名称: 牛胆粉, 胆酸
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 31.41%

分子结构信息

SMILES: CC(CCC(=O)O)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C
InChI: InChI=1S/C24H40O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-20,22,25-27H,4-12H2,1-3H3,(H,28,29)

描述信息

3alpha,7alpha,12beta-Trihydroxy-5beta-cholanoic acid, also known as lagocholic acid, is a bile acid. Bile acids with beta-hydroxyl and carbonyl groups at the C-3,7, and/or 12 positions are bile acids usually found in the urine of healthy humans (PMID: 8743575). Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending only on the presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g. membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues (PMID: 11316487, 16037564, 12576301, 11907135).
A - Alimentary tract and metabolism > A05 - Bile and liver therapy > A05A - Bile therapy > A05AA - Bile acids and derivatives
C78276 - Agent Affecting Digestive System or Metabolism > C66913 - Cholagogues or Choleretic Agents
D005765 - Gastrointestinal Agents > D001647 - Bile Acids and Salts
D005765 - Gastrointestinal Agents > D002793 - Cholic Acids
Same as: D10699
Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine. It facilitates fat absorption and cholesterol excretion. Cholic acid is orally active[1][2].
Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine. It facilitates fat absorption and cholesterol excretion. Cholic acid is orally active[1][2].

同义名列表

28 个代谢物同义名

(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R,16R)-5,9,16-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]pentanoic acid; (4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R,16R)-5,9,16-Trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoate; (3alpha,5beta,7alpha,12beta)-3,7,12-Trihydroxycholan-24-oic acid; 3alpha,7alpha,12alpha-Trihydroxy-5beta-cholan-24-oic acid; 3alpha,7alpha,12alpha-Trihydroxy-5beta-cholanic acid; 3alpha,7alpha,12beta-Trihydroxy-5beta-cholanoic acid; 3alpha,7alpha,12beta-Trihydroxy-5beta-cholanic acid; (3α,5β,7α,12β)-3,7,12-Trihydroxycholan-24-oic acid; 3alpha,7alpha,12alpha-Trihydroxy-5beta-cholanate; 3alpha,7alpha,12beta-Trihydroxy-5beta-cholanate; 3α,7α,12β-Trihydroxy-5β-cholanoic acid; 3α,7α,12β-trihydroxy-5β-cholanic acid; 3a,7a,12b-Trihydroxy-5b-cholanic acid; 3,7,12-Trihydroxycholan-24-oic acid; 3a,7a,12b-Trihydroxy-5b-cholanoate; 3a,7a,12b-Trihydroxy-5b-cholanate; 3α,7α,12β-trihydroxy-5β-cholanate; 12beta-Hydroxyisocholic acid; 12β-Hydroxyisocholic acid; 12b-Hydroxyisocholic acid; 12b-Hydroxyisocholate; Lagocholic Acid; Bile, extract; Cholic Acid; Lagocholate; ST 24:1;O5; cholate; Cholic acid



