Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Larson, JE; Rainer, PP; Watts, VL; Yang, R; Miller, KL; Phan, A; Barouch, LA.
Dependence of β3-adrenergic signaling on the adipokine leptin in cardiac myocytes.
Int J Obes (Lond). 2012; 36(6):876-879
Doi: 10.1038/ijo.2011.137
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- Co-Autor*innen der Med Uni Graz
- Rainer Peter
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- Abstract:
- β3-Adrenergic receptors (β3ARs) negatively regulate β-adrenergic signaling via nitric oxide and are dependent on the adipokine leptin for normal expression in adipocytes, thus making β3AR an attractive candidate for cross-talk with leptin in the heart. Accordingly, we tested the hypothesis that cardiac β3AR expression and function are dependent on leptin and are severely diminished in leptin-deficient ob/ob mice. Using isolated cardiac myocyte physiology studies, we found that β3AR function was significantly diminished in ob/ob myocytes and in wild-type myocytes treated with leptin antagonist. This finding was supported by quantitative PCR demonstrating markedly decreased β3AR mRNA levels in ob/ob mice. Both β3AR mRNA and function were restored in ob/ob mice after in vivo leptin repletion. We propose that diminished β3AR signaling may be the critical element to explain the direct effects of leptin on the myocardium and suggest that this work reveals a key feature in the role of leptin in obesity-related cardiac hypertrophy and heart failure.
- Find related publications in this database (using NLM MeSH Indexing)
- Adrenergic beta-Agonists - pharmacology
- Animals -
- Heart Failure - metabolism
- Leptin - metabolism
- Mice -
- Mice, Inbred Strains -
- Mice, Obese -
- Myocytes, Cardiac - metabolism
- Obesity - drug therapy
- Polymerase Chain Reaction - methods
- RNA, Messenger - metabolism
- Receptors, Adrenergic, beta-3 - genetics
- Receptors, Leptin - metabolism
- Signal Transduction -
- Find related publications in this database (Keywords)
- leptin
- beta-adrenergic receptors
- hypertrophy
- heart failure
- myocytes