ABSTRACT
Metabolites produced in the human gut are known modulators of host immunity. However, large-scale identification of metabolite-host receptor interactions remains a daunting challenge. Here, we employed computational approaches to identify 983 potential metabolite-target interactions using the Inflammatory Bowel Disease (IBD) cohort dataset of the Human Microbiome Project 2 (HMP2). Using a consensus of multiple machine learning methods, we ranked metabolites based on importance to IBD, followed by virtual ligand-based screening to identify possible human targets and adding evidence from compound assay, differential gene expression, pathway enrichment, and genome-wide association studies. We confirmed known metabolite-target pairs such as nicotinic acid-GPR109a or linoleoyl ethanolamide-GPR119 and inferred interactions of interest including oleanolic acid-GABRG2 and alpha-CEHC-THRB. Eleven metabolites were tested for bioactivity in vitro using human primary cell-types. By expanding the universe of possible microbial metabolite-host protein interactions, we provide multiple drug targets for potential immune-therapies.
Subject(s)
Anti-Inflammatory Agents/pharmacology , Bacteria/metabolism , Drug Discovery , Gastrointestinal Agents/pharmacology , Gastrointestinal Microbiome , Inflammatory Bowel Diseases/drug therapy , Machine Learning , Protein Interaction Maps , Bacteria/immunology , Cells, Cultured , Data Mining , Databases, Factual , Gene Expression Profiling , Host-Pathogen Interactions , Humans , Inflammatory Bowel Diseases/immunology , Inflammatory Bowel Diseases/metabolism , Inflammatory Bowel Diseases/microbiology , Ligands , Metabolome , Metabolomics , Molecular Targeted Therapy , Signal Transduction , TranscriptomeABSTRACT
Modulation of gastrointestinal nutrient sensing pathways provides a promising a new approach for the treatment of metabolic diseases including diabetes and obesity. The calcium-sensing receptor has been identified as a key receptor involved in mineral and amino acid nutrient sensing and thus is an attractive target for modulation in the intestine. Herein we describe the optimization of gastrointestinally restricted calcium-sensing receptor agonists starting from a 3-aminopyrrolidine-containing template leading to the identification of GI-restricted agonist 19 (GSK3004774).
Subject(s)
Receptors, Calcium-Sensing/agonists , Animals , Calcium/metabolism , Cell Membrane Permeability/drug effects , Dogs , Gastrointestinal Tract/metabolism , HEK293 Cells , Humans , Madin Darby Canine Kidney Cells , Pyrrolidines/chemistry , Pyrrolidines/metabolism , Pyrrolidines/pharmacology , Receptors, Calcium-Sensing/genetics , Receptors, Calcium-Sensing/metabolism , Structure-Activity RelationshipABSTRACT
Tapinarof (GSK2894512) is a naturally derived topical treatment with demonstrated efficacy for patients with psoriasis and atopic dermatitis, although the biologic target and mechanism of action had been unknown. We demonstrate that the anti-inflammatory properties of tapinarof are mediated through activation of the aryl hydrocarbon receptor (AhR). We show that tapinarof binds and activates AhR in multiple cell types, including cells of the target tissue-human skin. In addition, tapinarof moderates proinflammatory cytokine expression in stimulated peripheral blood CD4+ T cells and ex vivo human skin, and impacts barrier gene expression in primary human keratinocytes; both of these processes are likely to be downstream of AhR activation based on current evidence. That the anti-inflammatory properties of tapinarof derive from AhR agonism is conclusively demonstrated using the mouse model of imiquimod-induced psoriasiform skin lesions. Topical treatment of AhR-sufficient mice with tapinarof leads to compound-driven reductions in erythema, epidermal thickening, and tissue cytokine levels. In contrast, tapinarof has no impact on imiquimod-induced skin inflammation in AhR-deficient mice. In summary, these studies identify tapinarof as an AhR agonist and confirm that its efficacy is dependent on AhR.
Subject(s)
Basic Helix-Loop-Helix Transcription Factors/agonists , Dermatitis, Atopic/drug therapy , Inflammation/drug therapy , Psoriasis/drug therapy , Receptors, Aryl Hydrocarbon/agonists , Resorcinols/administration & dosage , Stilbenes/administration & dosage , Administration, Topical , Animals , Cells, Cultured , Cytokines/metabolism , Dermatitis, Atopic/metabolism , Dermatitis, Atopic/pathology , Disease Models, Animal , Humans , Inflammation/metabolism , Inflammation/pathology , Mice , Psoriasis/metabolism , Psoriasis/pathology , Skin/drug effects , Skin/metabolism , Skin/pathologyABSTRACT
The long chain free fatty acid receptor 4 (FFA4/GPR120) has recently been recognized as lipid sensor playing important roles in nutrient sensing and inflammation and thus holds potential as a therapeutic target for type 2 diabetes and metabolic syndrome. To explore the effects of stimulating this receptor in animal models of metabolic disease, we initiated work to identify agonists with appropriate pharmacokinetic properties to support progression into in vivo studies. Extensive SAR studies of a series of phenylpropanoic acids led to the identification of compound 29, a FFA4 agonist which lowers plasma glucose in two preclinical models of type 2 diabetes.
