Modulation of Ingestive Behavior and Gastrointestinal Motility by Ghrelin in Diabetic Animals and Humans

被引:85
作者
Chen, Chih-Yen [1 ,2 ]
Fujimiya, Mineko [3 ]
Laviano, Alessandro [4 ]
Chang, Full-Young [1 ,2 ]
Lin, Han-Chieh [1 ,2 ]
Lee, Shou-Doug [1 ,2 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Fac Med, Taipei 112, Taiwan
[3] Sapporo Med Univ, Sch Med, Dept Anat, Sapporo, Hokkaido, Japan
[4] Univ Roma La Sapienza, Dept Clin Med, Rome, Italy
关键词
acyl ghrelin; diabetes mellitus; feeding; gastrointestinal motility; ghrelin O-acyltransferase; INSULIN-SECRETION; ACYLATED PEPTIDE; GENE-PRODUCTS; FOOD-INTAKE; GLUCOSE; RATS; COMPLICATIONS; RECEPTORS; APPETITE; TRACTS;
D O I
10.1016/S1726-4901(10)70048-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acyl ghrelin, a 28-amino acid peptide hormone, is the endogenous cognate ligand for the growth hormone secretagogue receptor. Ghrelin is involved in stimulating growth hormone release, eliciting feeding behavior, inducing adiposity and stimulating gastrointestinal motility. Ghrelin is unique for its post-translational modification of O-n-octanoylation at serine 3 through ghrelin O-acyltransferase, and is the only peripheral signal to enhance food intake. Plasma ghrelin levels manifest "biphasic changes" in diabetes mellitus (DM). In the early stage of DM, the stomach significantly increases the secretion of ghrelin into the plasma, and elevated plasma ghrelin levels are correlated with diabetic hyperphagic feeding and accelerated gastrointestinal motility. In the late stage of DM, plasma ghrelin levels may be lower, which might be linked with anorexia/muscle wasting, delayed gastrointestinal transit, and even gastroparesis. Therefore, the unique ghrelin system may be the most important player compared to the other hindgut hormones participating in the "enteroinsular axis". Further studies using either knockdown or knockout of ghrelin gene products and ghrelin O-acyltransferase may unravel the pathogenesis of DM, and show benefits in combating this disease and metabolic syndrome. [J Chin Med Assoc 2010:73(5):225-229]
引用
收藏
页码:225 / 229
页数:5
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