Leptin inhibits directly glucocorticoid secretion by normal human and rat adrenal gland

被引:194
作者
Pralong, FP
Roduit, R
Waeber, G
Castillo, E
Mosimann, F
Thorens, B
Gaillard, RC
机构
[1] Univ Lausanne Hosp, Div Endocrinol Diabet & Metab, CH-1011 Lausanne, Switzerland
[2] Univ Lausanne Hosp, Inst Pharmacol & Toxicol, CH-1011 Lausanne, Switzerland
[3] Univ Lausanne Hosp, Serv Internal Med B, CH-1011 Lausanne, Switzerland
[4] Univ Lausanne Hosp, Dept Surg, CH-1011 Lausanne, Switzerland
关键词
D O I
10.1210/en.139.10.4264
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Different interactions have been described between glucocorticoids and the product of the ob gene leptin. Leptin can inhibit the activation of the hypothalamo-pituitary-adrenal axis by stressful stimuli, whereas adrenal glucocorticoids stimulate leptin production by the adipocyte. The present study was designed to investigate the potential direct effects of leptin to modulate glucocorticoid production by the adrenal. Human adrenal glands from kidney transplant donors were dissociated, and isolated primary cells were studied in vitro. These cells were preincubated with recombinant leptin (10(-10)-10(-7) M) for 6 Or 24 h, and basal or ACTH-stimulated cortisol secretion was subsequently measured. Basal cortisol secretion was unaffected by leptin, but a significant and dose-dependent inhibition of ACTH-stimulated cortisol secretion was observed [down by 29 +/- 0.18 of controls with the highest leptin dose, P < 0.01 vs. CT (unrelated positive control)]. This effect of leptin was also observed in rat primary adrenocortical cells, where leptin inhibited stimulated corticosterone secretion in a dose-dependent manner (down by 46 +/- 0.1% of controls with the highest leptin dose, P < 0.001 us. CT). These effects of leptin in adrenal cells are likely mediated by the long isoform of the leptin receptor (OB-R), because its transcript was found to be expressed in the adrenal tissue and leptin had no inhibitory effect in adrenal glands obtained from db/db mice. Therefore, leptin inhibits directly stimulated cortisol secretion from human and rat adrenal glands, and this may represent an important mechanism to modulate glucocorticoid levels in various metabolic states.
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页码:4264 / 4268
页数:5
相关论文
共 38 条
[31]   CHANGES IN THE HYPOTHALAMO-CORTICOTROPE AXIS AFTER BILATERAL ADRENALECTOMY - EVIDENCE FOR A MEDIAN-EMINENCE SITE OF GLUCOCORTICOID ACTION [J].
SPINEDI, E ;
GIACOMINI, M ;
JACQUIER, MC ;
GAILLARD, RC .
NEUROENDOCRINOLOGY, 1991, 53 (02) :160-170
[32]   THE ROLE OF NEUROPEPTIDE-Y IN THE ANTIOBESITY ACTION OF THE OBESE GENE-PRODUCT [J].
STEPHENS, TW ;
BASINSKI, M ;
BRISTOW, PK ;
BUEVALLESKEY, JM ;
BURGETT, SG ;
CRAFT, L ;
HALE, J ;
HOFFMANN, J ;
HSIUNG, HM ;
KRIAUCIUNAS, A ;
MACKELLAR, W ;
ROSTECK, PR ;
SCHONER, B ;
SMITH, D ;
TINSLEY, FC ;
ZHANG, XY ;
HEIMAN, M .
NATURE, 1995, 377 (6549) :530-532
[33]   Identification and expression cloning of a leptin receptor, OB-R [J].
Tartaglia, LA ;
Dembski, M ;
Weng, X ;
Deng, NH ;
Culpepper, J ;
Devos, R ;
Richards, GJ ;
Campfield, LA ;
Clark, FT ;
Deeds, J ;
Muir, C ;
Sanker, S ;
Moriarty, A ;
Moore, KJ ;
Smutko, JS ;
Mays, GG ;
Woolf, EA ;
Monroe, CA ;
Tepper, RI .
CELL, 1995, 83 (07) :1263-1271
[34]   Leptin activation of Stat3 in the hypothalamus of wildtype and ob/ob mice but not db/db mice [J].
Vaisse, C ;
Halaas, JL ;
Horvath, CM ;
Darnell, JE ;
Stoffel, M ;
Friedman, JM .
NATURE GENETICS, 1996, 14 (01) :95-97
[35]   Central leptin stimulates corticosterone secretion at the onset of the dark phase [J].
vanDijk, G ;
Donahey, JCK ;
Thiele, TE ;
Scheurink, AJW ;
Steffens, AB ;
Wilkinson, CW ;
Tenenbaum, R ;
Campfield, LA ;
Burn, P ;
Seeley, RJ ;
Woods, SC .
DIABETES, 1997, 46 (11) :1911-1914
[37]   Glucocorticoids as counterregulatory hormones of leptin - Toward an understanding of leptin resistance [J].
Zakrzewska, KE ;
Cusin, I ;
Sainsbury, A ;
RohnerJeanrenaud, F ;
Jeanrenaud, B .
DIABETES, 1997, 46 (04) :717-719
[38]   POSITIONAL CLONING OF THE MOUSE OBESE GENE AND ITS HUMAN HOMOLOG [J].
ZHANG, YY ;
PROENCA, R ;
MAFFEI, M ;
BARONE, M ;
LEOPOLD, L ;
FRIEDMAN, JM .
NATURE, 1994, 372 (6505) :425-432