Mechanism of growth inhibition by free bile acids in lactobacilli and bifidobacteria

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

Bligh, E. G., & Dyer, W. J. (1959) · Canadian Journal of Biochemistry and Physiology · doi:10.1139/o59-099 · Cited by 54,751 · see citing works

Quantitative estimation of the hydrophilic-hydrophobic balance of mixed bile salt solutions.

Heuman, D. M. (1989) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)38331-0 · Cited by 555 · see citing works

The influence of bile salt structure on self-association in aqueous solutions.

Roda, A., Hofmann, A. F., & Mysels, K. J. (1983) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)32418-9 · Cited by 529 · see citing works

Movement of fatty acids, fatty acid analogs, and bile acids across phospholipid bilayers

Kamp, F., & Hamilton, J. A. (1993) · Biochemistry · doi:10.1021/bi00092a017 · Cited by 310 · see citing works

pH gradients across phospholipid membranes caused by fast flip-flop of un-ionized fatty acids.

Kamp, F., & Hamilton, J. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.23.11367 · Cited by 299 · see citing works

Uncoupling by Acetic Acid Limits Growth of and Acetogenesis by Clostridium thermoaceticum

Baronofsky, J. J., Schreurs, W. J., & Kashket, E. R. (1984) · Applied and Environmental Microbiology · doi:10.1128/aem.48.6.1134-1139.1984 · Cited by 243 · see citing works

[32] Purification, reconstitution, and characterization of the lac permease of Escherichia coli

Viitanen, P. V., Newman, M. J., Foster, D. L., Wilson, T. H., & Kaback, H. R. (1986) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(86)25034-x · Cited by 170 · see citing works

Bile acid inhibition of intestinal anaerobic organisms

Binder, H., Filburn, B., & Floch, M. H. (1975) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/28.2.119 · Cited by 135 · see citing works

Transbilayer movement of bile acids in model membranes

Cabral, D. J., SMALL, D. M., Lilly, H. S., & Hamilton, J. A. (1987) · Biochemistry · doi:10.1021/bi00381a002 · Cited by 122 · see citing works

Bile-Mediated Aminoglycoside Sensitivity in Lactobacillus Species Likely Results from Increased Membrane Permeability Attributable to Cholic Acid

Elkins, C. A., & Mullis, L. B. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.12.7200-7209.2004 · Cited by 77 · see citing works

Resistance of Streptococcus bovis to acetic acid at low pH: relationship between intracellular pH and anion accumulation

Russell, J. B. (1991) · Applied and Environmental Microbiology · doi:10.1128/aem.57.1.255-259.1991 · Cited by 76 · see citing works

Cholic acid accumulation and its diminution by short-chain fatty acids in bifidobacteria

Kurdi, P., Tanaka, H., van Veen, H. W., Asano, K., Tomita, F., & Yokota, A. (2003) · Microbiology · doi:10.1099/mic.0.26376-0 · Cited by 70 · see citing works

Cholic Acid Is Accumulated Spontaneously, Driven by Membrane ΔpH, in Many Lactobacilli

Kurdi, P., van Veen, H. W., Tanaka, H., Mierau, I., Konings, W. N., Tannock, G. W., Tomita, F., & Yokota, A. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.22.6525-6528.2000 · Cited by 63 · see citing works

Biotransformation of Bile Acids, Cholesterol, and Steroid Hormones

Baron, S. F., & Hylemon, P. B. (1997) · Springer eBooks · doi:10.1007/978-1-4615-4111-0_13 · Cited by 50 · see citing works

Gastrointestinal ecosystems and fermentations

Mackie, R. I., & White, B. A. (1997) · Chapman & Hall eBooks · Cited by 43 · see citing works

Effects of carbonylcyanide-m-chlorophenylhydrazone (CCCP) and acetate on Escherichia coli O157:H7 and K-12: uncoupling versus anion accumulation

Diez‐Gonzalez, F. (1997) · FEMS Microbiology Letters · doi:10.1016/s0378-1097(97)00140-7 · Cited by 42 · see citing works

Effects of carbonylcyanide-m-chlorophenylhydrazone (CCCP) and acetate on Escherichia coli O157:H7 and K-12: uncoupling versus anion accumulation

Diez‐Gonzalez, F., & Russell, J. B. (2006) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1997.tb10396.x · Cited by 37 · see citing works