Subject(s)
Phenylpropionates/pharmacology , Receptors, G-Protein-Coupled/agonists , Animals , Blood Glucose/drug effects , Diabetes Mellitus, Type 2/drug therapy , Disease Models, Animal , Humans , Male , Mice , Phenylpropionates/chemistry , Phenylpropionates/pharmacokinetics , Phenylpropionates/therapeutic use , Protein Binding/drug effects , Rats , Receptors, G-Protein-Coupled/metabolism , Structure-Activity RelationshipABSTRACT
The identification of a low-permeability scavenger receptor BI (SR-BI) inhibitor starting from the ITX-5061 template is described. Structure-activity and structure-permeability relationships were assessed for analogs leading to the identification of compound 8 as a potent and nonabsorbable SR-BI inhibitor.
Subject(s)
Phenylenediamines/pharmacology , Scavenger Receptors, Class B/antagonists & inhibitors , Sulfonamides/pharmacology , Animals , Dogs , Dose-Response Relationship, Drug , Humans , Madin Darby Canine Kidney Cells , Molecular Structure , Organ Specificity , Phenylenediamines/administration & dosage , Phenylenediamines/chemistry , Rats , Structure-Activity Relationship , Sulfonamides/administration & dosage , Sulfonamides/chemistryABSTRACT
The exploration of a diarylsulfonamide series of free fatty acid receptor 4 (FFA4/GPR120) agonists is described. This work led to the identification of selective FFA4 agonist 8 (GSK137647A) and selective FFA4 antagonist 39. The in vitro profile of compounds 8 and 39 is presented herein.
Subject(s)
Receptors, G-Protein-Coupled/agonists , Sulfonamides/pharmacology , Animals , Cell Line , Dose-Response Relationship, Drug , HEK293 Cells , Humans , Insulin/agonists , Mice , Molecular Structure , Structure-Activity Relationship , Sulfonamides/chemical synthesis , Sulfonamides/chemistryABSTRACT
A series of 3-aryl-4-isoxazolecarboxamides identified from a high-throughput screening campaign as novel, potent agonists of the human TGR5 G-protein-coupled receptor is described. Many analogues were readily accessible via solution-phase synthesis which resulted in the rapid identification of key structure-activity relationships (SAR), and the discovery of potent exemplars (up to pEC50=9). Details of the SAR and optimization of this series are presented herein.
Subject(s)
Acrylamides/chemical synthesis , Drug Design , Isoxazoles/chemical synthesis , Receptors, G-Protein-Coupled/agonists , Acrylamides/chemistry , Acrylamides/pharmacology , Humans , Isoxazoles/chemistry , Isoxazoles/pharmacology , Molecular Structure , Structure-Activity RelationshipABSTRACT
A series of 3-aryl-4-isoxazolecarboxamides identified from a high-throughput screening campaign as novel, potent small molecule agonists of the human TGR5 G-protein coupled receptor is described. Subsequent optimization resulted in the rapid identification of potent exemplars 6 and 7 which demonstrated improved GLP-1 secretion in vivo via an intracolonic dose coadministered with glucose challenge in a canine model. These novel TGR5 receptor agonists are potentially useful therapeutics for metabolic disorders such as type II diabetes and its associated complications.
Subject(s)
Isoxazoles/pharmacology , Receptors, G-Protein-Coupled/agonists , Amides/chemistry , Amides/pharmacokinetics , Amides/pharmacology , Animals , Diabetes Mellitus, Type 2/drug therapy , Diabetes Mellitus, Type 2/metabolism , Disease Models, Animal , Dogs , Glucagon-Like Peptide 1/metabolism , Glucose/administration & dosage , Humans , Isoxazoles/chemistry , Isoxazoles/pharmacokinetics , RatsABSTRACT
The melanophore bioassay is a robust, sensitive, and versatile procedure for screening G protein-coupled receptors in a variety of formats. Because melanophores contain a wide variety of G proteins, they can be employed as a sensitive, real-time response system for studying transfected receptors and for defining equilibria for drug effects. This assay can be run in 96-well microtiter plates or in open-lawn 1536 format, and can yield conventional agonist-antagonist as well as constitutive assays.
Subject(s)
Drug Evaluation, Preclinical/methods , Melanophores/drug effects , Receptors, G-Protein-Coupled/physiology , Animals , Cell Line , Melanophores/physiology , Xenopus laevisABSTRACT
Screening in a 'well-less' or lawn format provides a means to screen large compound collections against many targets in a fast, versatile and cost effective manner. The development of generic lawn format assays to screen various gene families against large compound collections should facilitate the identification of hits and tools to use in drug discovery and chemogenomic endeavours. Lawn format holds particular promise for screening GPCRs and selected enzyme families with potential use in other gene families.
Subject(s)
Combinatorial Chemistry Techniques/methods , Drug Evaluation, Preclinical/methods , Animals , Anti-Infective Agents/chemical synthesis , Anti-Infective Agents/pharmacology , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Cells, Cultured , Drug Design , Enzymes/chemistry , Humans , Protein BindingABSTRACT
A method for rapidly evaluating functional interactions between ligands and G-protein--coupled receptors has been developed. The technology is based on the ability of animals to change color by controlling the position of pigmented organelles within skin cells called melanophores. cDNA coding for a receptor to be studied is expressed in immortalized frog melanophores. Stimulation of a receptor that normally functions to activate either adenyl cyclase or phospholipase C induces centrifugal melanosome translocation and cell darkening. Conversely, application of an agonist to cells expressing a receptor that operates to inhibit adenyl cyclase induces centripetal pigment movement and cell lightening. The simple optical change can be used to investigate ligand-receptor interactions at several levels, including single-cell analysis and high-throughput chemical screening. Current efforts are focused on (1) identifying small peptides that activate or block thromboxane. A(2) and platelet-activating factor (PAF) receptors and (2) cloning eicosanoid receptors.