Literature DB >> 12118913

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

Gennaro Illiano1, Silvio Naviglio, Mario Pagano, Annamaria Spina, Emilio Chiosi, Michelangela Barbieri, Giuseppe Paolisso.   

Abstract

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% v 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, Gai, 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.

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Year:  2002        PMID: 12118913     DOI: 10.1016/s0895-7061(02)02925-4

Source DB:  PubMed          Journal:  Am J Hypertens        ISSN: 0895-7061            Impact factor:   2.689


  5 in total

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Journal:  Acta Cardiol Sin       Date:  2016-11       Impact factor: 2.672

2.  Leptin repletion restores depressed {beta}-adrenergic contractility in ob/ob mice independently of cardiac hypertrophy.

Authors:  Khalid M Minhas; Shakil A Khan; Shubha V Y Raju; Alexander C Phan; Daniel R Gonzalez; Mike W Skaf; Kwangho Lee; Ankit D Tejani; Anastasios P Saliaris; Anastasies P Saliaris; Lili A Barouch; Christopher P O'Donnell; Charles W Emala; Dan E Berkowitz; Joshua M Hare
Journal:  J Physiol       Date:  2005-03-10       Impact factor: 5.182

3.  Reduced neuronal nitric oxide synthase expression contributes to cardiac oxidative stress and nitroso-redox imbalance in ob/ob mice.

Authors:  Roberto M Saraiva; Khalid M Minhas; Meizi Zheng; Eleanor Pitz; Adriana Treuer; Daniel Gonzalez; Karl H Schuleri; Koenraad M Vandegaer; Lili A Barouch; Joshua M Hare
Journal:  Nitric Oxide       Date:  2006-12-21       Impact factor: 4.427

4.  Cardiac Dysfunction Induced by Obesity Is Not Related to β-Adrenergic System Impairment at the Receptor-Signalling Pathway.

Authors:  Artur Junio Togneri Ferron; Bruno Barcellos Jacobsen; Paula Grippa Sant'Ana; Dijon Henrique Salomé de Campos; Loreta Casquel de Tomasi; Renata de Azevedo Mello Luvizotto; Antonio Carlos Cicogna; André Soares Leopoldo; Ana Paula Lima-Leopoldo
Journal:  PLoS One       Date:  2015-09-21       Impact factor: 3.240

5.  Saturated high-fat diet-induced obesity increases adenylate cyclase of myocardial β-adrenergic system and does not compromise cardiac function.

Authors:  Danielle F Vileigas; Adriana F de Deus; Danielle C T da Silva; Loreta C de Tomasi; Dijon H S de Campos; Caroline S Adorni; Scarlet M de Oliveira; Paula G Sant'Ana; Katashi Okoshi; Carlos R Padovani; Antonio C Cicogna
Journal:  Physiol Rep       Date:  2016-09
  5 in total

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