数据库引用编号

29 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

2 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 6 ABCB1, ABCB4, ALB, APOE, GPBAR1, PLA2G12A
Peripheral membrane protein 1 CYP27A1
Endosome membrane 1 LDLR
Endoplasmic reticulum membrane 3 CYP7A1, CYP8B1, HMGCR
Mitochondrion membrane 1 CYP27A1
Nucleus 3 ALB, APOE, PPARA
cytosol 4 ABCB4, ALB, APOA1, GPT
dendrite 1 APOE
centrosome 1 ALB
nucleoplasm 2 ABCB4, PPARA
Cell membrane 7 ABCB1, ABCB11, ABCB4, ABCG5, GPBAR1, LDLR, SLC10A1
Multi-pass membrane protein 9 ABCB1, ABCB11, ABCB4, ABCC2, ABCC3, ABCG5, GPBAR1, HMGCR, SLC10A1
cell surface 4 ABCB1, ABCB11, ABCC2, LDLR
glutamatergic synapse 1 APOE
Golgi apparatus 3 ALB, APOE, LDLR
Golgi membrane 2 ABCB11, INS
mitochondrial inner membrane 1 CYP27A1
neuronal cell body 1 APOE
Lysosome 1 LDLR
endosome 1 ABCB11
plasma membrane 11 ABCB1, ABCB11, ABCB4, ABCC2, ABCC3, ABCG5, APOA1, APOE, GPBAR1, LDLR, SLC10A1
Membrane 10 ABCB1, ABCB11, ABCB4, ABCC2, ABCC3, ABCG5, APOE, HMGCR, LDLR, SLC10A1
apical plasma membrane 5 ABCB1, ABCB11, ABCB4, ABCC2, ABCG5
basolateral plasma membrane 3 ABCC3, LDLR, SLC10A1
extracellular exosome 7 ABCB1, ABCB11, ABCB4, ALB, APOA1, APOE, GPT
endoplasmic reticulum 3 ALB, APOE, HMGCR
extracellular space 4 ALB, APOA1, APOE, INS
intercellular canaliculus 3 ABCB11, ABCB4, ABCC2
mitochondrion 1 CYP27A1
protein-containing complex 1 ALB
intracellular membrane-bounded organelle 1 CYP7A1
Microsome membrane 2 CYP7A1, CYP8B1
Single-pass type I membrane protein 1 LDLR
Secreted 5 ALB, APOA1, APOE, INS, PLA2G12A
extracellular region 5 ALB, APOA1, APOE, INS, PLA2G12A
Single-pass membrane protein 3 CYP7A1, CYP8B1, LDLR
mitochondrial matrix 1 CYP27A1
anchoring junction 1 ALB
external side of plasma membrane 1 LDLR
Endosome, multivesicular body 1 APOE
Extracellular vesicle 2 APOA1, APOE
Secreted, extracellular space, extracellular matrix 1 APOE
chylomicron 2 APOA1, APOE
high-density lipoprotein particle 2 APOA1, APOE
low-density lipoprotein particle 3 APOA1, APOE, LDLR
multivesicular body 1 APOE
very-low-density lipoprotein particle 2 APOA1, APOE
cytoplasmic vesicle 1 APOA1
Early endosome 3 APOA1, APOE, LDLR
Membrane, clathrin-coated pit 1 LDLR
apical part of cell 1 LDLR
clathrin-coated pit 1 LDLR
recycling endosome 1 ABCB11
Apical cell membrane 5 ABCB1, ABCB11, ABCB4, ABCC2, ABCG5
Mitochondrion inner membrane 1 CYP27A1
Membrane raft 1 ABCB4
focal adhesion 1 ABCB4
extracellular matrix 1 APOE
peroxisomal membrane 1 HMGCR
collagen-containing extracellular matrix 2 APOA1, APOE
Late endosome 1 LDLR
receptor complex 3 ABCG5, GPBAR1, LDLR
ciliary basal body 1 ALB
chromatin 1 PPARA
centriole 1 ALB
Secreted, extracellular space 1 APOE
spindle pole 1 ALB
blood microparticle 3 ALB, APOA1, APOE
Basolateral cell membrane 1 ABCC3
Recycling endosome membrane 1 ABCB11
Endomembrane system 1 LDLR
endosome lumen 1 INS
sorting endosome 1 LDLR
Melanosome 1 APOE
Peroxisome membrane 1 HMGCR
basal plasma membrane 1 ABCC3
clathrin-coated vesicle 1 ABCB4
secretory granule lumen 2 APOA1, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 4 ALB, APOA1, APOE, INS
platelet alpha granule lumen 1 ALB
Cytoplasmic vesicle, clathrin-coated vesicle 1 ABCB4
endocytic vesicle 1 APOA1
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
ATP-binding cassette (ABC) transporter complex 1 ABCG5
clathrin-coated endocytic vesicle membrane 2 APOE, LDLR
synaptic cleft 1 APOE
Basal cell membrane 1 ABCC3
external side of apical plasma membrane 1 ABCB1
endolysosome membrane 1 LDLR
somatodendritic compartment 1 LDLR
intracellular canaliculus 1 ABCB11
discoidal high-density lipoprotein particle 1 APOE
spherical high-density lipoprotein particle 1 APOA1
endocytic vesicle lumen 2 APOA1, APOE
PCSK9-LDLR complex 1 LDLR
chylomicron remnant 1 APOE
intermediate-density lipoprotein particle 1 APOE
lipoprotein particle 1 APOE
multivesicular body, internal vesicle 1 APOE
ciliary transition fiber 1 ALB


