GIP receptor mRNA expression in different fat tissue depots in postmenopausal non-diabetic women

被引:59
作者
Ruclovich, Natalia
Kaiser, Simone
Engeli, Stefan
Osterhoff, Martin
Gogebakan, Ozlem
Bluher, Matthias
Pfeiffer, Andreas F. H.
机构
[1] German Inst Human Nutr Potsdam Rehbrucke, Dept Clin Nutr, D-14558 Nuthetal, Germany
[2] Charite Med Univ Berlin, Dept Endocrinol Diabet & Nutr, Berlin, Germany
[3] Franz Volhard Clin Res Ctr, Berlin, Germany
[4] HELIOS Clin Berlin, Berlin, Germany
[5] Univ Leipzig, Dept Internal Med 3, D-7010 Leipzig, Germany
关键词
gastric inhibitory polypeptide; GIP; GIP receptor; insulin resistance; central obesity;
D O I
10.1016/j.regpep.2007.02.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: Gastric inhibitory polypeptide (GIP) is an insulinotropic duodenal hormone released in response to meals. Recent studies in rodents suggested that GEP directly links overnutrition to obesity. Despite evidence for GIP effects on fat metabolism in humans, the GIP receptor (GIPR) has not been identified in fat tissues. We identified the GIPR gene in human subcutaneous and visceral fat tissues and tested the hypothesis that that the expression of this gene is influenced by central obesity and weight loss. Methods: GIPR gene mRNA expression in subcutaneous fat tissue biopsies (n=70) and in paired subcutaneous and visceral fat tissue samples (n=25) of non-diabetic postmenopausal women was studied by real-time reverse transcription polymerase chain reaction. The effect of weight reduction on GIPR gene expression in subcutaneous fat tissue was studied in a subset of 14 women. Results: GIPR adipose tissue gene expression was significantly lower in insulin resistant obese non-diabetic women (p=0.004). The GIPR mRNA expression was higher in the visceral fat tissue compared with subcutaneous fat (p<0.001). Despite adjustment for obesity-associated variables, waist circumference was the most significant predictor of GIPR gene expression in subcutaneous fat depot (F=4.066; beta=-0.997;p=0.000l) and, together with fasting insulin levels, in visceral fat (F=3.553; beta=-0.507 and beta=0.495; p=0.0001). Moderate weight reduction did not change gene expression levels of the GIPR gene (p=0.085). Conclusions: Decreased expression of the GIPR gene in subcutaneous fat tissue is associated with signs of insulin resistance in non-diabetic women with central obesity and demonstrates that fasting hyperinsulinemia is a possible negative regulator of GIPR gene expression in subcutaneous fat. Higher GIPR gene expression levels in visceral fat vs. subcutaneous fat reflect regional differences in adipose tissue biology. Moderate weight reduction did not change gene expression levels of GIPR in subcutaneous fat. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
相关论文
共 42 条
[31]   PRESERVED INCRETIN ACTIVITY OF GLUCAGON-LIKE PEPTIDE-1 [7-36 AMIDE] BUT NOT OF SYNTHETIC HUMAN GASTRIC-INHIBITORY POLYPEPTIDE IN PATIENTS WITH TYPE-2 DIABETES-MELLITUS [J].
NAUCK, MA ;
HEIMESAAT, MM ;
ORSKOV, C ;
HOLST, JJ ;
EBERT, R ;
CREUTZFELDT, W .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) :301-307
[32]   Gastric inhibitory polypeptide and effects of glycation on glucose transport and metabolism in isolated mouse abdominal muscle [J].
O'Harte, FPM ;
Gray, AM ;
Flatt, PR .
JOURNAL OF ENDOCRINOLOGY, 1998, 156 (02) :237-243
[33]   Identification and validation of suitable endogenous reference genes for gene expression studies of human bladder cancer [J].
Ohl, F ;
Jung, M ;
Radonic, A ;
Sachs, M ;
Loening, SA ;
Jung, K .
JOURNAL OF UROLOGY, 2006, 175 (05) :1915-1920
[34]   WAIST CIRCUMFERENCE AND ABDOMINAL SAGITTAL DIAMETER - BEST SIMPLE ANTHROPOMETRIC INDEXES OF ABDOMINAL VISCERAL ADIPOSE-TISSUE ACCUMULATION AND RELATED CARDIOVASCULAR RISK IN MEN AND WOMEN [J].
POULIOT, MC ;
DESPRES, JP ;
LEMIEUX, S ;
MOORJANI, S ;
BOUCHARD, C ;
TREMBLAY, A ;
NADEAU, A ;
LUPIEN, PJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1994, 73 (07) :460-468
[35]   GIP INCREASES INSULIN-RECEPTOR AFFINITY AND CELLULAR-SENSITIVITY IN ADIPOCYTES [J].
STARICH, GH ;
BAR, RS ;
MAZZAFERRI, EL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (06) :E603-E607
[36]   Abundance of two human preadipocyte subtypes with distinct capacities for replication, adipogenesis, and apoptosis varies among fat depots [J].
Tchkonia, T ;
Tchoukalova, YD ;
Giorgadze, N ;
Pirtskhalava, T ;
Karagiannides, I ;
Forse, RA ;
Koo, A ;
Stevenson, M ;
Chinnappan, D ;
Cartwright, A ;
Jensen, MD ;
Kirkland, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2005, 288 (01) :E267-E277
[37]   Fat depot-specific characteristics are retained in strains derived from single human preadipocytes [J].
Tchkonia, Tamara ;
Giorgadze, Nino ;
Pirtskhalava, Tamar ;
Thomou, Thomas ;
DePonte, Matthew ;
Koo, Ada ;
Forse, R. Armour ;
Chinnappan, Dharmaraj ;
Martin-Ruiz, Carmen ;
von Zglinicki, Thomas ;
Kirkland, James L. .
DIABETES, 2006, 55 (09) :2571-2578
[38]   GASTRIC-INHIBITORY POLYPEPTIDE RECEPTOR, A MEMBER OF THE SECRETIN-VASOACTIVE INTESTINAL PEPTIDE RECEPTOR FAMILY, IS WIDELY DISTRIBUTED IN PERIPHERAL ORGANS AND THE BRAIN [J].
USDIN, TB ;
MEZEY, E ;
BUTTON, DC ;
BROWNSTEIN, MJ ;
BONNER, TI .
ENDOCRINOLOGY, 1993, 133 (06) :2861-2870
[39]   Incretin secretion in relation to meal size and body weight in healthy subjects and people with type 1 and type 2 diabetes mellitus [J].
Vilsboll, T ;
Krarup, T ;
Sonne, J ;
Madsbad, S ;
Volund, A ;
Juul, AG ;
Holst, JJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (06) :2706-2713
[40]  
VOH MC, 2004, OBES RES, V12, P1217