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Titlebook: Bile Acids and Their Receptors; Stefano Fiorucci,Eleonora Distrutti Book 2019 Springer Nature Switzerland AG 2019 Bile acids.Nuclear recep

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发表于 2025-3-21 18:20:42 | 显示全部楼层 |阅读模式
期刊全称Bile Acids and Their Receptors
影响因子2023Stefano Fiorucci,Eleonora Distrutti
视频video
发行地址Gives an overview on latest findings in the novel field of research of bile acids as signaling molecules.Offers a cross-country view of the functional role of bile acids as signaling molecules, virtua
学科分类Handbook of Experimental Pharmacology
图书封面Titlebook: Bile Acids and Their Receptors;  Stefano Fiorucci,Eleonora Distrutti Book 2019 Springer Nature Switzerland AG 2019 Bile acids.Nuclear recep
影响因子This book focusses on the latest results related to the field of  bile acids as signaling molecules  and describes how these receptors have become a major pharmacological target. It covers all major areas of research in this field, from genetics, chemistry, in silico modeling, molecular biology to clinical applications, offering a cross-country view of the functional role of bile acids as signaling molecules, virtually acting on all major areas of metabolism. While FXR  and GPBAR1 are essential bile acid sensors that  integrate the .de novo. bile acid synthesis with intestinal microbiota and  liver metabolism, in a broader sense,  BARs  play a pathogenic role in the development of common human alignments  including  liver, intestinal and metabolic disorders, such as steatosis (NAFLD) and steato-hepatitis (NASH), diabetes, obesity and atherosclerosis. 
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发表于 2025-3-22 02:32:02 | 显示全部楼层
Structural Insight into the Binding Mode of FXR and GPBAR1 Modulators,resenting promising pharmacological targets. We pay particular attention to the chemical and structural features of the ligand-receptor interaction, providing guidelines to achieve ligands endowed with selective or dual activity towards the receptor and paving the way to future drug design studies.
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发表于 2025-3-22 14:38:37 | 显示全部楼层
,Pflege der Isolieröle im Betrieb,lectively target GPBAR1 or FXR..In this review, we summarize the most recent acquisition on natural, semisynthetic, and synthetic steroidal and nonsteroidal ligands, able to interact with FXR and GPBAR1.
发表于 2025-3-22 19:58:58 | 显示全部楼层
https://doi.org/10.1007/978-3-663-07267-6d their activated receptors in mediating the beneficial metabolic effects of bariatric surgery. We also discuss the potential to target bile acid-activated receptors in order to treat obesity and other metabolic diseases.
发表于 2025-3-22 23:07:34 | 显示全部楼层
The Enterokine Fibroblast Growth Factor 15/19 in Bile Acid Metabolism,he liver. However, native FGF19 seems to retain peculiar hepatic pro-tumorigenic actions. Recently engineered FGF19 analogues have been recently synthetized, with fully retained BA regulatory activity but without intrinsic pro-tumoral action, thus opening bona fide novel pharmacological strategy for the treatment of gut-liver axis diseases.
发表于 2025-3-23 04:34:06 | 显示全部楼层
Chemistry and Pharmacology of GPBAR1 and FXR Selective Agonists, Dual Agonists, and Antagonists,lectively target GPBAR1 or FXR..In this review, we summarize the most recent acquisition on natural, semisynthetic, and synthetic steroidal and nonsteroidal ligands, able to interact with FXR and GPBAR1.
发表于 2025-3-23 08:08:18 | 显示全部楼层
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