The cannabinoid receptor type 2 promotes cardiac myocyte and fibroblast survival and protects against ischemia/reperfusion-induced cardiomyopathy

被引:102
作者
Defer, Nicole [1 ,2 ]
Wan, Jinghong [1 ,2 ]
Souktani, Richard [2 ,3 ]
Escoubet, Brigitte [4 ]
Perier, Magali [1 ,2 ]
Caramelle, Philippe [1 ,2 ]
Manin, Sylvie [1 ,2 ]
Deveaux, Vanessa [1 ,2 ]
Bourin, Marie-Claude [1 ,2 ]
Zimmer, Andreas [5 ]
Lotersztajn, Sophie [1 ,2 ]
Pecker, Francoise [1 ,2 ,6 ]
Pavoine, Catherine [1 ,2 ]
机构
[1] Hop Henri Mondor, INSERM, U955, IMRB, F-94010 Creteil, France
[2] Univ Paris 12, Fac Med, UMR S 955, Creteil, France
[3] IFR10 IM3, Creteil, France
[4] Univ Paris 07, INSERM, Assistance Publ Hop Paris, Hop Bichat,UFR Med,U872, Paris, France
[5] Univ Bonn, Inst Mol Psychiat, D-5300 Bonn, Germany
[6] Grp Hosp Henri Mondor Albert Chenevier, Assistance Publ Hop Paris, Creteil, France
关键词
in vivo; remodeling; apoptosis; heart failure; signaling; fibrosis; ISCHEMIA-REPERFUSION INJURY; NECROSIS-FACTOR-ALPHA; INFARCT SIZE; TNF-ALPHA; MYOCARDIAL-INFARCTION; HEART-FAILURE; CB2; RECEPTOR; ENDOCANNABINOIDS; MICE; RATS;
D O I
10.1096/fj.09-129478
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Post-myocardial infarction (MI) heart failure is a major public health problem in Western countries and results from ischemia/reperfusion (IR)-induced cell death, remodeling, and contractile dysfunction. Ex vivo studies have demonstrated the cardioprotective anti-inflammatory effect of the cannabinoid type 2 (CB2) receptor agonists within hours after IR. Herein, we evaluated the in vivo effect of CB2 receptors on IR-induced cell death, fibrosis, and cardiac dysfunction and investigated the target role of cardiac myocytes and fibroblasts. The infarct size was increased 24 h after IR in CB2(-/-) vs. wild-type (WT) hearts and decreased when WT hearts were injected with the CB2 agonist JWH133 (3 mg/kg) at reperfusion. Compared with WT hearts, CB2(-/-) hearts showed widespread injury 3 d after IR, with enhanced apoptosis and remodeling affecting the remote myocardium. Finally, CB2(-/-) hearts exhibited exacerbated fibrosis, associated with left ventricular dysfunction 4 wk after IR, whereas their WT counterparts recovered normal function. Cardiac myocytes and fibroblasts isolated from CB2(-/-) hearts displayed a higher H2O2-induced death than WT cells, whereas 1 mu M JWH133 triggered survival effects. Furthermore, H2O2-induced myofibroblast activation was increased in CB2(-/-) fibroblasts but decreased in 1 mu M JWH133-treated WT fibroblasts, compared with that in WT cells. Therefore, CB2 receptor activation may protect against post-IR heart failure through direct inhibition of cardiac myocyte and fibroblast death and prevention of myofibroblast activation.-Defer, N., Wan, J., Souktani, R., Escoubet, B., Perier, M., Caramelle, P., Manin, S., Deveaux, V., Bourin, M.-C., Zimmer, A., Lotersztajn, S., Pecker, F., Pavoine, C. The cannabinoid receptor type 2 promotes cardiac myocyte and fibroblast survival and protects against ischemia/reperfusion-induced cardiomyopathy. FASEB J. 23, 2120-2130 (2009)
引用
收藏
页码:2120 / 2130
页数:11
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