Bile acids — interaction with the intestinal mucosa

Rafter, J. J., & Branting, C. (1991) · European Journal of Cancer Prevention · doi:10.1097/00008469-199110002-00009 · Cited by 20 · see citing works

Diet and Precancerous Lesions of the Stomach

Reed, P. I. (1991) · Springer eBooks · doi:10.1007/978-94-011-3308-1_6 · Cited by 3 · see citing works

Gut microbiota functions: metabolism of nutrients and other food components

Rowland, I., Gibson, G., Heinken, A., Scott, K., Swann, J., Thiele, I., & Tuohy, K. (2018) · European Journal of Nutrition · doi:10.1007/s00394-017-1445-8 · Cited by 2,878 · see citing works

Gut microbiota-derived metabolites as key actors in inflammatory bowel disease

Lavelle, A., & Sokol, H. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0258-z · Cited by 2,015 · see citing works

Gut microbiota in cardiovascular health and disease

Tang, W. H. W., Kitai, T., & Hazen, S. L. (2017) · Circulation Research · doi:10.1161/circresaha.117.309715 · Cited by 1,670 · see citing works

Signals from the gut microbiota to distant organs in physiology and disease

Schroeder, B. O., & Bäckhed, F. (2016) · Nature Medicine · doi:10.1038/nm.4185 · Cited by 1,409 · see citing works

Consequences of bile salt biotransformations by intestinal bacteria

Ridlon, J. M., Harris, S. C., Bhowmik, S., Kang, D.-J., & Hylemon, P. B. (2016) · Gut Microbes · doi:10.1080/19490976.2015.1127483 · Cited by 1,097 · see citing works

Bile acid signaling in metabolic disease and drug therapy

Li, T., & Chiang, J. Y. L. (2014) · Pharmacological Reviews · doi:10.1124/pr.113.008201 · Cited by 935 · see citing works

Bile Acid Is a Host Factor That Regulates the Composition of the Cecal Microbiota in Rats

Islam, K. B. M. S., Fukiya, S., Hagio, M., Fujii, N., Ishizuka, S., Ooka, T., Ogura, Y., Hayashi, T., & Yokota, A. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.046 · Cited by 918 · see citing works

Stress Physiology of Lactic Acid Bacteria.

Papadimitriou, K., Alegría, Á., Bron, P. A., de Angelis, M., Gobbetti, M., Kleerebezem, M., Lemos, J. A., Linares, D. M., Ross, P., Stanton, C., et al. (2016) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00076-15 · Cited by 914 · see citing works

Lipotoxicity and the gut-liver axis in NASH pathogenesis

Marra, F., & Svegliati-Baroni, G. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2017.11.014 · Cited by 847 · see citing works

Modulation of the fecal bile acid profile by gut microbiota in cirrhosis

Kakiyama, G., Pandak, W. M., Gillevet, P. M., Hylemon, P. B., Heuman, D. M., Daita, K., Takei, H., Muto, A., Nittono, H., Ridlon, J. M., et al. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.01.003 · Cited by 782 · see citing works

Review: microbial transformations of human bile acids

Guzior, D. V., & Quinn, R. A. (2021) · Microbiome · doi:10.1186/s40168-021-01101-1 · Cited by 760 · see citing works

Intestinal transport and metabolism of bile acids

Dawson, P. A., & Karpen, S. J. (2015) · Journal of Lipid Research · doi:10.1194/jlr.r054114 · Cited by 598 · see citing works

Gut Microbiota and Colonization Resistance against Bacterial Enteric Infection

Ducarmon, Q. R., Zwittink, R. D., Hornung, B. V. H., van Schaik, W., Young, V. B., & Kuijper, E. J. (2019) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00007-19 · Cited by 566 · see citing works

Bile resistance mechanisms in Lactobacillus and Bifidobacterium

Ruiz, L., Margolles, A., & Sánchez, B. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00396 · Cited by 548 · see citing works

Molecular physiology of bile acid signaling in health, disease, and aging

Perino, A., Demagny, H., Velazquez-Villegas, L., & Schoonjans, K. (2021) · Physiological Reviews · doi:10.1152/physrev.00049.2019 · Cited by 481 · see citing works

