Adrenergic signaling and oxidative stress: a role for sirtuins?

被引:68
作者
Corbi, Graziamaria [1 ]
Conti, Valeria [2 ]
Russomanno, Giusy [2 ,3 ]
Longobardi, Giancarlo [4 ]
Furgi, Giuseppe [4 ]
Filippelli, Amelia [2 ,3 ]
Ferrara, Nicola [4 ,5 ]
机构
[1] Univ Molise, Dept Med & Hlth Sci, I-86100 Campobasso, Italy
[2] Univ Salerno, Dept Med & Surg, I-84100 Salerno, Italy
[3] Univ Salerno, Doctoral Sch Translat & Clin Med, I-84100 Salerno, Italy
[4] Fdn S Maugeri, Ist Telese, Telese Terme, Italy
[5] Univ Naples Federico II, Dept Med Translat Sci, Naples, Italy
来源
FRONTIERS IN PHYSIOLOGY | 2013年 / 4卷
关键词
oxidative stress; sirtuins; GRK2; beta-adrenergic system; exercise training; heart failure; reactive oxygen species; RECEPTOR KINASE 2; ACTIVATED PROTEIN-KINASE; MANGANESE SUPEROXIDE-DISMUTASE; HUMAN ENDOTHELIAL-CELLS; FATTY-ACID OXIDATION; FACTOR-KAPPA-B; REACTIVE OXYGEN; INSULIN-RESISTANCE; HEART-FAILURE; CARDIAC-HYPERTROPHY;
D O I
10.3389/fphys.2013.00324
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The adrenergic system plays a central role in stress signaling and stress is often associated with increased production of ROS. However, ROS overproduction generates oxidative stress, that occurs in response to several stressors. beta-adrenergic signaling is markedly attenuated in conditions such as heart failure, with downregulation and desensitization of the receptors and their uncoupling from adenylyl cyclase. Transgenic activation of beta 2-adrenoceptor leads to elevation of NADPH oxidase activity, with greater ROS production and p38MAPK phosphorylation. Inhibition of NADPH oxidase or ROS significantly reduced the p38MAPK signaling cascade. Chronic beta 2-adrenoceptor activation is associated with greater cardiac dilatation and dysfunction, augmented pro-inflammatory and profibrotic signaling, while antioxidant treatment protected hearts against these abnormalities, indicating ROS production to be central to the detrimental signaling of beta 2-adrenoceptors. It has been demonstrated that sirtuins are involved in modulating the cellular stress response directly by deacetylation of some factors. Sirt1 increases cellular stress resistance, by an increased insulin sensitivity, a decreased circulating free fatty acids and insulin-like growth factor (IGF-1), an increased activity of AMPK, increased activity of PGC-1a, and increased mitochondrial number. Sirt1 acts by involving signaling molecules such P-I-3-kinase-Akt, MARK and p38-MAPK-beta. beta AR stimulation antagonizes the protective effect of the AKT pathway through inhibiting induction of Hif-1 alpha and Sirt1 genes, key elements in cell survival. More studies are needed to better clarify the involvement of sirtuins in the beta-adrenergic response and, overall, to better define the mechanisms by which tools such as exercise training are able to counteract the oxidative stress, by both activation of sirtuins and inhibition of GRK2 in many cardiovascular conditions and can be used to prevent or treat diseases such as heart failure.
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页数:14
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