Peripheral metabolic actions of leptin

被引:148
作者
Muoio, DM
Dohm, GL
机构
[1] Duke Univ, Med Ctr, Durham, NC 27710 USA
[2] E Carolina Univ, Brody Sch Med, Greenville, NC USA
关键词
leptin; energy balance; obesity; type; 2; diabetes; lipid metabolism; beta-oxidation; triacylglycerol; glucose metabolism; insulin signalling; skeletal muscle; liver; pancreas; adipose tissue;
D O I
10.1053/beem.2002.0223
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The adipocyte-derived hormone, leptin, regulates food intake and systemic fuel metabolism; ob/ob mice, which lack functional leptin, exhibit an obesity syndrome that is similar to morbid obesity in humans. Leptin receptors are expressed most abundantly in the brain but are also present in several peripheral tissues. The role of leptin in controlling energy homeostasis has thus far focused on brain receptors and neuroendocrine pathways that regulate feeding behaviour and sympathetic nervous system activity. This chapter focuses on mounting evidence that leptin's effects on energy balance are also mediated by direct peripheral actions on key metabolic organs such as skeletal muscle, liver, pancreas and adipose tissue. Strong evidence indicates that peripheral leptin receptors regulate cellular lipid balance, favouring beta-oxidation over triacylglycerol storage. There are data to indicate that peripheral leptin also modulates glucose metabolism and insulin action; however, its precise role in controlling gluco-regulatory pathways remains uncertain and requires further investigation.
引用
收藏
页码:653 / 666
页数:14
相关论文
共 83 条
[1]   The stomach is a source of leptin [J].
Bado, A ;
Levasseur, S ;
Attoub, S ;
Kermorgant, S ;
Laigneau, JP ;
Bortoluzzi, MN ;
Moizo, L ;
Lehy, T ;
Guerre-Millo, M ;
Le Marchand-Brustel, Y ;
Lewin, MJM .
NATURE, 1998, 394 (6695) :790-793
[2]   Acute stimulation of glucose uptake by leptin in L6 muscle cells [J].
Bates, SH ;
Gardiner, JV ;
Jones, RB ;
Bloom, SR ;
Bailey, CJ .
HORMONE AND METABOLIC RESEARCH, 2002, 34 (03) :111-115
[3]   Leptin stimulates glucose transport and glycogen synthesis in C2C12 myotubes: Evidence for a PI3-kinase mediated effect [J].
Berti, L ;
Kellerer, M ;
Capp, E ;
Haring, HU .
DIABETOLOGIA, 1997, 40 (05) :606-609
[4]   Divergent signaling capacities of the long and short isoforms of the leptin receptor [J].
Bjorbaek, C ;
Uotani, S ;
da Silva, B ;
Flier, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32686-32695
[5]   The uncoupling proteins, a review [J].
Boss, O ;
Muzzin, P ;
Giacobino, JP .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1998, 139 (01) :1-9
[6]   Physiological increase in plasma leptin markedly inhibits insulin secretion in vivo [J].
Cases, JA ;
Gabriely, I ;
Ma, XH ;
Yang, XM ;
Michaeli, T ;
Fleischer, N ;
Rossetti, L ;
Barzilai, N .
DIABETES, 2001, 50 (02) :348-352
[7]   Leptin inhibits insulin-stimulated incorporation of glucose into lipids and stimulates glucose decarboxylation in isolated rat adipocytes [J].
Ceddia, RB ;
William, WN ;
Lima, FB ;
Curi, R .
JOURNAL OF ENDOCRINOLOGY, 1998, 158 (03) :R7-R9
[8]   Comparing effects of leptin and insulin on glucose metabolism in skeletal muscle: evidence for an effect of leptin on glucose uptake and decarboxylation [J].
Ceddia, RB ;
William, WN ;
Curi, R .
INTERNATIONAL JOURNAL OF OBESITY, 1999, 23 (01) :75-82
[9]   Leptin increases glucose transport and utilization in skeletal muscle in vitro [J].
Ceddia, RB ;
William, WN ;
Curi, R .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1998, 31 (05) :799-801
[10]   Leptin constrains acetylcholine-induced insulin secretion from pancreatic islets of ob/ob mice [J].
Chen, NG ;
Swick, AG ;
Romsos, DR .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) :1174-1179