Bile acid nuclear receptor FXR and digestive system diseases

Ding, L., Yang, L., Wang, Z., & Huang, W. (2015) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2015.01.004 · Cited by 477 · see citing works

Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis

Rusch, J. A., Layden, B. T., & Dugas, L. R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1130689 · Cited by 415 · see citing works

The Role of the Gut Microbiota in Bile Acid Metabolism

Ramírez-Pérez, O., Cruz-Ramón, V., Chinchilla-López, P., & Méndez‐Sánchez, N. (2017) · Annals of Hepatology · doi:10.5604/01.3001.0010.5672 · Cited by 393 · see citing works

Restructuring of the Gut Microbiome by Intermittent Fasting Prevents Retinopathy and Prolongs Survival in db/db Mice

Beli, E., Yan, Y., Moldovan, L., Vieira, C. P., Gao, R., Duan, Y., Prasad, R., Bhatwadekar, A. D., White, F. A., Townsend, S. D., et al. (2018) · Diabetes · doi:10.2337/db18-0158 · Cited by 372 · see citing works

Bile acid is a significant host factor shaping the gut microbiome of diet-induced obese mice

Zheng, X., Huang, F., Zhao, A., Lei, S., Zhang, Y., Xie, G., Chen, T., Qu, C., Rajani, C., Dong, B., et al. (2017) · BMC Biology · doi:10.1186/s12915-017-0462-7 · Cited by 323 · see citing works

Emerging roles of bile acids in mucosal immunity and inflammation

Chen, M. L., Takeda, K., & Sundrud, M. S. (2019) · Mucosal Immunology · doi:10.1038/s41385-019-0162-4 · Cited by 301 · see citing works

Exercise Attenuates PCB-Induced Changes in the Mouse Gut Microbiome

Choi, J. J., Eum, S. Y., Rampersaud, E., Daunert, S., Abreu, M. T., & Toborek, M. (2013) · Environmental Health Perspectives · doi:10.1289/ehp.1306534 · Cited by 298 · see citing works

Gut microbiota promotes cholesterol gallstone formation by modulating bile acid composition and biliary cholesterol secretion

Hu, H., Shao, W., Liu, Q., Liu, N., Wang, Q., Xu, J., Zhang, X., Weng, Z., Lu, Q., Jiao, L., et al. (2022) · Nature Communications · doi:10.1038/s41467-021-27758-8 · Cited by 288 · see citing works

The gut microbiome in obesity

Tseng, C.-H., & Wu, C. (2018) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2018.07.009 · Cited by 278 · see citing works

Gut microbiota influence in type 2 diabetes mellitus (T2DM)

Cunningham, A., Stephens, J. W., & Harris, D. A. (2021) · Gut Pathogens · doi:10.1186/s13099-021-00446-0 · Cited by 279 · see citing works

Dietary fat, bile acid metabolism and colorectal cancer

Ocvirk, S., & O’Keefe, S. J. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.10.003 · Cited by 263 · see citing works

The importance of the gut microbiota after bariatric surgery

Aron‐Wisnewsky, J., Dore, J. M., & Clément, K. (2012) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2012.161 · Cited by 259 · see citing works

Microbiota, cirrhosis, and the emerging oral-gut-liver axis

Acharya, C., Sahingur, S. E., & Bajaj, J. S. (2017) · JCI Insight · doi:10.1172/jci.insight.94416 · Cited by 256 · see citing works

The microbiome modulating activity of bile acids

Tian, Y., Gui, W., Koo, I., Smith, P. B. W., Allman, E. L., Nichols, R. G., Rimal, B., Cai, J., Liu, Q., & Patterson, A. D. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1732268 · Cited by 251 · see citing works

Role of microbiota-derived lipopolysaccharide in adipose tissue inflammation, adipocyte size and pyroptosis during obesity

Hersoug, L., Möller, P., & Loft, S. H. (2018) · Nutrition Research Reviews · doi:10.1017/s0954422417000269 · Cited by 246 · see citing works

Inflammaging as a common ground for the development and maintenance of sarcopenia, obesity, cardiomyopathy and dysbiosis

Livshits, G., & Kalinkovich, A. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.100980 · Cited by 239 · see citing works

New insights into bacterial bile resistance mechanisms: the role of bile salt hydrolase and its impact on human health