文献列表

  • Fengjing Jia, Liqing Du, Jinchao He, Zhaozhou Zhang, Xinxin Hou, Qinjun Dong, Zhaoxiang Bian, Ling Zhao. Tong-Xie-Yao-Fang strengthens intestinal feedback control of bile acid synthesis to ameliorate irritable bowel syndrome by enhancing bile salt hydrolase-expressing microbiota. Journal of ethnopharmacology. 2024 Sep; 331(?):118256. doi: 10.1016/j.jep.2024.118256. [PMID: 38677571]
  • Kexin Xiao, Hongyu Li, Yuening Li, Bo Zhan, Xiaohua Fang, Bingjie Zhao, Xiaofei Zhang, Yumei Wu, Fan Wang, Yanyan Jia. Protective effects and mechanism of Sangyu granule on acetaminophen-induced liver injury in mice. Journal of ethnopharmacology. 2024 Sep; 331(?):118282. doi: 10.1016/j.jep.2024.118282. [PMID: 38701935]
  • Yingkun Sheng, Guibing Meng, Min Zhang, Xiaopeng Chen, Xin Chai, Haiyang Yu, Lifeng Han, Qilong Wang, Yuefei Wang, Miaomiao Jiang. Dan-shen Yin promotes bile acid metabolism and excretion to prevent atherosclerosis via activating FXR/BSEP signaling pathway. Journal of ethnopharmacology. 2024 Aug; 330(?):118209. doi: 10.1016/j.jep.2024.118209. [PMID: 38663779]
  • Rui Song, Yu Wang, Gazang Drolma, Nima Drolga, Dawa Drolma, Bing Xia, Yan Zhou. Rapid analysis of the chemical constituents of traditional Tibetan medicine Sbyor-bzo-ghi-wang using ballpoint electrospray ionization technique. Rapid communications in mass spectrometry : RCM. 2024 Jul; 38(13):e9760. doi: 10.1002/rcm.9760. [PMID: 38682312]
  • Katarzyna Kłosowska, Teresa Del Castillo-Santaella, Julia Maldonado-Valderrama, Adam Macierzanka. The bile salt/phospholipid ratio determines the extent of in vitro intestinal lipolysis of triglycerides: Interfacial and emulsion studies. Food research international (Ottawa, Ont.). 2024 Jul; 187(?):114421. doi: 10.1016/j.foodres.2024.114421. [PMID: 38763671]
  • Siwei Deng, Yao Ge, Zhian Zhai, Haozhen Liu, Xinyu Zhang, Yinfeng Chen, Ying Yang, Zhenlong Wu. Fructose induces hepatic steatosis in adolescent mice linked to the disorders of lipid metabolism, bile acid metabolism, and autophagy. The Journal of nutritional biochemistry. 2024 Jul; 129(?):109635. doi: 10.1016/j.jnutbio.2024.109635. [PMID: 38561080]
  • Xingran Kou, Min Hong, Fei Pan, Xin Huang, Qingran Meng, Yunchong Zhang, Qinfei Ke. Inhibitory effects of nobiletin-mediated interfacial instability of bile salt emulsified oil droplets on lipid digestion. Food chemistry. 2024 Jun; 444(?):138751. doi: 10.1016/j.foodchem.2024.138751. [PMID: 38412567]
  • Jianjun Yu, Qing Zhu, Maofu Zhou, Xiaofang Huang, Yimin Le, Hui Ouyang, Shaomin Cheng. Mechanism of Tianma-Gouteng granules lowering blood pressure based on the bile acid-regulated Farnesoid X Receptor-Fibroblast Growth Factor 15- Cholesterol 7α-hydroxylase pathway. Journal of ethnopharmacology. 2024 Jun; 328(?):118091. doi: 10.1016/j.jep.2024.118091. [PMID: 38521427]
  • Jingyi Cai, Zhenyun Zhu, Yuanyuan Li, Qi Li, Tian Tian, Qian Meng, Tianming Wang, Yueming Ma, Jiasheng Wu. Artemisia capillaris Thunb. Polysaccharide alleviates cholestatic liver injury through gut microbiota modulation and Nrf2 signaling pathway activation in mice. Journal of ethnopharmacology. 2024 Jun; 327(?):118009. doi: 10.1016/j.jep.2024.118009. [PMID: 38447617]
