2022
DOI: 10.1007/s12265-022-10310-4
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Irisin Regulates Cardiac Responses to Exercise in Health and Diseases: a Narrative Review

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Cited by 7 publications
(2 citation statements)
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“…One of most common molecular mechanisms by which irisin counteracts the activity of RAAS and SAS is its ability to booster the activity of AMP kinase, but not Akt and MAP kinase, thereby protecting cardiomyocytes from hypertrophy induced by angiotensin II or phenylephrine, and suppressing fibrosis, gluconeogenesis, lipolysis, oxidative stress and inflammation [ 45 ]. The next mechanism is irisin-induced protective autophagy, which not only attenuates cardiac hypertrophy [ 46 ], but also improves the tolerability of cardiac myocytes against apoptosis and necrosis due to hypoxia and ischemia [ 47 ]. Moreover, irisin is able to regulate the metabolism of skeletal muscles in an autocrine manner [ 48 ], thereby reducing resistance to insulin, which plays a central role in altered reparative tissue potency in T2DM as well as in HF [ 49 ].…”
Section: Discussionmentioning
confidence: 99%
“…One of most common molecular mechanisms by which irisin counteracts the activity of RAAS and SAS is its ability to booster the activity of AMP kinase, but not Akt and MAP kinase, thereby protecting cardiomyocytes from hypertrophy induced by angiotensin II or phenylephrine, and suppressing fibrosis, gluconeogenesis, lipolysis, oxidative stress and inflammation [ 45 ]. The next mechanism is irisin-induced protective autophagy, which not only attenuates cardiac hypertrophy [ 46 ], but also improves the tolerability of cardiac myocytes against apoptosis and necrosis due to hypoxia and ischemia [ 47 ]. Moreover, irisin is able to regulate the metabolism of skeletal muscles in an autocrine manner [ 48 ], thereby reducing resistance to insulin, which plays a central role in altered reparative tissue potency in T2DM as well as in HF [ 49 ].…”
Section: Discussionmentioning
confidence: 99%
“…By reducing ROS/p38 mitogen-activated protein kinase (MAPK)/ NF-κB signaling, irisin reduces endothelial injury and inflammation, and prevents foam cell development and monocyte adhesion caused by ox-LDL [33]. Exogenous irisin delivery decreases mitogenactivated protein kinase (MAPK) activation, the nuclear factor light chain enhancer of NF-κB translocation from the cytoplasm to the nucleus, and ROS levels in HUVECs treated with ox-LDL.…”
Section: Nf-κbmentioning
confidence: 99%