Regulation of resistin by gonadal, thyroid hormone, and nutritional status

被引:94
作者
Nogueiras, R
Gualillo, O
Caminos, JE
Casanueva, FF
Diéguez, C
机构
[1] Univ Santiago de Compostela, Sch Med, Dept Physiol, Santiago De Compostela 15705, Spain
[2] Univ Santiago de Compostela, Complejo Hosp, Santiago De Compostela 15705, Spain
[3] Univ Santiago de Compostela, Sch Med, Dept Med, Mol Endocrinol Sect, Santiago De Compostela 15705, Spain
来源
OBESITY RESEARCH | 2003年 / 11卷 / 03期
关键词
insulin sensitivity; sex steroids; thyroid hormones; chronic food restriction; pregnancy;
D O I
10.1038/oby.2003.55
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Resistin was recently identified as a hormone secreted by adipocytes that is under hormonal and nutritional control. This hormone has been suggested to be the link between obesity and type 2 diabetes. The aim of this study was to assess the influence of gender, gonadal status, thyroid hormones, pregnancy, and food restriction on resistin mRNA levels in adipose tissue of rats. Research Methods and Procedures: We have determined resistin mRNA expression by Northern blot analysis in all experimental sets. Results: Resistin mRNA expression is influenced by age, with the highest hormone levels existing at 45 days after birth and decreasing thereafter. Resistin mRNA expression is higher in men than in women. Moreover, we studied the effect of orchidectomy and ovariectomy in rats of different ages and showed that gonadal hormones increase adipose tissue resistin mRNA expression in male rats. Resistin is also regulated by thyroid hormones; it is severely decreased in hyperthyroid rats. Our results clearly show that chronic food restriction (30% of ad libitum food intake) led to a decrease in adipose tissue mRNA levels in normal cycling female rats and pregnant rats. In pregnancy, resistin mRNA levels were enhanced particularly at midgestation. Discussion: Our observations indicate that resistin is influenced by gender, gonadal status, thyroid hormones, and pregnancy. These findings suggest that resistin could explain the decreased insulin sensitivity during puberty and could be the link between sex steroids and insulin sensitivity. Moreover, resistin could mediate the effect of thyroid hormones on insulin resistance and the state of insulin resistance present during pregnancy.
引用
收藏
页码:408 / 414
页数:7
相关论文
共 35 条
[1]   INSULIN RESISTANCE OF PUBERTY - A DEFECT RESTRICTED TO PERIPHERAL GLUCOSE-METABOLISM [J].
AMIEL, SA ;
CAPRIO, S ;
SHERWIN, RS ;
PLEWE, G ;
HAYMOND, MW ;
TAMBORLANE, WV .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 72 (02) :277-282
[2]   Dimerization of resistin and resistin-like molecules is determined by a single cysteine [J].
Banerjee, RR ;
Lazar, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (28) :25970-25973
[3]   PREGNANCY AND DIABETES - THE MATERNAL RESPONSE [J].
BENDER, HS ;
CHICKERING, WR .
LIFE SCIENCES, 1985, 37 (01) :1-9
[4]   PUBERTY DECREASES INSULIN SENSITIVITY [J].
BLOCH, CA ;
CLEMONS, P ;
SPERLING, MA .
JOURNAL OF PEDIATRICS, 1987, 110 (03) :481-487
[5]   Downregulated IRS-1 and PPARγ in obese women with gestational diabetes:: relationship to FFA during pregnancy [J].
Catalano, PM ;
Nizielski, SE ;
Shao, JH ;
Preston, L ;
Qiao, LP ;
Friedman, JE .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 282 (03) :E522-E533
[6]  
Damm P, 1998, DAN MED BULL, V45, P495
[7]   Diabetes - The missing link with obesity? [J].
Flier, JS .
NATURE, 2001, 409 (6818) :292-293
[8]   PERIPHERAL GLUCOSE-METABOLISM IN HUMAN HYPERTHYROIDISM [J].
FOSS, MC ;
PACCOLA, GMGF ;
SAAD, MJA ;
PIMENTA, WP ;
PICCINATO, CE ;
IAZIGI, N .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 70 (04) :1167-1172
[9]   The physiology and pathophysiology of intrauterine growth retardation [J].
Gluckman, PD ;
Harding, JE .
HORMONE RESEARCH, 1997, 48 :11-16
[10]   Effect of food restriction on ghrelin in normal-cycling female rats and in pregnancy [J].
Gualillo, O ;
Caminos, JE ;
Nogueiras, R ;
Seoane, LM ;
Arvat, E ;
Ghigo, E ;
Casanueva, FF ;
Diéguez, C .
OBESITY RESEARCH, 2002, 10 (07) :682-687