The current state of GPCR‐based drug discovery to treat metabolic disease
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P. Emmerson | F. Willard | M. Statnick | K. Sloop | Francis S Willard | Paul J Emmerson | Kyle W Sloop | Michael A Statnick
[1] M. Rodbell. The problem of identifying the glucagon receptor. , 1973, Federation proceedings.
[2] J. Raufman,et al. Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom. Further evidence for an exendin receptor on dispersed acini from guinea pig pancreas. , 1992, The Journal of biological chemistry.
[3] L. Lasagna,et al. Long‐term weight control study I (weeks 0 to 34) , 1992, Clinical pharmacology and therapeutics.
[4] F J Grant,et al. Expression cloning and signaling properties of the rat glucagon receptor. , 1993, Science.
[5] C. Bogardus,et al. Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene. , 1995, The New England journal of medicine.
[6] G. Gessa,et al. Appetite suppression and weight loss after the cannabinoid antagonist SR 141716. , 1998, Life sciences.
[7] B. Lowell,et al. Mice expressing human but not murine beta3-adrenergic receptors under the control of human gene regulatory elements. , 1998, Diabetes.
[8] P. Burn,et al. Melanocortin-4 receptor: A novel signalling pathway involved in body weight regulation , 1999, International Journal of Obesity.
[9] S. Toubro,et al. Effect of a 28-d treatment with L-796568, a novel beta(3)-adrenergic receptor agonist, on energy expenditure and body composition in obese men. , 2002, The American journal of clinical nutrition.
[10] Rachel L. Batterham,et al. Gut hormone PYY3-36 physiologically inhibits food intake , 2002, Nature.
[11] M. Fujimiya,et al. Antagonism of ghrelin receptor reduces food intake and body weight gain in mice , 2003, Gut.
[12] B. Lowell,et al. β-Adrenergic Receptors, Diet-induced Thermogenesis, and Obesity* , 2003, Journal of Biological Chemistry.
[13] J. Holst,et al. Double incretin receptor knockout (DIRKO) mice reveal an essential role for the enteroinsular axis in transducing the glucoregulatory actions of DPP-IV inhibitors. , 2004, Diabetes.
[14] N. Porksen,et al. Hepatic and glucagon-like peptide-1-mediated reversal of diabetes by glucagon receptor antisense oligonucleotide inhibitors. , 2004, The Journal of clinical investigation.
[15] Bengt Långström,et al. Neuropeptide Y5 receptor antagonism does not induce clinically meaningful weight loss in overweight and obese adults. , 2006, Cell metabolism.
[16] D. Drucker. The biology of incretin hormones. , 2006, Cell metabolism.
[17] R. Lefkowitz,et al. Seven transmembrane receptors: something old, something new , 2007, Acta physiologica.
[18] A. A. Jensen,et al. Allosteric Modulation of the Calcium-Sensing Receptor , 2007, Current neuropharmacology.
[19] B. Ahrén. Dipeptidyl Peptidase-4 Inhibitors , 2007, Diabetes Care.
[20] Bonnie J. Ahr. Dipeptidyl Peptidase-4 Inhibitors Clinical data and clinical implications , 2007 .
[21] P. Piazza,et al. Effects of CB1 antagonist on the control of metabolic functions in obese type 2 diabetic patients. , 2007, Diabetes & metabolism.
[22] Lawrence A Leiter,et al. Stimulation of Cholecystokinin‐A Receptors With GI181771X does not Cause Weight Loss in Overweight or Obese Patients , 2008, Clinical pharmacology and therapeutics.
[23] H. Davis,et al. Lack of FFAR1/GPR40 Does Not Protect Mice From High-Fat Diet–Induced Metabolic Disease , 2008, Diabetes.
[24] K. Gadde,et al. Rational Design of a Combination Medication for the Treatment of Obesity , 2009, Obesity.
[25] Y. Tao. Mutations in melanocortin-4 receptor and human obesity. , 2009, Progress in molecular biology and translational science.
[26] T. Kowalski,et al. GPR119 is required for physiological regulation of glucagon-like peptide-1 secretion but not for metabolic homeostasis. , 2009, The Journal of endocrinology.