  • Lei Zhang, Langqing Lu, Shiqin Jiang, Zhaokun Yin, Guoyao Tan, Fangqing Ning, Zhiyan Qin, Junyuan Huang, Min Huang, Jing Jin. Salvianolic acid extract prevents Tripterygium wilfordii polyglycosides-induced acute liver injury by modulating bile acid metabolism. Journal of ethnopharmacology. 2024 Jun; 327(?):117939. doi: 10.1016/j.jep.2024.117939. [PMID: 38382651]
  • Vita D'Amico, Antonio Lopalco, Rosa Maria Iacobazzi, Mirco Vacca, Sonya Siragusa, Maria De Angelis, Angela Assunta Lopedota, Nunzio Denora. Multistimuli responsive microcapsules produced by the prilling/vibration technique for targeted colonic delivery of probiotics. International journal of pharmaceutics. 2024 Jun; 658(?):124223. doi: 10.1016/j.ijpharm.2024.124223. [PMID: 38744413]
  • Wen Huang, Min Zhang, Qiong Qiu, Jing Zhang, Chao Hua, Geliang Chen, Hua Xie. Metabolomics of human umbilical vein endothelial cell-based analysis of the relationship between hyperuricemia and dyslipidemia. Nutrition, metabolism, and cardiovascular diseases : NMCD. 2024 Jun; 34(6):1528-1537. doi: 10.1016/j.numecd.2024.02.001. [PMID: 38508990]
  • Ioannis I Lazaridis, Angela J T Bosch, Lena Keller, Andy J Y Low, Jeanne Tamarelle, Seraina O Moser, Denise V Winter, Cristina Gómez, Caspar J Peterson, Romano Schneider, Marko Kraljević, Alex Odermatt, Pascale Vonaesch, Ralph Peterli, Tarik Delko, Claudia Cavelti-Weder. Metabolic outcomes in obese mice undergoing one-anastomosis gastric bypass (OAGB) with a long or a short biliopancreatic limb. American journal of physiology. Endocrinology and metabolism. 2024 Jun; 326(6):E819-E831. doi: 10.1152/ajpendo.00327.2023. [PMID: 38630050]
  • Ali Kiasat, Stefanie Prast-Nielsen, Susanne Rautiainen, Lars Engstrand, Fredrik Andersson, Johan Lindberg, Ina Schuppe-Koistinen, Anna Löf Granström, Ulf O Gustafsson. Plasma bile acids in association with Crohn's disease. Scandinavian journal of gastroenterology. 2024 Jun; 59(6):674-682. doi: 10.1080/00365521.2024.2328592. [PMID: 38505982]
  • Qing Guo, Wenwen Liu, Lu Zhao, Yiming Sui, Houfa Zhao, Yining Liu, Cuimin Mu, Xuepeng Wang. Fermented bile acids improved growth performance and intestinal health by altering metabolic profiles and intestinal microbiome in Micropterus salmoides. Fish & shellfish immunology. 2024 Jun; 149(?):109593. doi: 10.1016/j.fsi.2024.109593. [PMID: 38697374]
  • Xiaoliang He, Yingya Zhou, Jingtao Yu, Qinpo Huang, Zhengyuan Chen, Ru Xiao, Changhui Liu, Shuhua Gui, Tianqin Xiong. JiaGaSongTang improves chronic cholestasis via enhancing FXR-mediated bile acid metabolism. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jun; 128(?):155347. doi: 10.1016/j.phymed.2024.155347. [PMID: 38493717]
  • Jian Shi, Lin Zhu, Bang-Yi Tang, Wan-Qing Yang, Sheng-Yan Xi, Chen-Long Zhang, Peng-Fei Li, Yu-Jie Wang, Kai-Hang Guo, Jing-Ru Huang, Chen-Rui Huang, Zhou-Xin Yu, Bao-Kang Yu, Chun-Fang Zhang, Yu-Mei Zhang. Regulatory effect of Yinchenhao decoction on bile acid metabolism to improve the inflammatory microenvironment of hepatocellular carcinoma in mice. Journal of natural medicines. 2024 Jun; 78(3):633-643. doi: 10.1007/s11418-024-01812-3. [PMID: 38704807]
