Ginsenosides: chemistry, biosynthesis, analysis, and potential health effects

LP Christensen - Advances in food and nutrition research, 2008 - Elsevier
Ginsenosides are a special group of triterpenoid saponins that can be classified into two
groups by the skeleton of their aglycones, namely dammarane‐and oleanane‐type …

International union of basic and clinical pharmacology CXIII: Nuclear receptor superfamily—Update 2023

TP Burris, IMS de Vera, I Cote, CA Flaveny… - Pharmacological …, 2023 - Elsevier
The NR superfamily comprises 48 transcription factors in humans that control a plethora of
gene network programs involved in a wide range of physiologic processes. This review will …

The Synbiotic Combination of Akkermansia muciniphila and Quercetin Ameliorates Early Obesity and NAFLD through Gut Microbiota Resha** and Bile Acid …

M Juárez-Fernández, D Porras, P Petrov… - Antioxidants, 2021 - mdpi.com
Gut microbiota plays a key role in obesity and non-alcoholic fatty liver disease (NAFLD), so
synbiotics could be a therapeutic alternative. We aim to evaluate a nutritional intervention …

Chemogenomics for NR1 nuclear hormone receptors

L Isigkeit, E Schallmayer, R Busch, L Brunello… - Nature …, 2024 - nature.com
Nuclear receptors (NRs) regulate transcription in response to ligand binding and NR
modulation allows pharmacological control of gene expression. Although some NRs are …

Nuclear receptors and their selective pharmacologic modulators

TP Burris, LA Solt, Y Wang, C Crumbley… - Pharmacological …, 2013 - Elsevier
Nuclear receptors are ligand-activated transcription factors and include the receptors for
steroid hormones, lipophilic vitamins, sterols, and bile acids. These receptors serve as …

Review of the Structural and Dynamic Mechanisms of PPARγ Partial Agonism

AJ Kroker, JB Bruning - PPAR research, 2015 - Wiley Online Library
PPARγ (peroxisome proliferator activated receptor γ) is a ligand activated transcription factor
of the nuclear receptor superfamily that controls the expression of a variety of genes …

Peroxisome proliferator-activated receptor structures: ligand specificity, molecular switch and interactions with regulators

V Zoete, A Grosdidier, O Michielin - … Acta (BBA)-Molecular and Cell Biology …, 2007 - Elsevier
Peroxisome proliferator-activated receptors (PPARs) compose a family of nuclear receptors
that mediate the effects of lipidic ligands at the transcriptional level. In this review, we …

Partial agonists activate PPARγ using a helix 12 independent mechanism

JB Bruning, MJ Chalmers, S Prasad, SA Busby… - Structure, 2007 - cell.com
Binding to helix 12 of the ligand-binding domain of PPARγ is required for full agonist activity.
Previously, the degree of stabilization of the activation function 2 (AF-2) surface was thought …

The endocrine disruptor monoethyl-hexyl-phthalate is a selective peroxisome proliferator-activated receptor γ modulator that promotes adipogenesis

JN Feige, L Gelman, D Rossi, V Zoete, R Métivier… - Journal of Biological …, 2007 - jbc.org
The ability of pollutants to affect human health is a major concern, justified by the wide
demonstration that reproductive functions are altered by endocrine disrupting chemicals …

Medium chain fatty acids are selective peroxisome proliferator activated receptor (PPAR) γ activators and pan-PPAR partial agonists

MV Liberato, AS Nascimento, SD Ayers, JZ Lin… - PloS one, 2012 - journals.plos.org
Thiazolidinediones (TZDs) act through peroxisome proliferator activated receptor (PPAR) γ
to increase insulin sensitivity in type 2 diabetes (T2DM), but deleterious effects of these …