2010
DOI: 10.2337/db10-0362
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Expression of Human Chemerin Induces Insulin Resistance in the Skeletal Muscle but Does Not Affect Weight, Lipid Levels, and Atherosclerosis in LDL Receptor Knockout Mice on High-Fat Diet

Abstract: OBJECTIVEChemerin is a recently discovered hepatoadipokine that regulates adipocyte differentiation as well as chemotaxis and activation of dendritic cells and macrophages. Chemerin was reported to modulate insulin sensitivity in adipocytes and skeletal muscle cells in vitro and to exacerbate glucose intolerance in several mouse models in vivo. In humans, chemerin was shown to be associated with multiple components of the metabolic syndrome including BMI, triglycerides, HDL cholesterol, and hypertension. This … Show more

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Cited by 93 publications
(75 citation statements)
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References 24 publications
(44 reference statements)
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“…It is possible that in obesity, elevated levels of chemerin predominantly induce insulin resistance in muscle and even if chemerin stimulates β-cell function and suppresses gluconeogenesis in the liver, the net glucose tolerance may be deteriorated. It has been reported that serum chemerin levels were associated with insulin resistance in mice [35] and humans [17], which supports this hypothesis.…”
Section: Discussionsupporting
confidence: 74%
“…It is possible that in obesity, elevated levels of chemerin predominantly induce insulin resistance in muscle and even if chemerin stimulates β-cell function and suppresses gluconeogenesis in the liver, the net glucose tolerance may be deteriorated. It has been reported that serum chemerin levels were associated with insulin resistance in mice [35] and humans [17], which supports this hypothesis.…”
Section: Discussionsupporting
confidence: 74%
“…Hart and Greaves 31) showed that chemerin rapidly stimulated the adhesion of macrophages to the extracellular matrix protein, fibronectin, and to the adhesion molecule, vascular cell adhesion molecule-1, suggesting that chemerin might promote the progression of atherosclerosis. Although Becker et al 32) showed that the Independent variables in multiple stepwise regression analysis: gender, age, body mass index, waist circumference, systolic blood pressure, diastolic blood pressure, fasting blood glucose, LDL-cholesterol, HDL-cholesterol, triglycerides, high sensitivity C-reactive protein, and chemerin baPWV, brachial ankle pulse wave velocity; SE, standard error; R expression of chemerin did not significantly alter the extent of atherosclerosis in LDL receptor knockout mice, they hypothesized that chemerin may affect early atherosclerotic plaque development and plaque morphology rather than the extent of the atherosclerotic lesion area. Furthermore, Kaur et al 33) demonstrated the novel presence of a G-protein coupled chemerin receptor (CMKLR1) in human endothelial cells and its significant up-regulation by pro-inflammatory cytokines (TNF-, IL-1 , and IL-6).…”
Section: Fig 1 Correlation Between Circulating Chemerin Levels and mentioning
confidence: 98%
“…Chemerin is an attractant for immune cells and pro-and antiinflammatory effects of chemerin have been described . More recently it has been shown that chemerin impairs insulin signaling in adipocytes and skeletal muscle cells (Becker et al, 2010;Kralisch et al, 2009;Sell et al, 2009). …”
Section: Introductionmentioning
confidence: 99%