Potential therapies based on antidiabetic peptides

被引:10
作者
Billyard, Tom
McTernan, Philip [2 ]
Kumar, Sudhesh [1 ]
机构
[1] Univ Warwick, Warwick Med Sch, Clin Sci Res Inst, Coventry CV4 7AL, W Midlands, England
[2] Univ Warwick, Warwick Med Sch, Univ Hosp, Coventry CV2 2DX, W Midlands, England
关键词
type-2; diabetes; obesity; leptin; adiponectin; obestatin; peptide YY;
D O I
10.1016/j.beem.2007.07.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since adipose tissue was shown to be more than a storage organ, the many cytokines it produces have been identified, along with their roles in energy homeostasis, appetite, and insulin resistance. Concurrently, numerous gut hormones with a diversity of effects have been discovered. They include, amongst many others, peptide YY, ghrelin and oxyntomodulin. As these peptides have been investigated, the potential for their use as novel anti-obesity and antidiabetic therapies has been realized. In this chapter we describe the actions of four of the peptides that have been proposed as the basis for promising new therapies for diabetes: leptin, adiponectin, obestatin and peptide YY They each have an effect on appetite and, directly or indirectly, on glucose metabolism. We synthesize available data for these peptides and consider the therapeutic potential of each.
引用
收藏
页码:641 / 655
页数:15
相关论文
共 100 条
[91]   Generation of globular fragment of adiponectin by leukocyte elastase secreted by monocytic cell line THP-1 [J].
Waki, H ;
Yamauchi, T ;
Kamon, J ;
Kita, S ;
Ito, Y ;
Hada, Y ;
Uchida, S ;
Tsuchida, A ;
Takekawa, S ;
Kadowaki, T .
ENDOCRINOLOGY, 2005, 146 (02) :790-796
[92]   Impaired multimerization of human adiponectin mutants associated with diabetes - Molecular structure and multimer formation of adiponectin [J].
Waki, H ;
Yamauchi, T ;
Kamon, J ;
Ito, Y ;
Uchida, S ;
Kita, S ;
Hara, K ;
Hada, Y ;
Vasseur, F ;
Froguel, P ;
Kimura, S ;
Nagai, R ;
Kadowaki, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (41) :40352-40363
[93]   Adiponectin receptor 1 gene (ADIPOR1) as a candidate for type 2 diabetes and insulin resistance [J].
Wang, H ;
Zhang, HL ;
Jia, YW ;
Zhang, ZX ;
Craig, R ;
Wang, XQ ;
Elbein, SC .
DIABETES, 2004, 53 (08) :2132-2136
[94]   Microanalysis of eating behavior of three leptin deficient adults treated with leptin therapy [J].
Williamson, DA ;
Ravussin, E ;
Wong, ML ;
Wagner, A ;
DiPaoli, A ;
Caglayan, S ;
Ozata, M ;
Martin, C ;
Walden, H ;
Arnett, C ;
Licinio, J .
APPETITE, 2005, 45 (01) :75-80
[95]   Plasma leptin and prognosis in patients with established coronary atherosclerosis [J].
Wolk, R ;
Berger, P ;
Lennon, RJ ;
Brilakis, ES ;
Johnson, BD ;
Somers, VK .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 44 (09) :1819-1824
[96]   Adiponectin, an adipocyte-derived protein, predicts future insulin resistance: Two-year follow-up study in Japanese population [J].
Yamamoto, Y ;
Hirose, H ;
Saito, I ;
Nishikai, K ;
Saruta, T .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (01) :87-90
[97]   Cloning of adiponectin receptors that mediate antidiabetic metabolic effects [J].
Yamauchi, T ;
Kamon, J ;
Ito, Y ;
Tsuchida, A ;
Yokomizo, T ;
Kita, S ;
Sugiyama, T ;
Miyagishi, M ;
Hara, K ;
Tsunoda, M ;
Murakami, K ;
Ohteki, T ;
Uchida, S ;
Takekawa, S ;
Waki, H ;
Tsuno, NH ;
Shibata, Y ;
Terauchi, Y ;
Froguel, P ;
Tobe, K ;
Koyasu, S ;
Taira, K ;
Kitamura, T ;
Shimizu, T ;
Nagai, R ;
Kadowaki, T .
NATURE, 2003, 423 (6941) :762-769
[98]   Targeted disruption of AdipoR1 and AdipoR2 causes abrogation of adiponectin binding and metabolic actions [J].
Yamauchi, Toshimasa ;
Nio, Yasunori ;
Maki, Toshiyuki ;
Kobayashi, Masaki ;
Takazawa, Takeshi ;
Iwabu, Masato ;
Okada-Iwabu, Miki ;
Kawamoto, Sachiko ;
Kubota, Naoto ;
Kubota, Tetsuya ;
Ito, Yusuke ;
Kamon, Junji ;
Tsuchida, Atsushi ;
Kumagai, Katsuyoshi ;
Kozono, Hideki ;
Hada, Yusuke ;
Ogata, Hitomi ;
Tokuyama, Kumpei ;
Tsunoda, Masaki ;
Ide, Tomohiro ;
Murakami, Kouji ;
Awazawa, Motoharu ;
Takamoto, Iseki ;
Froguel, Philippe ;
Hara, Kazuo ;
Tobe, Kazuyuki ;
Nagai, Ryozo ;
Ueki, Kohjiro ;
Kadowaki, Takashi .
NATURE MEDICINE, 2007, 13 (03) :332-339
[99]   Obestatin, a peptide encoded by the ghrelin gene, opposes ghrelin's effects on food intake [J].
Zhang, JV ;
Ren, PG ;
Avsian-Kretchmer, O ;
Luo, CW ;
Rauch, R ;
Klein, C ;
Hsueh, AJW .
SCIENCE, 2005, 310 (5750) :996-999
[100]   POSITIONAL CLONING OF THE MOUSE OBESE GENE AND ITS HUMAN HOMOLOG [J].
ZHANG, YY ;
PROENCA, R ;
MAFFEI, M ;
BARONE, M ;
LEOPOLD, L ;
FRIEDMAN, JM .
NATURE, 1994, 372 (6505) :425-432