  • Monica D Chow, Katherine Otersen, Andrew Wassef, Bo Kong, Sowmya Yamarthy, Daniel Rizzolo, Ill Yang, Brian Buckley, Alexander Lu, Naomi Crook, Matthew Lee, Judy Gao, Sareena Naganand, Mary F Stofan, Laura Armstrong, Justin Schumacher, Rulaiha Taylor, Zakiyah Henry, Veronia Basaly, Zhenning Yang, Min Zhang, Mingxing Huang, Leonid Kagan, Luigi Brunetti, Ragui Sadek, Yi-Horng Lee, Grace L Guo. Effects of intestine-specific deletion of FGF15 on the development of fatty liver disease with vertical sleeve gastrectomy. Hepatology communications. 2024 Jun; 8(6):. doi: 10.1097/hc9.0000000000000444. [PMID: 38780301]
  • Yun Wang, Jiawei Wu, Yu Hong, Jiaying Zhu, Youcai Zhang, Jun Zhang, Chujie Ding, Yuan Che, Guangji Wang, Aiqin Jiang, Haiping Hao, Lijuan Cao. Ginsenosides retard atherogenesis via remodelling host-microbiome metabolic homeostasis. British journal of pharmacology. 2024 Jun; 181(12):1768-1792. doi: 10.1111/bph.16320. [PMID: 38355288]
  • Teresa Padro, Victoria Santisteban, Pol Huedo, Montserrat Puntes, Meritxell Aguiló, Jordi Espadaler-Mazo, Lina Badimon. Lactiplantibacillus plantarum strains KABP011, KABP012, and KABP013 modulate bile acids and cholesterol metabolism in humans. Cardiovascular research. 2024 May; 120(7):708-722. doi: 10.1093/cvr/cvae061. [PMID: 38525555]
  • Rulaiha Taylor, Zhenning Yang, Zakiyah Henry, Gina Capece, Vik Meadows, Katherine Otersen, Veronia Basaly, Anisha Bhattacharya, Stephanie Mera, Peihong Zhou, Laurie Joseph, Ill Yang, Anita Brinker, Brian Buckley, Bo Kong, Grace L Guo. Characterization of individual bile acids in vivo utilizing a novel low bile acid mouse model. Toxicological sciences : an official journal of the Society of Toxicology. 2024 May; 199(2):316-331. doi: 10.1093/toxsci/kfae029. [PMID: 38526215]
  • Zhenxing Ren, Ling Zhao, Mingliang Zhao, Tianhao Bao, Tianlu Chen, Aihua Zhao, Xiaojiao Zheng, Xinru Gu, Tao Sun, Yuhuai Guo, Yajun Tang, Guoxiang Xie, Wei Jia. Increased intestinal bile acid absorption contributes to age-related cognitive impairment. Cell reports. Medicine. 2024 May; 5(5):101543. doi: 10.1016/j.xcrm.2024.101543. [PMID: 38697101]
  • Annika Wahlström, Ariel Brumbaugh, Wilhelm Sjöland, Lisa Olsson, Hao Wu, Marcus Henricsson, Annika Lundqvist, Kassem Makki, Stanley L Hazen, Göran Bergström, Hanns-Ulrich Marschall, Michael A Fischbach, Fredrik Bäckhed. Production of deoxycholic acid by low-abundant microbial species is associated with impaired glucose metabolism. Nature communications. 2024 May; 15(1):4276. doi: 10.1038/s41467-024-48543-3. [PMID: 38769296]
  • Romain Riscal, Sarah M Gardner, Nathan J Coffey, Madeleine Carens, Clementina Mesaros, Jimmy P Xu, Yizheng Xue, Leah Davis, Sara Demczyszyn, Austin Vogt, Adam Olia, Jennifer M Finan, Jason Godfrey, David C Schultz, Ian A Blair, Brian Keith, Ronen Marmorstein, Nicolas Skuli, M Celeste Simon. Bile Acid Metabolism Mediates Cholesterol Homeostasis and Promotes Tumorigenesis in Clear Cell Renal Cell Carcinoma. Cancer research. 2024 May; 84(10):1570-1582. doi: 10.1158/0008-5472.can-23-0821. [PMID: 38417134]
  • Aleksandra Boldys, Lukasz Buldak. Metabolic dysfunction-associated steatotic liver disease: Navigating terminological evolution, diagnostic frontiers and therapeutic horizon-an editorial exploration. World journal of gastroenterology. 2024 May; 30(18):2387-2390. doi: 10.3748/wjg.v30.i18.2387. [PMID: 38764762]