Bustos, A. Y., Font de Valdez, G., Fadda, S., & Taranto, M. P. (2018) · Food Research International · doi:10.1016/j.foodres.2018.06.035 · Cited by 232 · see citing works

Secondary bile acid-induced dysbiosis promotes intestinal carcinogenesis

Cao, H., Xu, M., Dong, W., Deng, B., Wang, S., Zhang, Y., Wang, S., Luo, S., Wang, W., Qi, Y., et al. (2017) · International Journal of Cancer · doi:10.1002/ijc.30643 · Cited by 230 · see citing works

Impact of Diet on Human Intestinal Microbiota and Health

Salonen, A., & de Vos, W. M. (2014) · Annual Review of Food Science and Technology · doi:10.1146/annurev-food-030212-182554 · Cited by 215 · see citing works

The Effects of Nutrition on the Gastrointestinal Microbiome of Cats and Dogs: Impact on Health and Disease

Wernimont, S. M., Radosevich, J., Jackson, M. I., Ephraim, E., Badri, D. V., MacLeay, J. M., Jewell, D. E., & Suchodolski, J. S. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01266 · Cited by 220 · see citing works

Is bile acid a determinant of the gut microbiota on a high-fat diet?

Yokota, A., Fukiya, S., Islam, K. B. M. S., Ooka, T., Ogura, Y., Hayashi, T., Hagio, M., & Ishizuka, S. (2012) · Gut Microbes · doi:10.4161/gmic.21216 · Cited by 207 · see citing works

Interactive relationships between intestinal flora and bile acids

Guo, X., Okpara, E. S., Hu, W., Yan, C., Wang, Y., Liang, Q., Chiang, J. Y. L., & Han, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158343 · Cited by 206 · see citing works

Spatial Heterogeneity and Co-occurrence of Mucosal and Luminal Microbiome across Swine Intestinal Tract

Zhang, L., Wu, W., Lee, Y. K., Xie, J., & Zhang, H. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00048 · Cited by 198 · see citing works

Bile salt hydrolase/aminoacyltransferase shapes the microbiome

Guzior, D., Okros, M., Hernandez, C. M., Shivel, M., Armwald, B., Hausinger, R., & Quinn, R. (2022) · doi:10.21203/rs.3.rs-2050406/v1 · Cited by 187 · see citing works

Targeting fatty acid metabolism to improve glucose metabolism

Stinkens, R., Goossens, G. H., Jocken, J. W. E., & Blaak, E. E. (2015) · Obesity Reviews · doi:10.1111/obr.12298 · Cited by 183 · see citing works

In Vitro Antibacterial Activity of Unconjugated and Conjugated Bile Salts on Staphylococcus aureus

Sannasiddappa, T. H., Lund, P. A., & Clarke, S. R. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01581 · Cited by 183 · see citing works

Intestinal microbiota and type 2 diabetes: From mechanism insights to therapeutic perspective

Han, J.-L., & Lin, H. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i47.17737 · Cited by 179 · see citing works

Influence of Bile Acids on Colorectal Cancer Risk: Potential Mechanisms Mediated by Diet-Gut Microbiota Interactions

Ocvirk, S., & O’Keefe, S. J. (2017) · Current Nutrition Reports · doi:10.1007/s13668-017-0219-5 · Cited by 176 · see citing works

Contribution of the 7β-hydroxysteroid dehydrogenase from Ruminococcus gnavus N53 to ursodeoxycholic acid formation in the human colon

Lee, J., Arai, H., Nakamura, Y., Fukiya, S., Wada, M., & Yokota, A. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m039834 · Cited by 169 · see citing works

Bile salts and cholestasis

Wenniger, L. J. M. D. B., & Beuers, U. H. (2010) · Digestive and Liver Disease · doi:10.1016/j.dld.2010.03.015 · Cited by 161 · see citing works

Characterization of a Novel Bile-Inducible Operon Encoding a Two-Component Regulatory System in<i>Lactobacillus acidophilus</i>

Pfeiler, E. A., Azcarate-Peril, M. A., & Klaenhammer, T. R. (2007) · Journal of Bacteriology · doi:10.1128/jb.00337-07 · Cited by 154 · see citing works

