Leptin affects adenylate cyclase activity in H9c2 cardiac cell line: Effects of short- and long-term exposure

被引:26
作者
Illiano, G
Naviglio, S
Pagano, M
Spina, A
Chiosi, E
Barbieri, M
Paolisso, G
机构
[1] Univ Naples 2, Dept Biochem & Biophys F Cedrangolo, I-80138 Naples, Italy
[2] Univ Naples 2, Dept Geriatr Med & Metab Dis, I-80138 Naples, Italy
关键词
leptin; cardiac cells; adenylate cyclase; catecholamine; G protein;
D O I
10.1016/S0895-7061(02)02925-4
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Leptin has been hypothesized to be a pathophysiologic link between obesity and cardiovascular diseases, Because the adenylate cyclase (AC) system is a main effector of beta-adrenergic receptors and leptin has been shown to modulate AC activity in other cell lines. a leptin impact on cardiac AC activity was hypothesized. Therefore. acute and chronic effects of leptin on a rat cardiac cell line (H9c2) were investigated. Leptin affected both basal (+13% at 30 min and -16.4% after 18 h v untreated cells) and catecholamine-stimulated AC activity (isoproterenol + leptin at 30 min or 18 h was +21% untreated cells: norepinephrine + leptin at 30 min was +38.8% v untreated cells: and norepinephrine + leptin at 18 h was +6% v untreated cells). Thus. long-term leptin treatment was associated with a reduced AC activity and a different responsiveness to catecholamines. The AC activity on leptin treatment was accompanied by changes in levels of proteins structurally or functionally related to AC complex (AC, Gas, Galphai, p21-ras). These data indicate that the AC complex is profoundly affected at more than one level by leptin treatment in the H9c2 cardiac cell line. Differences in AC activity after short- and long-term exposure to leptin and the interaction between leptin and catecholamine might provide further insight to the Understanding of the development of hypertension and congestive heart failure in obese patients. (C) 2002 American Journal of Hypertension. Ltd.
引用
收藏
页码:638 / 643
页数:6
相关论文
共 25 条
[1]   Leptin [J].
Ahima, RS ;
Flier, JS .
ANNUAL REVIEW OF PHYSIOLOGY, 2000, 62 :413-437
[2]   Leptin inhibits insulin secretion induced by cellular cAMP in a pancreatic B cell line (INS-1 cells) [J].
Ahrén, B ;
Havel, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 277 (04) :R959-R966
[3]  
BIORBAEK C, 1997, J BIOL CHEM, V272, P32686
[4]  
Braunwald E, 2000, CIRCULATION, V102, P14
[5]   β-adrenergic receptor blockade in chronic heart failure [J].
Bristow, MR .
CIRCULATION, 2000, 101 (05) :558-569
[6]   Increasing complexity of Ras signaling [J].
Campbell, SL ;
Khosravi-Far, R ;
Rossman, KL ;
Clark, GJ ;
Der, CJ .
ONCOGENE, 1998, 17 (11) :1395-1413
[7]  
Dzimiri N, 1999, PHARMACOL REV, V51, P465
[8]   Leptin-induced lipolysis opposes the tonic inhibition of endogenous adenosine in white adipocytes [J].
Frühbeck, G ;
Gómez-Ambrosi, J ;
Salvador, J .
FASEB JOURNAL, 2001, 15 (02) :333-340
[9]   Leptin can induce proliferation, differentiation, and functional activation of hemopoietic cells [J].
Gainsford, T ;
Willson, TA ;
Metcalf, D ;
Handman, E ;
McFarlane, C ;
Ng, A ;
Nicola, NA ;
Alexander, WS ;
Hilton, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14564-14568
[10]   The leptin receptor activates janus kinase 2 and signals for proliferation in a factor-dependent cell line [J].
Ghilardi, N ;
Skoda, RC .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (04) :393-399