Latest approaches for the treatment of obesity

被引:92
作者
Jackson, V. Margaret [1 ]
Breen, Danna M. [1 ]
Fortin, Jean-Philippe [1 ]
Liou, Alice [1 ]
Kuzmiski, J. Brent [1 ]
Loomis, A. Katrina [2 ]
Rives, Marie-Laure [1 ]
Shah, Bhavik [1 ]
Carpino, Philip A. [3 ]
机构
[1] Pfizer PharmaTherapeut, Cardiovasc & Metab Dis Res Unit, Cambridge, MA 02139 USA
[2] Pfizer PharmaTherapeut, Clin Res, Groton, CT 06340 USA
[3] Pfizer PharmaTherapeut, Cardiovasc & Metab Dis Med Chem, Cambridge, MA 02139 USA
关键词
central nervous system; devices; FGF21; FGFR1c/beta-Klotho; GLP-1; GLP-1R; LepRb; leptin system; MC4R; melanocortin system; microbiome; obesity; GLUCAGON-LIKE PEPTIDE-1; ENDOPLASMIC-RETICULUM STRESS; BLOOD-BRAIN-BARRIER; EARLY-ONSET OBESITY; BODY-MASS INDEX; MELANOCORTIN-4; RECEPTOR; WEIGHT-LOSS; LEPTIN RECEPTOR; ENERGY-EXPENDITURE; CELL-SURFACE;
D O I
10.1517/17460441.2015.1044966
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Obesity is a body weight disorder characterized by excess adiposity that increases the risk for developing co-morbidities such as type 2 diabetes. A large medical need exists for new anti-obesity treatments capable of promoting 10% or greater weight loss, with minimal side effects. Areas covered: The authors describe the application of monogenic forms of rare obesity and genome-wide association studies in selecting critical pathways for drug discovery. Furthermore, they review in detail several pathways and pharmacological targets in the central nervous system (e.g., the leptin-melanocortin axis, the opioid system, GLP-1/GLP-1 system, and FGF21/FGFR1c/beta-Klotho axis) that play an important role in the regulation of feeding behavior and energy homeostasis. Special focus is given to new strategies that engage well-known targets via novel mechanisms in order to circumvent issues seen with previous drug candidates that failed in the clinic. Finally, the authors discuss the recent developments around fixed-dose combinations, targeted polypharmacology, and non-traditional combinations of drugs and devices. Expert opinion: The future for new weight-loss approaches to treat obesity looks promising. Current therapies have shown modest effects on weight loss in the general obese population but will have greater impact in smaller homogeneous sub-populations of obese subjects using personalized medicine. Drug combinations that target multiple, complementary pathways have the potential to promote double-digit weight loss in a broader, heterogeneous patient population. Furthermore, the development of advanced subcutaneous delivery technologies has opened up opportunities to develop breakthrough peptide and biologic agents for the treatment of obesity.
引用
收藏
页码:825 / 839
页数:15
相关论文
共 171 条
[21]   Naltrexone/bupropion for obesity: An investigational combination pharmacotherapy for weight loss [J].
Billes, Sonja K. ;
Sinnayah, Puspha ;
Cowley, Michael A. .
PHARMACOLOGICAL RESEARCH, 2014, 84 :1-11
[22]   The role of SOCS-3 in leptin signaling and leptin resistance [J].
Bjorbæk, C ;
El-Haschimi, K ;
Frantz, JD ;
Flier, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) :30059-30065
[23]   Endogenous opioids and feeding behavior: a 30-year historical perspective [J].
Bodnar, RJ .
PEPTIDES, 2004, 25 (04) :697-725
[24]  
Caixas A, 2014, DRUG DES DEV THER, V8, P9
[25]   Naltrexone sustained-release/bupropion sustained-release for the management of obesity: review of the data to date [J].
Caixas, Assumpta ;
Albert, Lara ;
Capel, Ismael ;
Rigla, Mercedes .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2014, 8 :1419-1427
[26]   Targeting endoplasmic reticulum stress in metabolic disease [J].
Cao, Stewart Siyan ;
Kaufman, Randal J. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2013, 17 (04) :437-448
[27]  
Chambers E. S., 2014, GUT
[28]   RM-493, a Melanocortin-4 Receptor (MC4R) Agonist, Increases Resting Energy Expenditure in Obese Individuals [J].
Chen, Kong Y. ;
Muniyappa, Ranganath ;
Abel, Brent S. ;
Mullins, Katherine P. ;
Staker, Pamela ;
Brychta, Robert J. ;
Zhao, Xiongce ;
Ring, Michael ;
Psota, Tricia L. ;
Cone, Roger D. ;
Panaro, Brandon L. ;
Gottesdiener, Keith M. ;
Van der Ploeg, Lex H. T. ;
Reitman, Marc L. ;
Skarulis, Monica C. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2015, 100 (04) :1639-1645
[29]   Novel locus including FGF21 is associated with dietary macronutrient intake [J].
Chu, Audrey Y. ;
Workalemahu, Tsegaselassie ;
Paynter, Nina P. ;
Rose, Lynda M. ;
Giulianini, Franco ;
Tanaka, Toshiko ;
Ngwa, Julius S. ;
Qi, Qibin ;
Curhan, Gary C. ;
Rimm, Eric B. ;
Hunter, David J. ;
Pasquale, Louis R. ;
Ridker, Paul M. ;
Hu, Frank B. ;
Chasman, Daniel I. ;
Qi, Lu .
HUMAN MOLECULAR GENETICS, 2013, 22 (09) :1895-1902
[30]  
Clemmensen C, 2015, EMBO MOL MED