Ursodeoxycholic Acid and Its Taurine- or Glycine-Conjugated Species Reduce Colitogenic Dysbiosis and Equally Suppress Experimental Colitis in Mice

den Bossche, L. V., Hindryckx, P., Devisscher, L., Devriese, S., Welden, S. V., Holvoet, T., Vilchez‐Vargas, R., Vital, M., Pieper, D. H., Bussche, J. V., et al. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.02766-16 · Cited by 146 · see citing works

Bile acids: a communication channel in the gut-brain axis

Monteiro-Cardoso, V. F., Corlianò, M., & Singaraja, R. R. (2021) · NeuroMolecular Medicine · doi:10.1007/s12017-020-08625-z · Cited by 145 · see citing works

Role of immune responses in the development of NAFLD-associated liver cancer and prospects for therapeutic modulation

Yahoo, N., Dudek, M., Knolle, P. A., & Heikenwälder, M. F. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.02.033 · Cited by 145 · see citing works

Mechanistic links between gut microbial community dynamics, microbial functions and metabolic health

Ha, C. W. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i44.16498 · Cited by 137 · see citing works

Comprehensive evaluation of the bactericidal activities of free bile acids in the large intestine of humans and rodents

Watanabe, M., Fukiya, S., & Yokota, A. (2017) · Journal of Lipid Research · doi:10.1194/jlr.m075143 · Cited by 137 · see citing works

Interplay between bile acids and the gut microbiota promotes intestinal carcinogenesis

Wang, S., Dong, W., Liu, L., Xu, M., Wang, Y., Liu, T., Zhang, Y., Wang, B., & Cao, H. (2019) · Molecular Carcinogenesis · doi:10.1002/mc.22999 · Cited by 132 · see citing works

Inflammation meets metabolic disease: Gut feeling mediated by GLP-1

Zietek, T., & Rath, E. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00154 · Cited by 131 · see citing works

Intestinal dysbiosis in nonalcoholic fatty liver disease (NAFLD): focusing on the gut–liver axis

Han, H. L., Jiang, Y., Wang, M., Melaku, M., Liu, L., Zhao, Y. M., Everaert, N., Yi, B., & Zhang, H. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1966738 · Cited by 130 · see citing works

How do bifidobacteria counteract environmental challenges? Mechanisms involved and physiological consequences

Ruíz, L., Ruas‐Madiedo, P., Gueimonde, M., Reyes‐Gavilán, C. G. D. L., Margollés, A., & Sánchez, B. (2011) · Genes & Nutrition · doi:10.1007/s12263-010-0207-5 · Cited by 127 · see citing works

Cross-talk between bile acids and intestinal microbiota in host metabolism and health

Nie, Y., Hu, J. P., & Yan, X. (2015) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1400327 · Cited by 128 · see citing works

Effects of various polysaccharides (alginate, carrageenan, gums, chitosan) and their combination with prebiotic saccharides (resistant starch, lactosucrose, lactulose) on the encapsulation of probiotic bacteria Lactobacillus casei 01 strain

Ta, L. P., Bujna, E., Antal, O., Ladányi, M., Juhász, R., Szécsi, A., Kun, S., Sudheer, S. M., Gupta, V. K., & Nguyen, Q. D. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.04.170 · Cited by 124 · see citing works

Changes in the Intestinal Microbiome and Alcoholic and Nonalcoholic Liver Diseases: Causes or Effects?

Betrapally, N. S., Gillevet, P. M., & Bajaj, J. S. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.02.073 · Cited by 123 · see citing works

The role of the gut microbiota in health and cardiovascular diseases

Wang, L., Wang, S., Zhang, Q., He, C., Fu, C., & Wei, Q. (2022) · Molecular Biomedicine · doi:10.1186/s43556-022-00091-2 · Cited by 124 · see citing works

Recent Advances in the Understanding of Stress Resistance Mechanisms in Probiotics: Relevance for the Design of Functional Food Systems

Bustos, A. Y., Taranto, M. P., Gerez, C. L., Agriopoulou, S., Smaoui, S., Varzakas, T. H., & Enshasy, H. A. E. (2024) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-024-10273-9 · Cited by 130 · see citing works

Importance of microbial defence systems to bile salts and mechanisms of serum cholesterol reduction

Horáčková, Š., Plocková, M., & Demnerová, K. (2017) · Biotechnology Advances · doi:10.1016/j.biotechadv.2017.12.005 · Cited by 119 · see citing works

