Influence of estrogenic status on the lipolytic activity of parametrial adipose tissue in vivo: An in situ microdialysis study

被引:34
作者
Darimont, C
Delansorne, R
Paris, J
Ailhaud, G
Negrel, R
机构
[1] UNIV NICE, CTR BIOCHIM, UMR 6543 CNRS, FAC SCI, F-06108 NICE 2, FRANCE
[2] LAB THERAMEX, PRECLIN R&D DEPT, MC-98000 MONACO, MONACO
关键词
D O I
10.1210/en.138.3.1092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ovarian hormones have been shown to modulate the metabolism of adipose cells obtained from adipose tissue of different animals. The aim of this study was to better understand the short- and long-term influences of estrogens on the in vivo lipolytic response of rat parametrial fat pads, determined by measurement of extracellular glycerol concentrations using in situ microdialysis. Possible direct effects of estrogens on lipolysis were studied by perfusion of a potent estrogenic analogue such as moxestrol. Moxestrol (10(-6) M) failed to increase glycerol concentrations in estrus, diestrus, or 8-day ovariectomized animals. However, the basal glycerol concentrations and the Lipolytic responses stimulated by 10(-6) M isoproterenol were decreased in parametrial fat pads of diestrus, compared with estrus, rats. Greater decreases in basal and stimulated glycerol concentrations were observed in rats that had been ovariectomized for 8, 15, or 30 days. Ln ovariectomized rats, isoproterenol-induced lipolysis was restored to the levels observed in diestrus animals by a daily injection of 17 beta-estradiol for a period of? days. These results implicate estrogens as long-term modulators of in vivo basal and stimulated lipolytic responses of rat parametrial fat pad.
引用
收藏
页码:1092 / 1096
页数:5
相关论文
共 45 条
[1]   POTENTIATION OF EPINEPHRINE-INDUCED LIPOLYSIS BY CATECHOL ESTROGENS AND THEIR METHOXY DERIVATIVES [J].
ACKERMAN, GE ;
MACDONALD, PC ;
GUDELSKY, G ;
MENDELSON, CR ;
SIMPSON, ER .
ENDOCRINOLOGY, 1981, 109 (06) :2084-2088
[2]   MICRODIALYSIS OF ADIPOSE-TISSUE AND BLOOD FOR INVIVO LIPOLYSIS STUDIES [J].
ARNER, P ;
BOLINDER, J ;
ELIASSON, A ;
LUNDIN, A ;
UNGERSTEDT, U .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (05) :E737-E742
[3]   ESTROGEN ACTION VIA THE CAMP SIGNALING PATHWAY - STIMULATION OF ADENYLATE-CYCLASE AND CAMP-REGULATED GENE-TRANSCRIPTION [J].
ARONICA, SM ;
KRAUS, WL ;
KATZENELLENBOGEN, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (18) :8517-8521
[4]   In situ assessment of the role of the beta(1)-, beta(2)- and beta(3)-adrenoceptors in the control of lipolysis and nutritive blood flow in human subcutaneous adipose tissue [J].
Barbe, P ;
Millet, L ;
Galitzky, J ;
Lafontan, M ;
Berlan, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 117 (05) :907-913
[5]   POTENTIATION OF EPINEPHRINE-INDUCED LIPOLYSIS IN FAT-CELLS FROM ESTROGEN-TREATED RATS [J].
BENOIT, V ;
VALETTE, A ;
MERCIER, L ;
MEIGNEN, JM ;
BOYER, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 109 (04) :1186-1191
[6]   RADIOMETRIC ASSAYS FOR GLYCEROL, GLUCOSE, AND GLYCOGEN [J].
BRADLEY, DC ;
KASLOW, HR .
ANALYTICAL BIOCHEMISTRY, 1989, 180 (01) :11-16
[7]   DIVERGENCE BETWEEN OVARIAN AROMATASE-ACTIVITY, ESTROGEN, AND ANDROGEN LEVELS IN THE CYCLING RAT [J].
BRANDT, ME ;
PUETT, D ;
ZIMNISKI, SJ .
ENDOCRINOLOGY, 1990, 126 (01) :72-79
[8]   EMERGING DIVERSITIES IN THE MECHANISM OF ACTION OF STEROID-HORMONES [J].
BRANN, DW ;
HENDRY, LB ;
MAHESH, VB .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 52 (02) :113-133
[9]  
BRODIE AMH, 1977, ENDOCRINOLOGY, V100, P1384
[10]  
BUTCHER RL, 1974, ENDOCRINOLOGY, V94, P1734