Involvement of β3-Adrenoceptor in Altered β-Adrenergic Response in Senescent Heart

被引:34
作者
Birenbaum, Aurelie [1 ,2 ]
Tesse, Angela
Loyer, Xavier
Michelet, Pierre [3 ]
Andriantsitohaina, Ramaroson
Heymes, Christophe
Riou, Bruno
Amour, Julien [1 ,2 ]
机构
[1] Univ Paris 06, EA 3975, Paris, France
[2] CHU Pitie Salpetriere, AP HP, Dept Anesthesiol & Crit Care, F-75651 Paris 13, France
[3] Hop St Maguerite, Dept Anesthesiol & Crit Care, Marseille, France
关键词
D O I
10.1097/ALN.0b013e31818d7e5a
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: In senescent heart beta-adrenergic response in parallel with beta(1)- and beta(2)-adrenoceptor down-regulation. A negative inotropic effect of beta(3)-adrenoceptor could be involved. In this study, the authors tested die hypothesis that beta(3)-adrenoceptor plays a role in beta-adrenergic dysfunction in senescent heart. Methods: beta-Adrenergic responses were investigated in vivo (echocardiography-dobutamine. electron paramagnetic resonance) and in vitro (isolated left ventricular papillary muscle, electron paramagnetic resonance) in young, adult (3-month-old) and senescent (24-month-old) rats. Nitric oxide synthase (NOS) immunolabeling (confocal microscopy), nitric oxide production (electron paramagnetic resonance) and beta-adrenoceptor Western blots were performed in vitro. Data are mean percentages of baseline +/- SD. Results: An impaired positive inotropic effect (isoproterenol) was confirmed in senescent hearts in vivo (117 +/- 23 vs. 162 +/- 16%; P < 0.05) and in vitro (127 +/- 10 vs. 179 +/- 15%; P < 0.05). In the young adult group, the positive inotropic effect was not significantly modified by the nonselective NOS inhibitor N-G-nitro-L-arginine methylester (L-NAME; 183 +/- 19%), the selective NOS1 inhibitor vinyl-L-N-5(1-imino-3-butenyl)-L-ornithine (L-VNIO; 172 +/- 13%), or the selective NOS2 inhibitor 1400W (193 19%). In the senescent group, in parallel with beta(3)-adrenoceptor up-regulation and increased nitric oxide production, the positive inotropic effect was partially restored by L-NAME (151 +/- 8%; P < 0.05) and L-VNIO (149 +/- 7%; P < 0.05) but not by 1400W (132 +/- 11%; not significant). The positive inotropic effect induced by dibutyryl-cyclic adenosine monophosphate was decreased in the senescent group with the specific beta(3)-adrenoceptor agonist BRL 37344 (167 +/- 10 vs. 142 +/- 10%; P < 0.05). NOS1 and NOS2 were significantly up-regulated in the senescent rat. Conclusions: In senescent cardiomyopathy beta(3)-adrenoceptor overexpression plays all important role it] the altered beta-adrenergic response via induction of NOS1-nitric oxide.
引用
收藏
页码:1045 / 1053
页数:9
相关论文
共 37 条
[1]   Interaction of halogenated anesthetics with α- and β-adrenoceptor stimulations in diabetic rat myocardium [J].
Amour, J ;
David, JS ;
Vivien, B ;
Coriat, P ;
Riou, B .
ANESTHESIOLOGY, 2004, 101 (05) :1145-1152
[2]   Preservation of the positive lusitropic effect of β-adrenoceptors stimulation in diabetic cardiomyopathy [J].
Amour, Julien ;
Loyer, Xavier ;
Michelet, Pierre ;
Birenbaum, Aurelie ;
Riou, Bruno ;
Heymes, Christophe .
ANESTHESIA AND ANALGESIA, 2008, 107 (04) :1130-1138
[3]   Diabetic cardiomyopathy and anesthesia: Bench to bedside [J].
Amour, Julien ;
Kersten, Judy R. .
ANESTHESIOLOGY, 2008, 108 (03) :524-530
[4]   Altered contractile response due to increased β3-adrenoceptor stimulation in diabetic cardiomyopathy -: The role of nitric oxide synthase 1-derived nitric oxide [J].
Amour, Julien ;
Loyer, Xavier ;
Le Guen, Morgan ;
Mabrouk, Nejma ;
David, Jean-Stephane ;
Camors, Emmanuel ;
Carusio, Nunzia ;
Vivien, Benoit ;
Andriantsitohaina, Ramaroson ;
Heymes, Christophe ;
Riou, Bruno .
ANESTHESIOLOGY, 2007, 107 (03) :452-460
[5]   Senescent heart compared with pressure overload-induced hypertrophy [J].
Assayag, P ;
Charlemagne, D ;
deLeiris, J ;
Boucher, F ;
Valere, PE ;
Lortet, S ;
Swynghedauw, B ;
Besse, S .
HYPERTENSION, 1997, 29 (01) :15-21
[6]   Role of myocardial neuronal nitric oxide synthase-derived nitric oxide in β-adrenergic hyporesponsiveness after myocardial infarction-induced heart failure in rat [J].
Bendall, JK ;
Damy, T ;
Ratajczak, P ;
Loyer, X ;
Monceau, V ;
Marty, I ;
Milliez, P ;
Robidel, E ;
Marotte, F ;
Samuel, JL ;
Heymes, C .
CIRCULATION, 2004, 110 (16) :2368-2375
[7]   NORMAL AND HYPERTROPHIED SENESCENT RAT-HEART - MECHANICAL AND MOLECULAR CHARACTERISTICS [J].
BESSE, S ;
ASSAYAG, P ;
DELCAYRE, C ;
CARRE, F ;
CHEAV, SL ;
LECARPENTIER, Y ;
SWYNGHEDAUW, B .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (01) :H183-H190
[8]   Increased neuronal nitric oxide synthase-derived NO production in the failing human heart [J].
Damy, T ;
Ratajczak, P ;
Shah, AM ;
Camors, E ;
Marty, I ;
Hasenfuss, G ;
Marotte, F ;
Samuel, JL ;
Heymes, C .
LANCET, 2004, 363 (9418) :1365-1367
[9]   Up-regulation of cardiac nitric oxide synthase 1-derived nitric oxide after myocardial infarction in senescent rats [J].
Damy, T ;
Ratajczak, P ;
Robidel, E ;
Bendall, JK ;
Oliviéro, P ;
Boczkowski, J ;
Ebrahimian, T ;
Marotte, F ;
Samuel, JL ;
Heymes, C .
FASEB JOURNAL, 2003, 17 (11) :1934-+
[10]   Myocardial effects of halothane and sevoflurane in diabetic rats [J].
David, JS ;
Tavernier, B ;
Amour, J ;
Vivien, B ;
Coriat, P ;
Riou, B .
ANESTHESIOLOGY, 2004, 100 (05) :1179-1187