  • Xiaobo Zhang, Jie Zhang, Zubing Zhou, Peiyu Xiong, Li Cheng, Jingru Ma, Yueqiang Wen, Tao Shen, Xiaoyan He, Long Wang, Yong Zhang, Chong Xiao. Integrated network pharmacology, metabolomics, and transcriptomics of Huanglian-Hongqu herb pair in non-alcoholic fatty liver disease. Journal of ethnopharmacology. 2024 May; 325(?):117828. doi: 10.1016/j.jep.2024.117828. [PMID: 38325669]
  • Runhao Xu, Jianan Shen, Yan Song, Jingbo Lu, Yijing Liu, Yun Cao, Zhenhua Wang, Jie Zhang. Exploration of the application potential of serum multi-biomarker model in colorectal cancer screening. Scientific reports. 2024 05; 14(1):10127. doi: 10.1038/s41598-024-60867-0. [PMID: 38698075]
  • Wenwen Zhang, Hefei Wu, Shiman Luo, Xiaohua Lu, Xiyue Tan, Li Wen, Xiao Ma, Thomas Efferth. Molecular insights into experimental models and therapeutics for cholestasis. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2024 May; 174(?):116594. doi: 10.1016/j.biopha.2024.116594. [PMID: 38615607]
  • Zijie Jin, Ruotong Yin, Yan Yuan, Chen Zheng, Peng Zhang, Yalin Wang, Hongbo Weng. Dapagliflozin ameliorates hepatic steatosis via suppressing LXRα-mediated synthesis of lipids and bile acids. Biochemical pharmacology. 2024 May; 223(?):116167. doi: 10.1016/j.bcp.2024.116167. [PMID: 38527558]
  • Natalia Łozińska, Julia Maldonado-Valderrama, Teresa Del Castillo-Santaella, Yanija Zhou, Dorota Martysiak-Żurowska, Yuanqi Lu, Christian Jungnickel. Bile conjugation and its effect on in vitro lipolysis of emulsions. Food research international (Ottawa, Ont.). 2024 May; 184(?):114255. doi: 10.1016/j.foodres.2024.114255. [PMID: 38609233]
  • Wei Jia, Yitao Li, Kenneth C P Cheung, Xiaojiao Zheng. Bile acid signaling in the regulation of whole body metabolic and immunological homeostasis. Science China. Life sciences. 2024 May; 67(5):865-878. doi: 10.1007/s11427-023-2353-0. [PMID: 37515688]
  • Yoriko Heianza, Qiaochu Xue, Jennifer Rood, Clary B Clish, George A Bray, Frank M Sacks, Lu Qi. Changes in bile acid subtypes and improvements in lipid metabolism and atherosclerotic cardiovascular disease risk: the Preventing Overweight Using Novel Dietary Strategies (POUNDS Lost) trial. The American journal of clinical nutrition. 2024 May; 119(5):1293-1300. doi: 10.1016/j.ajcnut.2024.02.019. [PMID: 38428740]
  • Zilu Cheng, Yixiong Chen, Bernd Schnabl, Huikuan Chu, Ling Yang. Bile acid and nonalcoholic steatohepatitis: Molecular insights and therapeutic targets. Journal of advanced research. 2024 May; 59(?):173-187. doi: 10.1016/j.jare.2023.06.009. [PMID: 37356804]
  • Mengcheng Jin, Tangbin Zou, Hairong Huang, Ming Chen, Haoqi Zou, Baoyan Chen, Chengze Lai, Huawen Li, Peiwen Zhang. The Effect of Coenzyme Q10 Supplementation on Bile Acid Metabolism: Insights from Network Pharmacology, Molecular Docking, and Experimental Validation. Molecular nutrition & food research. 2024 May; 68(9):e2400147. doi: 10.1002/mnfr.202400147. [PMID: 38643378]
  • Amanda Morrison, Bahaa Elgendy. Tailoring FXR Modulators for Intestinal Specificity: Recent Progress and Insights. Molecules (Basel, Switzerland). 2024 Apr; 29(9):. doi: 10.3390/molecules29092022. [PMID: 38731514]
  • Joshua S Fleishman, Sunil Kumar. Bile acid metabolism and signaling in health and disease: molecular mechanisms and therapeutic targets. Signal transduction and targeted therapy. 2024 Apr; 9(1):97. doi: 10.1038/s41392-024-01811-6. [PMID: 38664391]
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