2017
DOI: 10.4062/biomolther.2016.128
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β-Adrenergic Receptor and Insulin Resistance in the Heart

Abstract: Insulin resistance is characterized by the reduced ability of insulin to stimulate tissue uptake and disposal of glucose including cardiac muscle. These conditions accelerate the progression of heart failure and increase cardiovascular morbidity and mortality in patients with cardiovascular diseases. It is noteworthy that some conditions of insulin resistance are characterized by up-regulation of the sympathetic nervous system, resulting in enhanced stimulation of β-adrenergic receptor (βAR). Over-stimulation … Show more

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Cited by 36 publications
(27 citation statements)
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References 138 publications
(199 reference statements)
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“…Chronic activation of the sympathetic nervous system and the associated increase in catecholamines such as epinephrine and norepinephrine are another hallmark of PS [ 127 ]. These catecholamines contribute to insulin resistance in the heart by activating β -adrenergic receptors ( β -AR) [ 128 ]. Activation of β -AR induces oxidative stress in cardiomyocytes, adipocytes, and endothelial cells, at least partly by β 2-AR-mediated upregulation of Nox [ 128 132 ].…”
Section: Pathways To Cellular Stresses In Insulin Target Cellsmentioning
confidence: 99%
See 1 more Smart Citation
“…Chronic activation of the sympathetic nervous system and the associated increase in catecholamines such as epinephrine and norepinephrine are another hallmark of PS [ 127 ]. These catecholamines contribute to insulin resistance in the heart by activating β -adrenergic receptors ( β -AR) [ 128 ]. Activation of β -AR induces oxidative stress in cardiomyocytes, adipocytes, and endothelial cells, at least partly by β 2-AR-mediated upregulation of Nox [ 128 132 ].…”
Section: Pathways To Cellular Stresses In Insulin Target Cellsmentioning
confidence: 99%
“…These catecholamines contribute to insulin resistance in the heart by activating β -adrenergic receptors ( β -AR) [ 128 ]. Activation of β -AR induces oxidative stress in cardiomyocytes, adipocytes, and endothelial cells, at least partly by β 2-AR-mediated upregulation of Nox [ 128 132 ]. The β 3-AR activates hormone-sensitive lipase in adipocytes and thus promotes accumulation of free fatty acids and the associated increase in ceramide synthesis and MAPK activation [ 133 ].…”
Section: Pathways To Cellular Stresses In Insulin Target Cellsmentioning
confidence: 99%
“…Insulin promotes glucose uptake in cardiomyocytes through activation of an InsR-mediated phosphatidylinositol 3-kinase (PI3K)-Akt pathway, which mobilizes glucose transporter 4 (GLUT4) vesicles to the cell surface for glucose uptake [1]. Interestingly, stimulation of βAR in heart also induces an additive effect on insulin-induced glucose uptake; and this effect is mediated by phosphorylation of Akt in threonine 308 through protein kinase A (PKA)/Ca 2+ -dependent pathway [2, 3]. On the cellular level, stimulation with either insulin or catecholamines antagonizes the ability of the other to activate glucose transport and to modulate cardiomyocyte survival [4, 5].…”
Section: Sympathetic Nervous Activity and Insulin Resistance In Heartmentioning
confidence: 99%
“…These effects are also associated with suppression of myocardial fatty acid oxidation, greater glucose consumption, increased SERCA2a and phospholamban mRNA expression [91, 92]. In contrary, long-term βAR stimulation inhibits insulin-induced phosphorylation of ERK1/2 and JNK [2], which are required for insulin to exert its protective effect against the hypoxia-induced activation of pro-apoptotic caspase-3 [2]. Together, these data suggests that the correlation between cardiac sympathetic function and insulin sensitivity contributes to IR and subsequently outcomes in failing ischemic human hearts, supporting the use of insulin and/or a combination of selective β 1 AR-blocker and β 2 AR agonist in treatment of acute I/R injury.…”
Section: Insulin and βAr Signaling In Ischemia And Reperfusionmentioning
confidence: 99%
“…And HTSeq v6.0 was used to count the number of fragments for each gene in each sample. Selection of the insulin signaling pathway [64,65]. The candidate genes under selection in duck domestication are shown in red.…”
Section: Rna-seq and Gene Expression Analysismentioning
confidence: 99%