[27] R. DeFronzo,et al. Skeletal Muscle Insulin Resistance Is the Primary Defect in Type 2 Diabetes , 2009, Diabetes Care.
[28] G. Bray,et al. Potent and Selective Agonism of the Melanocortin Receptor 4 With MK‐0493 Does Not Induce Weight Loss in Obese Human Subjects: Energy Intake Predicts Lack of Weight Loss Efficacy , 2009, Clinical pharmacology and therapeutics.
[29] Charles C. Persinger,et al. How to improve R&D productivity: the pharmaceutical industry's grand challenge , 2010, Nature Reviews Drug Discovery.
[30] S. Kliewer,et al. The G protein-coupled bile acid receptor, TGR5, stimulates gallbladder filling. , 2011, Molecular endocrinology.
[31] P. Rorsman,et al. The Effects of TAK-875, a Selective G Protein-Coupled Receptor 40/Free Fatty Acid 1 Agonist, on Insulin and Glucagon Secretion in Isolated Rat and Human Islets , 2012, Journal of Pharmacology and Experimental Therapeutics.
[32] Sean P. Brown,et al. A Potent Class of GPR40 Full Agonists Engages the EnteroInsular Axis to Promote Glucose Control in Rodents , 2012, PloS one.
[33] L. Xi,et al. Effects of JNJ‐38431055, a novel GPR119 receptor agonist, in randomized, double‐blind, placebo‐controlled studies in subjects with type 2 diabetes , 2012, Diabetes, obesity & metabolism.
[34] R. Coppari,et al. Direct leptin action on POMC neurons regulates glucose homeostasis and hepatic insulin sensitivity in mice. , 2012, The Journal of clinical investigation.
[35] Randy J. Seeley,et al. Cooperation between brain and islet in glucose homeostasis and diabetes , 2013, Nature.
[36] Sang-Uk Kang,et al. GPR119 agonists: a promising approach for T2DM treatment? A SWOT analysis of GPR119. , 2013, Drug discovery today.
[37] D. Nunez,et al. Safety, Pharmacokinetics, and Pharmacodynamic Effects of a Selective TGR5 Agonist, SB‐756050, in Type 2 Diabetes , 2013, Clinical pharmacology in drug development.
[38] J. Jaén,et al. Evaluation of AMG 076, a potent and selective MCHR1 antagonist, in rodent and primate obesity models , 2013, Pharmacology research & perspectives.
[39] Bin Yang,et al. Unimolecular Dual Incretins Maximize Metabolic Benefits in Rodents, Monkeys, and Humans , 2013, Science Translational Medicine.
[40] J. Holst,et al. Exaggerated Glucagon-Like Peptide 1 Response Is Important for Improved β-Cell Function and Glucose Tolerance After Roux-en-Y Gastric Bypass in Patients With Type 2 Diabetes , 2013, Diabetes.
[41] J. Shaw,et al. Diabetes: a 21st century challenge. , 2014, The lancet. Diabetes & endocrinology.
[42] R. Evans,et al. A Gpr120 Selective Agonist Improves Insulin Resistance and Chronic Inflammation , 2014, Nature Medicine.
[43] L. Corsino,et al. Gut Hormone Pharmacology of a Novel GPR119 Agonist (GSK1292263), Metformin, and Sitagliptin in Type 2 Diabetes Mellitus: Results from Two Randomized Studies , 2014, PloS one.
[44] D. Dodick,et al. Safety and efficacy of LY2951742, a monoclonal antibody to calcitonin gene-related peptide, for the prevention of migraine: a phase 2, randomised, double-blind, placebo-controlled study , 2014, The Lancet Neurology.
[45] Kira B. Harris,et al. Efficacy and tolerability of glucagon-like peptide-1 receptor agonists in patients with type 2 diabetes mellitus , 2015, Therapeutic advances in endocrinology and metabolism.
[46] K. Kaku,et al. Efficacy and safety of fasiglifam (TAK-875), a G protein-coupled receptor 40 agonist, in Japanese patients with type 2 diabetes inadequately controlled by diet and exercise: a randomized, double-blind, placebo-controlled, phase III trial , 2015, Diabetes, obesity & metabolism.
