Stimulation of leptin release by actinomycin D in rat adipocytes

被引:8
作者
Fain, JN [1 ]
Bahouth, SW
机构
[1] Univ Tennessee, Coll Med, Dept Biochem, Memphis, TN 38163 USA
[2] Univ Tennessee, Coll Med, Dept Pharmacol, Memphis, TN 38163 USA
关键词
leptin; leptin mRNA; dexamethasone; adipocytes; 18S RNA; actinomycin D; cycloheximide; GAPDH mRNA;
D O I
10.1016/S0006-2952(97)00638-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A greater understanding of the factors causing the enhanced release of leptin by adipocytes in obesity is needed. Experiments were designed to determine the effects of actinomycin D on leptin release by isolated rat adipocytes during primary culture for 24 hr. In adipocytes from fed hypothyroid rats, the initial rate of leptin release over the first 6 hr was not maintained over the next 18 hr. The decline in leptin release by adipocytes in primary culture between 6 and 24 hr was reduced markedly by either dexamethasone or actinomycin D. Both actinomycin D and dexamethasone also reduced the loss of leptin mRNA seen over the 24-hr incubation. Maximal effects on leptin release and leptin mRNA accumulation required only 0.1 mu M of actinomycin D, a concentration that had no significant effect on the 18S RNA content of adipocytes at the end of a 24-hr incubation. In contrast to the reduced loss of leptin mRNA seen at 24 hr, the loss of glyceraldehyde 3-phosphate dehydrogenase messenger ribonucleic acid (GAPDH mRNA) was enhanced in the presence of 0.1 mu M of actinomycin D. The effects of dexamethasone could be differentiated from those of actinomycin D by the finding that cycloheximide blocked the reduced loss of leptin mRNA due to dexamethasone while having no effect on that due to actinomycin D. These results point to a unique regulation of leptin release and leptin mRNA levels by actinomycin D. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:1309 / 1314
页数:6
相关论文
共 23 条
[1]   Role of leptin in the neuroendocrine response to fasting [J].
Ahima, RS ;
Prabakaran, D ;
Mantzoros, C ;
Qu, DQ ;
Lowell, B ;
MaratosFlier, E ;
Flier, JS .
NATURE, 1996, 382 (6588) :250-252
[2]  
ALTUS MS, 1991, J BIOL CHEM, V266, P21190
[3]   DIET-INDUCED AND DIABETES-INDUCED CHANGES OF OB GENE-EXPRESSION IN RAT ADIPOSE-TISSUE [J].
BECKER, DJ ;
ONGEMBA, LN ;
BRICHARD, V ;
HENQUIN, JC ;
BRICHARD, SM .
FEBS LETTERS, 1995, 371 (03) :324-328
[4]   A SIMPLE ONE-STEP ENZYMATIC FLUOROMETRIC METHOD FOR THE DETERMINATION OF GLYCEROL IN 20-MU-1 OF PLASMA [J].
BOOBIS, LH ;
MAUGHAN, RJ .
CLINICA CHIMICA ACTA, 1983, 132 (02) :173-179
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]  
Fain J N, 1967, Adv Enzyme Regul, V5, P39, DOI 10.1016/0065-2571(67)90007-6
[7]   Expression of leptin and beta(2)-adrenergic receptors in rat adipose tissue in altered thyroid states [J].
Fain, JN ;
Coronel, EC ;
Beauchamp, MJ ;
Bahouth, SW .
BIOCHEMICAL JOURNAL, 1997, 322 :145-150
[8]   The beta(3)-adrenergic receptor inhibits insulin-stimulated leptin secretion from isolated rat adipocytes [J].
Gettys, TW ;
Harkness, PJ ;
Watson, PM .
ENDOCRINOLOGY, 1996, 137 (09) :4054-4057
[9]   Insulin sensitizes beta-agonist and forskolin-stimulated lipolysis to inhibition by 2',5'-dideoxyadenosine [J].
GokmenPolar, Y ;
Coronel, EC ;
Bahouth, SW ;
Fain, JN .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (02) :C562-C569
[10]   WEIGHT-REDUCING EFFECTS OF THE PLASMA-PROTEIN ENCODED BY THE OBESE GENE [J].
HALAAS, JL ;
GAJIWALA, KS ;
MAFFEI, M ;
COHEN, SL ;
CHAIT, BT ;
RABINOWITZ, D ;
LALLONE, RL ;
BURLEY, SK ;
FRIEDMAN, JM .
SCIENCE, 1995, 269 (5223) :543-546