Bile acid homeostasis and intestinal dysbiosis in alcoholic hepatitis

Ciocan, D. M., Voican, C. S., Wrzosek, L., Hugot, C., Rainteau, D. P., Humbert, L., Cassard, A., & Perlemuter, G. (2018) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.14949 · Cited by 116 · see citing works

Intestinal flora imbalance affects bile acid metabolism and is associated with gallstone formation

Wang, Q., Hao, C., Yao, W., Zhu, D., Lu, H., Li, L., Ma, B., Sun, B., Xue, D., & Zhang, W. (2020) · BMC Gastroenterology · doi:10.1186/s12876-020-01195-1 · Cited by 113 · see citing works

Role of farnesoid X receptor and bile acids in alcoholic liver disease

Manley, S., & Ding, W. (2015) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2014.12.011 · Cited by 114 · see citing works

Microbial Hydroxysteroid Dehydrogenases: From Alpha to Omega

Doden, H. L., & Ridlon, J. M. (2021) · Microorganisms · doi:10.3390/microorganisms9030469 · Cited by 110 · see citing works

Effect of dietary bile acids on growth, body composition, lipid metabolism and microbiota in grass carp (Ctenopharyngodon idella)

Zhou, J., Chen, H. J., Ji, H., Shi, X., Li, X. X., Chen, L., Du, Z., & Yu, H. (2017) · Aquaculture Nutrition · doi:10.1111/anu.12609 · Cited by 110 · see citing works

NMN Maintains Intestinal Homeostasis by Regulating the Gut Microbiota

Huang, P., Jiang, A., Wang, X., Zhou, Y., Tang, W., Ren, C., Qian, X., Zhou, Z., & Gong, A. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.714604 · Cited by 110 · see citing works

Swine gut microbiota and its interaction with host nutrient metabolism

Wang, H., Xu, R., Zhang, H., Su, Y., & Zhu, W. (2020) · Animal nutrition · doi:10.1016/j.aninu.2020.10.002 · Cited by 109 · see citing works

The gut microbiota at the intersection of bile acids and intestinal carcinogenesis: An old story, yet mesmerizing

Liu, T., Song, X., Khan, S., Li, Y., Guo, Z., Li, C., Wang, S., Dong, W., Liu, W., Wang, B., et al. (2019) · International Journal of Cancer · doi:10.1002/ijc.32563 · Cited by 106 · see citing works

Interactions between bile salts, gut microbiota, and hepatic innate immunity

Schubert, K. A., Damink, S. W. M. O., von Bergen�, M., & Schaap, F. G. (2017) · Immunological Reviews · doi:10.1111/imr.12579 · Cited by 102 · see citing works

Dietary nutrition and gut microflora: A promising target for treating diseases

Nie, Y., Luo, F., & Lin, Q. (2018) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2018.03.002 · Cited by 104 · see citing works

Is It Time to Use Probiotics to Prevent or Treat Obesity?

Brusaferro, A., Cozzali, R., Orabona, C., Biscarini, A., Farinelli, E., Cavalli, E., Grohmann, U., Principi, N., & Esposito, S. (2018) · Nutrients · doi:10.3390/nu10111613 · Cited by 102 · see citing works

Early Salmonella Typhimurium infection in pigs disrupts Microbiome composition and functionality principally at the ileum mucosa

Argüello, H., Estellé, J., Zaldívar‐López, S., Jiménez-Marín, Á., Carvajal, A., López-Bascón, M. A., Crispie, F., O’Sullivan, Ó., Cotter, P. D., Priego‐Capote, F., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-26083-3 · Cited by 100 · see citing works

Bile acid–microbiota crosstalk in gastrointestinal inflammation and carcinogenesis: a role for bifidobacteria and lactobacilli?

