Latest approaches for the treatment of obesity

被引:85
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
    Billes, Sonja K.
    Sinnayah, Puspha
    Cowley, Michael A.
    [J]. PHARMACOLOGICAL RESEARCH, 2014, 84 : 1 - 11
  • [22] The role of SOCS-3 in leptin signaling and leptin resistance
    Bjorbæk, C
    El-Haschimi, K
    Frantz, JD
    Flier, JS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) : 30059 - 30065
  • [23] Endogenous opioids and feeding behavior: a 30-year historical perspective
    Bodnar, RJ
    [J]. 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
    Caixas, Assumpta
    Albert, Lara
    Capel, Ismael
    Rigla, Mercedes
    [J]. DRUG DESIGN DEVELOPMENT AND THERAPY, 2014, 8 : 1419 - 1427
  • [26] Targeting endoplasmic reticulum stress in metabolic disease
    Cao, Stewart Siyan
    Kaufman, Randal J.
    [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
    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.
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2015, 100 (04) : 1639 - 1645
  • [29] Novel locus including FGF21 is associated with dietary macronutrient intake
    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
    [J]. HUMAN MOLECULAR GENETICS, 2013, 22 (09) : 1895 - 1902
  • [30] Clemmensen C, 2015, EMBO MOL MED