[47] F. Gao,et al. GSK256073 acutely regulates NEFA levels via HCA2 agonism but does not achieve durable glycaemic control in type 2 diabetes. A randomised trial. , 2015, European journal of pharmacology.
[48] Kak‐Shan Shia,et al. A novel peripheral cannabinoid receptor 1 antagonist, BPR0912, reduces weight independently of food intake and modulates thermogenesis , 2015, Diabetes, obesity & metabolism.
[49] Jianhua Shen,et al. Discovery of Intestinal Targeted TGR5 Agonists for the Treatment of Type 2 Diabetes. , 2015, Journal of medicinal chemistry.
[50] Tamara S. Roman,et al. New genetic loci link adipose and insulin biology to body fat distribution , 2014, Nature.
[51] R. Cone,et al. RM-493, a melanocortin-4 receptor (MC4R) agonist, increases resting energy expenditure in obese individuals. , 2015, The Journal of clinical endocrinology and metabolism.
[52] Bryan L Roth,et al. Integrated Approaches for Genome-wide Interrogation of the Druggable Non-olfactory G Protein-coupled Receptor Superfamily* , 2015, The Journal of Biological Chemistry.
[53] A. Mancini,et al. GPR40 agonists for the treatment of type 2 diabetes: life after ‘TAKing’ a hit , 2015, Diabetes, obesity & metabolism.
[54] K. Clément,et al. Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist. , 2016, The New England journal of medicine.
[55] H. Stark,et al. Cherry-picked ligands at histamine receptor subtypes , 2016, Neuropharmacology.
[56] Elizabeth G. Mietlicki-Baase. Amylin-mediated control of glycemia, energy balance, and cognition , 2016, Physiology & Behavior.
[57] P. Sexton,et al. Glucagon-Like Peptide-1 and Its Class B G Protein–Coupled Receptors: A Long March to Therapeutic Successes , 2016, Pharmacological Reviews.
[58] G. Shulman,et al. The pathogenesis of insulin resistance: integrating signaling pathways and substrate flux. , 2016, The Journal of clinical investigation.
[59] D. Drucker. The Cardiovascular Biology of Glucagon-like Peptide-1. , 2016, Cell metabolism.
[60] Lawrence A Leiter,et al. Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes. , 2016, The New England journal of medicine.
[61] P. Blandina,et al. The histaminergic system as a target for the prevention of obesity and metabolic syndrome , 2016, Neuropharmacology.
[62] R. Unger,et al. Clinical Trials, Triumphs, and Tribulations of Glucagon Receptor Antagonists , 2016, Diabetes Care.
[63] C. Buning,et al. G Protein-Coupled Receptor 119 (GPR119) Agonists for the Treatment of Diabetes: Recent Progress and Prevailing Challenges. , 2016, Journal of medicinal chemistry.
[64] Tudor I. Oprea,et al. A comprehensive map of molecular drug targets , 2016, Nature Reviews Drug Discovery.
[65] Arthur Christopoulos,et al. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: G protein‐coupled receptors , 2017, British journal of pharmacology.
[66] Adam J Pawson,et al. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Enzymes , 2017, British journal of pharmacology.
[67] Adam J Pawson,et al. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Transporters , 2017, British journal of pharmacology.
[68] M. Tschöp,et al. The New Biology and Pharmacology of Glucagon. , 2017, Physiological reviews.
[69] Adam J Pawson,et al. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Nuclear hormone receptors , 2017, British journal of pharmacology.
[70] T. Schwartz,et al. Gq and Gs signaling acting in synergy to control GLP-1 secretion , 2017, Molecular and Cellular Endocrinology.
[71] F. Willard,et al. Regulation of Endogenous (Male) Rodent GLP-1 Secretion and Human Islet Insulin Secretion by Antagonism of Somatostatin Receptor 5 , 2017, Endocrinology.
[72] A. Howard,et al. GPR40 reduces food intake and body weight through GLP-1. , 2017, American journal of physiology. Endocrinology and metabolism.
[73] Margaret S. Wu,et al. GPR120 suppresses adipose tissue lipolysis and synergizes with GPR40 in antidiabetic efficacy[S] , 2017, Journal of Lipid Research.
[74] Alasdair J. G. Gray,et al. The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY , 2017, Nucleic Acids Res..