Sánchez, B. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2018.23 · Cited by 98 · see citing works

Role of bile acids in carcinogenesis of pancreatic cancer: An old topic with new perspective

Feng, H., & Chen, Y. (2016) · World Journal of Gastroenterology · doi:10.3748/wjg.v22.i33.7463 · Cited by 94 · see citing works

Antibiotics, gut microbiome and obesity

Leong, K. S. W., Derraik, J. G. B., Hofman, P. L., & Cutfield, W. S. (2017) · Clinical Endocrinology · doi:10.1111/cen.13495 · Cited by 91 · see citing works

Bile acids affect intestinal barrier function through FXR and TGR5

Song, G., Xie, Y., Yi, L., Cheng, W., Jia, H., Shi, W., Liu, Q., Fang, L., Xue, S., Liu, D., et al. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1607899 · Cited by 98 · see citing works

Bile acid-based therapies for non-alcoholic steatohepatitis and alcoholic liver disease

Li, T., & Chiang, J. Y. L. (2020) · HepatoBiliary Surgery and Nutrition · doi:10.21037/hbsn.2019.09.03 · Cited by 86 · see citing works

Cell envelope changes inBifidobacterium animalisssp.lactisas a response to bile

Ruíz, L., Sánchez, B., Ruas‐Madiedo, P., Reyes‐Gavilán, C. G. D. L., & Margollés, A. (2007) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2007.00854.x · Cited by 87 · see citing works

Proteomic and transcriptomic analysis of the response to bile stress of Lactobacillus casei BL23

Alcántara, C., & Zúñiga, M. (2012) · Microbiology · doi:10.1099/mic.0.055657-0 · Cited by 87 · see citing works

Current Research on the Pathogenesis of NAFLD/NASH and the Gut–Liver Axis: Gut Microbiota, Dysbiosis, and Leaky-Gut Syndrome

Kobayashi, T., Iwaki, M., Nakajima, A., Nogami, A., & Yoneda, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911689 · Cited by 85 · see citing works

Advances in Fecal Microbiota Transplantation for Gut Dysbiosis‐Related Diseases

Hou, S., Yu, J., Li, Y., Zhao, D., & Zhang, Z. (2025) · Advanced Science · doi:10.1002/advs.202413197 · Cited by 93 · see citing works

Alteration of gut microbiota in association with cholesterol gallstone formation in mice

Wang, Q., Jiao, L. R., He, C., Sun, H., Cai, Q., Han, T., & Hu, H. (2017) · BMC Gastroenterology · doi:10.1186/s12876-017-0629-2 · Cited by 85 · see citing works

Gut Microbiome Modulation Based on Probiotic Application for Anti-Obesity: A Review on Efficacy and Validation

Barathikannan, K., Chelliah, R., Rubab, M., Daliri, E. B., Elahi, F., Kim, D.-H., Agastian, P., Oh, S.-Y., & Oh, D. H. (2019) · Microorganisms · doi:10.3390/microorganisms7100456 · Cited by 84 · see citing works

Gut microbiota in pathophysiology, diagnosis, and therapeutics of inflammatory bowel disease

Pandey, H., Jain, D., Tang, D. W. T., Wong, S. H., & Lal, D. (2023) · Intestinal Research · doi:10.5217/ir.2023.00080 · Cited by 89 · see citing works

Effect of antibiotics on gut microbiota, glucose metabolism and body weight regulation: a review of the literature

Mikkelsen, S. U., Allin, K. H., & Knop, F. K. (2016) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12637 · Cited by 80 · see citing works

Bile acids in immunity: Bidirectional mediators between the host and the microbiota

Godlewska, U., Bulanda, E., & Wypych, T. P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.949033 · Cited by 77 · see citing works

Bile Acid Signaling in Metabolic and Inflammatory Diseases and Drug Development

Li, T., & Chiang, J. Y. L. (2024) · Pharmacological Reviews · doi:10.1124/pharmrev.124.000978 · Cited by 83 · see citing works

Targeting the Gut Microbiome as a Treatment for Primary Sclerosing Cholangitis: A Conceptional Framework

Shah, A., Macdonald, G. A., Morrison, M., & Holtmann, G. (2020) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000000604 · Cited by 77 · see citing works

Manipulation of epithelial integrity and mucosal immunity by host and microbiota‐derived metabolites

Kayama, H., & Takeda, K. (2020) · European Journal of Immunology · doi:10.1002/eji.201948478 · Cited by 74 · see citing works

Soil metabolome correlates with bacterial diversity and co-occurrence patterns in root-associated soils on the Tibetan Plateau

Liu, K., Ding, X., & Wang, J. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.139572 · Cited by 71 · see citing works

Commensal Obligate Anaerobic Bacteria and Health: Production, Storage, and Delivery Strategies

