Effects of high-fat feeding and fasting on ghrelin expression in the mouse stomach

被引:56
作者
Moesgaard, SG
Ahrén, B
Carr, RD
Gram, DX
Brand, CL
Sundler, F
机构
[1] Lund Univ, Dept Med, Lund, Sweden
[2] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[3] Lund Univ, Dept Physiol Sci, Lund, Sweden
关键词
ghrelin; fasting; high fat; insulin resistance; mouse; immunocytochemistry; in situ hybridization;
D O I
10.1016/j.regpep.2004.03.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ghrelin is a peptide identified as an endogenous ligand for the growth hormone secretagogue receptor. Studies have shown that ghrelin stimulates growth hormone, promotes food intake and decreases energy expenditure. Furthermore, feeding status seems to influence plasma ghrelin levels, as these are increased during fasting, whereas feeding and oral glucose intake reduce plasma ghrelin. This study examined whether standardized obesity and fasting affect cellular expression of ghrelin. Specimens from the gastrointestinal tract of fed or 18-h fasted, low-fat or high-fat fed (10 weeks on diet) C5713L/6J mice were studied by immunocytochemistry (ICC) for ghrelin and in situ hybridization (ISH) for ghrelin mRNA. Ghrelin was expressed in especially the corpus but also the antrum of the stomach of all groups studied. Cells positive for ghrelin and ghrelin mRNA in the stomach were reduced in high-fat fed mice. In contrast, ghrelin expression was not affected by fasting. The reduction in ghrelin expression in the high-fat fed mice was associated with a reduction in plasma levels of ghrelin, whereas after fasting, when expression rate was not altered, there was an increase in plasma ghrelin. In conclusion, ghrelin is highly expressed in the corpus and antrum of the stomach of C57BL/6J mice. This expression is reduced in obesity, whereas fasting has no effect. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:261 / 267
页数:7
相关论文
共 27 条
[1]   Dissociated insulinotropic sensitivity to glucose and carbachol in high-fat diet-induced insulin resistance in C57BL/6J mice [J].
Ahren, B ;
Simonsson, E ;
Scheurink, AJW ;
Mulder, H ;
Myrsen, U ;
Sundler, F .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (01) :97-106
[2]  
Ahrén B, 1999, ACTA PHYSIOL SCAND, V165, P233, DOI 10.1046/j.1365-201x.1999.00518.x
[3]   Delayed short-term secretory regulation of ghrelin in obese animals: Evidenced by a specific RIA for the active form of ghrelin [J].
Ariyasu, H ;
Takaya, K ;
Hosoda, H ;
Iwakura, H ;
Ebihara, K ;
Mori, K ;
Ogawa, Y ;
Hosoda, K ;
Akamizu, T ;
Kojima, M ;
Kangawa, K ;
Nakao, K .
ENDOCRINOLOGY, 2002, 143 (09) :3341-3350
[4]   Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Yuzuriha, H ;
Nagata, T ;
Ueno, N ;
Makino, S ;
Fujimiya, M ;
Niijima, A ;
Fujino, MA ;
Kasuga, M .
GASTROENTEROLOGY, 2001, 120 (02) :337-345
[5]   Antagonism of ghrelin receptor reduces food intake and body weight gain in mice [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Katsuura, G ;
Fujimiya, M ;
Fujino, MA ;
Kasuga, M .
GUT, 2003, 52 (07) :947-952
[6]   Ghrelin, macronutrient intake and dietary preferences in Long-Evans rats [J].
Beck, B ;
Musse, N ;
Stricker-Krongrad, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 292 (04) :1031-1035
[7]   Ghrelin, a novel growth hormone-releasing acylated peptide, is synthesized in a distinct endocrine cell type in the gastrointestinal tracts of rats and humans [J].
Date, Y ;
Kojima, M ;
Hosoda, H ;
Sawaguchi, A ;
Mondal, MS ;
Suganuma, T ;
Matsukura, S ;
Kangawa, K ;
Nakazato, M .
ENDOCRINOLOGY, 2000, 141 (11) :4255-4261
[8]   Glucose-mediated glucose disposal in insulin-resistant normoglycemic relatives of type 2 diabetic patients [J].
Henriksen, JE ;
Levin, K ;
Thye-Ronn, P ;
Alford, F ;
Hother-Nielsen, O ;
Holst, JJ ;
Beck-Nielsen, H .
DIABETES, 2000, 49 (07) :1209-1218
[9]   Ghrelin is a growth-hormone-releasing acylated peptide from stomach [J].
Kojima, M ;
Hosoda, H ;
Date, Y ;
Nakazato, M ;
Matsuo, H ;
Kangawa, K .
NATURE, 1999, 402 (6762) :656-660
[10]   Ghrelin, a new gastrointestinal endocrine peptide that stimulates insulin secretion: Enteric distribution, ontogeny, influence of endocrine, and dietary manipulations [J].
Lee, HM ;
Wang, GY ;
Englander, EW ;
Kojima, M ;
Greeley, GH .
ENDOCRINOLOGY, 2002, 143 (01) :185-190