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Circulation ; 112(9 Suppl): I51-6, 2005 Aug 30.
Article in English | MEDLINE | ID: mdl-16159865

ABSTRACT

OBJECTIVE: Chronic mechanical unloading induces left ventricular (LV) atrophy, which may impair functional recovery during support with an LV-assist device. Clenbuterol, a beta2-adrenergic receptor (AR) agonist, is known to induce myocardial hypertrophy and might prevent LV atrophy during LV unloading. Furthermore, beta2-AR stimulation is reported to improve Ca2+ handling and contribute to antiapoptosis. However, there is little information on the effects of clenbuterol during LV unloading. METHODS AND RESULTS: We investigated LV atrophy and function after LV unloading produced by heterotopic heart transplantation in isogenic rats. After transplantation, rats were randomized to 1 of 2 groups (n=10 each). The clenbuterol group received 2 mg.kg(-1).d(-1) of the drug for 2 weeks; the control group received normal saline. The weight of unloaded control hearts was 48% less than that of host hearts after 2 weeks of unloading. Clenbuterol significantly increased the weight of the host hearts but did not prevent unloading-induced LV atrophy. Papillary muscles were isolated and stimulated, and there was no difference in developed tension between the 2 groups. However, the inotropic response to the beta-AR agonist isoproterenol significantly improved in the clenbuterol group. The mRNA expression of myocardial sarco(endo)plasmic reticulum Ca2+-ATPase 2a (SERCA2a) and fetal gene shift (myosin heavy chain [MHC] mRNA isozyme) was also significantly improved by clenbuterol treatment. There was no difference in beta1-AR mRNA expression between the 2 groups. In contrast, beta2-AR mRNA was significantly decreased in the clenbuterol-treated, unloaded heart. This indicates that clenbuterol may downregulate beta2-ARs. In the evaluation of apoptosis, mRNA expression of caspase-3, which is the central pathway for apoptosis, tended to be better in the clenbuterol group. CONCLUSIONS: During complete LV unloading, clenbuterol did not prevent myocardial atrophy but improved gene expression (SERCA2a, beta-MHC) and beta-adrenergic responsiveness and potentially prevented myocardial apoptosis. However, chronic administration of clenbuterol may be associated with downregulation of beta2-ARs.


Subject(s)
Adrenergic beta-Agonists/therapeutic use , Clenbuterol/therapeutic use , Heart/drug effects , Adrenergic beta-Agonists/pharmacology , Animals , Atrophy , Calcium-Transporting ATPases/biosynthesis , Calcium-Transporting ATPases/genetics , Caspase 3 , Caspases/biosynthesis , Caspases/genetics , Clenbuterol/pharmacology , Down-Regulation/drug effects , Drug Evaluation, Preclinical , Enzyme Induction/drug effects , Gene Expression Regulation/drug effects , Heart Transplantation , Heart Ventricles/drug effects , Heart Ventricles/pathology , Heart Ventricles/physiopathology , Isoproterenol/pharmacology , Male , Myocardial Contraction/drug effects , Myocardium/pathology , Myosin Heavy Chains/biosynthesis , Myosin Heavy Chains/genetics , Organ Size , Papillary Muscles/drug effects , Papillary Muscles/physiopathology , Protein Isoforms/biosynthesis , Protein Isoforms/genetics , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Random Allocation , Rats , Rats, Inbred Lew , Receptors, Adrenergic, beta-1/biosynthesis , Receptors, Adrenergic, beta-1/genetics , Receptors, Adrenergic, beta-2/biosynthesis , Receptors, Adrenergic, beta-2/drug effects , Receptors, Adrenergic, beta-2/genetics , Sarcoplasmic Reticulum Calcium-Transporting ATPases , Stress, Mechanical , Transplantation, Heterotopic , Transplantation, Isogeneic , Ventricular Function, Left/drug effects
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