Andrade, J. C., Almeida, D., Domingos, M., Seabra, C. L., Machado, D., Freitas, A. C., & Gomes, A. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00550 · Cited by 77 · see citing works

Modulation of the Gut Microbiota-farnesoid X Receptor Axis Improves Deoxycholic Acid-induced Intestinal Inflammation in Mice

Xu, M., Shen, Y. S., Cen, M., Zhu, Y., Cheng, F., Tang, L., Zheng, X., Kim, J. J., Dai, N., & Hu, W. (2021) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjab003 · Cited by 71 · see citing works

Gut Microbiota‐Bile Acid Crosstalk in Diarrhea‐Irritable Bowel Syndrome

Zhan, K., Zheng, H., Jian-qing, L., Wu, H., Qin, S., Luo, L., & Huang, S. (2020) · BioMed Research International · doi:10.1155/2020/3828249 · Cited by 70 · see citing works

Characterization of the bile and gall bladder microbiota of healthy pigs

Jiménez, E., Sánchez, B., Farina, A., Margollés, A., & Rodríguez, J. M. (2014) · MicrobiologyOpen · doi:10.1002/mbo3.218 · Cited by 69 · see citing works

Development of a Double-Crossover Markerless Gene Deletion System in Bifidobacterium longum: Functional Analysis of the α-Galactosidase Gene for Raffinose Assimilation

Hirayama, Y., Sakanaka, M., Fukuma, H., Murayama, H., Kano, Y., Fukiya, S., & Yokota, A. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.00588-12 · Cited by 69 · see citing works

Changes seen in gut bacteria content and distribution with obesity: causation or association?

Bell, D. S. H. (2015) · Postgraduate Medicine · doi:10.1080/00325481.2015.1098519 · Cited by 69 · see citing works

Changes in the composition of the human intestinal microbiome in alcohol use disorder: a systematic review

Litwinowicz, K., Choroszy, M., & Waszczuk, E. (2019) · The American Journal of Drug and Alcohol Abuse · doi:10.1080/00952990.2019.1669629 · Cited by 67 · see citing works

Cholestasis: exploring the triangular relationship of gut microbiota-bile acid-cholestasis and the potential probiotic strategies

Yu, L., Liu, Y., Wang, S., Zhang, Q., Zhao, J., Zhang, H., Narbad, A., Tian, F., Zhai, Q., & Chen, W. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2181930 · Cited by 68 · see citing works

Detection of Gut Dysbiosis due to Reduced Clostridium Subcluster XIVa Using the Fecal or Serum Bile Acid Profile

Murakami, M., Iwamoto, J., Honda, A., Tsuji, T., Tamamushi, M., Ueda, H., Monma, T., Konishi, N., Yara, S., Hirayama, T. T., et al. (2018) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izy022 · Cited by 65 · see citing works

Cholic acid accumulation and its diminution by short-chain fatty acids in bifidobacteria

Kurdi, P., Tanaka, H., van Veen, H. W., Asano, K., Tomita, F., & Yokota, A. (2003) · Microbiology · doi:10.1099/mic.0.26376-0 · Cited by 70 · see citing works

Comprehensive evaluation of the bactericidal activities of free bile acids in the large intestine of humans and rodents

Watanabe, M., Fukiya, S., & Yokota, A. (2017) · Journal of Lipid Research · doi:10.1194/jlr.m075143 · Cited by 137 · see citing works

The Mechanism of Antimicrobial Activity of Conjugated Bile Acids against Lactic Acid Bacilli

Chai, L., Wu, H. J., Wang, X., He, L., & Guo, C. (2023) · Microorganisms · doi:10.3390/microorganisms11071823 · Cited by 18 · see citing works

Effect of bile acid on the cell membrane functionality of lactic acid bacteria for oral administration

Taranto, M. P., Pérez‐Martínez, G., & de Valdez, G. F. (2006) · Research in Microbiology · doi:10.1016/j.resmic.2006.04.002 · Cited by 76 · see citing works

Molecular Insight into the Response of Lactic Acid Bacteria to Bile Acids

Moreno, C. N., Gomez, J. N., Taranto, M. P., Ledesma, A. E., & Bustos, A. Y. (2024) · BioTech · doi:10.3390/biotech13030029 · Cited by 8 · see citing works