PYY3-36 as an anti-obesity drug target

被引:84
作者
Boggiano, MM
Chandler, PC
Oswald, KD
Rodgers, RJ
Blundell, JE
Ishii, Y
Beattie, AH
Holch, P
Allison, DB
Schindler, M
Arndt, K
Rudolf, K
Mark, M
Schoelch, C
Joost, HG
Klaus, S
Thöne-Reineke, C
Benoit, SC
Seeley, RJ
Beck-Sickinger, AG
Koglin, N
Raun, K
Madsen, K
Wulff, BS
Stidsen, CE
Birringer, M
Kreuzer, OJ
Deng, XY
Whitcomb, DC
Halem, H
Taylor, J
Dong, J
Datta, R
Culler, M
Ortmann, S
Castañeda, TR
Tschöp, M
机构
[1] Univ Alabama Birmingham, Dept Psychol, Birmingham, AL 35294 USA
[2] Univ Leeds, Behav Neurosci Lab, Inst Psychol Sci, Leeds, W Yorkshire, England
[3] Univ Alabama Birmingham, Sect Stat Genet, Dept Biostat, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Clin Nutr Res Ctr, Birmingham, AL 35294 USA
[5] Boehringer Ingelheim Pharma GmbH & Co KG, Biberach, Germany
[6] German Inst Human Nutr, Potsdam, Germany
[7] Univ Med Berlin, Charite, Inst Pharmacol & Toxicol, Cardiovasc Res Ctr, Berlin, Germany
[8] Univ Cincinnati, Dept Psychiat, Genome Res Inst, Cincinnati, OH USA
[9] Univ Leipzig, Inst Biochem, D-7010 Leipzig, Germany
[10] Novo Nordisk AS, Discovery, Copenhagen, Denmark
[11] Peptides & Elephants GmbH, Potsdam, Germany
[12] Univ Pittsburgh, Dept Med, Div Gastroenterol Hepatol & Nutr, Pittsburgh, PA USA
[13] Biomeasure Inc, Ipsen Grp, Paris, France
[14] Biomeasure Inc, Ipsen Grp, Milford, MA USA
[15] Inst Zoo & Wildlife Res, Berlin, Germany
关键词
food intake; obesity; peptide YY; PYY; PYY(3-36); Y-2; receptor;
D O I
10.1111/j.1467-789X.2005.00218.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The neuropeptide Y (NPY)/peptide YY (PYY) system has been implicated in the physiology of obesity for several decades. More recently, Batterham et al. 2002 ignited enormous interest in PYY3-36, an endogenous Y2-receptor agonist, as a promising anti-obesity compound. Despite this interest, there have been remarkably few subsequent reports reproducing or extending the initial findings, while at the same time studies finding no anti-obesity effects have surfaced. Out of 41 different rodent studies conducted (in 16 independent labs worldwide), 33 (83%) were unable to reproduce the reported effects and obtained no change or sometimes increased food intake, despite use of the same experimental conditions (i.e. adaptation protocols, routes of drug administration and doses, rodent strains, diets, drug vendors, light cycles, room temperatures). Among studies by authors in the original study, procedural caveats are reported under which positive effects may be obtained. Currently, data speak against a sustained decrease in food intake, body fat, or body weight gain following PYY3-36 administration and make the previously suggested role of the hypothalamic melanocortin system unlikely as is the existence of PYY deficiency in human obesity. We review the studies that are in the public domain which support or challenge PYY3-36 as a potential anti-obesity target.
引用
收藏
页码:307 / 322
页数:16
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